ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Inorganic Chemistry  (6.914)
  • Analytical Chemistry and Spectroscopy  (6.520)
  • Ocean Drilling Program; ODP
  • 1995-1999  (4.028)
  • 1980-1984  (7.824)
  • 1940-1944  (1.631)
Sammlung
Schlagwörter
Verlag/Herausgeber
Erscheinungszeitraum
Jahr
  • 1
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Wallrabe-Adams, Hans-Joachim; Werner, Reinhard (1999): Date report: Chemical Composition of Middle Miocene to Early Pliocene ash from Sites 982 and 985. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-14, https://doi.org/10.2973/odp.proc.sr.162.021.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: The Cenozoic volcanic activity on Iceland has been recorded in North Atlantic sediments drilled during several Ocean Drilling Program (ODP)/Deep Sea Drilling Project legs (Legs 104, 151, 152, 162, and 163). Leg 162 (North Atlantic-Arctic Gateways II) recovered ash layers at Sites 982, 985, and 907 (Jansen, Raymo, Blum, et al., 1996, doi:10.2973/odp.proc.ir.162.1996). The revisited Site 907 was first drilled during Leg 151, and the ash from this site has been described in detail by Lacasse et al. (1996, doi:10.2973/odp.proc.sr.151.122.1996) and Werner et al. (1996, doi:10.2973/odp.proc.sr.151.123.1996). Site 982 is located within the Hatton-Rockall Basin on the Rockall Plateau, which is situated west of the British Isles. Site 985 is located northeast of Iceland at the foot of the eastern slope of the Iceland Plateau, adjacent to the Norwegian Basin. Here we report chemical analyses of Neogene tephra layers from Holes 982A, 983B, 982C, 985A, and 985B. The sedimentary sequence at Site 982 spans the lower Miocene-Holocene; Site 985 recovered sediments spanning the upper Oligocene-Holocene. Twenty-two distinct ash layers and ash-bearing sediments were sampled in Holes 982A-982C (Cores 162-982A-16H through 24H, 162-982B-14H through 56X, and 162-982C-15H through 27H), and 59 ash layers were sampled in Holes 985A and 985B (Cores 162-985A-11H through 59X, and 162-985B-11H through 14H). Almost 50% of the sampled ash is strongly altered (predominantly from Site 985). A cluster of altered thin layers in the lower Pliocene of Site 985 (top of Unit III) is remarkable.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Ortiz, Joseph D; O'Connell, Suzanne B; Mix, Alan C (1999): Data Report: Spectral reflectance observations from recovered sediments. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-6, https://doi.org/10.2973/odp.proc.sr.162.029.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Sediment spectral reflectance measurements were generated aboard the JOIDES Resolution during Ocean Drilling Program Leg 162 shipboard operations. The large size of the raw data set (over 1.3 gigabytes) and limited computer hard disk storage space precluded detailed analysis of the data at sea, although broad band averages were used as aids in developing splices and determining lithologic boundaries. This data report describes the methods used to collect these data and their shipboard and postcruise processing. These initial results provide the basis for further postcruise research.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Zuleger, Evelyn; Alt, Jeffrey C; Erzinger, Jörg (1995): Primary and secondary variations in major and trace element geochemistry of the lower sheeted dike complex: Hole 504B, Leg 140. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 65-80, https://doi.org/10.2973/odp.proc.sr.137140.022.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Rocks of the lower sheeted dike complex of Hole 504B sampled during Leg 140 were analyzed for major and trace element compositions to investigate the effects of igneous processes and hydrothermal alteration on the compositions of the rocks. The rocks are relatively uniform in composition and similar to the shallower dikes. They are moderately evolved mid-ocean-ridge basalts (MORB) with relatively high MgO (7.9-10 wt%) and Mg# (0.60-0.70), and have unusually low incompatible element contents (TiO2 = 0.42-1.1 wt%, Zr = 23-62 ppm). Discrete compositional intervals in the hole reflect varying degrees of differentiation, and olivine and plagioclase accumulation in the rocks, and may be related to injection of packets of dikes having similar compositions. Systematic depletions of total REE, Zr, Y, TiO2, and P2O5 in centimeter-size patches are most likely attributed to exclusion of highly differentiated, late-stage interstitial liquids from small portions of the rocks. The rocks exhibit increased H2O+ reflecting hydrothermal alteration. Replacement of primary plagioclase by albite and oligoclase led to local gains of Na2O, losses of CaO, and slightly positive Eu anomalies. Some mobility of P2O5 led to minor increases and decreases in P2O5 contents, and some local mobility of Ti may have occurred during alteration of titanomagnetite to titanite. Higher temperatures of alteration in the lower sheeted dikes led to breakdown of pyroxene and sulfide minerals and losses of Zn, Cu, and S to hydrothermal fluids. Later addition of anhydrite to the rocks in microfractures and replacing plagioclase caused local increases in sulfur contents. The lower sheeted dikes are a major source of metals to hydrothermal fluids for the formation of metal sulfide deposits on and within the seafloor.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Sparks, Joel W (1995): Geochemistry of the lower sheeted dike complex, Hole 504B, Leg 140. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 81-97, https://doi.org/10.2973/odp.proc.sr.137140.021.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Sixty-three samples representing 379 m of sheeted dikes from Deep Sea Drilling Project/Ocean Drilling Program Site 504B have been analyzed for major and selected trace elements by X-ray fluorescence. The samples range from microcrystalline aphyric basalts to moderately phyric (2%-10% phenocrysts) diabase that are typically multiply saturated with plagioclase, olivine, and clinopyroxene, in order of relative abundance. All analyzed samples are classified as Group D compositions with moderate to slightly elevated compatible elements (MgÆ-value = 0.65% ± 0.03%; Al2O3 = 15.5% ± 0.8%; CaO = 13.0% ± 0.3%; Ni = 114 ± 29 ppm), and unusually depleted levels of moderate to highly incompatible elements (Nb 〈 1 ppm; Zr = 44 ± 7 ppm; Rb 〈 0.5 ppm; Ba ~ 1 ppm; P2O5 = 0.07% ± 0.02%). These compositions are consistent with a multistage melting of a normal ocean ridge basaltic mantle source followed by extensive fractionation of olivine, plagioclase, and clinopyroxene. Leg 140 aphyric to sparsely phyric (0%-2% phenocrysts) basalts and diabases are compositionally indistinguishable from similarly phyric samples at higher levels in the hole. An examination of the entire crustal section, from the overlying volcanics through the sheeted dikes observed in Leg 140, reveals no significant trends indicating the enrichment or depletion of Costa Rica Rift Zone source magmas over time. Similarly, significant trends toward increased or decreased differentiation cannot be identified, although compositional patterns reflecting variable amounts of phenocryst addition are apparent at various depths. Below ? 1700 mbsf to the bottom of the Leg 140 section, there is a broadly systematic pattern of Zn depletion with depth, the result of high-temperature hydrothermal leaching. This zone of depletion is thought to be a significant source of Zn for the hydrothermal fluids depositing metal sulfides at ridge-crest hydrothermal vents and the sulfide-mineralization zone, located in the transition between pillow lavas and sheeted dikes. Localized zones of intense alteration (60%-95% recrystallization) are present on a centimeter to meter scale in many lithologic units. Within these zones, normally immobile elements Ti, Zr, Y, and rare-earth elements are strongly depleted compared with "fresher" samples centimeters away. The extent of compositional variability of these elements tends to obscure primary igneous trends if the highly altered samples are not identified or removed. At levels up to 40% (or possibly 60%) recrystallization, Ti, Zr, and Y retain their primary signatures. Although the mechanisms are unclear, it is possible that these intense alteration zones are a source of Y and rare-earth elements for the typically rare-earth-element-enriched hydrothermal vent fluids of mid-ocean ridges.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Johnson, Kevin T M; Fisk, Martin R; Naslund, Howard Richard (1995): Geochemical characteristics of refractory silicate melt inclusions from Leg 140 diabases. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 131-139, https://doi.org/10.2973/odp.proc.sr.137140.004.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Geochemical data from plagioclase-hosted silicate melt inclusions from Leg 140, Hole 504B diabase dikes are reported. Hand-picked plagioclase grains were heated to 1260°-1280°C to remelt the glass inclusions and to infer trapping temperatures. The samples were then polished to expose the inclusions, which were analyzed by electron and ion microprobes. Inclusion compositions are mainly in equilibrium with the host plagioclase and are more depleted in incompatible elements than the host rock. Simple crystal-liquid equilibrium calculations show that the melt inclusions could have been in equilibrium with depleted abyssal peridotite diopsides, whereas whole-rock basalt compositions generally could not have been. The melt inclusions are significantly more depleted than normal (N-type) mid-ocean-ridge basalt (MORB) and are consistent with being produced by 8%-16% incremental or open-system melting with 2% residual porosity in the peridotite source. These magmas were formed during pressure-release melting of the mantle over a range of depths between 30 and 15 km.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Alt, Jeffrey C; Zuleger, Evelyn; Erzinger, Jörg (1995): Mineralogy and stable isotopic compositions of the hydrothermally altered lower sheeted dike complex, Hole 504B, Leg 140. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 155-166, https://doi.org/10.2973/odp.proc.sr.137140.013.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Drilling during Legs 137 and 140 of the Ocean Drilling Program deepened Hole 504B, the only hole to penetrate through the volcanic section and into the underlying hydrothermally altered sheeted dike complex, by 438.1 m to a total depth of 2000.4 meters below seafloor. This paper presents the secondary mineralogy, bulk-rock sulfur contents, and stable isotopic (O, S) compositions, plus oxygen isotopic compositions of secondary minerals from the lower sheeted dike complex drilled during Legs 137 and 140. Various evidence indicates higher temperatures of hydrothermal alteration in the lower dikes than in the upper dikes, including: the local presence of secondary clinopyroxene in the lower dikes; secondary anorthite and hornblende in the lower dikes vs. mainly actinolite and albite-oligoclase in the upper dikes; generally increasing Al and Ti contents of amphibole downward in the dike section; and greater 18O depletions of the lower dikes (d18O = 3.6-5.0 per mil) compared with the upper dikes. Early high-temperature alteration stages (T = 350°-500°C) resulted in 18O depletions and losses of metals (Cu, Zn) and sulfur from the rocks. Local incorporation of reduced seawater sulfate led to elevated d34S values of sulfide in the rocks (up to 2.5 per mil). Quartz + epidote formed in crosscutting veins at temperatures of 310°-320°C from more evolved fluids (d18O = 1 per mil). Late-stage lower-temperature (~250°C) reactions producing albite, prehnite, and zeolites in the rocks caused slight 18O enrichments, but these were insufficient to offset the 18O depletions caused by earlier higher-temperature reactions. Addition of anhydrite to the rocks during seawater recharge led to increased S contents of rocks that had previously lost S during axial hydrothermal alteration, and to further increases in d34S values of total S in the rocks (up to 12 per mil). Despite the evidence for seawater recharge to near the base of the sheeted dike complex, the paucity of late zeolites in the lower dikes suggests that late-stage, off-axis circulation was mainly restricted to the volcanics and shallowest dikes, or to localized high-permeability zones (faults) at depth.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Kelley, Deborah S; Vanko, David A; Gu, Chifeng (1995): Fluid evolution in oceanic crustal layer 2: fluid inclusion evidence from the sheeted dike complex, Hole 504B, Costa Rica Rift. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 191-198, https://doi.org/10.2973/odp.proc.sr.137140.015.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Fluid inclusions in variably altered diabase recovered from Ocean Drilling Program Legs 137 and 140 at Hole 504B, Costa Rica Rift, exhibit fluid salinities up to 3.7 times that of seawater values (11.7 wt% NaCl equivalent) and exhibit uncorrected homogenization temperatures of 125°C to 202°C. The liquid-dominated inclusions commonly are entrapped in zones of secondary plagioclase and may be primary in origin. Fluid salinities are similar to compositions of fluids venting on the seafloor (0.4-7.0 wt% NaCl) and overlap with those measured in metabasalt samples recovered from near the Kane Fracture Zone on the Mid-Atlantic Ridge and from the Troodos ophiolite, Cyprus. The salinity variations may reflect hydration reactions involving formation of secondary mineral assemblages under rock-dominated conditions, which modify the ionic strength of hydrothermal fluids by consuming or liberating water and chloride ion. Rare CO2-CH4-bearing inclusions, subjacent to zones where talc after olivine becomes an important secondary mineral phase (1700 mbsf), may have formed due to local interaction of seawater and olivine at low water to rock ratios. Corrected average fluid inclusion homogenization temperatures exhibit a gradient from 159°C at a depth of 1370 mbsf to 183°C at a depth of 1992 mbsf and are in apparent equilibrium with the present conductive downhole temperatures. These data indicate that fluid inclusions may be used to estimate downhole temperatures if logging data are unavailable. The compositional and thermal evolution of the diabase-hosted fluids may reflect late-stage, off-axis circulation and conductive heating of compositionally modified seawater in the sheeted dike complex at Hole 504B.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Laverne, Christine; Vanko, David A; Tartarotti, Paola; Alt, Jeffrey C (1995): Chemistry and geothermometry of secondary minerals from the deep sheeted dike complex, Hole 504B. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 167-189, https://doi.org/10.2973/odp.proc.sr.137140.014.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Dolerites sampled from the lower sheeted dikes from Hole 504B during Ocean Drilling Program Legs 137 and 140, between 1562.4 and 2000.4 mbsf, were examined to document the mineralogy, petrography, and mineral parageneses associated with secondary alteration, to constrain the thermal history and composition of hydrothermal fluids. The main methods used were mineral chemical analyses by electron microprobe, X-ray diffraction, and cathodoluminescence microscopy. Temperatures of alteration were estimated on the basis of single and/or coexisting mineral chemistry. Permeability is important in controlling the type and extent of alteration in the studied dike section. At the meter-scale, intervals of weakly altered dolerites containing fresh olivine are interpreted as having experienced restricted exposure to hydrothermal fluids. At the centimeter- or millimeter-scale, alteration patches and extensively altered halos adjacent to veins reflect the permeability related to intergranular primary porosity and cracks. Most of the sheeted dike alteration in this case resulted from non-focused, pervasive fluid-rock interaction. This study confirms and extends the previous model for hydrothermal alteration at Hole 504B: hydrothermal alteration at the ridge axis followed by seawater recharge and off-axis alteration. The major new discoveries, all related to higher temperatures of alteration, are: (1) the presence of hydrothermal plagioclase (An80-95), (2) the presence of deuteric and/or hydrothermal diopside, and (3) the general increasing proportion of amphiboles, and particularly magnesio-hornblende with depth. We propose that the dolerites at Hole 504B were altered in five stages. Stage 1 occurred at high temperatures (less than 500° to 700°C) and involved late-magmatic formation of Na- and Ti-rich diopside, the hydrothermal formation of Na, Ti-poor diopside and the hydrothermal formation of an assemblage of An-rich plagioclase + hornblende. Stage 2 occurred at lower temperatures (250°-320°C) and is characterized by the appearance of actinolite, chlorite, chlorite-smectite, and/or talc (in low permeability zones) and albite. During Stage 3, quartz and epidote precipitated from evolved hydrothermal fluids at temperatures between 310° and 320°C. Anhydrite appeared during Stage 4 and likely precipitated directly from heated seawater. Stage 5 occurred off-axis at low temperatures (250°C) with laumontite and prehnite from evolved fluids.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 9 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Iturrino, Gerardo J; Christensen, Nikolas I; Becker, Keir; Boldreel, Lars O; Harvey, Peter K H; Pezard, Philippe A (1995): Physical properties and elastic constants of upper crustal rocks from core-log measurements in Hole 504B. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 273-291, https://doi.org/10.2973/odp.proc.sr.137140.031.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Seismic velocities have been measured at confining pressures of 100 MPa and 600 MPa for sheeted dike samples recovered during Ocean Drilling Program Legs 137 and 140. The compressional- and shear-wave velocities show an increase with depth at Hole 504B, which is in sharp contrast to the atmospheric pressure velocity measurements performed as part of the shipboard analyses. Rocks exposed to different types of alteration and fracture patterns show distinct changes in their physical properties. The seismic reflectors observed on the vertical seismic profile (VSP) experiment performed during Leg 111 may have been caused by low velocity zones resulting from alteration. The amount of fracturing and hydrothermal alteration in several zones also may have contributed to the acoustic impedance contrast necessary to produce the E5 reflector. Poisson's ratios calculated from laboratory velocity measurements show several low values at depths ranging from 1600 mbsf to 2000 mbsf, which tends to follow similar trends obtained from previous oceanic refraction experiments. A comparison of physical properties between samples recovered from Hole 504B and ophiolite studies in the Bay of Islands and Oman shows a good correlation with the Bay of Islands but significant differences from the measurements performed in the Oman complex.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Stokking, Laura B; Heise, Elizabeth A; Pariso, Janet E; Allerton, Simon A (1995): Data report: Magnetic mineralogy, major- and trace-element geochemistry, and rock magnetic properties of Hole 504B upper crustal rocks. In: Erzinger, J; Becker, K; Dick, HJB; Stokking, LB (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 137, 327-337, https://doi.org/10.2973/odp.proc.sr.137140.029.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Leg 140 of the Ocean Drilling Program deepened Hole 504B to a total depth of 2000.4 m below seafloor (mbsf), making it the deepest hole drilled into ocean crust. Site 504, south of the Costa Rica Rift, is considered the most important in-situ reference section for the structure of shallow ocean crust. We present the results of studies of magnetic mineralogy and magnetic properties of Hole 504B upper crustal rocks recovered during Legs 137 and 140. Results from this sample set are consistent with those discussed in Pariso et al. (this volume) from Legs 111, 137, and 140. Coercivity (Hc) ranges from 5.3 to 27.7 mT (mean 12 mT), coercivity of remanence (HCR) ranges from 13.3 to 50.6 mT (mean 26 mT), and the ratio HCR/HC ranges from 1.6 to 3.19 (mean 2.13). Saturation magnetization (JS) ranges from 0.03 to 5.94 * 10**-6 Am**2, (mean 2.52 * 10**-6 Am**2), saturation remanence (JR) ranges from 0.01 to 0.58 * 10**-6 Am2 (mean 0.37 * 10**-6 Am**2), and the ratio JR/JS ranges from 0.08 to 0.29 (mean 0.16), consistent with pseudo-single-domain behavior. Natural remanent magnetization (NRM) intensity ranges from 0.029 to 7.18 A/m (mean 2.95 A/m), whereas RM10 intensity varies only from 0.006 to 4.8 A/m and has a mean of only 1.02 A/m. Anhysteretic remanent magnetization (ARM) intensity ranges from 0.04 to 6.0 A/m, with a mean of 2.46 A/m, and isothermal remanent magnetization (IRM) intensity ranges from 0.5 to 1683 A/m, with a mean of 430.7 A/m. Volume susceptibility ranges from 0.0003 to 0.043 SI (mean 0.011 SI). In all samples examined, high-temperature oxidation of primary titanomagnetite has produced lamellae or pods of magnetite and ilmenite. Hydrothermal alteration has further altered the minerals in some samples to a mixture of magnetite, ilmenite, titanite, and a high-titanium mineral (either rutile or anatase). Electron microprobe analyses show that magnetite lamellae are enriched in the trivalent oxides Cr2O3, Al2O3, and V2O5, whereas divalent oxides (MnO and MgO) are concentrated in ilmenite lamellae.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 11
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Farrell, John W; Raffi, Isabella; Janecek, Thomas R; Murray, David W; Levitan, Mikhail A; Dadey, Kathleen A; Emeis, Kay-Christian; Lyle, Mitchell W; Flores, José-Abel; Hovan, Steven A (1995): Late Neogene sedimentation patterns in the eastern equatorial Pacific Ocean. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 717-756, https://doi.org/10.2973/odp.proc.sr.138.143.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: The post-middle Miocene evolution of sedimentary patterns in the eastern equatorial Pacific Ocean has been deduced from a compilation and synthesis of CaCO3, opal, and nannofossil assemblage data from 11 sites drilled during Leg 138. Improvements in stratigraphic correlation and time scale development enabled the construction of lithostratigraphic and chronostratigraphic frameworks of exceptional quality. These frameworks, and the high sedimentation rates (often exceeding 4 cm/k.y.) provided a detailed and synoptic paleoceanographic view of a large and highly productive region. The three highlights that emerge are: (1) a middle late Miocene "carbonate crash" (Lyle et al., this volume); (2) a late Miocene-early Pliocene "biogenic bloom"; and (3) an early Pliocene "opal shift". During the carbonate crash, an interval of dissolution extending from -11.2 to 7.5 Ma, CaCO3 accumulation rates declined to near zero over much of the eastern equatorial Pacific, whereas opal accumulation rates remained substantially unchanged. The crash nadir, near 9.5 Ma, was marked by a brief shoaling of the regional carbonate compensation depth by more than 1400 m. The carbonate crash has been correlated over the entire tropical Pacific Ocean, and has been attributed to tectonically-induced changes in abyssal flow through the Panamanian seaway. The biogenic bloom extended from 6.7 to 4.5 Ma, and was characterized by an overall increase in biogenic accumulation and by a steepening of the latitudinal accumulation gradient toward the equator. The bloom has been observed over a large portion of the global ocean and has been linked to increased productivity. The final highlight, is a distinct and permanent shift in the locus of maximum opal mass accumulation rate at 4.4 Ma. This shift was temporally, and perhaps causally, linked to the final closure of the Panamanian seaway. Before 4.4 Ma, opal accumulation was greatest in the eastern equatorial Pacific Basin (near 0°N, 107°W). Since then, the highest opal fluxes in the equatorial Pacific have occurred in the Galapagos region (near 3°S, 92°W).
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 12
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Oyun, S; Elderfield, Henry; Klinkhammer, Gary P (1995): Strontium isotopes in pore waters of east equatorial Pacific sediments: Indicators of seawater advection through oceanic crust and sediments. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 813-819, https://doi.org/10.2973/odp.proc.sr.138.156.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Pore-water samples from the equatorial sedimentary bulge area show reversals in depth profiles of 87Sr/86Sr ratios at the sediment/basement interface. Results of this work support inferences made from previous pore-water data (from DSDP drilling in the area) that large-scale horizontal advection of seawater has occurred through the basement underlying the thick sedimentary sequence in this region. The area of apparent advection includes the eastern part of the equatorial high-productivity zone and part of the Guatemala Basin. We attempted to find links between the observed near-basement reversals in pore-water chemistry and sedimentary thickness, age, and topography of the area. Most of the sites that show horizontal advection have disturbed basement topography or outcrops within 10 to 20 km, suggesting that the cooling effects of outcrops may extend for at least 20 km horizontally. Heat-flow data from the area were compared to determine whether sites showing near-bottom chemistry reversals were consistent with areas of low conductive heat flow. This was generally true for the area of the sedimentary bulge and Guatemala Basin. Not enough pore-water data from the Nazca Plate were available to establish any reliable systematics. Because the high-productivity area is well-sealed from hydrothermal circulation, the missing heat must be lost by horizontal advective heat transport. From profiles of strontium isotopes and other elements that show departure from seawater values with increasing depth in the sediments, but return to seawater values near the basement, it appears that water flows relatively freely through much of the oceanic crust, even when sealed by considerable sedimentary cover.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 13
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Lyle, Mitchell W; Dadey, Kathleen A; Farrell, John W (1995): The late Miocene (11–8 Ma) eastern Pacific carbonate crash: evidence for reorganization of deep-water circulation by the closure of the Panama gateway. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 821-838, https://doi.org/10.2973/odp.proc.sr.138.157.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: In the eastern and central Pacific Ocean the most profound change in Neogene calcium carbonate deposition occurred at the late/middle Miocene boundary (about 10 Ma), when carbonate mass accumulation rates (MARs) abruptly dropped. East of the East Pacific Rise (EPR), carbonate deposition essentially ceased. The carbonate compensation depth (CCD) in the Guatemala Basin, for example, rose by 800 m in less than 0.5 Ma. Even the rise crests suffered carbonate losses - Site 846, at the time less than 300 meters deeper than the EPR axis, experienced intervals between 10 and 9 Ma where no carbonate at all was buried. By about 8 Ma carbonate deposition resumed and was concentrated along an equatorial band, suggestive of high surface water carbonate production. East of the EPR, however, CCDs remained shallow since 10 Ma. This event which we have termed the late Miocene carbonate crash marks a fundamental paleoceanographic change that occurred in the eastern Pacific Ocean. Here, we document the changing pattern of carbonate deposition from 13 Ma to 5 Ma by using maps of carbonate MAR reconstructed from ODP Leg 138 and DSDP data. Comparisons to modern oceanographic conditions demonstrate that the late Miocene carbonate crash could not have been caused by an abrupt increase in productivity at 10 Ma or by loss of Corg from continental shelves. Instead it was probably caused by a relatively small reduction in deep-water exchange between the Atlantic and Pacific Oceans through the Panama Gateway prior to the emergence of the isthmus. A small restriction of deep-water exchange through this gateway is sufficient to radically change carbonate MARs in the eastern Pacific.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 14
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Baldauf, Jack G; Iwai, Masao (1995): Neogene diatom biostratigraphy for the eastern Equatorial Pacific Ocean, Leg 138. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 105-128, https://doi.org/10.2973/odp.proc.sr.138.107.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Ocean Drilling Program (ODP) Leg 138 recovered more than 5500 m of Quaternary to middle Miocene (~17 Ma) sediments from 11 sites in the eastern equatorial Pacific Ocean. These sediments represent the most complete stratigraphic sequence recovered since the start of scientific ocean drilling by the Deep Sea Drilling Project (DSDP) and ODP. The diatoms observed generally are common to abundant and well-preserved throughout the samples examined. The assemblages are characterized by species typical of low-latitudes and regions of high surface-water productivity and are dominated by Thalassiothrix longissima, Thalassionema nitzschioides, Azpeitia nodulifer, and numerous species of Thalassiosira and Nitzschia. Fifty-six biostratigraphic events were identified at Sites 844 through 852, allowing us, in part, to use the diatom zonation of Barron (1985a). This zonation was modified by replacing the Rhizosolenia preabergonii Zone and the upper portion of the Nitzschia jouseae Zone, as used by Barron (1985a), with the Nitzschia marina and Nitzschia jouseae zones, as used by Baldauf (1984, 1987). Twenty-nine biostratigraphic events have been correlated to the Leg 138 paleomagnetic stratigraphy of Schneider (this volume). Nineteen of these events are well constrained to permit recalibration. Diatoms were rare or absent in samples examined from Sites 853 and 854. As such, these sites are not included in the following discussion.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 15
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Schneider, David A (1995): Paleomagnetism of some Leg 138 sediments: detailing Miocene magnetostratigraphy. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 59-72, https://doi.org/10.2973/odp.proc.sr.138.105.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: The aims of this study are twofold. First, the study tries to provide the most reliable chronology possible for two critical sections by correlating the magnetic polarity stratigraphy measured in these sediments with a newly revised geomagnetic polarity time scale. Second, this study attempts to examine in detail the nature of seven short events not included in the shipboard standard time scale, but for which abundant magnetostratigraphic evidence was obtained during the Leg. Data presented here force some modifications of the shipboard interpretations of the magnetostratigraphy of Sites 845 and 844 on the basis of new data generated using discrete samples and from a greater appreciation of the magnetostratigraphic signature of Miocene-age short events. Those short events can be classified into two groups: those that probably reflect short, full-polarity intervals and those that more likely represent an interval of diminished geomagnetic intensity. Three of the seven events documented here correspond well with three subtle features, as seen in marine magnetic profiles, that have been newly included in the geomagnetic polarity time scale as short, full-polarity chrons. One of the seven events corresponds to a poorly defined feature of the marine magnetic record that has also been newly included in the geomagnetic polarity time scale, but which was considered of enigmatic origin. The three remaining events investigated here, although they have not been identified with features in the seafloor magnetic record, are suggested to be events of a similar nature, most likely times of anomalously low geomagnetic intensity. In addition to the Miocene magnetostratigraphic results given, several sets of averaged paleomagnetic inclinations are presented. Although these results clearly show the effects of a residual coring overprint, they demonstrate that paleomagnetic estimates of paleolatitudes can be made which are in good general agreement with ancient site positions calculated using hot spot-based plate reconstructions.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 16
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Farrell, John W; Murray, David W; McKenna, V S; Ravelo, Ana Christina (1995): Upper ocean temperature and nutrient contrasts inferred from Pleistocene planktonic foraminifer d18O and d13C in the eastern Equatorial Pacific. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 289-319, https://doi.org/10.2973/odp.proc.sr.138.115.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: We present Pleistocene oxygen and carbon isotope records from two planktonic foraminifer species (Globigerinoides sacculifer and Neogloboquadrina dutertrei) from Ocean Drilling Program Site 847 (0°16'N, 95°19'W; 3334 m water depth). An average sample resolution of 4500 yr was obtained by sampling at an interval of 15 cm through a continuous 35-m section from 0 to 1.15 Ma. Our d18O-based chronology is similar to that derived independently by astronomically tuning the gamma-ray attenuation porosity evaluator (GRAPE) record (Shackleton et al., 1995), though offsets as large as ± 30 k.y. occur on occasion. The surface waters at eastern equatorial Pacific Site 847, 380 km west of the Galapagos, are characterized by strong and constant upwelling, elevated nutrient concentrations, and high productivity. The isotopic composition of G. sacculifer (300-355 µm) reflects conditions in the thin-surface mixed layer, and the composition of N. dutertrei (355-425 µm) monitors the subsurface waters of the permanent shallow (10-40 m) thermocline. The Pleistocene d18O difference (N. dutertrei minus G. sacculifer, Dd18Od-s) averages 0.9 per mil and ranges from 0 per mil to 1.7 per mil. Neglecting species effects and shell size, the average Pleistocene d13C difference (G. sacculifer minus N. dutertrei, Dd13Cs-d) is 0.0 per mil and ranges from -0.5 per mil to 0.5 per mil. The Dd18Od-s and Dd13Cs-d records are used to infer vertical contrasts in upper ocean water temperature and nutrient concentration, though d13C may also be influenced by other factors, such as CO2 gas exchange. Variations in the isotopic differences are often synchronous with glacial/interglacial climate change. Glacial periods are characterized by smaller vertical contrasts in both temperature and nutrient concentration, and by notably greater accumulation rates of N. dutertrei and CaCO3. We attribute these responses to greater upwelling at the equatorial divergence. Superimposed on the glacial/interglacial Dd18Od-s pattern is a long-term trend possibly associated with the advection of Peru Current waters. The temporal fluctuations in the isotopic contrasts are strikingly similar to those observed at Site 851 (Ravelo and Shackleton, this volume), suggesting that the inferred changes in thermal and chemical profiles occurred over a broad region in the equatorial Pacific.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 17
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Ravelo, Ana Christina; Shackleton, Nicholas J (1995): Evidence for surface-water circulation changes at Site 851 in the eastern Tropical Pacific Ocean. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 503-514, https://doi.org/10.2973/odp.proc.sr.138.126.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: This study investigates changes in the upper water column hydrography at Site 851 of the eastern tropical Pacific Ocean since the late Pliocene, using the oxygen and carbon isotopic composition of three species of planktonic foraminifers, each calcifying at different depths in the photic zone. The upper ocean seasonal hydrography in this region responds to the seasonally changing trade winds and thus is expected to respond to past changes in trade winds. One major change occurs at about 1.5 Ma, when the thermocline adjusts from a deep position to a shallower position. The thermocline remains in a relatively shallow position throughout the record up to recent time, with slight variations occurring synchronously with glacial/interglacial stages. In glacials, SSTs are probably a few degrees cooler and the thermocline is slightly deeper. From our knowledge of seasonal and interannual adjustments of the thermocline in this location, a deeper thermocline might be interpreted as either a decrease in the strength of the Equatorial Undercurrent (EUC) that results from lower mean wind strength or an increase in the Equatorial Countercurrent (ECC), which results from an increase in the strength of the southeasterly trade winds. A major shift from higher to lower carbon isotope values occurred at about 1.9 Ma, marking a transition to reduced planktonic-benthic d13C differences after 1.9 Ma. The carbon isotopic data indicate that changes in the carbon isotopic composition of intermediate upwelling water occurs at higher frequencies than the glacial/interglacial changes in ice volume.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 18
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Pisias, Nicklas G; Moore, Theodore C (1995): Radiolarian response to oceanographic changes in the eastern Equatorial Pacific at 2.3 and 4.8 Ma: Relationship between changing carbonate deposition and surface oceanography. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 461-478, https://doi.org/10.2973/odp.proc.sr.138.124.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Two short time intervals centered at 2.3 and 4.7 Ma were studied to investigate short-term variations in surface-ocean processes as indicated by changes in the radiolarian microfossil population. These time intervals represent two different settings of late Neogene climate. The older interval represents a time when tropical circulation between the Pacific and Atlantic oceans was not blocked by the Isthmus of Panama, whereas the younger interval represents a time when Northern Hemisphere glaciation was present but did not display the dominance of the 100,000-yr cycle that characterizes the late Pleistocene. The younger time slice at 2.3 Ma was sampled at all Leg 138 sites except Site 844, where significant reworking was evident. All sites except 844, 853, and 854 were sampled for the older time slice. Samples were taken at 10- to 20-cm intervals at each site and spanned a GRAPE density maximum and minimum. Thus, it was possible to investigate whether the changes in carbonate content (as indicated by GRAPE density) were associated with changes in surface-ocean conditions (indicated by radiolarian assemblage variations). For both time slices, the radiolarian data indicate that intervals of decreased carbonate content are periods of cooler water conditions and possibly enhanced biogenic production. Times of increased carbonate content are associated with inferred warmer oceanographic conditions, as indicated by the dominance of tropical assemblages at 2.3 Ma and tropical and western Pacific assemblages during the time slice centered at 4.8 Ma. However, the spatial patterns of change during each time slice show a distinct difference in the mapped patterns of radiolarian assemblage dominance. The older time slice, representing a period before the closing of the Isthmus of Panama, shows more zonal patterns presumably associated with a more zonal character of equatorial circulation. After the closing of the isthmus, the shifts in faunal patterns between times of high and low carbonates are characterized by shifts in the dominance of the tropical and transitional assemblages, respectively, throughout the region.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 19
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Moore, Theodore C (1995): Radiolarian stratigraphy, Leg 138. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 191-232, https://doi.org/10.2973/odp.proc.sr.138.111.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: A group of 46 radiolarian species was used in this study of Leg 138 sites. The recovery of the sections was complete in the intervals that were cored using the APC system and nearly complete in the deeper sections. The northeastern sites (844 and 845) were sampled down through the middle Miocene into the uppermost part of the lower Miocene (middle part of the Calocycletta costata Zone). In the southeastern sites and those of the eastern transect (846 through 854) sediments were of late Miocene age (Diartus petterssoni Zone) and younger. Preservation of the radiolarian fauna was good to moderately good in most of the sites. Only in Sites 853 and 854 was the section older than late Pliocene barren of radiolarians. Reworked older radiolarians were found in the upper Miocene and Pliocene parts of the sections in most sites. Reworked upper Miocene radiolarians were even found in the upper Pliocene of Sites 853 and 854 where the upper Miocene part of the sections were barren of radiolarians. The development of an orbitally tuned time scale for the last 10 m.y. allowed the differentiation between radiolarian datums that appear to be synchronous (within 150,000 yr) in the eastern equatorial Pacific Ocean and those which appear to be diachronous. Of the 39 datums examined in this time interval, only 10 met this working definition of synchrony within the study area.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 34 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 20
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Filippelli, Gabriel M; Delaney, Margaret Lois (1995): Phosphorus geochemistry and accumulation rates in the eastern equatorial Pacific Ocean: results from Leg 138. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 757-767, https://doi.org/10.2973/odp.proc.sr.138.144.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: We determined phosphorus (P) concentrations in Leg 138 sediment samples from Sites 844, 846, and 851, using a sequential extraction technique to identify the P associated with five sedimentary components. Total concentrations of P (sum of the five components) ranged from 4 to 35 µmol P/g sediment, with mean values relatively similar between the three sites (11, 14, and 12 for Sites 844,846, and 851, respectively). Authigenic/biogenic P was the most important component in terms of percentage of total P (about 75%), with iron-bound P (13%), adsorbed P (2%-9%), and organic P (4%) of secondary importance; detrital P was a minor P sink (1%) in these sediments. Profiles of adsorbed P and iron-bound P show decreasing concentrations with age, indicating that these components have been affected by diagenesis and reorganization of P. A peak in iron-bound P may reflect higher fluxes of hydrothermally derived Fe to eastern equatorial Pacific Ocean sediments from 11 to 8 Ma. Lower detrital P values for western Site 851 reflect a greater distance of this site from a terrigenous source area, compared to that of Sites 844 and 846. Phosphorus mass accumulation rates (P-MARs; units of µmol P/cm**2/k.y.) were calculated using total P concentrations (not including the minor and oceanically unreactive detrital P component) and sedimentation rates and dry-bulk densities averaged over time intervals of 0.5 m.y. P-MARs generally decrease from 17 Ma to the present. Eastern transect Sites 844 and 846 display a decrease in P-MARs from about 30 to 10 in the interval from 17 to 8 Ma, while western transect Site 851 is highly variable during this interval. P-MARs increase to about 45 and stay relatively high from 8 to 6 Ma, then decrease toward the present to some of the lowest values of the record (about 10). The general trend of high P-MARs at about 6 Ma and decreasing values toward the present is correlated with other geochemical and sedimentary trends through this interval and may reflect (1) a change in net sediment and P burial, (2) a reorganization of fluxes with no change of net burial, or (3) a combination of the two.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 21
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Vincent, Edith; Toumarkine, M (1995): Data Report: Miocene planktonic foraminifers from the eastern equatorial Pacific. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 895-907, https://doi.org/10.2973/odp.proc.sr.138.159.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Neogene calcareous sediments were recovered at 11 sites along two north-south transects in the eastern equatorial Pacific Ocean during Ocean Drilling Program (ODP) Leg 138. An overview of planktonic foraminifer distribution in these sediments was presented in Mayer, Pisias, Janecek, et al. (1992) based on a preliminary examination of core-catcher samples. In general, the preservation state of the foraminifers is poor throughout most of the sedimentary sequences, making this microfossil group here of much less value for biostratigraphy than other microfossil groups. Pliocene-Pleistocene planktonic foraminifers from several sites have been analyzed in great detail for their oxygen and carbon isotope composition in various high-resolution studies (Farrell et al., this volume; Mix et al., this volume; Ravello et al., this volume; Shackleton et al., this volume). Planktonic foraminiferal datums of biostratigraphic value have been identified in several of these studies. This report presents planktonic foraminiferal distribution in selected Miocene sediments.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 5 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 22
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: McCartney, Kevin; Churchill, J H; Woestendiek, Linda (1995): Silicoflagellates and ebridians from Leg 138, eastern equatorial Pacific. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 129-162, https://doi.org/10.2973/odp.proc.sr.138.108.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: The biostratigraphic distribution and abundance of middle Miocene to Pleistocene silicoflagellates is documented from Ocean Drilling Program (ODP) Leg 138 Holes 844B, 847B, 848B, 849B, 850B, 85 IB, 852B, and 854B from the eastern Equatorial Pacific Ocean. The silicoflagellates were generally abundant and well preserved and frequently exhibited an unusually large range of variation. The upper Miocene of near-equatorial sites includes an assemblage of Bachmannocena diodon nodosa, which includes a bridge across the width of the basal ring. Stratigraphically below this, at sites within 5° of the equator is a lengthy interval of specimens of Distephanus speculum tenuis, which have a fragile apical structure. Both the intervals of Bachmannocena diodon nodosa plexus and Distephanus speculum tenuis are biostratigraphically useful within 5° of the equator, but are less useful beyond that. An unusual range of variation also is observed for Dictyocha in the Pliocene sediments at about the point where D. perlaevis and D. messanensis appear in the geologic record. This variation may be explained by hybridization between diverging species.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 8 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 23
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Rea, David K; Snoeckx, Hilde; Joseph, Leah H (1998): Late Cenozoic Eolian deposition in the North Pacific: Asian drying, Tibetan uplift, and cooling of the northern hemisphere. Paleoceanography, 13(3), 215-224, https://doi.org/10.1029/98PA00123
    Publikationsdatum: 2024-01-09
    Beschreibung: A newly constructed record of eolian dust accumulation from the central North Pacific shows that dust deposition increased by an order of magnitude quite rapidly at 3.6 Ma. We associate this sudden drying with the uplift of at least the northern portion of the Tibetan Plateau, shutting off the Indian Ocean moisture source to central and western China. This ten-fold increase in atmospheric dust loading appears to be associated with the 1-m.y.-long shift toward heavy d18O values that occurred at 3.6-2.6 Ma. The dust grain-size record of wind intensity begins its late Cenozoic coarsening a million years before the drying event, at ~4.5 Ma. The northern hemisphere cooling that results in intensification of the subpolar westerly winds may have as its ultimate cause the drawdown of atmospheric CO2 in the latest Miocene and the early Pliocene closing of the Panamanian Seaway.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 5 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 24
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Hoefs, Marcel JL; Versteegh, Gerard J M; Rijpstra, W Irene C; de Leeuw, Jan W; Sinninghe Damsté, Jaap S (1998): Postdepositional oxic degradation of alkenones: Implications for the measurement of palaeo sea surface temperatures. Paleoceanography, 13(1), 42-49, https://doi.org/10.1029/97PA02893
    Publikationsdatum: 2024-01-09
    Beschreibung: Free and 'bound' long-chain alkenones (C37:2 and C37:3) in oxidized and unoxidized sections of four organic matter-rich Pliocene and Miocene Madeira Abyssal Plain turbidites (one from Ocean Drilling Program site 951B and three from site 952A) were analyzed to determine the effect of severe post depositional oxidation on the value of Uk'37. The profiles of both alkenones across the redox boundary show a preferential degradation of the C37:3 compared to the C37:2 compound. Because of the high initial Uk'37 values and the way of calculating the Uk'37 this degradation hardly influences the Uk'37 profiles. However, for lower Uk'37 values, measured selective degradation would increase Uk'37 up to 0.17 units, equivalent to 5°C. For most of the Uk'37 band-width, much smaller degradation already increases Uk'37 beyond the analytical error (0.017 units). Consequently, for interpreting the Uk'37 record in terms of past sea surface temperatures, selective degradation needs serious consideration.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 25
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Raymo, Maureen E (1997): The timing of major climate terminations. Paleoceanography, 12(4), 577-585, https://doi.org/10.1029/97PA01169
    Publikationsdatum: 2024-01-09
    Beschreibung: A simple, untuned "constant sedimentation rate" timescale developed using three radiometric age constraints and eleven d18O records longer than 0.8 Myr provides strong support for the validity of the SPECMAP timescale of the late Quaternary (Imbrie et al., 1984). In particular, the present study independently confirms the link between major deglaciations (terminations) and increases in northern hemisphere summer radiation at high latitudes and shows that this correlation is not an artifact of orbital tuning. In addition, the excess ice characteristic of late Quaternary "100-kyr" climate cycles typically accumulates when July insolation at 65°N has been unusually low for more than a full precessional cycle, or 〉21 kyr, and once established does not last beyond the next increase in summer insolation. Thus, the timing of the growth and decay of large 100-kyr ice sheets, as depicted in the deep sea d18O record, is strongly (and semipredictably) influenced by eccentricity through its modulation of the orbital precession component of northern hemisphere summer insolation.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 5 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 26
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: St. John, Kristen E Kudless (1999): Data Report: Site 918 IRD mass accumulation rate record, late Miocene-Pleistocene. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-4, https://doi.org/10.2973/odp.proc.sr.163.119.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: To understand the late Cenozoic glacial history of the Northern Hemisphere, continuous long-term proxy records from climatically sensitive regions must be examined. Ice-rafted debris (IRD) from Ocean Drilling Program (ODP) Site 918, located in the Irminger Basin, is one such record. IRD in marine sediments is a direct indicator of the presence of glacial ice extending to sea level on adjacent landmasses, and, therefore, is an important paleoclimatic signal from the mid- to high latitudes. The IRD record at Site 918 is the first long-term ice-rafting record available for southeast Greenland, a region that may have been a key nucleation area for widespread glaciation during the late Cenozoic (Larsen et al, 1994, doi:10.2973/odp.proc.ir.152.1994). This data report presents the results of coarse sand-size IRD mass accumulation rate (MAR) analyses for Site 918 from the late Miocene through the Pleistocene. In addition, a preliminary analysis of IRD compositions is included. Detailed discussions of the local, regional, and global paleoclimatic implications of this data, and of the companion Site 919 Pleistocene IRD MAR data (Krissek, 1999, doi:10.2973/odp.proc.sr.163.118.1999), are in preparation. Such future work will include comparisons of these IRD MAR data sets to the Site 919 oxygen isotope stratigraphy developed by Flower (1998, doi:10.2973/odp.proc.sr.152.219.1998).
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 27
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Allan, James F; Forsythe, Lance; Natland, James H (1999): Determination of primitive melt composition in the North Atlantic seaward-dipping reflector sequences from Cr-rich spinel compositions. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-16, https://doi.org/10.2973/odp.proc.sr.163.121.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Coring during Ocean Drilling Program and Deep Sea Drilling Project Legs 163, 152, 104, 81, and 38 recovered sequences of altered basalt from North Atlantic seaward-dipping reflector sequences (SDRS) erupted during the initial rifting of Greenland from northern Europe and likely associated with excessive mantle temperatures caused by an impacting mantle plume head. Cr-rich spinel is found abundantly as inclusions and groundmass crystals within the olivine-rich lavas of Hole 917A (Leg 152) cored into the Southeast Greenland SDRS, but only rarely as inclusions within plagioclase in the lavas of the Vøring Plateau SDRS, and it is absent from other cored SDRS lavas from the Rockall Plateau and Southeast Greenland. Eruptive melt compositions determined from inferred, thermodynamically-defined, spinel-melt exchange equilibria indicate that the most primitive melts represented by Hole 917A basalts have Mg/(Mg + Fe2+) at least as high as 0.70 and approach near-primary mantle melt compositions. In contrast, Cr-rich spinels from Hole 338 (Leg 38) lavas on the Vøring Plateau SDRS give evidence for melt with Mg/(Mg + Fe2+) only as high as 0.64. This study underlines that primitive melts similar to those from Hole 917A comprise only a small fraction of the eruptive North Atlantic SDRS melts, and that most SDRS basalts were, in fact, too evolved to have precipitated Cr-rich spinel, with true melt Mg/(Mg + Fe2+) likely below 0.60. The evolved nature of the SDRS basalts implies large amounts of fractionation at the base of the crust or deep within it, consistent with seismic results that indicate an abnormally thick Layer 3 underlying the SDRS.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 5 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 28
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Channell, James E T; Amigo, Alejandro E; Fronval, Torben; Rack, Frank R; Lehman, Benoît (1999): Magnetic stratigraphy at Sites 907 and 985 in the Norwegian-Greenland Sea and a revision of the Site 907 composite section. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-18, https://doi.org/10.2973/odp.proc.sr.162.036.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: The magnetic polarity stratigraphy at Site 907 obtained from the shipboard pass-through magnetometer and from discrete samples is readily interpretable back to the onset of the Gilbert Chron (5.89 Ma). From this level to the base of the section at ~14 Ma, the interpretation is corroborated by silicoflagellate datums with predictable correlation to polarity chrons. The resulting magnetostratigraphic interpretation differs from those proposed in the Leg 151 (Hole 907A) and 162 (Holes 907B and 907C) Initial Reports volumes. An important hiatus in the 7-10 Ma interval at Site 907 caused sedimentation to slow or cease for ~2.7 m.y. We have revised the shipboard correlation among the three holes at Site 907, resulting in a new composite section splice and recalculation of composite depths. For Site 985, magnetostratigraphic interpretation is possible down to ~150 meters below seafloor (mbsf) (C3An/C3Ar) at ~6 Ma. There are no useful biostratigraphic datums from Site 985 to support this interpretation; however, the interpretation is supported by the correlation of Sites 985 and 907 using natural gamma data from the shipboard multisensor track. Below ~150 mbsf at Site 985, drilling-related deformation at the onset of extended core barrel drilling precluded magnetostratigraphic interpretation.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 29
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Channell, James E T; Smelror, Morten; Jansen, Eystein; Higgins, Sean M; Lehman, Benoît; Eidvin, Tor; Solheim, Anders (1999): Age models for glacial fan deposits off East Greenland and Svalbard (Sites 986 and 987). In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-18, https://doi.org/10.2973/odp.proc.sr.162.008.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Cores recovered at Sites 986 and 987 comprise glacial fan sedimentation associated with the Svalbard-Barents Sea and Greenland Ice Sheets, respectively. At Site 986, the top 150 m and the basal 250 m yielded interpretable magnetic stratigraphies. The record from the intervening 550 m is compromised by drilling-related core deformation, poor recovery, and numerous debris flows. The uppermost 150 m appears to record the Brunhes/Matuyama boundary and the Jaramillo Subchron. The base of the drilled section (at ~950 meters below seafloor [mbsf]) is interpreted to lie within the Matuyama Chron (age 〈2.58 Ma) with an apparent normal polarity interval in the ~730-750 mbsf interval. Dinoflagellate cyst biostratigraphy and Sr isotopic ratios are consistent with a Matuyama age for the base of the drilled section and with the normal polarity interval as the Olduvai Subchron. On the other hand, the last occurrence of Neogloboquadrina atlantica (sinistral) and the last common occurrence of the warm-dwelling Globigerina bulloides at 647-650 mbsf in Hole 986D indicate an age for this level of ~2.3 Ma, inconsistent with the designation of the Olduvai Subchron in the ~730-750 mbsf interval. If the age at 647-650 mbsf in Hole 986D is taken as 2.3 Ma and the base of the hole lies within the Matuyama Chron, then the sedimentation rate in the basal 300 m of the cored section averages 1 m/k.y. At Site 987, the magnetic stratigraphy is fairly unambiguous throughout the section and yields an age of 7.5 Ma (Chron 4n) for the base of the drilled section. The paucity of calcareous and siliceous microfossils precludes biostratigraphic corroboration of the magnetostratigraphic interpretation, although dinoflagellate cysts provide general support, particularly at the base of the section. The age model indicates relatively low sedimentation rates (~5 cm/k.y.) at the base of the section with rates at least four to five times greater during intervals of debris flows at ~5-4.6 and ~2.6 Ma.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 30
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Raffi, Isabella; Rio, Domenico; d'Atri, Anna; Fornaciari, Eliana; Rocchetti, Silvana (1995): Quantitative distribution patterns and biomagnetostratigraphy of middle and late Miocene calcareous nannofossils from equatorial Indian and Pacific oceans (Leg 115, 130, and 138). In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 479-502, https://doi.org/10.2973/odp.proc.sr.138.125.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Selected calcareous nannofossils were investigated by means of quantitative methods in middle and upper Miocene sediments from the tropical Indian Ocean (ODP Leg 115) and equatorial Pacific Ocean (DSDP Leg 85, ODP Legs 130 and 138). Our goal was to test the reliability of the classic biohorizons used in the standard zonations of Martini (1971) and Bukry (1973) and, possibly, to improve biostratigraphic resolution in the Miocene. In a time interval of about 8 m.y., from the last occurrence (LO) of S. heteromorphus (~13.6 Ma) to the LO of D. quinqueramus (~5.5 Ma), a total 37 events were investigated, using both the conventional and some additional markers proposed in the literature. At least 17 of these events proved to be distinct biostratigraphic correlation lines between the two considered areas. This integrated biostratigraphic framework increases the biostratigraphic resolution in the middle-upper Miocene interval (of the order of about 0.5 m.y). All the investigated events were tied to the geomagnetic polarity time scale (GPTS) and compared to biomagnetostratigraphy from mid-latitude North Atlantic Site 94-608 (Olafsson, 1991; Gartner, 1992), thus obtaining further information about the biostratigraphic and biochronologic reliability of the investigated events and a significant improvement of the available nannofossil biomagnetostratigraphic model for the middle and late Miocene.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 11 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 31
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Ravizza, Gregory E (1998): Osmium-isotope geochemistry of Site 959: implications for Re-Os sedimentary geochronology and reconstruction of past variations in the Os-isotopic composition of seawater. In: Mascle, J, Lohman; GP; Moullard, M (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 159, 181-186, https://doi.org/10.2973/odp.proc.sr.159.035.1998
    Publikationsdatum: 2024-01-09
    Beschreibung: Analyses of Re, Os, and Ir concentrations, as well as Os-isotopic compositions, are reported for a suite of sediments from Ocean Drilling Program Site 959. These samples vary in age from late Neogene to Late Cretaceous, and represent a range in depositional oxidation-reduction conditions from suboxic in the Neogene to anoxic in the Late Cretaceous. Age assignments based on shipboard biostratigraphic data are used to calculate initial 187Os/186Os ratios of Neogene nannofossil/foraminifer oozes and Eocene to upper Oligocene laminated diatomites. These calculated initial ratios are in general agreement with published data constraining the Os-isotopic evolution of seawater through time, indicating that the Os-isotopic composition of these sediments is controlled largely by the Os isotopic composition of contemporaneous seawater. Results from analyses of Upper Cretaceous to lower Paleocene claystones do not exhibit elevated Ir concentrations and exhibit Re-Os systematics that are highly consistent with closed-system production of 187Os by in situ 187Re decay. Scatter in both the Cretaceous and Cenozoic data sets is likely the result of the influence of nonhydrogenous Os, carried by clastics, on the bulk sediment Os-isotopic composition, or post-depositional mobility of Re and/or Os.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 32
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Ortiz, Joseph D; Mix, Alan C; Harris, Sara E; O'Connell, Suzanne B (1999): Diffuse spectral reflectance as a proxy for percent carbonate content in North Atlantic sediments. Paleoceanography, 14(2), 171-186, https://doi.org/10.1029/1998PA900021
    Publikationsdatum: 2024-01-09
    Beschreibung: Diffuse reflectance records from Feni Drift in the North Atlantic faithfully record sediment percent carbonate. A high-resolution, reflectance-based age model for these sediments derived from an orbitally tuned age model for western equatorial Atlantic, Ceara Rise sediments was generated by spectral frequency mapping. Power spectra of the Feni Drift record indicate statistically significant sub-Milankovitch cyclicity at 7.6-8.4 and 4.8-6.1 kyr. We infer that these ~8 and ~5 kyr cycles document a linkage between North and equatorial Atlantic climate given our ability to correlate these records. These climate cycles influence Atlantic basin carbonate prior to the intensification of Northern Hemisphere glaciation and thus must arise from some portion of the climate system other than the dynamics of large ice sheets. The presence of these peaks, which could be related to equatorial clipped precession, implies a possible non-linear response to Milankovitch forcing.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 33
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Kroon, Dick; Alexander, Ian T; Little, Mark G; Lourens, Lucas Joost; Matthewson, A; Robertson, Alastair H F; Sakamoto, Tatsuhiko (1998): Oxygen isotope and sapropel stratigraphy in the eastern Mediterranean during the last 3.2 million years. In: Robertson, AHF; Emeis, K-C; Richter, C; Camerlenghi, A (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, 160: College Station, TX (Ocean Drilling Program), 160, 181-189, https://doi.org/10.2973/odp.proc.sr.160.071.1998
    Publikationsdatum: 2024-01-09
    Beschreibung: Stable oxygen isotope data from four holes drilled at the Ocean Drilling Program Site 967, which is located on the lower northern slope of the Eratosthenes Seamount, provide a continuous record of Eastern Mediterranean surface-water conditions during the last 3.2 Ma. A high-resolution stratigraphy for the Pliocene-Pleistocene sequence was established by using a combination of astronomical calibration of sedimentary cycles, nannofossil stratigraphy, and stable oxygen isotope fluctuations. Sapropels and color cycles are present throughout the last 3.2 Ma at Site 967, and their ages, as determined by calibration against the precessional component of the astronomical record, are consistent with those estimated for the sapropels of the classical land-based marine sequences of the Punta Piccola, San Nicola, Singa, and Vrica sections (southern Italy). The Site 967 oxygen isotope record shows large amplitude fluctuations mainly caused by variations in surface water salinity throughout the entire period. Spectral analysis shows that fluctuations in the d18O record were predominantly influenced by orbital obliquity and precessional forcing from 3.2 to 1 Ma, and all main orbital frequencies characterize the d18O record for the last million years. The start of sapropel formation at 3.2 Ma indicates a possible link between sapropel formation and the build up of northern hemisphere ice sheets. The dominance of the obliquity cycle in the interval from 3.2-1 Ma further points to the sensitivity of Eastern Mediterranean climate to the fluctuations in the volume of Arctic ice sheets. An intensification of negative isotope anomalies at Site 967, relative to the open ocean, supports a link between high run-off (during warm periods) and sapropel formation. freshwater input would have inhibited deep-water formation, which led to stagnation of deeper waters. Comparison with the land sections also confirms that differential preservation and diagenesis play a key role in sapropel occurrence.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 34
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Bralower, Timothy J; Zachos, James C; Thomas, Ellen; Parrow, Matthew; Paull, Charles K; Kelly, Daniel Clay; Premoli Silva, Isabella; Sliter, William V; Lohmann, Kyger C (1995): Late Paleocene to Eocene paleoceanography of the equatorial Pacific Ocean: Stable isotopes recorded at Ocean Drilling Program Site 865, Allison Guyot. Paleoceanography, 10(4), 841-865, https://doi.org/10.1029/95PA01143
    Publikationsdatum: 2024-01-09
    Beschreibung: An expanded and largely complete upper Paleocene to upper Eocene section was recovered from the pelagic cap overlying Allison Guyot, Mid-Pacific Mountains at Ocean Drilling Program (ODP) Site 865 (18°26'N, 179°33'W; paleodepth 1300-1500 m). Reconstructions show that the site was within a few degrees of the equator during the Paleogene. Because no other Paleogene sections have been recovered in the Pacific Ocean at such a low latitude, Site 865 provides a unique record of equatorial Pacific paleoceanography. Detailed stable isotopic investigations were conducted on three planktonic foraminiferal taxa (species of Acarinina, Morozovella, and Subbotina). We studied benthic foraminiferal isotopes at much lower resolution on species of Cibicidoides and Lenticulina, Nuttallides truempyi and Gavelinella beccariiformis, because of their exceptional rarity. The d18O and d13C stratigraphies from Site 865 are generally similar to those derived from other Paleocene and Eocene sections. The planktonic foraminiferal records at Site 865, however, include significantly less short-term, single-sample variability than those from higher-latitude sites, indicating that this tropical, oligotrophic location had a comparatively stable water column structure with a deep mixed layer and less seasonal variability. Low-amplitude (0.1-0.8 per mil) oscillations on timescales of 250,000 to 300,000 years correlate between the d13C records of all planktonic taxa and may represent fluctuations in the mixing intensity of surface waters. Peak sea surface temperatures of 24°-25°C occurred in the earliest Eocene, followed by a rapid cooling of 3-6°C in the late early Eocene. Temperatures remained cool and stable through the middle Eocene. In the late Eocene, surface water temperatures decreased further. Vertical temperature gradients decreased dramatically in the late Paleocene and were relatively constant through much of the Eocene but increased markedly in the late Eocene. Intermediate waters warmed through the late Paleocene, reaching a maximum temperature of 10°C in the early Eocene. Cooling in the middle and late Eocene paralleled that of surface waters, with latest Eocene temperatures below 5°C. Extinction patterns of benthic foraminifera in the latest Paleocene were similar to those observed at other Pacific sites and were coeval with a short-term, very rapid negative excursion in d13C values in planktonic and benthic taxa as at other sites. During this excursion, benthic foraminiferal d18O values decreased markedly, indicating warming of 4 to 6°C for tropical intermediate waters, while planktonic taxa show slight warming (1°C) followed by 2°C of cooling. Convergence of d18O values of planktonic and benthic foraminifera suggests that thermal gradients in the water column in this tropical location collapsed during the excursion. These data are consistent with the hypothesis that equatorial Pacific surface waters were a potential source of warm, higher salinity waters which filled portions of the deep ocean in the latest Paleocene. Oxygen isotopic data indicate that equator to high southern latitude sea surface thermal gradients decreased to as little as 4°C at the peak of the excursion, suggesting some fundamental change in global heat transport.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 35
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Shackleton, Nicholas J; Crowhurst, Simon J; Hagelberg, Teresa King; Pisias, Nicklas G; Schneider, David A (1995): A new Late Neogene timescale: Application to leg 138 sites. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 73-101, https://doi.org/10.2973/odp.proc.sr.138.106.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: The sediments recovered during Leg 138 provide a remarkable opportunity to improve the geological time scale of the late Neogene. We have developed new time scales in the following steps. First, we constructed age models on the basis of shipboard magnetostratigraphy and biostratigraphy, using the time scale of Berggren, Kent, and Flynn (1985). Second, we refined these age models using shipboard GRAPE density measurements to provide more accurate correlation points. Third, we calibrated a time scale for the past 6 m.y. by matching the high-frequency GRAPE density variations to the orbital insolation record of Berger and Loutre (1991); we also took into account d18O records, where they were available. Fourth, we generated a new seafloor anomaly time scale using our astronomical calibration of C3A.n (t) at 5.875 Ma and an age of 9.639 Ma for C5n.1n (t) that is based on a new radiometric calibration (Baksi, 1992). Fifth, we recalibrated the records older than 6 Ma to this new scale. Finally, we reconsidered the 6- to 10-Ma interval and found that this could also be partially tuned astronomically.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 25 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 36
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Thy, Peter; Lesher, Charles E; Mayfield, J D (1999): Low-pressure melting studies of basalt and basaltic andesite from the Southeast Greenland continental margin and the origin of dacites at Site 917. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-18, https://doi.org/10.2973/odp.proc.sr.163.114.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: A series of 1-atm. melting experiments on basaltic flows collected from Holes 918D and 989B in the oceanic succession of the East Greenland continental margin can be used to define possible phase equilibria and liquid lines of descent. A sample from Site 918 (Section 152-918D-108R-2) shows the melting order low-Ca pyroxene (1153ºC), augite (1182ºC), olivine (1192ºC), and plagioclase (1192ºC). A sample from Site 989 (Section 163-989B-10R-7) melts in the order of low-Ca pyroxene (1113ºC), augite (1167ºC), plagioclase (1177ºC), and olivine (1184ºC). In particular, the relatively early appearance of low-Ca pyroxene distinguishes the melting relations for the oceanic succession from those observed for the basaltic continental succession at Site 917. A basaltic andesite flow from the Middle Series at Site 917 (Section 152-917A-27R-4) shows the melting order of low-Ca pyroxene (1142ºC), plagioclase (1173ºC), and olivine (1173ºC). This melting order is difficult to reconcile with the observed large compositional variations in SiO2 and FeO for the Middle Series, which imply early magnetite fractionation. Major element considerations and rare-earth element modeling of the dacites of the Middle Series suggest that they formed by low extent of melting (〈20%) of continental hydrated gabbroic or mafic amphibolite at pressures 〈8 kbar. These crustally derived melts represent possible contaminants of basaltic magmas of the Lower and Middle Series at Site 917.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 6 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 37
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Hooper, Peter R; Rehacek, Jakub; Morris, George (1999): Data Report: Major and trace element composition, strontium, neodymium, and oxygen isotope ratios, and mineral compositions of samples. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-5, https://doi.org/10.2973/odp.proc.sr.163.117.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Thirty-five samples from the drill core of the three Leg 163 sites (Sites 988, 989, and 990) off the southeast coast of Greenland were analyzed for 27 major, minor, and trace elements by X-ray fluorescence (XRF) and for 25 trace elements, including 14 rare-earth elements (REEs), by an inductively coupled plasma source mass spectrometer (ICP/MS). Sr- and Nd-isotope data are reported for seven samples and oxygen-isotope data are reported for 19 plagioclase separates. In addition, a reconnaissance survey of the composition of the main mineral phases, plagioclase, pyroxene, and oxides was determined on an electron microprobe to provide the basic information required for petrogenetic modeling. Olivine pseudomorphs are present in many of the samples, but in no case was an olivine grain found that was fresh enough to give a reliable analysis. The chemical and isotopic data recorded here were determined to provide a comparison with the larger data sets acquired by the Edinburgh, Copenhagen, and Leicester laboratories from both Legs 152 and 163 drill cores. This will permit a detailed comparison of the North Atlantic flood basalt province as a whole with the better known Columbia River, Deccan, and Karoo continental flood basalt provinces, for which substantial chemical data sets are already available at Washington State University.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 38
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Saunders, Andrew D; Kempton, Pamela D; Fitton, J Godfrey; Larsen, Lotte M (1999): Sr, Nd, and Pb isotopes and trace element geochemistry of basalts from the Southeast Greenland margin. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-17, https://doi.org/10.2973/odp.proc.sr.163.122.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Voluminous, subaerial magmatism resulted in the formation of extensive seaward-dipping reflector sequences (SDRS) along the Paleogene Southeast Greenland rifted margin. Drilling during Leg 163 recovered basalts from the SDRS at 66ºN (Site 988) and 63ºN (Sites 989 and 990). The basalt from Site 988 is light rare-earth-element (REE) enriched (La(n)/Yb(n) = 3.4), with epsilon-Nd(t=60) = 5.3, 87Sr/86Sr = 0.7034, and 206Pb/204Pb = 17.98. It is similar to tholeiites recovered from the Irminger Basin during Leg 49 and to light-REE-enriched tholeiites from Iceland. Drilling at Site 989, the innermost of the sites on the 63ºN transect, was proposed to extend recovery of the earliest part of the SDRS initiated during Leg 152. These basalts are, however, younger than those from Site 917 and are compositionally similar to basalts from the more seaward Sites 990 and 915. Many of the basalts from Sites 989 and 990 show evidence of contamination by continental crust (e.g., epsilon-Nd(t=60) extends down to -3.7, 206Pb/204Pb extends down to 15.1). We suggest that the contaminant is a mixture of Archean granulite and amphibolite and that the most contaminated basalts have assimilated ~5% of crust. Uncontaminated basalts are isotopically similar to basalts from Site 918, on the main body of the SDRS, and are light-REE depleted. Consistent with previous models of the development of this margin, we show that at the time of formation of the basalts from Sites 989 and 990 (1) melting was at relatively shallow levels in a fully-fledged rift zone; (2) fragments of continental crust were present in the lithosphere above the zones of melt generation; and (3) the sublithospheric mantle was dominated by a depleted Icelandic plume component.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 39
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Teagle, Damon A H; Alt, Jeffrey C (1999): Data Report: Alteration and vein log of Holes 917A and 918D, Southeast Greenland margin. In: Larsen, HC; Duncan, RA; Allan, JF; Brooks, K (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 163, 1-5, https://doi.org/10.2973/odp.proc.sr.163.116.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: This data report provides a systematic documentation of the low-temperature alteration associated with the formation of a volcanic-rifted margin by the quantification of alteration effects and vein mineralogy and distributions in basalts recovered on Leg 152 (Larsen, Saunders, Clift, et al., 1994, doi:10.2973/odp.proc.ir.152.1994). Basaltic rocks from Holes 917A and 918D have been investigated to provide a quantitative description of the extents of recrystallization and secondary mineral abundance resulting from low-temperature alteration and weathering. Only limited descriptions of alteration and secondary mineral distributions were undertaken on board ship during Leg 152, and the data presented here provide an essential complement to the shipboard logs of the limited amount of basalt recovered during Leg 163 from Sites 988, 989, and 990 (Duncan, Larsen, Allan, et al., 1996, doi:10.2973/odp.proc.ir.163.1996).
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 40
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Flower, Benjamin P (1999): Data Report: Planktonic foraminifers from the subpolar North Atlantic and Nordic Seas: Sites 980-987 and 907. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-16, https://doi.org/10.2973/odp.proc.sr.162.038.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: During Ocean Drilling Program (ODP) Leg 162, five sites were drilled in the subpolar North Atlantic (Sites 980-984), three sites in the Nordic Seas (Sites 985-987), and two holes at Iceland Sea Site 907 (first drilled during ODP Leg 151). Carbonate sediments at the subpolar sites have generally common to abundant and well-preserved planktonic foraminifers, especially at Feni Drift Sites 980/981 and Rockall Plateau Site 982. Gardar Drift Site 983 and Bjorn Drift Site 984 featured greater concentrations of clay material and ice-rafted debris, diluting carbonate material in some intervals (particularly before ~1.8 Ma at Site 984). Nordic Seas Sites 907 and 985-987 feature generally rare to common and moderately well-preserved planktonic foraminifers only within the past 1 m.y., although Pliocene taxa are sparsely recorded at Site 986 on the Svalbard margin. Planktonic foraminifer datum levels are located to the section level where possible for the subpolar North Atlantic sites. Comparison to an integrated magnetostratigraphy and calcareous nannofossil stratigraphy shows that several datum levels are synchronous to within 5% of their published ages. In particular, the start of the Neogloboquadrina pachyderma (sinistral) Acme Zone (1.8 Ma), the first occurrence (FO) of Globorotalia inflata (2.09 Ma), the last occurrence (LO) of Globorotalia cf. crassula (3.3 Ma), and the FO of Globorotalia puncticulata (4.5 Ma) are judged synchronous in eastern sections of the subpolar North Atlantic. The LO of Neogloboquadrina atlantica (sinistral) occurs ~100-200 k.y. later relative to its mid-latitude North Atlantic age (2.41 Ma).
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 10 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 41
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Amigo, Alejandro E (1999): Miocene silicoflagellate stratigraphy: Iceland and Rockall Plateaus. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-19, https://doi.org/10.2973/odp.proc.sr.162.001.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Silicoflagellate assemblages were analyzed for the Miocene intervals recovered during Ocean Drilling Program (ODP) Leg 162. The middle and late Miocene are represented in Holes 907B (Iceland Plateau) and 982B (Rockall Plateau) by well-preserved silicoflagellates. A zonal scheme is presented, which improves previous attempts to establish a comprehensive silicoflagellate stratigraphy for this realm, based on an increased resolution given by the analysis of this largest-ever number of samples for the given interval (about three times as many as those studied for ODP Leg 104). The most important change is the replacement of the last appearance of Corbisema triacantha by the first appearance of Bachmannocena circulus apiculata as the top of the upper C. triacantha Zone/bottom of the B. c. apiculata Zone. In addition, two important bioevents (the first appearance of Bachmannocena diodon nodosa and the last appearance of Distephanus crux stradneri) allow the subdivision of the B. c. apiculata Zone into three new subzones: Caryocha spp. Subzone, D. c. stradneri Subzone, and B. d. nodosa Subzone (oldest to youngest, respectively). This zonal scheme is correlated with the standard calcareous nannoplankton zonation and tentatively correlated with the magnetic polarity time scale. A qualitative analysis of the changes in surface-water characteristics is given, based on the variation in abundances of the several silicoflagellate groups. This shows a replacement of silicoflagellates that are adapted to warm surface waters by those adapted to temperate surface waters during the middle Miocene. In turn, the latter are gradually replaced by those adapted to cool surface waters during the late Miocene. The taxonomy of the taxa encountered has been revised in an effort to bring together differing schools. Only one new taxon, Distephanus crux lockerii, is described herein.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 42
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Channell, James E T; Lehman, Benoît (1999): Magnetic stratigraphy of North Atlantic Sites 980-984. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-18, https://doi.org/10.2973/odp.proc.sr.162.002.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Magnetic polarity stratigraphies for Sites 980-984 are based on shipboard measurements from the pass-through magnetometer after alternating field (AF) demagnetization at a peak field of 25 mT and shore-based stepwise AF demagnetization of discrete samples. The characteristic magnetization component was determined after AF demagnetization removed the steep downward drill-string-related magnetic overprint. Peak AF fields in the 20-30 mT range were required to resolve the component, carried by magnetite, that was used to produce unambiguous Pliocene-Pleistocene magnetic stratigraphies at all five sites. At Sites 980 and 983, magnetic stratigraphies were resolved to the base of the recovered advanced hydraulic piston corer (APC) section, which lies in the Matuyama Chron (1r.2r) and Olduvai Subchron (2n), respectively. At Sites 981 and 982, magnetization intensities decrease sharply in the normal polarity zone corresponding to the Gauss Chron (2An), and magnetic stratigraphies below this level could not be resolved. At Site 984, the resolution of magnetic stratigraphy was curtailed at ~250 meters below seafloor (Olduvai Subchron) by core deformation at the base of the APC section and in the underlying extended core barrel section. As the magnetic stratigraphies at all four sites are unequivocal, polarity chron interpretations can be made without aid from the biostratigraphy. Mean sedimentation rates within polarity chrons have been calculated and Pliocene-Pleistocene biomagnetostratigraphic correlations tested.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 43
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Carter, Susan J; Raymo, Maureen E (1999): Sedimentological and mineralogical control of multisensor track data at Sites 981 and 984. In: Raymo, ME; Jansen, E; Blum, P; Herbert, TD (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 162, 1-11, https://doi.org/10.2973/odp.proc.sr.162.022.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Multisensor track data, including magnetic susceptibility, gamma-ray attenuation porosity evaluator (GRAPE) wet bulk density, and natural gamma emission, were collected on all cores recovered during Ocean Drilling Program Leg 162. Data from the upper Pliocene and lower Pleistocene of Sites 981 and 984 are here compared to results from analyses of a limited set of discrete samples, including benthic foraminiferal isotopic composition, grain size, carbonate content, abundance of foraminifers and lithic particles, and clay mineralogy. Natural gamma emission most closely monitors the input of felsic terrigenous material to these two sites. Magnetic susceptibility also tracks felsic terrigenous input at Site 981 but appears to reflect a separate, more mafic, terrigenous component at Site 984. The GRAPE record does not correlate well with any discretely measured variable at Sites 981 or 984.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 44
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Marsaglia, Kathleen M; Tribble, Jane S (1999): Petrography and mineralogy of the uppermost Messinian section and the Pliocene/Miocene boundary at Site 975, Western Mediterranean Sea. In: Zahn, R; Comas, MC; Klaus, A (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 161, 1-18, https://doi.org/10.2973/odp.proc.sr.161.201.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Ocean Drilling Program Site 975 is located near the base of the Menorca Rise in the South Balearic Basin of the western Mediterranean Sea. Coring at this site penetrated the Pliocene/Miocene boundary and recovered a sequence of sediments that represent the final stages of salt deposition and the transition from evaporitic to open marine conditions at the end of the Miocene (Messinian). Detailed petrographic observations and bulk mineralogical analyses by X-ray diffraction form the basis for preliminary interpretations of depositional environments for this section. Gypsum is thought to have been deposited in an evaporating basin below wave base. Cycles consisting of a clay layer overlain by gypsiferous chalk, laminated gypsum, and finally pinch-and-swell gypsum suggest upsection increases in salinity. The gypsum section is overlain by two exotic sand layers thought to mark events of fresher water (marine or meteoric) inflow to the basin. Gypsum deposition terminated and was replaced by inorganic precipitation of micritic calcite with periodic, variable dilution by fine-grained terrigenous sediment. The micritic sediments have fine, slightly wavy, laminations indicating either an algal/microbial mat origin, or varve-like fluctuations in deposition, perhaps in a deep basin. The Pliocene/Miocene boundary falls within an interval of banded micritic silty clays that reflect the final environmental fluctuations during the transition to the open marine conditions of the Pliocene.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 45
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Martinez-Ruiz, Francisca C; Comas, Maria C; Alonso, Belen (1999): Mineral associations and geochemical indicators in upper Miocene to Pleistocene sediments in the Alboran Basin. In: Zahn, R; Comas, MC; Klaus, A (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 161, 1-16, https://doi.org/10.2973/odp.proc.sr.161.203.1999
    Publikationsdatum: 2024-01-09
    Beschreibung: Upper Miocene to Pleistocene hemipelagites and resedimented facies recovered at Holes 976B and 977A (Leg 161) in the Alboran Basin consist mainly of biogenic and detrital components, with a minor contribution of neoformed mineral phases. Diagenetic processes have not obliterated the primary deposition signal, and therefore detrital components (quartz, feldspar, detrital dolomite, rock fragments, and clays) provide information about source rocks and provenances. No major bulk or clay mineralogy differences were recognized between resedimented and hemipelagic facies; in fact, similar mineral assemblages in both types of facies suggest common source rocks. However, mineral abundance fluctuations can be related to climate variations and tectonic factors, as the main controls of sediment fill of this basin. A marked increase in smectites in Messinian sediments suggests an extensive development of soils during that time, probably favored by the alternation of wet and dry climate episodes and the relative aridification of the Mediterranean borderlands. A notable increase in detrital components suggests a sea-level fall and/or tectonic uplift during the late Pliocene. The significant increase in detrital dolomite in the uppermost Pliocene deposits suggests the uplift of dolomite-rich rocks as source areas. Mineral components in Pleistocene sediments indicate increasing tectonic stability, and clay-mineral fluctuations during the Pleistocene can be related not only to tectonic events, but also to alternating cooling and warming periods.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 9 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 46
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Mix, Alan C; Harris, Sara E; Janecek, Thomas R (1995): Estimating lithology from nonintrusive reflectance spectra: Leg 138. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 413-427, https://doi.org/10.2973/odp.proc.sr.138.121.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: During Leg 138, we measured reflectance spectra in the visible and near-infrared bands (455-945 nm) every few centimeters on split core surfaces from eastern tropical Pacific Ocean sediments. Here, we evaluate predictions of the content of biogenic calcite, biogenic opal, and nonbiogenic sediments from the reflectance spectra. For Sites 844 through 847, which contain a significant nonbiogenic component, reflectance spectra yielded a useful proxy for the percentages of CaCO3 over a wide range of values from nearly 0% to 100%, with root-mean-square (RMS) errors of about 9%. Direct estimates of "nonbiogenic" sediment percentages, approximated by 100 - (CaCO3 + opal), were reasonably successful (RMS error of 10%), however, were incorrect in some intervals. This suggests that mineralogy of the nonbiogenic material changes through time and that further subdivision of this component will be needed for useful estimation from reflectance. For percentages of biogenic opal, calibration equations appear to work well (RMS error of 6%) at concentrations of less than 30%, but for higher opal concentrations, reflectance equations often underestimate the true contents of opal. Improvements in multiparameter lithologic estimates from reflectance spectra may come from (1) expanding the wavelengths measured to better capture unique mineral reflectance bands, and (2) adding the ability to measure diffuse, rather than directional, reflectance to minimize the effects of surface roughness.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 3 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 47
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Chaisson, William P (1995): Planktonic foraminiferal assemblages and paleoceanographic change in the trans-tropical Pacific Ocean: A comparison of West (Leg 130) and East (Leg 138), latest Miocene to Pleistocene. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 555-597, https://doi.org/10.2973/odp.proc.sr.138.129.1995
    Publikationsdatum: 2024-01-09
    Beschreibung: Cores from four Ocean Drilling Program (ODP) sites were examined for planktonic foraminifers. One sample per core (from core-catchers in Holes 806B and 807B and from Section 4 in Holes 847B and 852B) was examined through the interval representing the last 5.8 m.y. Sites 806 (0°19.1'N; 159°21.7'E) and 847 (0o12.1'N; 95°19.2'W) are beneath the equatorial divergence zone. Sites 807 (3°36.4'N; 156°37.5'E) and 852 (5°19.6'N; 110°4.6'W) are located north of the equator in the convergence zone created by the interaction of the westward-flowing South Equatorial Current (SEC) and the eastward-flowing North Equatorial Countercurrent (NECC). Specimens were identified to species and then grouped according to depth habitat and trophic level. Species richness and diversity were also calculated. Tropical neogloboquadrinids have been more abundant in the eastern than in the western equatorial Pacific Ocean throughout the last 5.8 m.y. During the mid-Pliocene (3.8-3.2 Ma), their abundance increased at all sites, while during the Pleistocene (after ~ 1.6 Ma), they expanded in the east and declined in the west. This suggests an increase in surface-water productivity across the Pacific Ocean during the closing of the Central American seaway and an exacerbation of the productivity asymmetry between the eastern and western equatorial regions during the Pleistocene. This faunal evidence agrees with eolian grain-size data (Hovan, 1995) and diatom flux data (Iwai, this volume), which suggest increases in tradewind strength in the eastern equatorial Pacific that centered around 3.5 and 0.5 Ma. The present longitudinal zonation of thermocline dwelling species, a response to the piling of warm surface water in the western equatorial region of the Pacific, seems to have developed after 2.4 Ma, not directly after the closing of the Panama seaway (3.2 Ma). Apparently, after 2.4 Ma, the piling warm water in the west overwhelmed the upwelling of nutrients into the photic zone in that region, creating the Oceanographic asymmetry that exists in the modern tropical Pacific and is reflected in the microfossil record. In the upper Miocene and lower Pliocene sediments, the ratio of thermocline-dwelling species to mixed-layer dwellers is 60%:40%. During the mid-Pliocene, the western sites became 40% thermocline and 60% mixed-layer dwellers. Subsequent to -2.4 Ma, the asymmetry increased to 20%: 80% in the west and the reverse in the east. This documents the gradual thickening of the warm-water layer piled up in the western tropical Pacific over the last 5.8 m.y. and reveals two "steps" in the biotic trend that can be associated with specific events in the physical environment.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 48
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Altabet, Mark A; Murray, David W; Prell, Warren L (1999): Climatically linked oscillations in Arabian Sea denitrification over the past 1 m.y.: Implications for the marine N cycle. Paleoceanography, 14(6), 732-743, https://doi.org/10.1029/1999PA900035
    Publikationsdatum: 2024-01-09
    Beschreibung: Water column and core-top d15N data show that Arabian Sea denitrification produces large nitrogen isotopic enrichments that are regionally recorded with fidelity in the sediments. These results facilitate interpretation of a 1 m.y. d15N record for Ocean Drilling Program site 722B on the Owen Ridge in terms of climatically linked oscillations in denitrification at the major orbital periods. As at present, denitrification was greatest during interglacial periods and, apparently, was not active during most glacial intervals. Cross-spectral analysis of d15N with foraminiferal d18O (global climate/sea level index) and lithogenic grain size (monsoon strength index) suggests forcings by changes in hydrography and productivity acting through the extent and intensity of the oxygen minimum zone. The data suggest that denitrification may be an internal forcing mechanism for climate change during major glacial/interglacial transitions through influence on marine N inventory and atmospheric CO2. However, compensation or amplification may occur from other sinks (sediment denitrification) or sources (nitrogen fixation).
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 2 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 49
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Hovan, Steven A (1995): Late Cenozoic atmospheric circulation intensity and climatic history recorded by eolian deposition in the eastern Equatorial Pacific Ocean, Leg 138. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 615-625, https://doi.org/10.2973/odp.proc.sr.138.132.1995
    Publikationsdatum: 2024-02-12
    Beschreibung: Sediments recovered during Ocean Drilling Program (ODP) Leg 138 in the eastern equatorial Pacific Ocean were analyzed for variations in eolian accumulation rate and mean grain-size. Latitudinal and temporal patterns of these parameters showed important changes in the intensity of atmospheric circulation and eolian flux associated with the intertropical convergence zone (ITCZ) and suggested that eolian input parameters could be used to define its paleoposition through time. Modern atmospheric circulation in the equatorial region is weakest in the intertropical convergence zone and increases as the trade winds are approached to the north and south. Thus, the expected spatial pattern of eolian grain size would have the finest material deposited beneath the ITCZ and a coarsening of material in both directions away from this zone. Sediments from ODP Leg 138 show this pattern for much of the Pleistocene and Pliocene but, prior to about 4 Ma, begin to lose the northern coarse component suggesting that the ITCZ was located north of its present position during the late Miocene. Eolian flux records also show a latitudinal pattern of deposition associated with the position of the ITCZ that, similar to eolian grain-size variability, suggests a more northerly position of the ITCZ during the late Miocene. Overall, the regional input of eolian material to the equatorial Pacific has decreased throughout the late Neogene. This reduction in eolian input reflects climatic changes to relatively wetter conditions in the continental eolian source regions beginning during the late Pliocene.
    Schlagwort(e): Ocean Drilling Program; ODP
    Materialart: Dataset
    Format: application/zip, 4 datasets
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 50
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Synthesis of 3-Oxo-8-oxabicyclo[3.2.1]oct-6-ene-2-carbonitriles from γ-Bromo-β-oxonitriles and Furan via [4 + 3] Cycloaddition of 1-Cyanoallylium-2-olatesSome γ-bromo-β-oxonitriles 3 react with furan in the presence of silver oxide to form stereoselectively the title compounds 7. Satisfying yields are obtained only with those bromides 3, whose γ-carbon ist tertiary or which are monoalkylated both at the α- and γ-carbon atoms. The results are explained by a [4 + 3] cycloaddition of 1-cyanoallylium-2-olate intermediates (14) to the 1,3-diene system of the furan. With cyclic γ-bromo-β-oxonitriles (6) two types of cycloadducts were observed: 3-bromo-3-methyl-2-oxocyclohexanecarbonitrile (6b) and 3-bromo-2-oxocyclododecanecarbonitrile (6d) form the tricyclic [4 + 3] cycloadducts 10b and d, analogs of the bicyclic adducts 7. With 3-bromo-2-oxocyclohexanecarbonitrile (6a) and 3-bromo-5-tert-butyl-2-oxocyclohexanecarbonitrile (6e), however, the carbonyl oxygen is connected with an α-carbon of the furan to give the tricyclic [3 + 2] cycloadducts 12Aa and Ae. The structure of endo-2,endo-4-dimethyl-3-oxo-8-oxabicyclo[3.2.1]oct-6-ene-exo-2-carbonitrile (7eα) was determined by X-ray analysis.
    Notizen: Verschiedene γ-Brom-β-oxonitrile 3 reagieren in Gegenwart von Silberoxid mit Furan stereoselektiv zu den Titelverbindungen 7. Befriedigende Ausbeuten werden nur mit solchen Bromiden 3 erhalten, deren γ-Kohlenstoff tertiär ist oder die sowohl am α- als auch γ-Kohlenstoff monoalkyliert sind (3c, e-h). Die Befunde werden durch eine [4 + 3]-Cycloaddition von intermediären 1-Cyanallylium-2-olaten (14) an das 1,3-Dien-System des Furans erklärt. Mit cyclischen γ-Brom-β-oxonitrilen (6) wurden zwei Typen von Cycloaddukten beobachtet: 3-Brom-3-methyl-2-oxocyclohexancarbonitril (6b) und 3-Brom-2-oxocyclododecancarbonitril (6d) reagieren zu den tricyclischen [4 + 3]-Cycloaddukten 10b und d, Analoga der Bicyclen 7. Bei 3-Brom-2-oxocyclohexancarbonitril (6a) und 3-Brom-5-tert-butyl-2-oxocyclohexancarbonitril (6e) wurde jedoch der Carbonyl-Sauerstoff mit einem α-Kohlenstoffatom des Furans verknüpft, wobei die tricyclischen [3 + 2]-Cycloaddukte 12Aa und Ae entstanden. Die Struktur von endo-2,endo-4-Dimetyl-3-oxo-8-oxabicyclo[3.2.1]oct-6-en-exo-2-carbonitril (7eα) wurde durch eine Röntgenstrukturanalyse bestimmt.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 51
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Metal-π-Complexes of Benzene Derivatives, XV. Bis(η6-naphthalene)chromium(0): X-Ray Structure Determination and Investigation by Nuclear Magnetic Resonance SpectroscopyBis(η6-naphthalene)chromium(0) (2) crystallizes in the space group P21/n with two molecules in the unit cell. The ligands in individual molecules of 2 are syn-oriented. The implied presence of a center of symmetry in 2 is caused by disorder that consists in the statistical occupation by chromium atoms of two equivalent sites between the six membered ring of pairs of parallel naphthalene ligands. The 1H and 13C NMR spectra of 2 are analysed and the spectroscopic parameters are discussed with reference to the respective data of free naphthalene as well as other (η-naphthalene)metal complexes.
    Notizen: Bis(η6-naphthalin)chrom(0) (2) kristallisiert in der Raumgruppe P21/n mit zwei Molekülen in der Elementarzelle. Die Liganden in individuellen Molekülen von 2 nehmen dabei eine syn-Anordnung ein. Das Vorliegen eines Symmetriezentrums in 2 wird durch eine Fehlordnung vorgetäuscht, die darin besteht, daß in Paaren parallel angeordneter Naphthalin-Liganden linke und rechte Lücken zwischen den Sechsringen statistisch mit Chromatomen besetzt sind. Die 1H- und 13C-NMR-Spektren von 2 werden analysiert, und die spektroskopischen Parameter werden im Vergleich mit entsprechenden Daten des freien Naphthalins sowie anderer (η-Naphthalin)metall-Komplexe diskutiert.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 52
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 393-395 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Refinement of the Crystal Structure of (Ethylenediamine)zinc(II) Benzohydroxamate Hydrate, ZnC23H29N5O7The already known structure1) of the title compound has been refined and slightly corrected from new data.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 53
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 54
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 800-805 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 2,2-Disubstituted 1,3-Dithianes from β-Dicarbonyl Compounds1,3-Dicarbonyl compounds 2 can be condensed with 1,3-propanedithiol (1) to yield 2,2-disubstituted 1,3-dithianes 3 which are remarkably stable in contrast to analogous open-chain thioacetals 6. Compounds with alkoxycarbonyl functions are easily hydrolysed to the corresponding carboxylic acids 11 which by further esterification with alkanols 12 yield estermodified 1,3-dithianes 3. All new compounds are characterized by 13C NMR spectroscopy.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 55
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 806-807 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Perchloro-2-methylene-2H-pyranThe synthesis of the title compound 4 is described. 4 is thermally and chemically very stable.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 56
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 808-810 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Anchimerically Enhanced Homolyses, V. Fluoride Ion Catalysed Rearrangements of Benzyl 9-(Trimethylgermyl)-9-fluorenyl EtherThe thermal rearrangement (homolysis) of the germanium compound 1d into 4d is considerably slower than that of the analogous Si compound 1c. Thus, a correlation is suggested between the velocity of the rearrangement and the strength of the new bond to oxygen. The rearrangement 1d→4d is also induced by fluoride ions at room temperature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 57
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 58
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 3904-3907 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reactions of Allylidenephosphoranes with Heterocumulenes, II. New Syntheses of 1,2,4-Pentatrienes and 2-Pentene-1,5-dionesCinnamylidenetriphenylphosphorane (2a) undergoes Wittig reaction with ketenes to afford monomeric and dimeric 1,2,4-pentatrienes 4 and 5, resp. 4b reacts further with an excess of ketene via a [2 + 2]-cycloaddition, whereby the 3-styryl-1-naphthyl diphenylacetate 12 is formed. In contrast, with the α-phenylsubstituted phosphorane 2b, instead of the Wittig reaction addition of ketene takes place at both the α- and the γ-positions. The 1,3-diacyl-3-triphenylphosphonio-1-propen-3-enolate 6 readily hydrolyzes to the 2-pentene-1,5-dione 9.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 59
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 55-65 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Cycloaddition Reactions of Heterocumulenes, XXVI. Cycloadducts from Aryl Isothiocyanates and 2,2-Disubstituted EnaminesAryl isothiocyanates 1 react with enamines 2 to give two types of 2:1 cycloadducts. Below 50°C, 1a - g and 2 give rise to 6-imino-1,3-thiazine-2-thiones 5, the constitutions of which are proved by an X-ray analysis of 5c. Above 50°C or starting from 4-nitrophenyl isothiocyanate (1h),2,4-dithiouracils 6 are formed. 1:1 cycloadducts of the reactants are detected spectroscopically; on workup, they hydrolyze to give 2-formylthiopropionanilides 9.
    Notizen: Arylisothiocyanate 1 und Enamine 2 reagieren zu zwei Typen von 2:1-Cycloaddukten. Unterhalb von 50°C entstehen aus 1a - g und 2 6-Imino-1,3-thiazin-2-thione 5, deren Konstitution durch die Röntgenstrukturanalyse von 5c bewiesen wurde. Oberhalb 50°C oder aus 4-Nitrophenylisothio-cyanat (1h) bilden sich 2,4-Dithiouracile 6. 1:1-Cycloaddukte der Reaktanten lassen sich spektroskopisch nachweisen; bei der Aufarbeitung hydrolysieren sie zu 2-Formylthiopropionaniliden 9.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 60
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2668-2673 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Contributions to the Chemistry of Boron, 127. Hexamethylborazine-Gallium Trichloride: Structure in Solution and in the Solid StateHexamethylborazine forms a 1:1 adduct 1 with gallium trichloride. It is isostructural with hexamethylborazine-aluminium tribromide. The BN heterocycle is no longer planer, and the molecule adapts almost Cs symmetry and contains a tetracoordinated nitrogen atom. 1 shows fluctional behavior in toluene solution at room temperature. The coordinated GaCl3 will no longer change its coordination site at T 〈 220 K (two signals each for the CH3N-and CH3B-protons). However, at T 〈 195 K an additional splitting of the signals is observed - three signals for each type of CH3 groups: this would be consistent with a pentacoordinated gallium atom and a bidentate borazine ligand.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 61
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 62
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2679-2681 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Preparation of Cyclic Nitrones from Heterocyclic N-(Benzyloxy)aminesTreatment of heterocyclic N-(benzyloxy)amines 1 with concentrated hydrogen peroxide solution in acetic acid enables the preparation of 7-membered cyclic nitrones in respectable yields. This one-pot procedure offers some advantages compared with conventional routes.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 63
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2674-2678 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Vinyl Carbanions, 13. Convenient Synthesis of Oxaloacetic Acid DerivativesThe vinyllithium derivatives 2a, b and 9a, b, obtained by direct lithiation of the functionally substituted acrylic acid derivatives 1a, b and 8a, b, respectively, react with heterocumulenes A-E such as phenyl isocyanate, phenyl isothiocyanate, and carbon dioxide to give derivatives of oxaloacetic acid. In a single step reaction the oxaloacetic acid monoester 6a and monoamide 6b were synthesized.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 64
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2683-2696 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Synthesis of a [3]-PrecatenaneStarting from the previously synthesised compound 9a, the cyclophane 13 is prepared. Acetalisation with 1,25-dichloro-13-pentacosanone followed by nitration and reduction afforded the diamine 16. By cyclization of this compound in isoamyl alcohol with sodium carbonate and sodium iodide under high dilution conditions the monomeric products 17, 18, and 19 are obtained in yields of 5.0, 2.4, and 0.1%, respectively. On the basis of mass, 13C and 1H NMR spectra the structures of these compounds are discussed. The attempted transformation of the [3]-precatenane 17 into the [3]-catenane 24 gives a mixture of products among which 24 could not be identified with certainty.
    Notizen: Ausgehend von der bereits früher hergestellten Verbindung 9a wird das Cyclophan 13 synthetisiert. Durch dessen Acetalisierung mit 1,25-Dichlor-13-pentacosanon, nachfolgende Nitrierung und Reduktion wird das Diamin 16 erhalten. Dessen Cyclisierung in Isoamylalkohol in Gegenwart von Natriumcarbonat und Natriumiodid unter Verdünnungsbedingungen ergibt die monomeren Cyclisierungsprodukte 17, 18 und 19 in Ausbeuten von 5.0, 2.4 und 0.1%. Die Struktur dieser Verbindungen wird anhand der Massen-, 13C-und 1H-NMR-Spektren diskutiert. Die versuchte Umwandlung des [3]-Praecatenans 17 in das [3]-Catenan 24 führt zu einem Produktgemisch, in dem 24 nicht mit Sicherheit identifiziert werden konnte.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 65
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2697-2706 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Ozonolysis of Symmetrically 1,2-Disubstituted Ethylenes in HCl/Methanol Solutions: Acid Catalyzed Reactions of Primary Cleavage ProductsThe ozonolysis of olefins in 1 M anhydrous solutions of hydrogen chloride in methanol at ≤ 0°C was investigated. Upon warm-up of the ozonolysis products, the peroxidic primary fragmentation products were converted into non-peroxidic end-products by HCl-catalyzed reactions. Cyclopentene (1a) and cyclohexene (1b), e.g., afforded mixtures of the corresponding α,ω-dialdehyde-bis(dimethyl acetals) (8), dimethyl α,ω-dicarboxylates (9), and methyl ω-aldehyde dimethyl acetal carboxylates (10). Norbornene (1c) gave a mixture of the correspondingly substituted 1,3-cyclopentane compounds (8c-10c), phenanthrene (22) gave a mixture of methyl 2′-formyl-2-biphenyl-carboxylate (24a), 2,2′-biphenyldicarbaldehyde (24b), and dimethyl 2,2′-biphenyldicarboxylate (24c). A reaction scheme was advanced for the rationalization of the types and the distribution of the products. It was partly substantiated by model reactions.
    Notizen: Die Ozonolyse von Olefinen in wasserfreien 1 M Lösungen von Chlorwasserstoff in Methanol bei ≤ 0°C wurde untersucht. Beim Erwärmen der Ozonolyseprodukte traten HCI-katalysierte Folgereaktionen ein, in deren Verlauf die peroxidischen Primärspaltprodukte in peroxidfreie Endprodukte umgewandelt wurden. Z. B. lieferten Cyclopenten (1a) und Cyclohexen (1b) Gemische der entsprechenden α,ω-Dialdehyd-bis(dimethylacetale) (8), α,ω-Dicarbonsäure-dimethylester (9) und ω-Aldehyd-dimethylacetal-carbonsäure-methylester (10). Norbornen (1c) ergab ein Gemisch der entsprechend substituierten 1,3-Cyclopentanverbindungen (8c-10c), Phenanthren (22) ein Gemisch von 2′-Formyl-2-biphenylcarbonsäure-methylester (24a), 2,2′-Biphenyldicarbaldehyd (24b) und 2,2′-Biphenyldicarbonsäure-dimethylester (24c). Für die Entstehungsweise und die Verteilung der Produkte wurde ein Reaktionsweg formuliert, welcher z. T. durch Modellreaktionen bestätigt wurde.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 66
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 544-548 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Crystal and Molecular Structure of the Anthraquinonophane [2.0.0](1,4)Benzeno(1,8)anthraquinono(1,4)benzenophaneBoth phenylene rings in the [5.2]paracyclophane subunit of the anthraquinonophane [2.0.0](1,4)benzeno(1,8)anthraquinono(1,4)benzenophane (1) are tilted by 37.6°. They show a boat-like deformation. The carbonyl group pointing towards the interior of the molecule interacts with the paracyclophane system. From this a strong boat-like deformation of the quinone ring of the anthraquinone moiety results.
    Notizen: Die beiden Phenylenringe in der [5.2]Paracyclophan-Untereinheit des [2.0.0](1,4)Benzeno(1,8)-anthrachinono(1,4)benzenophans (1) sind um 37.6° gegeneinander geneigt und wannenförmig deformiert. Die Wechselwirkungen der ins Molekülinnere zeigenden Carbonylgruppe mit dem Paracyclophan-System verursachen eine starke wannenförmige Deformation des Chinonringes in der Anthrachinon-Einheit.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 67
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Four- and Five-membered Phosphorus Heterocycles, 55. 1,2,4-Diazaphospholo-[1,2,3]diazaphospholes - Preparation by Phosphaalkene + Nitrilimine Cycloaddition, Decomposition by Nitrile Elimination, and Structural Comparison of Addend and Adduct2,5-Dimethyl-1,2,3-diazaphosphole (1a) reacts with N-Phenylbenzohydrazonoyl chloride (6a) and a base in a sequence of nitrilimine cycloaddition, benzonitrile elimination, and another cycloaddition to give in the second step the 4-anilino derivative 7 of 1a, in the first and third step the 7a-unsubstituted and 7a-anilino-substituted title compound, 3a and 8, respectively. - As shown by the molecular structures, determined by X-ray analysis, there is a 6 π delocalization in 7 which is lost in 8 with remarkably little geometrical change at the phosphorus. - Other nitrilimines add to 1a in the same direction, that is with PC- and CN-bond formation.
    Notizen: 2,5-Dimethyl-1,2,3-diazaphosphol (1a) reagiert mit N-Phenylbenzohydrazonoylchlorid (6a) und einer Base in einer Folge von Nitrilimin-Cycloaddition, Benzonitril-Eliminierung und neuerlicher Cycloaddition. In der zweiten Stufe bilden sich dabei das 4-Anilinoderivat 7 von 1a, in der ersten und dritten Stufe entstehen die 7a-unsubstituierte und 7a-anilinosubstituierte Titelverbindung, 3a bzw. 8. - Die röntgenographisch bestimmten Molekülstrukturen zeigen für den Übergang von 7 in 8 die Aufhebung einer 6 π-Delokalisierung bei nur geringen geometrischen Veränderungen am Phosphor. - Auch andere Nitrilimine addieren sich an 1a in gleicher Richtung, also unter PC- und CN-Verknüpfung.
    Zusätzliches Material: 6 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 68
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 919-933 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Thiono and Dithio Esters, XXII. α,β-Unsaturated Thiono and Dithio Estersα,β-Unsaturated thiono and dithio esters such as O-ethyl thiocinnamate (3), methyl dithiocinnamate (7), O-ethyl thiocrotonate (17), and O,O-diethyl dithiofumarate (28) have been prepared by thiolysis between 20 and -75°C from the corresponding O- or S-alkylated tertiary amides or thioamides. They tend to dimerize in part by [4 + 2] cycloadditions. Methyl dithiocrotonate (24) could only be isolated as the endo-dimer 25.
    Notizen: α,β-Ungesättigte Thion- und Dithioester wie Thiozimtsäure-O-ethylester (3), Dithiozimtsäure-methylester (7), Thiocrotonsäure-O-ethylester (17) und Dithiofumarsäure-O,O-diethylester (28) sind durch Thiolyse aus den entsprechenden O- oder S-alkylierten tertiären Amiden oder Thio-amiden bei Temperaturen von 20 bis -75°C zugänglich. Sie dimerisieren zum Teil in [4 + 2]-Cycloadditionen. Dithiocrotonsäure-methylester (24) ist nur als endo-Dimeres 25 erhältlich.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 69
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 875-901 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Thermolysis of Compounds with a Geometrically Fixed Vinyloxirane Unit: Stereospecific Synthesis of 4,5-Fused cis-and trans-2,3-DihydrofuransThe conformationally fixed vinyloxiranes 7c - f, 8a - f, and 9b - d are transformed thermally into the bicyclic ethers 23 - 25. Starting with the spiro-derivatives c - f, which are monosubstituted at the vinyl group, the ring expansion takes place with high stereospecificity leading to 4,5-fused cis-(c/e) and trans-2,3-dihydrofurans (d/f), respectively. On heating 8b and 9b in the presence of dimethylfumarate besides the isomerisation to 24b/25b two cycloadducts are formed in each case to which the structures of 29/31 and 30/32 have been assigned. Oxapentadienyl dipoles (3) are proposed as intermediates in which the rotation of C/O-bonds is energetically more favorable than rotation of C/C-bonds. The activation parameters for the transformation 8b → 24b are determined and discussed together with the reported data of some analogous ring expansion reactions.
    Notizen: Die konformativ fixierten Vinyloxirane 7c - f, 8a - f und 9b - d wandeln sich thermisch mit Ausbeuten zwischen 50 und 80% in die bicyclischen Ether 23 - 25 um. Ausgehend von den an der Vinylgruppe monosubstituierten Spiro-Derivaten c - f erfolgt die Ringerweiterungsreaktion mit hoher Stereospezifität zu 4,5-anellierten cis- (c/e) bzw. trans-2,3-Dihydrofuranen (d/f). Beim Erhitzen von 8b und 9b in Gegenwart von Fumarsäuredimethylester entstehen neben den Isomeren 24b bzw. 25b jeweils zwei Cycloaddukte im Verhältnis 10: 1, denen die Strukturen 29/31 und 30/32 zugeordnet werden. Als Zwischenstufen werden Oxapentadienyl-Dipole (3) angenommen, in welchen die Rotation um C/O-Bindungen energetisch günstiger ist als die um C/C-Bindungen. Die Aktivierungsparameter der Umwandlung 8b → 24b werden bestimmt und im Zusammenhang mit denen einiger analoger Ringerweiterungen diskutiert.
    Zusätzliches Material: 12 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 70
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 941-954 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Statistical Syntheses of RotaxanesThe acetalisation of the 28-membered cyclic diols 11a, b with the long-chain dibromo ketone 12 gives acetals 13a, b. These compounds react with triphenylmethyllithium to give 17a, b and 18a, b from which the rotaxanes 20a, b are obtained in 0.066 or 0.18 and 0.12% yield, respectively, after hydrolysis of the acetal bonds. The reacetalisation of rotaxane 20b affords, by an intraannular reaction, the prerotaxane 18b in pure form.
    Notizen: Die Acetalisierung der 28-gliedrigen cyclischen Diole 11a, b mit dem langkettigen Dibromketon 12 ergibt die Acetale 13a, b. Nach Umsetzung mit Triphenylmethyllithium zu 17a, b und 18a, b werden nach Hydrolyse der Acetalbindungen die Rotaxane 20a, b in Ausbeuten von 0.066 und 0.18 bzw. 0.12% als farblose Öle isoliert. Durch Reacetalisierung von 20b wird in einer intraannularen Reaktion das Prärotaxan 18b in reiner Form erhalten.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 71
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 934-940 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Rearrangement of α-Isocyanato-N2-(arylsulfonyl)amidines to 1-Arylsulfonyl-3-imidazolin-2-onesThe reaction of the azirines 1 with the isocyanates 2 leads to the α-isocyanato-N2-(arylsulfonyl)-amidines 6. Starting from 1b, also considerable amounts of 7b and 8b are formed as a result of a retro-ene reaction of 6b. The heterocumulenes 6 readily rearrange with a shift of the sulfonyl group to give the heterocycles 10. The mobility of the sulfonyl residue is also obvious from the reaction of 6a with hydrogen chloride to afford tosyl chloride and 8a as well as from the reaction with amines, which, however, does not only yield the tosylamides 15, but also the ureas 13 and their secondary products 14.
    Notizen: Die Reaktion der Azirine 1 mit den Isocyanaten 2 führt zu den α-Isocyanato-N2-(arylsulfonyl)-amidinen 6. Ausgehend von 1b werden auch beträchtliche Mengen 7b und 8b als Folge einer Retro-En-Reaktion von 6b gebildet. Die Heterocumulene 6 lagern sich unter Wanderung der Sulfonyl-Gruppe leicht in die Heterocyclen 10 um. Die Beweglichkeit des Sulfonyl-Rests wird auch in der Reaktion von 6a mit Chlorwasserstoff zu Tosylchlorid und 8a sowie in der Umsetzung mit Aminen deutlich, die neben Tosylamiden 15 allerdings auch Harnstoffe 13 und deren Folgeprodukte 14 liefert.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 72
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 989-994 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Di-μ-(carboxylato)-bis[dicarbonyl(tri-tert-butylphosphane)ruthenium(I)](Ru - Ru)Ru3(CO)12 reacts with tri-tert-butylphosphane and formic acid, acetic acid, propionic acid, butyric acid, or stearic acid to form di-μ-(carboxylato)-bis[dicarbonyl(tri-tert-butylphosphane)-ruthenium(I)](Ru - Ru). The IR and NMR spectroscopic data are discussed.
    Notizen: Ru3(CO)12 reagiert mit Tri-tert-butylphosphan und Ameisensäure. Essigsäure, Propionsäure, Buttersäure oder Stearinsäure unter Bildung von Di-μ-(carboxylato)-bis[dicarbonyl(tri-tert-butylphosphan)ruthenium(I)](Ru - Ru). Die IR- und NMR-spektroskopischen Daten der neuen Komplexe werden diskutiert.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 73
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 979-988 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Addition of Aldehydes to Activated Double Bonds, XXIII. Syntheses of 1,3,6-TriketonesThiazolium salt-catalyzed addition of aldehydes to monoacetals of vinyl-1,3-diketones (1, 2; 23, 24) leads to 1,4-diketones (3 - 10; 25 - 31), which are hydrolyzed to 1,3,6-triketones (11 - 18; 32 - 38). A way to the mono-acetalized vinyl-1,3-diketones 1, 2; 23, 24 using the norbornenyl group with following pyrolysis is given.
    Notizen: Thiazoliumsalz-katalysierte Additionen von Aldehyden an mono-acetalisierte Vinyl-1,3-diketone (1,2; 23, 24) führen zu 1,4-Diketonen (3 - 10; 25 - 31), die sich zu den 1,3,6-Triketonen (11 - 18; 32 - 38) hydrolysieren lassen. Ein Syntheseweg zu den mono-acetalisierten Vinyl-1,3-diketonen 1, 2; 23, 24 über die Norbornenyl-Gruppierung und nachfolgende Pyrolyse wird angegeben.
    Zusätzliches Material: 6 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 74
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 970-978 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Introduction of the (Dimethylhydrazono)ethyl Group into Methylene Active Compounds and PhenolsIn [2-(dimethylhydrazono)ethyl]trimethylammonium iodide the trimethylammonium group can be substituted by several nucleophiles. With this reagent (dimethylhydrazono)ethyl derivatives of CH-acidic compounds, phenols, and indole can be prepared.
    Notizen: In [2-(Dimethylhydrazono)ethyl]trimethylammonium-iodid (19) läßt sich die Trimethylammoniumgruppe durch verschiedenartige Nucleophile verdrängen. CH-acide Verbindungen sowie Phenole und Indole kann man mit diesem Reagenz zu den entsprechenden Hydrazonoethyl-Derivaten umsetzen.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 75
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 955-969 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Preparation of Novel Mono- and Disaccharide Glycals for the Synthesis of Oligodeoxy OligosaccharidesUnder various conditions opening of the 6-deoxy-allo-epoxide 1 with lithium iodide yields a mixture of the 3-iodo-gluco-(3) and, predominantly, the 2-iodo-altro-hydrine (2), the reaction of which with methyllithium is studied. By a simplified procedure rendering a separation of 2a and 3a unnecessary the preparation of crystalline D-digitoxal (4a) in approximately 50% yield based on 1 is described. The condensation of 1 and 4b in the presence of N-iodosuccinimide yields the α,1→4-linked altro-allo disaccharide derivative 8a, and only minor amounts of the isomeric β,1→4-linked allo-allo disaccharide 10. Following the opening of the epoxide ring in 8a with lithium iodide and subsequent separation of the iodo hydrines by reduction of the bis-altro derivative 11a a synthesis of the methyl glycoside of the terminal disaccharide (12a) in neodigoxin is achieved. Starting with a reduction of 8a to 13b the subsequent opening of the epoxide ring with lithium iodide and separation of the isomers gives an access to the ribo-altro derivative 16b. By its reaction with methyllithium the disaccharide glycal digitoxosyl-digitoxal 15a is synthesized. The linkage of 15b with 1 is effected by application of the N-iodosuccinimide procedure and yields the trisaccharide derivative 17. The structures and conformations of all derivatives are characterized by comprehensive 1H NMR spectroscopy.
    Notizen: Die Öffnung des 6-Desoxy-allo-epoxid-Derivats 1 mit Lithiumiodid gibt unter verschiedenen Bedingungen ein Gemisch aus dem 3-Iod-gluco-(3) und überwiegend dem 2-Iod-altro-Hydrin (2), deren Umsetzungen mit Methyllithium untersucht werden. Ein vereinfachtes Verfahren ermöglicht ohne Trennung von 2a und 3a die Herstellung des kristallinen D-Digitoxals (4a) mit ca. 50% Ausbeute, bezogen auf 1. Die Kondensation von 1 mit 4b und N-Iodsuccinimid gibt glatt das α,1→4-verknüpfte altro-allo-Disaccharid-Derivat 8a und nur in geringen Mengen das isomere β,1→4-gebundene allo-allo-Disaccharid 10. Nach Öffnung des Epoxidringes in 8a mit Lithiumiodid und Trennung der Iodhydrine wird durch Reduktion des bis-altro-Derivats 11a das Methylglycosid des terminalen Disaccharids (12a) aus Neodigoxin gewonnen. Durch vorgelagerte Reduktion von 8a zu 13b läßt sich nach Öffnung des Epoxidringes mit Lithiumiodid und Trennung der Isomeren aus dem ribo-altro-Derivat 16b mit Methyllithium das Disaccharidglycal Digitoxosyl-digitoxal 15a darstellen. Die Verknüpfung von 15b mit 1 nach dem N-Iodsuccinimid-Verfahren liefert das Trisaccharid-Derivat 17. Alle Derivate wurden hinsichtlich der Struktur und Konformation durch 1H-NMR-Spektren charakterisiert.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 76
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1010-1019 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Transition Metal Carbyne Complexes, LII. (Tricarbonylchromium)-η6-phenyl as Substituent in Carbene- and Carbyne Complexes of the VI. SubgroupThe reaction of tricarbonyl(η6-phenyllithium)chromium with the metalhexacarbonyls of the VI. subgroup and subsequent alkylation by triethyloxonium tetrafluoroborate yields pentacarbonyl-{ethoxy[(tricarbonylchromium)-η6-phenyl]carbene} complexes of chromium, molybdenum, and tungsten (1 - 3). 1 and 3 react with boron trihalides BX3 (X = Cl, Br) by cleavage of the ethoxy group to form trans-tetracarbonylhalogeno[(tricarbonylchromium)-η6-phenylcarbyne]metal complexes 4 - 7. Properties, spectroscopic results, and the X-ray structure analysis of 6 are discussed.
    Notizen: Die Umsetzung von Tricarbonyl(η6-phenyllithium)chrom mit den Metallhexacarbonylen der VI. Nebengruppe und anschließende Alkylierung mittels Triethyloxonium-tetrafluoroborat führt zu Pentacarbonyl{ethoxy[(tricarbonylchrom)-η6-phenyl]carben}-Verbindungen des Chroms, Molybdäns und Wolframs (1 - 3). 1 und 3 reagieren mit den Bortrihalogeniden BX3 (X = Cl, Br) unter Abspaltung der Ethoxygruppe zu den trans-Tetracarbonylhalogeno[(tricarbonylchrom)-η6-phenylcarbin]metall-Komplexen 4 - 7. Eigenschaften und spektroskopische Ergebnisse sowie die Röntgenstrukturanalyse von 6 werden diskutiert.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 77
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 995-1009 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Contributions to the Chlorination - Dehydrochlorination of Perhydro-1,4-thiazepin-5-onesThe synthesis of unsaturated derivatives of perhydro-1,4-thiazepin-5-ones 3 is investigated. Depending on the substitution the thiazepin-5-ones 3 thereby react with sulfuryl chloride to yield 7- and 2-chloro derivatives 6 and 7; the latter eliminate hydrogen chloride only in the presence of a base (PVP, 8) to give the Δ2-thiazepines 9a,b,d,e,g, whereas the 7-chloro derivatives in situ afford the Δ6-thiazepines 10a - f, the 1,4-thiazepinium chloride 11c being isolated as intermediate. tert-Butyl hypochlorite forms according to the substituent size and solvent polarity 2- and 7-halogenation products, as well as 1,4-thiazepin-5-one-S-oxides 22. Further halogenation of the Δ6-1,4-thiazepines 10a - c results in the formation of unsaturated halogen derivatives 24, 25, and 26.
    Notizen: Es wird versucht, ungesättigte Derivate von Perhydro-1,4-thiazepin-5-onen 3 herzustellen. Die Thiazepin-5-one 3 reagieren dabei je nach Substitution mit Sulfurylchlorid zu 7- und 2-Chlorderivaten 6 und 7; letztere eliminieren Chlorwasserstoff erst in Basen-Gegenwart (PVP, 8) zu den Δ2-Thiazepinen 9a,b,d,e,g, die 7-Chlorderivate dagegen in situ zu den Δ6-Thiazepinen 10a - f, wobei das 1,4-Thiazepinium-chlorid 11c in Substanz erhalten wird. tert-Butylhypochlorit ergibt je nach Substituentengröße und Solvenspolarität neben 2- und 7-Halogenierung auch durch Umlagerung 1,4-Thiazepin-5-on-S-oxide 22. Erneute Halogenierung der Δ6-1,4-Thiazepine 10a - c ergibt die ungesättigten Halogenderivate 24, 25 und 26.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 78
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Organic Lewis Acids, 341. Thermal [4π + 2π]-Cycloaddition of Enol Ethers to 1,1-Dicarbonyl Substituted EthenesEnol ethers such as ethyl vinyl ether and 1,1-dimethoxyethene (3f) react thermally, in some instances below 0°C, with cyclic 2-alkylidene-1,3-dicarbonyl compounds such as 1 and 2 to give [4π + 2π]-cycloadducts 4 and 5, respectively (cyclic enol acetals and enol orthoesters), and with 1,1-dicyanoethenes 6 to give [2π + 2π]-cycloadducts 7. On passing from toluene to acetonitrile as the solvent, rates of formation of 4bf from 1b and 3f increase about tenfold and those of 7b from 6b and 3f about sixfold. A discussion of these rates, including rates of related reactions, the relative Lewis acid strengths of 1b and 6b, and the behaviour of 1b/3f towards methanol leads to the conclusion that the degree of concert of the formation of 4bf is below 6.5 kJ · mol-1. - The configurations and conformations of adducts 4 and 5 are discussed.
    Notizen: Enolether wie Ethylvinylether und 1,1-Dimethoxyethen (3f) bilden mit exocyclisch 1,1-dicarbonylsubstituierten Ethenen wie 1 und 2 z.T. schon unterhalb von 0°C thermisch die [4π + 2π]-Addukte 4 bzw. 5 (cyclische Enolacetale und Enolorthoester) und mit den 1,1-Dicyanethenen 6 die [2π + 2π]-Addukte 7. Die Bildungsgeschwindigkeit von 4bf aus 1b und 3f steigt auf etwa das Zehnfache und die von 7b aus 6b und 3f auf etwa das Sechsfache beim Übergang von Toluol auf Acetonitril als Lösungsmittel. Eine Diskussion dieser Bildungsgeschwindigkeiten unter Einbeziehung verwandter Reaktionsgeschwindigkeiten sowie der relativen Lewis-Säurestärken von 1b und 6b und des Verhaltens des Systems 1b/3f gegenüber Methanol führt zum Schluß, daß der energetische Konzertiertheitsgrad der Bildung von 4bf unter 6.5 kJ · mol-1 liegt. Die Konfigurationen und Konformationen der Addukte 4 und 5 werden diskutiert.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 79
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1940-1953 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Charge-Transfer Complexes of Tetrathiafulvalene (TTF) with 1,2,5-Thiadiazolequinones1)The syntheses and the X-ray structure analyses of the charge-transfer complexes of tetrathiafulvalene (TTF) with naphtho[2,3-c][1,2,5]thiadiazole-4,9-dione (1 : 2) (2) and benzol[1,2-c: 4,5-c′]-bis[1,2,5]thiadiazole-4,8-dione (1 : 1) (4) are reported. In their crystal structures both compounds are built up by mixed columnar stacks of donors and acceptors, forming a characteristic packing motive for organic D-A complexes with properties of an electrical insulator.
    Notizen: Es wird über die Synthese und die Einkristallröntgenstrukturanalysen der Charge-Transfer-Komplexe von Tetrathiafulvalen mit Naphtho[2,3-c][1,2,5]thiadiazol-4,9-dion (1 : 2) (2) und Benzo-[1,2-c: 4,5-c′]bis[1,2,5]thiadiazol-4,8-dion (1 : 1) (4) berichtet. Beide Verbindungen weisen in ihrer Kristallstruktur aus Donoren und Acceptoren gemischte kolumnare Stapel auf, ein charakteristisches Packungsmotiv organischer D-A-Komplexe mit elektrischen Isolatoreigenschaften.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 80
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1973-1976 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Generation of Nitrosyl Salts in Dry Organic MediaTrimethylsilyl halides (CH3)3SiX (2a - c, X = Cl, Br, I) are sufficiently electrophilic to cleave, in an equilibrium reaction, alkyl nitrites O = NOR (1a, b, R = i-C5H11, C2H5) with formation of O = NX (3a - c) and (CH3)3SiOR (4a, b). This reaction serves as a convenient in-situ-method to generate nitrosyl compounds NOX in chlorinated hydrocarbons as inert organic media.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 81
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1954-1964 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Iminoboranes from the Thermal Decomposition of DialkylazidoboranesIminoboranes RB = NR (1a - f) are formed by the thermal decomposition of azidoboranes R2BN3 (5a - f) in the gas phase or in solution. At low temperature, the iminoboranes 1b, d, e (R = iPr, iBu, sBu) can be trapped from the gas phase. They are characterized and brought to reaction as isolated species. Without other reactands, the iminoboranes dimerize or trimerize to form the cyclic products 2 or 3, respectively, or polymerize to the wax-like solids 4. Produced in solution below 100 °C, the iminoboranes are azidoborated by the educts 5 to give the (azidoboryl)amines 6 which are transformed into the borazines 3 at 160 - 180 °C. Iminoboranes undergo an ethyloboration with BEt3, a cycloaddition with PhN3, and in the absence of the strongly reactive R2BN3 a concurring cycloaddition and azidosilation with Me3SiN3 with formation of 7 - 10, respectively.
    Notizen: Iminoborane RB = NR (1a - f) entstehen beim thermischen Zerfall von Azidoboranen R2BN3 (5a - f) in der Gasphase oder in Lösung. Die aus der Gasphase abgeschiedenen Produkte 1b, d, e (R = iPr, iBu, sBu) lassen sich bei tiefer Temperatur isolieren, charakterisieren und isoliert umsetzen. Mit sich selbst reagieren die in der Gasphase ergzeugten Iminoborane 1a - f unter Cyclodi-oder -trimerisierung oder unter Polymerisierung zu Produkten von Typ 2, 3 bzw. 4. In Lösung unterhalb 100 °C erzeugt, werden die Iminoborane von den Edukten 5 zu Produkten 6 azidoboriert; diese lassen sich bei 160 - 180 °C in Borazine 3 überführen. Iminoborane erfahren durch BEt3 eine Ethyloborierung zu 7, mit PhN3 eine Cycloaddition zu 8 und mit Me3SiN3 nebeneinander eine Cycloaddition zu 9 und eine Azidosilierung zu 10, sofern nicht das Edukt R2BN3 zugegen ist, das dem Azid Me3SiN3 in der Reaktivität gegenüber 1 überlegen ist.
    Zusätzliches Material: 6 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 82
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1965-1972 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Azodesilylation - a Novel Aprotic Diazotization TechniqueNitrosyl compounds NOA (4a - e, A = Cl, Br, BF4, CF3SO3, I) - generated partially in situ from O = N - OR/(CH3)3SiA (7a, b, R = i-C5H11, C2H5/8a, b, e, A = Cl, Br, I) - react in aprotic organic media with N,N-bissilylated organylamines RN[Si(CH3)3]2 (3b, R = C6H5; 15, R = CH3) under generation of diazonium systems R - N2+ A- and formation of non-nucleophilic hexamethyldisiloxane (6b). This method represents the first nucleophile excluding diazotization technique on the basis of three-coordinated nitrogen and is termed „azodesilylation“.
    Notizen: Nitrosylverbindungen NOA (4a - e, A = Cl, Br, BF4, CF3SO3, I) - teilweise in situ hergestellt aus O = N - OR/(CH3)3SiA (7a, b, R = i-C5H11, C2H5/8a, b, e, A = Cl, Br, I) - reagieren mit N,N-bissilylierten Organylaminen RN[Si(CH3)3]2 (3b, R = C6H5; 15, R = CH3) in aprotischen organischen Medien unter Bildung von Diazonium-Systemen R - N2+ A- und nicht-nucleophilem Hexamethyldisiloxan (6b). Diese Methode repräsentiert die erste, Nucleophile ausschließende Diazotierungstechnik auf der Basis von 3fach koordiniertem Stickstoff und wird als „Azodesilylierung“ bezeichnet.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 83
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1977-1979 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Säurekatalysierte Cyclisierung des En-Produkts aus α-Pinen und PTADAluminiumchlorid-katalysierte Reaktion des En-Produkts 2 aus 4-Phenyl-4H-1,2,4-triazol-3,5-dion (PTAD) und α-Pinen (1), des 1-(6,6-Dimelthyl-2-methylenbicyclo[3.1.1]hept-3-yl)-4-phenyl-1,2,4-triazolidin-3,5-dions, ergab 3,8,8-Trimelthyl-N-phenyl-4,5-diazatricyclo[4.2.1.03,7]nonan-4,5-dicarboxamid (6) in 78% Ausbeute. Auch Bortrifluorid-etherat, trockener Chlorwasserstoff und p-Toluolsulfonsäure katalysieren die Cyclisierung von 2 zu 6, aber nicht in diesem Maße. Der Mechanismus der Cyclisierung wird über eine Gerüstumlagerung der Carbenium-Ionen-Zwischenstufen gedeutet.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 84
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1980-1981 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Chain Lengthening of Tetrafluoro-1,2-ethanedisulfenyl Dichloride by the Reaction with Hydrogen PeroxideThe reaction of the little compound ClSCF2CF2SCl (1) with aqueous H2O2 results in the formation of ClS2CF2CF2SSCF2CF2SO2Cl(2), which is characterized on the basis of 19F NMR, mass, IR, and Raman spectroscopy.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 85
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1982-1986 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Fluorination of Adamantane Derivatives with Oxygen DifluorideFluorination of adamantane and adamantane derivatives 1 with OF2 in the absence of an HF-trap gives fluoroadamantanes 2 and adamantanols 3 in varying amounts. Increasing yields of 2 are obtained in the presence of Na2CO3 as an HF-trap. In addition, the fluorooxahomoadamantanes 4b and e are formed in this reaction. The fluorination of adamantanone (5) with OF2 leads to analogous products.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 86
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1987-1990 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Photoelektronenspektren einiger Reduktionsprodukte von [2.2]ParacyclophanAnhand des He(I)-Photoelektronen(PE)-Spektrums von 2,3′,5,6′-Tetrahydro[2.2]paracyclophan (2) wird gezeigt, daß die Through-Bond-Wechselwirkung zwischen den Sechsringen klein, innerhalb der Cyclohexadienringe aber groß ist. Über die PE-Spektren der weiteren Hydrierungsprodukte 3 und 4 wird berichtet.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 87
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1991-1993 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Syntheses with Cyclobutadienes, 51). 5,5,6,6-Tetracyano-5,6-dihydro-Dewar benzene/3,3,4,4-Tetracyano-3,4-dihydrobenzvalene - a Novel Equilibrating SystemThe cyclobutadiene 3 reacts with tetracyanoethylene to give a 1 : 1-mixture of the dihydro-Dewar benzene 5 and the dihydrobenzvalene 6, which can be separated by crystallisation. In deuteriochloroform solution 5 and 6 are in a 1 : 1 equilibrium.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 88
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 89
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 1415-1421 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Thermolysis of Ansarane, Ansarene and CubaneThe thermolysis and kinetics of decomposition of cubane 4 and of ring enlarged cubanes, the ansaranes 1 - 3, are described. The relief of strain which will be observed breaking specific bonds has been estimated by the aid of force-field calculations thereby disclosing probable reaction pathways. The gas phase pyrolysis of cubane 4 yields vibrationally excited cyclooctatetraene 5 which fragmentates to benzene and acetylene. The gas kinetics of cyclooctatetraene 5 is reported on as well.
    Notizen: Die Thermolyse und Zerfallskinetik ringerweiterter Cubane, der Ansarane 1 - 3, sowie des Cubans 4 selbst, werden beschrieben. Mit Hilfe von Kraftfeldrechnungen wird die Spannungserleichterung beim Bruch bestimmter Bindungen abgeschätzt, und wahrscheinliche Thermolysewege werden aufgezeigt. Das bei der Gasphasenthermolyse von Cuban 4 gebildete schwingungsangeregte Cyclooctatetraen 5 fragmentiert zu Benzol und Acetylen. Über die Gasphasenkinetik von Cyclooctatetraen wird ebenfalls berichtet.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 90
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1755-1764 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Triarylmethyl Systems, III. Synthesis of α-Aryl[1.n]paracyclophanesAs triarylmethyl systems with unusual sterical orientation of the aryl rings α-aryl[1.n]paracyclophanes with n = 5-8 (1a-d, 8a,b) were synthesized via the corresponding dithia[1.(n + 2)]-paracyclophanes (2a-d, 6a,b) and the disulfones (3a-d, 7a,b) derived therefrom. The sterical situation in these α-aryl[1.n]paracyclophanes is discussed, especially on the basis of 1H NMR data.
    Notizen: Als Triarylmethyl-Systeme mit ungewöhnlicher räumlicher Orientierung der Aryl-Ringe wurden α-Aryl[1.n]paracyclophane mit n = 5-8 (1a-d, 8a,b) über die entsprechenden Dithia-[1.(n + 2)]paracyclophane (2a-d, 6a,b) und die davon abgeleiteten Disulfone (3a-d, 7a,b) dargestellt. Die sterischen Verhältnisse dieser α-Aryl[1.n]paracyclophane werden, besonders anhand von 1H-NMR-Spektren, diskutiert.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 91
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Desulfurization Reactions with Iron Carbonyl Compounds: Carbonyl(dioxolanylidene)iron Complexes from ThionocarbonatesDesulfurizations of thionocarbonates 3 with Fe(CO)5 and Fe2(CO)9 yield tetracarbonyl(dioxolanylidene)iron(0) complexes 4 and olefins 2 under thermal conditions. Photochemical conditions lead to 4 and cluster compounds with the formula Fe3(CO)9S(dioxolanylidene) (5). In all reactions Fe3(CO)9S2 (6) was also isolated. The carbene complexes are characterized spectroscopically. An X-ray structure analysis of the tetracarbonyliron carbene complex 4j shows the dioxolanylidene ligand in the axial position of a distorted trigonal bipyramid. (Dioxolanylidene)iron(0) complexes are „ylides with inverse bond polarizations“ (15).
    Notizen: Die Desulfurierung von Thionocarbonaten 3 mit Fe(CO)5 und Fe2(CO)9 gibt je nach Energiequelle unterschiedliche Reaktionsprodukte. Bei der thermischen Reaktion (105°C, Toluol) entstehen Tetracarbonyl(dioxolanyliden)eisen(0)-Komplexe 4 und Olefine 2. Durch Bestrahlung entsteht ebenfalls 4, außerdem werden Clusterverbindungen der Zusammensetzung Fe3(CO)9S(dioxolanyliden) (5) isoliert. Bei allen Reaktionen wird außerdem Fe3(CO)9S2 (6) gebildet. Eine Röntgenstrukturanalyse von 4j zeigte den Dioxolanyliden-Liganden in der axialen Position einer trigonalen Bipyramide. (Dioxolanyliden)eisen(0)-Verbindungen sind „Ylide mit inverser Bindungspolarisation“ (15).
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 92
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1810-1817 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: New Reagents, XX. (Triphenylstannyl)methyllithium and Analogous Trialkylstannyl Compounds, Synthesis and Reactions(Triphenylstannyl)methyllithium (1a) and analogous trialkylstannyl compounds (1b, c) were synthesized by halogen-lithium exchange reactions from 3a-c. As shown by high yields, stannyl groups are capable of stabilizing a carbanionic centre. 1a reacts with aldehydes and ketones to give β-hydroxystannanes 5 which tend to form olefins.
    Notizen: (Triphenylstannyl)methyllithium (1a) sowie analoge Trialkylstannyl-Verbindungen (1b, c) wurden durch Halogen-Lithium-Austausch aus 3a-c synthetisiert. Die erzielten hohen Ausbeuten zeigen, daß Stannylgruppen ein carbanionisches Zentrum stabilisieren. 1a reagiert mit Aldehyden und Ketonen zu β-Hydroxystannanen 5, die zur Olefinbildung neigen.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 93
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1765-1774 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Triarylmethyl Systems, IV. Synthesis and Reactions of α-Hydroxy- and α-Halo-α-aryl[1.n]paracyclophanesBy bromination of hydrocarbons 1a-d and 6 α-bromo-α-aryl[1.n]paracyclophanes with n = 5-8 (2a-d, 7) were prepared. Via 2a-d α-hydroxy-α-aryl[1.n]paracyclophanes 3a-d were obtained, starting from which the α-chloro and α-fluoro derivatives 4a-d and 5a,b, resp., were synthesized. - Compounds of the types 2-5 were of interest as representatives of a special triarylmethyl system for which, due to the [1.n]paracyclophane structure, unusual steric and electronic effects were to be expected. The formation of p,p′-bridged triarylmethyl radicals 8 from 2a-d and their dimerisation were investigated. Rate constants for the hydrolysis of α-bromo and α-chloro compounds 2a-d and 4a-d proceeding via the carbenium ions 9 were determined in water/acetone by conductivity measurements. Stabilities of 9 (n = 5-8), formed from the hydroxy compounds 3a-d in conc. sulfuric acid, were determined; their dependence on n is discussed in terms of specific steric and electronic effects of the α-aryl[1.n]paracyclophane system. Some spectroscopic data are reported for the carbanions 10.
    Notizen: Durch Bromierung der Kohlenwasserstoffe 1a-d und 6 wurden α-Brom-α-aryl[1.n]paracyclophane mit n = 5-8 (2a-d,7) dargestellt. Aus 2a-d erhielt man die α-Hydroxy-Verbindungen 3a-d, von denen aus die α-Chlor- und α-Fluor-Derivate 4a-d bzw. 5a,b zugänglich waren. - Verbindungen des Typs 2-5 interessierten als Vertreter eines besonderen Triarylmethyl-Systems, für das als Folge der [1.n]Paracyclophan-Struktur ungewöhnliche sterische und elektronische Effekte zu erwarten waren. Die Bildung der p,p′-überbrückten Triarylmethyl-Radikale 8 aus 2a-d und ihre Dimerisierung wurden untersucht. Die Geschwindigkeiten der über Carbenium-Ionen 9 verlaufenden Hydrolysen der α-Brom- und α-Chlor-Verbindungen 2a-d bzw. 4a-d in Wasser/Aceton wurden durch Leitfähigkeitsmessungen bestimmt und mit denen der entsprechenden Di- und Triphenylmethyl-Derivate verglichen. Die Stabilitäten der aus den α-Hydroxy-Verbindungen 3a-d in konz. Schwefelsäure erzeugten Carbenium-Ionen 9 mit n = 5-8 wurden ermittelt; ihre Abhängigkeit von n wird unter dem Gesichtspunkt der sterischen und elektronischen Effekte des α-Aryl[1.n]paracyclophan-Systems diskutiert. Einige spektroskopische Daten der Carbanionen 10 werden mitgeteilt.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 94
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1825-1834 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Protophanes and Polyaromatics, XXVI. Synthesis and Properties of Dehydrooligomers of 2-(3-Thienyl)- and 2-(Benzo[b]thien-3-yl)quinoxalineMonolithiated 2-(3-thienyl)- (1a′) and 2-(benzo[b]thien-3-yl)quinoxaline (2a′) react in each case by selfaddition to polyadducts from which polyaromatics can be prepared by hydrolysis and subsequent oxidation. From the reaction mixtures open-chain polyaromatics with 4 to 12 aromatic units (1b-f, 2b-d) were isolated. Starting from 2a′, in addition to open-chain polyaromatics the cyclotetraaromatic 7 has been obtained in low yield.
    Notizen: Monolithiiertes 2-(3-Thienyl)- (1a′) und 2-(Benzo[b]thien-3-yl)chinoxalin (2a′) reagieren jeweils durch Selbstaddition zu Polyaddukten, aus denen durch Hydrolyse und anschließende Oxidation Polyaromaten entstehen. Aus den Reaktionsgemischen konnten offenkettige Polyaromaten mit 4-12 Aromateneinheiten (1b-f, 2b-d) isoliert werden. Aus 2a′ entstand zusätzlich zu den offenkettigen Polyaromaten in geringer Ausbeute der Cyclotetraaromat 7.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 95
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1835-1856 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: The Chemistry of Biquadricyclanylidene Inter- and Intramolecular [π2+σ2+σ2]-Cycloaddition ReactionsThe value of biquadricyclanylidene 6 for the synthesis of polychromophoric frameworks of the type 1-5 through [π2+σ2+σ2]-cycloaddition of bishomodienophilic partners is elucidated. Thus, dimethyl acetylenedicarboxylate, dicyanoacetylene, maleic anhydride, and dimethyl azodicarboxylate are added with very good to good yields (90-50%) exo-specifically and in the case of the bis-adducts with high anti-selectivity. N-Phenyl-1,2,4-triazolinedione, however, attacks the central C=C-double bond of 6 forming a 1:1-adduct considered to be the 1,2,4-triazolium-3-olate 40. With the conversion of 41 into 42 an intramolecular [π2+σ2+σ2]-cycloaddition has been realized for the first time. X-ray structural analyses of tetramethyl anti-9,9′-bi[(1α,2β,5β,6α)-tricyclo[4.2.1.02,5]nona-3,7-dienylidene]-3,3′,4,4′-tetracarboxylate (14a) and its exo-epoxide 23 have been performed.
    Notizen: Die Brauchbarkeit des Biquadricyclanylidens 6 zum Aufbau polychromophorer Gerüste vom Typ 1-5 durch [π2+σ2+σ2]-Cycloaddition von bishomodienophilen Partnern wird untersucht. Acetylendicarbonsäure-dimethylester, Dicyanacetylen, Maleinsäureanhydrid und Azodicarbonsäure-dimethylester werden in diesem Sinn mit sehr guten bis guten Gesamtausbeuten (90-50%) exo-spezifisch, bei zweifacher Addition mit hoher Bevorzugung der anti-Isomeren, addiert. N-Phenyl-1,2,4-triazolindion greift 6 an der zentralen C=C-Doppelbindung unter Ausbildung eines vorläufig als 1,2,4-Triazolium-3-olat 40 angesprochenen 1:1-Adduktes an. Mit der Umwandlung 41 → 42 wird erstmals eine intramolekulare [π2+σ2+σ2]-Thermocycloaddition verwirklicht. Von anti-9,9′-Bi[(1α,2β,5β,6α)-tricyclo[4.2.1.02,5]nona-3,7-dienyliden]-3,3′,4,4′-tetracarbonsäuretetramethylester (14a) und seinem exo-Epoxid 23 wurden Röntgenstrukturanalysen durchgeführt.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 96
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Thermolysis of Tetramethyl anti-9,9′-Bi[(1α,2β,5β,6α)-tricyclo[4.2.1.02,5]nona-3,7-dienylidene]-3,3′,4,4′-tetracarboxylate An Efficient Intramolecular 1,4-Cyclohexanediyl Interception - A Multistep Isomerisation SequenceThe thermolysis of the anti-pentaene-tetraester 1, which is of interest in connection with its photochemistry, is examined. At 120°C 1 undergoes a uniform isomerisation with participation of four bonds to the octacycle 4. From the behaviour of several model compounds (2, 10-14) it is concluded that the transformation 1 → 4 begins with the 1,6-bridging between one of the orthogonal 1,5-diene segments and proceeds via a cascade of stabilised diradicals (5-7). This implies a quantitative, intramolecular interception of the 1,4-diyl intermediate (5) of the Cope reaction. Starting from 4 four additional, consecutively formed hepta- and hexacyclic isomerisation products (21 and 24-26) are isolated between 160 and 210°C. An x-ray structural analysis confirms the structure of 24.
    Notizen: Die im Zusammenhang mit der Photochemie interessierende Thermolyse des anti-Pentaen-tetraesters 1 wird untersucht. 1 geht bei 120°C unter Beteiligung von vier Bindungen einheitlich in den isomeren Octacyclus 4 über. Aus dem Verhalten mehrerer Modellverbindungen (2, 10-14) wird geschlossen, daß die Umwandlung 1 → 4 mit der 1,6-Überbrückung in einem der orthogonalen 1,5-Diensegmente eingesetzt und über eine Kaskade stabilisierter Diradikale (5-7) abläuft. Damit ist impliziert, daß die 1,4-Diyl-Vorstufe der Cope-Reaktion (5) quantitativ intramolekular abgefangen wird. Ausgehend von 4 werden zwischen 160 und 210°C mit 21 und 24-26 vier weitere konsekutiv gebildete hepta- bzw. hexacyclische Isomerisierungsprodukte isoliert. Davon ist die Struktur 24 durch Röntgenstrukturanalyse bewiesen.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 97
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2125-2134 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Polycyclic Compounds, XXI. Synthesis of Isomeric Benz[c]azepine Derivatives by 1,3-Transposition of the Nitrogen Function in the Seven-membered Ring SystemThe easily available oxanorbornadienes 1a and 1b are converted to various isomeric benz[c]azepine derivatives. The change of the position of the acetylated nitrogen in the seven-membered ring relative to the methoxycarbonyl groups in the six-membered ring by the reaction sequence 1 → 4 → 5 can be considered as a 1,3-transposition of the nitrogen function.
    Notizen: Die leicht zugänglichen Oxanorbornadiene 1a und 1b können zu verschiedenen isomeren Benz[c]azepin-Derivaten abgewandelt werden. Die Änderung der Stellung des acetylierten Stickstoffs im Siebenring relative zu den Methoxycarbonylgruppen im Sechsring durch die Reaktionsfolge 1 → 4 → 5 kann als 1,3-Transposition der Stickstoff-Funktion aufgefaßt werden.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 98
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2076-2124 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Element-Organic Amine/Imine Compounds, XXIII. Rotamers of Aminophosphanes and AminophosphoranesThe diazaphosphasiletidines 3a-h can be synthesized from R2Si(NCR3Li)2 and Cl2PNR1R2 (1) as well as from (2) and MNR1R2 (R = CH3). At ambient temperature they show hindered rotation about the P—NR1R2 bond. 3g is separated as a pair of E/Z-rotamers, whose structure has been elucidated by NMR and X-ray analyses. The kinetically measured P—N rotation barriers (ΔG± ≍ 30 kcal · mol-1) are until now the highest that have been measured. The isomerization of 3g(E) → 3g(Z) (P—N) rotation, P inversion, or both) is a P—N rotation which has been established by the synthesis and the NMR spectroscopically measured rearrangement of (3i) (R = CH3, four isomers). The interaction of 3a-h with sulfur, selenium, and methyl iodide gives 4-6a-h. Below 0°C they all show hindered rotation about the P - NR1R2 bond. 4 and 5 are suitable for the study of the structure dependence of 1H NMR ASIS effects. The oxidation of 3g(E/Z) to the isomers 4g-6g(E/Z) occurs with retention of configuration. These compounds show significant differences with respect to their thermal stability and their reaction with methanol. The comparison of the ΔG± values of the P—N rotation barriers of 3-6 shows that the steric influence of the exo-amino substituents R1 and R2 is most important. The E/Z equilibrium of the unsymmetrically substituted compounds gives evidence that the two ground states of P—;N rotation are mostly influenced sterically, possible also electronically.
    Notizen: Die Diazaphosphasiletidine 3a-h lassen sich aus R2Si(NCR3Li)2 und Cl2PNR1R2 (1) sowie aus (2) und MNR1R2 (R = CH3) darstellen. Sie weisen bei Raumtemperatur eine Rotationsbehinderung um die P—NR1R2-Bindung auf; 3g wird als E/Z-Rotamerenpaar getrennt und durch NMR- und Röntgenstrukturanalyse charakterisiert. Seine kinetisch ermittelten P—N-Rotationsbarrieren (ΔG± = ca. 30 kcal · mol-1) sind die bislang höchsten bestimmten Werte. Die Umlagerung von 3g(E) → 3g(Z) (P—N-Rotation, P-Inversion oder beides) ist eine P—N-Rotation, was durch Synthese und NMR-spektroskopische Verfolgung der Umlagerung des Isomerengemisches (3i) (R = CH3, vier Isomere) bewiesen wurde. Die Umsetzung von 3a-h mit Schwefel, Selen und Methyliodid ergibt 4-6a-h, die alle unterhalb 0°C eine Rotationsbehinderung um die P—NR1R2-Bindung aufweisen. 4 und 5 sind für das Studium der Strukturabhängigkeit von 1H-NMR-ASIS-Effekten geeignet. Die unter Konfigurationserhalt ablaufende Oxidation von 3g(E/Z) ergibt die Isomerenpaare 4g-6g(E/Z), die bemerkenswerte Unterschiede in bezug auf ihre Methanolyse- bzw. thermische Stabilität aufweisen. Der Vergleich der ΔG±-Werte für die P—N-Rotationsbarriere bei 3-6 zeigt, daß hier vorrangig der sterische Einfluß der exoständigen Aminosubstituenten R1, R2 verantwortlich ist. Aus den E/Z-Gleichgewichtslagen der unsymmetrisch substituierten Verbindungen erkennt man, daß auch die beiden Grundzustände der P—N-Rotation stark sterisch, möglicherweise aber auch elektronisch beeinflußt sind.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 99
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2135-2140 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Fluorination Reactions at 3,4-Dichloro-1,2,5-thiadiazoleFrom the title compound 1 and KF in sulfolane 3-chloro-4-fluoro- (2) and 3,4-difluoro-1,2,5-thiadiazole (3) are obtained. In the reaction with oxidizing fluorinating agents, e. g. XeF2, BrF3, or AgF2, 2 is the primary product. Cleavage of the ring system at one of the S=N bonds gives the bifunctional ethane derivatives ClNCClCF2NSF2 (5), ClNCFCF2NSF2 (6), Cl2NCF2CF2NSF2 (7), and (=NCF2CF2NSF2)2 (8).
    Notizen: Durch Umsetzung der Titelverbindung 1 mit KF in Sulfolan werden 3-Chlor-4-fluor-(2) und 3,4-Difluor-1,2,5-thiadiazol (3) erhalten. Die Reaktionen mit oxidierenden Fluorierungsmitteln wie XeF2, BrF3 oder AgF2 führen über 2 als Zwischenprodukt zur Spaltung des Ringsystems an einer der S=N-Bindungen. Dabei entstehen die bifunktionellen Ethanderivate CINCCICF2NSF2 (5), ClNCFCF2NSF2 (6), Cl2NCF2CF2NSF2 (7) und (=NCF2CF2NSF2)2 (8).
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 100
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2141-2152 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Cyclic Diazastannylenes, XIII. [SnN2(CH3)2]4 and [SnNCH(CH3)2]4, Molecules with Cubane-like Structures1,3-Di-tert-butyl-2,2-dimethyl-1,3,2,4λ2-diazasilastannetidine (1) reacts in benzene with N,N-dimethylhydrazine spontanously and with isopropylamine after warming shortly to yield N,N′-di-tert-butyl-Si,Si-dimethylsilazane (2) and the tetrameric molecules (SnN2Me2)4 (5) and (SnNCHMe2)4 (6). An X-ray structure determination (R = 0.026) proves 5 to be built of a very distorted Sn4N4-cube, the nitrogen atoms being attached to dimethylamino groups. In the crystal the molecules are linked together by Sn—Sn contacts (351 pm) forming a zick-zack band, which runs in the direction of the hexagonal axis. Typical Sn—N bond lengths are found to be 220.9 and 225.1 pm, while the mean N—N distance is 146.2 pm. When heated or by contact with oxygen the crystals of 5 decompose vehemently: the products are found to be β-tin, molecular nitrogen, and varying amounts of methane, ethane, and dimethylamine (by contact with oxygen small amounts of tin(II)-oxide are formed as well).
    Notizen: 1,3-Di-tert-butyl-2,2-dimethyl-1,3,2,4λ2-diazasilastannetidin (1) reagiert in Benzol mit N,N-Dimethylhydrazin spontan und mit Isopropylamin nach kurzem Erwärmen zu N,N′-Di-tert-butyl-Si,Si-dimethylsilazan (2) und den Tetrameren (SnN2Me2)4 (5) und (SnNCHMe2)4 (6). Eine Röntgenstrukturbestimmung (R = 0.026) zeigt, daß 5 einen stark verzerrten Sn4N4-Kubus besitzt, an dessen Stickstoffatome Dimethylaminogruppen gebunden sind. Im Kristall sind die Moleküle über Sn—Sn-Kontakte (351 pm) zu einem Zickzack-Band verknüpft, das in Richtung der hexagonalen Achse verläuft. Typische Sn—N-Bindungslängen liegen bei 220.9 und 225.1 pm, während für N—N 146.2 pm ermittelt werden. Beim Erhitzen sowie bei Sauerstoffzufuhr zersetzen sich die Kristalle von 5 heftig: als Produkte erhält man β-Zinn, molekularen Stickstoff und in wechselnden Mengen Methan, Ethan und Dimethylamin (bei Sauerstoffeinwirkung auch geringe Mengen an Zinn(II)-oxid).
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...