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  • Polymer and Materials Science  (8)
  • 159-959; Accumulation rate, mass; AGE; Biozone; COMPCORE; Composite Core; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Epoch; Gulf of Guinea; Joides Resolution; Leg159; Lithologic unit/sequence; Lithology/composition/facies; Ocean Drilling Program; ODP; Reference/source; Sample code/label; Sedimentation rate  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 493-500 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this article we describe the preparation of poly[2,3,9,10,16,17,23,24-octakis(dodecyloxycarbonyl)phthalocyaninatogermoxane] by thermal polycondensation of 2,3,9,10,16,17,23,24-octakis(dodecyloxycarbonyl)phthalocyaninatogermanium dihydroxide, and its characterization. The average molar mass of the resulting polymer was determined. High molar masses are assessible, e.g., M̄w = 360000 g/mol, M̄n = 140000 g/mol, at moderate temperature for the polycondensation (200°C). The polymer shows a liquid-crystalline phase in an extremely large temperature range. Furthermore, Langmuir-Blodgett films (LB films) of the polymer and of the monomer were prepared and characterized. In LB films the phthalocyanine rings are preferentially oriented normal to the dipping direction.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An improved procedure for the anionic polymerization of hexamethylcyclotrisiloxane (D3) initiated by a monofunctional lithium derivative is reported. The initiator seeding solution is preferably prepared in benzene, and tetrahydrofuran is used as a cosolvent which makes the presence of additional promoters useless. The main advantage of this procedure is that it delays the appearance of bimodality which is believed to result from a sudden change in aggregate molecularity during the course of the reaction. Applying this method, poly(dimethylsiloxane) samples having a single functional endgroup and possessing high molecular weights and narrow molecular weight distributions (1,03 ≤ M̄w/M̄n ≤ 1,06) were prepared on the 100 g scale.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1119-1124 
    ISSN: 0887-624X
    Keywords: poly(vinyl alcohol) ; silylation ; hexamethyldisilazane ; liquid ammonia ; kinetics ; properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Silylation of poly(vinyl alcohol) has been performed with hexamethyldisilazane in liquid ammonia in an autoclave. This novel procedure has the advantage that the educt, the reagent, and the product are soluble in ammonia, which works under homogeneous conditions. No salt like by-products are formed and no tedious purification of the product is necessary. The degree of silylation has been adjusted through the ratio of silylating agent to hydroxy groups. Random incorporation of trimethylsilyl groups was proven by the linear dependence of the glass transition temperature from the degree of silylation and the solubility of the partially silylated material. Quantitative investigation of the silylation reaction showed first-order kinetics for the initial and final stages of the reaction indicative of a reaction where k1 〉 k2 〉 k3. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 12 (1973), S. 201-221 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Theoretical calculations of the circular dichroism of double-helical DNA and RNA by the method of Johnson and Tinoco were performed in order to investigate the origins of the optical activity spectral differences between these polynucleotides. Calculations were performed using transition moment directions arising from molecular orbital calculations as well as a transition moment directions in agreement with experimental directions. The results of these calculations indicate that the conservative circular dichroism spectrum of B-form DNA and the nonconservative spectrum of RNA (and A-form DNA) arise as a consequence of the distance between the paired bases and the helix axis. The negative nonconservative spectrum of C-form DNA was calculated and shown also to result from the distance of the paired bases from the helix axis. Several other conspicuous geometric parameters of DNA and RNA were investigated and were found to be less significant in their effects upon the spectral differences. Theoretical calculations on a four-stranded DNA model which has paired bases similarly related to the helix axis as RNA and A-form DNA was found to yield a low intensity, nonconservative circular dichroism spectrum.
    Additional Material: 12 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 977-986 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Theoretical calculations of the near ultraviolet (uv) circular dichroism of double-helical DNA and RNA models were performed in order to evaluate the effects, on the calculated circular dichroism, of including the interactions of near uv quantum transitions of the nucleic acid bases with classical polarizable bonds of the sugar-phosphate backbone. Double-helical models (A-form, B-form, and C-form DNA and RNA-11) from X-ray diffraction data were used in the calculations. The results indicate that the contributions to the circular dichroism in the near uv region, of these types of interactions, provide calculated spectra that are slightly altered from calculated spectra when only base-base transition interactions were considered.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 573-582 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies are described which strongly support a cholesteric liquid crystal-like quaternary structure for the DNA molecules of a biologically native chromosomal preparation from equine sperm cells. Discrete chromosomal fibers released from the head pieces of equine spermatozoon cells were prepared intact and probed for liquid crystalline ordering using reflectance and linear dichroism spectroscopy. Assuming cholesteric liquid crystalline order for the DNA molecules within the chromatin fibers, parameters measured experimentally were used to calculate the circular dichroism (CD) of the fibers. The calculated results compare remarkably well with the experimentally measured CD of the sperm chromosomal fibers and suggest a specific cholesteric liquid crystal-like quanternary structural ordering of DNA molecules in equine sperm chromatin fibers. The potential of CD spectroscopy as a tool for the study of long-range ordering of macromolecules is discussed.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 515-522 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Silylation of cellulose and some low-molecular-weight hydroxy compounds (1,2-propanediol, D-glucose, methyl α-D-glucoside, sucrose and β-cyclodextrin) has been performed with hexamethyldisilazane (HMDS) in liquid ammonia at elevated temperature in an autoclave. No salt-like by-products are formed and no tedious purification of the products is necessary. As indicated by size-exclusion chromatography the silylation of cellulose with HMDS/NH3 proceeds without degradation of the polymer chain. The degree of silylation of the trimethylsilylcellulose obtained is higher than with other silylation procedures reported in the literature. The temperature/composition diagram of HMDS/NH3 proved complete miscibility above 24°C.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 3463-3471 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acylation of (partially) silylated poly(vinyl alcohol) with acyl chlorides and anhydrides was investigated under different conditions. In the presence of an acid acceptor (triethylamine) at temperatures below 50°C selective acylation of hydroxy groups was observed in agreement with literature data. At elevated temperature (160°C) without the use of an acid acceptor hydroxy and trimethylsiloxy groups react in an unselective manner. In addition, significant amounts of chlorine were found in the resulting polymers under these conditions, though no double bonds were detected. A polymer analogous reaction without incorporated chlorine was achieved with benzoic anhydride as acylating agent. Random distribution of chlorine and benzoyloxy groups most likely is obtained.
    Additional Material: 4 Ill.
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  • 9
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    PANGAEA
    In:  Supplement to: Wagner, Thomas (2002): Late Cretaceous to early Quaternary organic sedimentation in the eastern Equatorial Atlantic. Palaeogeography, Palaeoclimatology, Palaeoecology, 179(1-2), 113-147, https://doi.org/10.1016/S0031-0182(01)00415-1
    Publication Date: 2024-02-02
    Description: Reconstructing the long-term evolution of organic sedimentation in the eastern Equatorial Atlantic (ODP Leg 159) provides information about the history of the climate/ocean system, sediment accumulation, and deposition of hydrocarbon-prone rocks. The recovery of a continuous, 1200 m long sequence at ODP Site 959 covering sediments from Albian (?) to the present day (about 120 Ma) makes this position a key location to study these aspects in a tropical oceanic setting. New high resolution carbon and pyrolysis records identify three main periods of enhanced organic carbon accumulation in the eastern tropical Atlantic, i.e. the late Cretaceous, the Eocene-Oligocene, and the Pliocene-Pleistocene. Formation of Upper Cretaceous black shales off West Africa was closely related to the tectonosedimentary evolution of the semi-isolated Deep Ivorian Basin north of the Côte d'Ivoire-Ghana Transform Margin. Their deposition was confined to certain intervals of the last two Cretaceous anoxic events, the early Turonian OAE2 and the Coniacian-Santonian OAE3. Organic geochemical characteristics of laminated Coniacian-Santonian shales reveal peak organic carbon concentrations of up to 17% and kerogen type I/II organic matter, which qualify them as excellent hydrocarbon source rocks, similar to those reported from other marginal and deep sea basins. A middle to late Eocene high productivity period occurred off equatorial West Africa. Porcellanites deposited during that interval show enhanced total organic carbon (TOC) accumulation and a good hydrocarbon potential associated with oil-prone kerogen. Deposition of these TOC-rich beds was likely related to a reversal in the deep-water circulation in the adjacent Sierra Leone Basin. Accordingly, outflow of old deep waters of Southern Ocean origin from the Sierra Leone Basin into the northern Gulf of Guinea favored upwelling of nutrient-enriched waters and simultaneously enhanced the preservation potential of sedimentary organic matter along the West African continental margin. A pronounced cyclicity in the carbon record of Oligocene-lower Miocene diatomite-chalk interbeds indicates orbital forcing of paleoceanographic conditions in the eastern Equatorial Atlantic since the Oligocene-Miocene transition. A similar control may date back to the early Oligocene but has to be confirmed by further studies. Latest Miocene-early Pliocene organic carbon deposition was closely linked to the evolution of the African trade winds, continental upwelling in the eastern Equatorial Atlantic, ocean chemistry and eustatic sea level fluctuations. Reduction in carbonate carbon preservation associated with enhanced carbon dissolution is recorded in the uppermost Miocene (5.82-5.2 Ma) section and suggests that the latest Miocene carbon record of Site 959 documents the influence of corrosive deep waters which formed in response to the Messinian Salinity Crisis. Furthermore, sea level-related displacement of higher productive areas towards the West African shelf edge is indicated at 5.65, 5.6, 5.55, 5.2, 4.8 Ma. In view of humid conditions in tropical Africa and a strong West African monsoonal system around the Miocene-Pliocene transition, the onset of pronounced TOC cycles at about 5.6 Ma marks the first establishment of upwelling cycles in the northern Gulf of Guinea. An amplification in organic carbon deposition at 3.3 Ma and 2.45 Ma links organic sedimentation in the tropical eastern Equatorial Atlantic to the main steps of northern hemisphere glaciation and testifies to the late Pliocene transition from humid to arid conditions in central and western African climate. Aridification of central Africa around 2.8 Ma is not clearly recorded at Site 959. However, decreased and highly fluctuating carbonate carbon concentrations are observed from 2.85 Ma on that may relate to enhanced terrigenous (eolian) dilution from Africa.
    Keywords: 159-959; Accumulation rate, mass; AGE; Biozone; COMPCORE; Composite Core; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Epoch; Gulf of Guinea; Joides Resolution; Leg159; Lithologic unit/sequence; Lithology/composition/facies; Ocean Drilling Program; ODP; Reference/source; Sample code/label; Sedimentation rate
    Type: Dataset
    Format: text/tab-separated-values, 478 data points
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