ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (11)
  • Qinling Mountain; Age–elevation-relationship; Thermochronology; Yanshanian orogeny; Tibetan Plateau uplift  (1)
  • 1
    Publication Date: 2021-03-29
    Description: The western sector of the Qinling–Dabie orogenic belt plays a key role in both Late Jurassic to Early Cretaceous “Yanshanian” intracontinental tectonics and Cenozoic lateral escape triggered by India–Asia collision. The Taibai granite in the northern Qinling Mountains is located at the westernmost tip of a Yanshanian granite belt. It consists of multiple intrusions, constrained by new Late Jurassic and Early Cretaceous U–Pb zircon ages (156 ± 3 Ma and 124 ± 1 Ma). Applying various geochronometers (40Ar/39Ar on hornblende, biotite and K-feldspar, apatite fission-track, apatite [U–Th–Sm]/He) along a vertical profile of the Taibai Mountain refines the cooling and exhumation history. The new age constraints record the prolonged pre-Cenozoic intracontinental deformation as well as the cooling history mostly related to India–Asia collision. We detected rapid cooling for the Taibai granite from ca. 800 to 100 °C during Early Cretaceous (ca. 123 to 100 Ma) followed by a period of slow cooling from ca. 100 Ma to ca. 25 Ma, and pulsed exhumation of the low-relief Cretaceous peneplain during Cenozoic times. We interpret the Early Cretaceous rapid cooling and exhumation as a result from activity along the southern sinistral lithospheric scale tear fault of the recently postulated intracontinental subduction of the Archean/Palaeoproterozoic North China Block beneath the Alashan Block. A Late Oligocene to Early Miocene cooling phase might be triggered either by the lateral motion during India–Asia collision and/or the Pacific subduction zone. Late Miocene intensified cooling is ascribed to uplift of the Tibetan Plateau.
    Keywords: Qinling Mountain; Age–elevation-relationship; Thermochronology; Yanshanian orogeny; Tibetan Plateau uplift ; 551
    Language: English
    Type: article , publishedVersion
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 487-504 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatization of Amines with 4-Substitured 7-NitrobenzofurazansElectrophilc derivatives of 4-nitro-benzofurazan with different reactivities were used to synthesize 28 new mono- and disubstituted 4-amino-7-nitrobenzofurazans 2b, 2d, 2f-2i, 2l, 2m-2n, 3b-3f, 3h-3j, 4e-4d, 4f-4k, 4m, 4o-4p. A reaction mechanism is proposed on the basis of the differences of the reactivities and a preliminary kinetic examination. The acid character of the N—H-function in monosubstituted compounds is demonstrated by means of spectroscopical investigation of pKa-values.Data from i.r., u. v./vis, and fluorescence studies are offered.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 385-400 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical Reduction of 4-Substituted 7-Nitro-benzo-furazansThe electrochemical properties of 4-methoxy-, hydroxy-, alkylamino, and arylaminosubstituted 7-nitrobenzofurazans (1a-1h) are studied between pH 1,7 and 11,6 by use of buffer solutions containing different portions of various organic solvents. Reduction waves which are present in polarograms, are well reproducible and practicable for qualitative and quantitative analysis of amines. A mechanism of reduction is suggested by reason of polarographic and coulometric results. The half wave potentials are correlated with various substituent constants. A value of ϱ = + 0,32 follows from the determination of the reaction constant from the slope of the E 1/2 - σp - relation for the polarographic reduction of each nitro-function.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 261-274 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: UV-VIS- and IR-Spectroscopic Studies with N-Substituted 4-Amino-7-nitro-benzofurazansStarting from spectra of parent substance benzofurazan the influence of different functional groups (NO2, OH, NH2, NHAlk, NAlk2, NHAr, NArAlk) in 4- and (or) 7-position on the shape of spectra and the intensity of individual bands was examinated. It was tried to assign spectral bands to defined absorptions in the u.v./vis and i.r. range. The long-wave band in the solution-VIS-spectra of N-substituted 4-amino-7-nitrobenzofurazans was identified as a charge-transfer band. By the use of constants α, β, and π* by Kamlet and Taft the influence of different properties of solvents was correlated with band shifts in the UV/VIS range. A qualitative correlation was found between \documentclass{article}\pagestyle{empty}\begin{document}$ \bar \nu _{{\rm max}} $\end{document} of the long-wave band in the VIS-spectra, the polarographic half wave potential E 1/2 and the sum of polar substituent constants Σσ* of Taft. These proportions were plotted in a three-dimensional diagram.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 318 (1976), S. 635-642 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Electrochemical Behaviour of Asymmetrically Bridged DiquinonesRedox potentials and pK-values of tetravalent asymmetrically bridged diquinones, quinhydrones, and hydroquinones are described and the influences of substituents on these characteristics are discussed.
    Notes: Es werden Redoxpotentiale und pK-Werte von tetravalenten, unsymmetrisch verbrückten Dichinonen, Chinhydronen und Hydrochinonen beschrieben und Substituenten-einflüsse auf diese Eigenschaften diskutiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 745-754 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Intramolecular Quinhydrones. II. Synthesis and Oxidation Characteristics of Unsymmetrically Bridged DihydroquinonesBy ether cleavage with AlCl3 or AlBr3 the synthesized unsymmetrically bridged tetramethoxy derivatives 2a-w were converted into the corresponding tetravalent hydroquinones 3a-r and these were oxidized to the yellow diquinones 4a-p or partially to the deeply coloured intramolecular quinhydrones 6a-o.
    Notes: Die synthetisierten unsymmetrisch verbrückten Tetramethoxyderivate 2a-w wurden durch Ätherspaltung mit AICl3 oder AlBr3 in die entsprechenden tetravalenten Hydrochinone 3a-r übergeführt und diese zu den gelben Dichinonen 4a-P oder partiell zu den tieffarbigen intramolekularen Chinhydronen 6a-o oxidiert.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 1015-1020 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Intramolecular Quinhydrones. III. Colour and Charge-transfer InteractionsThe intensive colour of the crystalline intramolecular quinhydrones 2a-o depends on the substitution and the unsymmetrical bridge-structure. The solutions are yellow coloured. According to the x-ray, i.r.- and u.v./vis-results there are for 2a-o inter, but no intramolecular CT-complexes.
    Notes: Die intensive Farbe der kristallinen intramolekularen Chinhydrone 2a-o hängt von der Kernsubstition und der unsymmetrischen Brückenstruktur ab. Lösungen sind nur gelb gefärbt. Nach den Ergebnissen röntgenkristallographischer, IR- und UV/VIS-spektroskopischer Untersuchungen bilden 2a-o inter-, aber keine intramolekularen CT-Komplexe.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 299-310 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential scanning calorimetry (DSC) and in situ small-angle x-ray scattering (SAXS) indicate that in an α ω-methoxy-poly(ethylene oxide) (MPEO) fraction (MW 3000) a transient nonintegral folding (NIF) crystal initially forms during crystallization throughout a wide range of crystallization temperatures. Subsequent transformations of the NIF to IF (integral folding) crystals at low temperatures occur mainly through isothermal thickening or thinning via perfection processes or, at higher temperatures, through primary crystal formation. The NIF crystal is thermodynamically the least stable state among the crystal forms, but its growth is the most rapid. The overall crystallization and crystal melting of this MPEO fraction reveal that the NIF crystal and the NIF → IF crystal transformations are common to low-molecular mass PEO fractions without regard to the end group. Nevertheless, diffusion coefficient and viscosity measurements provide clear evidence of an end-group effect in PEO and MPEO fractions. The difference in the overall crystallization and isothermal thickening and thinning kinetics of low-molecular mass PEO and MPEO fractions can lead to further understanding of end-group effects.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1877-1894 
    ISSN: 0887-6266
    Keywords: liquid crystals ; crystallization metastable phases ; rates of phase transformation ; morphology ; competition between phases ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of the monotropic liquid crystal forming polyether, poly-n-nonyl-4 4′-biphenyl-2-chloroethane, was investigated using DSC calorimetry and polarizing optical microscopy. The principal theme was the nature of crystallization from the nematic liquid crystalline state, which in the monotropic system could be directly compared with the more familiar crystallization from the isotropic melt using one and the same compound. Novel, polarizing optical structures were observed that combine features of both the usual LCPs (fine “grains”) and those of the conventional crystallizeable polymers (spherulites) with differing degrees of prominence of each according to crystallization conditions. The considerations of such structural observations, combined with the calorimetric results and the newly gained information on the kinetics of the crystallization process, reveal an acceleration of the overall crystallization rate at the stage where liquid crystal formation sets in as assessed by calorimetry but not as registered with the polarizing microscope, leading to wider issues regarding the conception of “amorphous crystalline ratio” and its extension to the liquid crystal state. Beyond polymers, the new findings lead to the more general considerations on metastable phases, specifically to their emergence and competition with the phases of ultimate stability. In this respect the present study on a monotropic LCP provides an illustrative example of a more general treatment presented previously. © 1995 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1941-1950 
    ISSN: 0887-6266
    Keywords: rigid-rod polymer ; cation ; dialysis ; molecular weight ; cast ; aggregated ; isotropic ; anisotropic ; film ; depletion measurement ; ionic conductivity ; x-ray scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[(1,7-dihydrobenzo[1,2-d:4,5-d′] diimidazole-2,6-diyl)-2-(2-sulfo)-p-phenylene], a conjugated rigid-rod polymer, was derivatized with pendants of propane-sulfonated ionomers. The derivatized rigid-rod polymer was soluble in aprotic solvents as well as in water for isotropic solutions that were processed into isotropic films. Direct-current electrical conductivity σ of the films was measured using the four-probe technique. Room-temperature σ as high as 2.9 × 10-4S/cm was achieved on pristine isotropic films without using dopants. When the rigid-rod polymer concentration exceeded 25 wt %, the isotropic solution could be transformed into a liquid-crystalline solution that allowed deformations to be applied to produce anisotropic films. Significant increase in σ was obtained in a sheared film along both the parallel direction (∥) and the transverse direction (⊥) with a σ∥/σ⊥ = 5. Additionally, enhanced σ was realized in films heat-treated at about 100°C, in the derivatized polymer with higher molecular weight from dialysis, and in substituting the sulfonated ion Na+ by H+ in the pendants of the polymers. Constant-voltage measurements were applied to the polymers to monitor the σ stability for ascertaining the nature of the conductivity. No electronic contribution in σ was detected. Instead, a monotonically decreasing σ was consistently observed indicative of ionic conductivity. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...