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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 2529-2534 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The proton NMR line shapes of the anhydrous alkali metal hydroxides at 27 and 200 MHz are presented. The structure in the proton resonances of NaOH, KOH, and RbOH is explained using a four-spin planar zig–zag chain model calculation. Second moment calculations show that the observed line shapes are consistent with known crystal structures. The crystal structures of KOH and RbOH, as determined by x-ray powder diffraction, are confirmed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1383-1392 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homogeneous copolymers of ethylene and 1-alkenes have been prepared using an ethyl aluminum sesquichloride-vanadium oxychloride catalyst system. Branches were varied from CH3 to C16H33 by appropriate choice of 1-alkene. Size exclusion studies of copolymers of ethylene-d4 and 1-alkenes show that the comonomer content of a given sample is essentially constant over the whole molecular weight range. A random distribution of branches is inferred from the simplicity of the 13C-NMR spectra and from the melting behaviour of the copolymers. Comonomer contents varying from 1 mol% to 15 mol% were readily determined by 13C-NMR spectroscopy. The copolymers can be used to study the separate effects of branch length, branch frequency, and molecular weight on physical properties including melting point and crystallinity.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2447-2458 
    ISSN: 0887-6266
    Keywords: side-chain crystallization ; ethylene copolymers ; 13C NMR ; x-ray diffraction ; solid state NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase structure of random copolymers of ethylene and ethylene-d4 with 1-octadecene and other 1-alkenes has been investigated. CPMAS 13C NMR spectra show that a fraction of the central sections of C16H33 side chains in ethylene-d4 copolymers are in ordered environments at 298 K. They give rise to resonances from 32.9 ppm to 33.8 ppm, which show that they are in trans conformations; T1C values for this group of resonances range from 1 s to 7 s. The remaining side chains are in an amorphous environment, the internal methylenes having a chemical shift of 30.8 ppm and a T1C close to 0.4 s. A Raman band at 1062 cm-1 in the spectrum of an ethylene-d4-1-octadecene copolymer is consistent with partial crystallization of side chains. Some side-chain crystallization also occurs in a 1-tetradecene copolymer. X-ray diffraction studies suggest that smaller side chains do not crystallize to a significant extent at 298 K. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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