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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 364-366 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2259-2266 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Allyl vinyl ether can be polymerized to highly isotactic polymer with SbCl5 in toluene at ca. -10°C. The stereospecificity is not significantly lower than that of polymer made at ca. -75°C; The reproducibility of the process is greatly improved at the higher temperature. BF3.O(C2H5)2 proved to be an ineffective initiator, in contrast with literature data. NMR analysis, previously published for diads only from NMR data, was performed (1H and 13C) for triads as well, and partly for hexads. No evidence for stereocontrol other than the relationship between active chain end HC⊕OAllyl and incoming monomer can be inferred1cf. Part 2 of this series10.. A simple mechanism, featuring association between incoming monomer and counterion, invoking only steric hindrance is proposed as an explanation of these findings.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2385-2393 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stereoregularity of poly(allyl vinyl ether), (poly[1-(allyloxy)ethylene], 1) was studied by both 1H- and 13C NMR-spectroscopy at 6,34 tesla. Even at this field the 1H NMR-resonances severely overlap, thus hampering a reliable analysis. The situation is far better for the 13C NMR-resonances; here even hexad splittings could be observed. Relaxation time ratios of the backbone carbon atoms are consistent with a dipolar relaxation mechanism. The relaxation time for the racemic peak is longer than that for the meso peaks, which is in contrast with literature data for other polymers7,8. This deviating behaviour could be accounted for by the higher magnetic field used in our measurements.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 877-881 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Segmented block copolymers consisting of nylon 6 and polyoxypropylene blocks were prepared and characterized. Pronounced phase separation in the solid phase was deduced from differential calorimetry and from small-angle X-ray scattering, as well as from dynamic mechanical measurements. The morphology (from X-ray diffraction) and anisotropy in mechanical properties strongly suggest phase separation in the melt (which is optically clear). Elastomerlike properties are described and discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 3523-3529 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Carboxymethyl cellulose grafted with dextrin (CMC-g-dextrin) products are easily accessible by reacting freshly prepared CMC with the acid alcoholysis product from starch and glycerol monochlorohydrin. The success of the grafting reaction depends on adjusting the alkalinity of the grafting reaction mass prior to addition of the dextrin chlorohydrin reagent. In all, less NaOH should be applied than theoretically necessary for all chlorine substitution. In some cases the products show interesting rheology at very low shear, but rather CMC-like rheology or more Newtonian behavior than CMC at shearing rates over a few reciprocal seconds. These results reinforce the credibility of the view that natural polysaccharide gums with unusual rheologies derive their special properties from their well-defined substitution pattern rather than from their overall degree of substitution with (oligo)saccharide units.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Publication Date: 1989-01-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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