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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 215-221 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dependence of the molecular dimension of polypeptides in helicogenic solvents on molecular weight was calculated by using the Zimm-Bragg-Nagai theory in collaboration with the broken-rod model, in which the excluded volume effect was taken into account by setting the equivalent chain to be a nonintersecting chain. Our calculated results for PBLG in helicogenic solvents were compared with experiment with good agreement. The flexibility of the helices of PCBL and PELG as broken rods corresponded to that of PBLG without excluded volume effect (i.e., the broken rod of a self-intersecting chain) in a comparison of their experimental data with our calculated results for PBLG of self-intersecting and nonintersecting chains. Over a wide range of molecular weights M our theory explains the dependence of the length per monomeric residue h on M, even for short chains in which h 〉 1.5 Å.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1119-1124 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For calculating the ratio of the intrinsic viscosities of branched and linear polymers of the same molecular weight, [η]B/[η]L, a new theory taking into account the excluded volume effect is presented. By using the modified Flory equation, the excluded volume effect of branched polymers is predicted with the aid of the first-order perturbation theory. The linear expansion factor αs is converted to the hydrodynamic expansion factor αη by using the Kurata-Yamakawa theory. Our calculated results, i.e., [η]B/[η]L and 〈s2〉B/〈s2〉L, agree well with experiment for various type branched polymers, i.e., randomly branched and comb-shaped polymers of poly(vinyl acetate).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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