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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 1279-1285 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of β-pinene with styrene oxide (SO) and β-pinene with N-vinylpyrrolidone (VP) was investigated by using SnCl4 in dichloromethane diluent at low temperature. Monomer reactivity ratios were evaluated for both copolymers at -80°C; these are r1(SO) = 2.979 and r2(β-pinene) = 0.002 and r1(VP) = 0.096 and r2(β-pinene) = 0.294.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 2399-2413 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A spectroscopic and conductimetric study of the cationic polymerization of 2-vinylfuran (1) and 2-methyl-5-venylfuran (2) showed the existence of an important side reaction originating from a hydride-ion shift from an unsaturated polymer molecule to an active species. The resulting allylic carbocation, in equilibrium with a doubly unsaturated polymer molecule, can react further and the repetition of the mechanism on progressively more conjugated species leads to the formation of a series of highly charge-delocalized carbenium ions absorbing throughout the visible region of the spectrum (and giving high electrical conductivity) and of neutral polyconjugated polymer molecules. Since the hydride-ion abstraction occurs from the tertiary carbon atom of the vinylic chain, vinylidene polymers of monomers such as 2-isopropenylfuran (3) and 2-isopropenyl-5-methylfuran (4) are not susceptible to it. Indeed, their cationic polymerization proceeds without colour formation and conductivity increase.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1717-1732 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This article is part of the general project laid out in Part I (ref. 9) and is concerned with obtaining information on primary (unthickened) crystals of polyethylene formed at low supercoolings. For this, a technique had to be devised by which crystallization could be speeded up so as to eliminate or at least reduce lamellar thickening. Indeed we were able to increase the rate of crystallization by an order of magnitude using a technique which we have called enhanced self-nucleation. Using this technique we find that when viewed under an optical microscope, spherulites crystallize uniformly over the field of view, and not, as is usual, by a radial growth process. Isothermal crystallization in bulk linear polyethylene has been studied by means of the enhanced self-nucleation technique as a function of crystallization time by using Raman LAM and melting points to assess variations of fold length Data have been obtained at very much shorter times than before. At short times, we find a constant fold length; at longer times the crystals thicken linearly with the logarithm of time. Values of the initial fold length for crystallization temperatures between 118 and 130°C are presented. Associated with the thickening at short times we find an induction time which increases with temperature.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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