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  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The formation of a charge-transfer complex between 1-vinylindole (1a) and maleic anhydride (MA) was detected by 1H NMR analysis, and the corresponding Keq was measured (Keq=0,251 mol in CDCl3 at 25°C). It could be shown that this complex can be involved both in the initiation and propagation steps of the 1a-MA copolymerization by carrying out spontaneous copolymerization experiments and studying the influence of the feed composition on the conversion and [η] of the copolymer. The structure of the 1a-MA copolymer, investigated by 13C NMR spectroscopy, was found to be complicated due to the formation of indoline rings along the chains by an attack of the propagating MA radical at position 2 in the indole ring. As a consequence an excess of MA, with respect to a 1:1 mole ratio of monomer feed, was usually found in the copolymer. The mechanism of the cyclization reaction was clarified by copolymerizing MA with 2-methyl-1-vinylindole (1b), 3-methyl-1-vinylindole (1c), or 2,3-dimethyl-1-vinylindole (1d). An alternating copolymer with MA (mole ratio 1:1 of monomeric units), without irregularities, was obtained only by employing 1d as a comonomer.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 8 (1970), S. 573-584 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerizations of “endo” -dicyclopentadience (I), 1,2-dihydro-“endo”-dicyclopentadiene (II) and 9,10-dihydro-“endo”-dicyclopentadiene (III), initiated by cationic systems, have been investigated under different conditions. Linear polymers with M̄n in the range 1300-4500 have been obtained with (I) and (II): poly-(I) shows less than one double bond for structural unit. In the case of (III) only oligomers were observed. Copolymerization runs show a reactivity of (III) lower than (II). Spectroscopic and chemical analyses of the polymers obtained indicate that besides the norbornene double bond, also the cyclopentenic unsaturation, present in (I) and (III), reacts.Some evidences for a hydride shift in cyclopentence ring, after the attack of the initiator, were collected. In the case of poly-(I) the main enchainment resulted from the norbornene double bond opening, but about 30% of nortricyclene repeating unit was also observed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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