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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 853-872 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl-type monomers containing the pyrrole ring, such as 2-vinylpyrrole (2-VPyrr), N-(pyrrol-2-yl)methylacrylamide (PMA), N-methyl, N-(pyrrol-2-yl)methylacrylamide (MPMA), 2-allylpyrrole (2-AP), β-(pyrrol-1-yl)ethyl vinyl ether (PEVE), 2-diallyl-aminomethylpyrrole (DAMP), and 3-(2-pyrrolylmethyleneimino)propene-1 (PIP) were synthesized by various reactions involving characteristic properties of the pyrrole ring. Radical homopolymerizations and copolymerizations of these monomers were studied. In the homopolymerization of conjugated monomers such as 2-VPyrr and PMA, chain transfer to the pyrrole-containing monomer was remarkable but not degradative. The copolymerization parameters, that is, the values of r1, r2, Q1, and e1 of 2-VPyrr, were determined to be 0.066, 0.69, 5.53, and -1.36, respectively in the copolymerization of 2-VPyrr (M1) with MMA (M2). The Q and e values of the monomers containing a heteroaromatic ring such as 2-vinylpyrrole, 2-vinylfuran, and 2-vinylthiophene were evaluated by the molecular orbital theory. The e value of PMA was found to be negative (-0.64) in the copolymerization with styrene, although e for acrylamide derivatives is generally positive. This may be explained by the intermolecular hydrogen bonding between the carbonyl group and NH group of PMA. That is, attraction or polarization of π-electrons in the vinyl group of PMA is weakened by such hydrogen bonding. From the results of copolymerization of 2-AP with various comonomers, the comonomers could be classified into three categories: class a monomers, in which both Q and e values are largely positive, can copolymerize with 2-AP; class b monomers, having small e values, homopolymerize and can not copolymerize with 2-AP; class c monomers, in which both Q and e values are small. The Q and e values of the comonomer must be largely positive in order to permit copolymerization with an allyl-type monomer.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1243-1255 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copper complexes and the cobalt complex with the ligand of 3-(2-pyrrolylmethyl-enimino)propene-1 (PIP) or p-(2-pyrrolylmethylenimino)styrene (PIS) were synthesized and homopolymerizations and the copolymerization with styrene, acrylonitrile, methyl methacrylate and acrylic acid studied. In the polymerization of chelate monomers, inhibition of radical polymerization by the central metal ion was observed, but the chelate polymer could be obtained only if the initiator was present in higher concentrations in the feed. It is considered that the strength of inhibition depends on the electronic configuration of d-orbitals of the central metal ion. The initiation mechanism of the cupric chelate monomer may be reduction of the metal ion by the redox reaction with a primary radical via the intramolecular electron transfer through the π-conjugated system of the ligand prior to the propagation step. This mechanism was verified by studying the redox reaction of various copper complexes with DPPH. In the system of the copper complex containing PIS and acylic acid the alternating copolymer could be obtained at any mole fraction of monomer mixture in feed.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2379-2387 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The spectral sensitivity of poly(vinyl p-azidocinnamate)(PVACi) was discussed by comparison with poly(vinyl cinnamate)(PVCi) and poly(vinyl p-azidobenzoate). The photochemical reaction of PVACi was investigated with respect to the reactivity of two functional groups, namely, azido and cinnamoyl groups. It was found that cinnamoyl groups dimerized like PVCi and azido groups did not add to double bonds appreciably. The quantum yield of photolysis of azido groups was two times that of dimerization of cinnamoyl groups. A marked wavelength dependence of π-π* and n-π* absorption was observed in both the reactions of azido and cinnamoyl groups.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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