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  • Polymer and Materials Science  (4)
  • 1980-1984  (4)
  • 1983  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 4 (1983), S. 297-301 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 33-43 
    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: Four poly(vinyl chloride) (PVC) samples, 1, 2, 3, and 4, were prepared in bulk using 2,2′-azodiisobutyronitrile at 90°C and 60°C and the same initiator together with UV irradiation at 0°C and -50°C, respectively. Fractions were obtained from samples 2,3, and 4 by extracting with acetone, sample 1 being completely soluble in this solvent. The whole PVC's as well as their acetone soluble and insoluble fractions, were characterized by determining the intrinsic viscosity, the osmometric molecular weight, and the tacticity; then they were thermally degraded up to conversion of 0.3% in powder state. The values of degradation rate for both the insoluble fractions and the whole PVC's were in agreement with some prior results on the influence of syndiotactic sequences on propagation step. The soluble fractions proved to be very unstable in comparison with the insoluble, which, despite the lower molecular weight of the former, seems to obey their higher content of isotactic conformations. The fine polyene distribution in the degraded polymers was carried out by UV-visible spectroscopy. The results reveal the occurrence of two different polyene distributions, and allow for the peculiar one of the soluble fractions to be related to polyenes consisting of two sequences of trans conjugated double bonds separated by a single cis double bond. The results clearly shows that there are two mechanisms for initiation of the PVC degradation, depending on whether it occurs by random unstable structures or by the normal GTTG isotactic or TTTG heterotactic triads. Moreover, these two initiation processes are proved to give rise to different types of polyenes, which accounts for the occurrence of two unlike mechanisms of propagation.
    Additional Material: 6 Ill.
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anionic polymerization of p-triphenylgermylstyrene (1a) and p-tributylgermylstyrene (1b) were investigated under high vacuum conditions (≈10-6 mbar). Both 1a and 1b were readily polymerized with sodium naphthalide, potassium naphthalide, or α-methylstyrylsodium oligomers to form “living polymers”. The addition of α-methylstyrene to these living systems gave the triblock copolymer, poly(α-methylstyrene-b-p-triphenylgermylstyrene-b-α-methylstyrene). Both monomers were also polymerized radically with AIBN as initiator. Some physical properties of the resulting polymers were examined.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A spectroscopic (UV, IR, 1H NMR) study of the cationic polymerisation of 2-vinylfuran (1a) and 2-isopropenylfuran (2a) showed the existence of an important alkylation reaction at C5 which competes with normal propagation. The extent of this competition depends on the monomer used and the polymerisation temperature. A comparison of the spectra of standard polymers (prepared by radical or stereospecific polymerisation) with those of polymers obtained by cationic initiation allowed to assess the extent of alkylation and its regiospecificity at C5 2-Methyl-5-vinylfuran (1b) and 2-methyl-5-isopropenylfuran (2b) were found to undergo cationic polymerisation without any interference from alkylation reactions. Reactions between these four monomers and 2-methylfuran in the presence of typical acidic catalysts gave very high yields of alkylated products and no polymerisation, thus confirming the importance of this electrophilic reaction and its possible application to synthetic uses.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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