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  • 1985-1989  (2)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 2327-2349 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of linear methyl ω-epoxyalkanoates of C-3 to C-10 carboxylic acids (0 to 7 methylene groups between oxirane ring and carbomethoxy group) was accomplished with a triethylaluminum/water/acetylacetone (1.0/0.5/1.0) initiator system to yield polymers of high molecular weight, apparently via a coordinative anionic mechanism. The rate of polymerization increased as the number of methylene groups between the oxirane ring and the carbomethoxy group increased, up to three methylene groups. When more than three methylene groups separate the polymerizable oxirane group and the carbomethoxy group, the rate of polymerization becomes essentially constant. The polymers were characterized by their infrared and 13C-NMR spectra, DSC, GPC, and inherent viscosity. The lower members of the series (ω-epoxyalkanoates of n 〈 3) gave polymers of lower molecular weight and wider-molecular-weight distribution (Mw/Mn 〉 2), while the higher members had molecular weight distributions between 1.5 and 2. The glass transition temperatures of the polymers also decreased from -26°C for n = 1 to around -50 to -55°C for n ≥ 3.
    Additional Material: 3 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. 649-671 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Selected methyl ω-epoxyalkanoates ranging from methyl 3,4-epoxybutanoate to methyl 7,8-epoxyoctanoate were copolymerized with a number of oxiranes and with oxetane. Tetrahydrofuran did not take part in the attempted methyl ω-epoxyalkanote-tetrahydrofuran copolymerization, but acted only as the solvent. The oxirane copolymers had polymer compositions similar to the comonomer feed ratio. Oxirane comonomers used were propylene oxide (1,2-epoxypropane), butylene oxide (1,2-epoxybutane), 1,2-epoxyhexane, epichlorohydrin, and phenylglycidyl ether. The initiator system used was triethylaluminum/water/acetylacetone (1.0/0.5/1.0) in about 5 mol %. In the copolymerizations using methyl 3,4-epoxybutanoate as a comonomer, only small yields of polymer (in the range of 1 to 2%) were realized, while for methyl 4,5-epoxypentanoate the yields were generally in the range of 20 to 60%. Methyl 7,8-epoxyoctanoate copolymerized readily and gave yields of copolymers of 50 to 90%.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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