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  • Articles  (3)
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  • 1965-1969  (3)
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  • Articles  (3)
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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
    Description / Table of Contents: Die kationische Polymerisation von 3-Chlor-3-methylbuten-1 wurde im Temperaturbereich von -30 bis -130°C untersucht. Die Struktur des Polymeren wurde durch NMR-Spektroskopie bestimmt und erweist sich als eine Mischung fast gleicher Anteile von Grundbausteinen. Temperaturänderungen zwischen -30 und -130°C beeinflussen das Verhältnis dieser Strukturen nur schwach. Für eine Polymerisation unter Wanderung eines Methylanions (Methide Shift Polymerization) wurde kein Hinweis gefunden. Diese Ergebnisse werden aufgrund eines früher vorgeschlagenen Mechanismus diskutiert.
    Notes: The cationic polymerization of 3-chloro-3-methyl-1-butene was investigated in the temperature range from -30° to -130°C. The structure of the polymer was characterized by NMR spectroscopy and was found to be a mixture of about equal portions of repeating units. Changing the temperature from -30° to -130°C. affects only slightly the respective amounts of these structures. No evidence for methide shift polymerization was found. These results are discussed in terms of an earlier proposed mechanism.
    Additional Material: 3 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 3 (1965), S. 729-734 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Certain aluminum alkyls and aluminum dialkyl halides in conjunction with suitable simple cocatalysts generating proton or carbonium ion exhibit high polymerization activity and produce high molecular weight polyolefins, diolefins and/or copolymers at comparatively high temperatures. In this paper we report our investigations with AlEt2Cl-Brönsted acid systems used for polymerizing isobutylene and copolymerizing isobutene-isoprene mixtures for high molecular weight products. The cocatalyst is not specific in these reactions. Highly active systems can be obtained with HCl, HBr, CCl3COOH, etc. Evidently proton donors in general (Brönsted acids) may function as cocatalysts in this system. The sequence of polymerization initiation activity of various Brönsted acids in conjunction with AlEt2Cl is HCl, HBr ≫ HF, H2O 〉 CCl3COOH ≫ CH3OH 〉 CH3COCH3. The effect of temperature on the molecular weights was studied. In contrast to linear plots of log molecular weight versus 1/T, obtained for polyisobutylene or isobutylene-isoprene copolymers with conventional Friedel-Crafts halides in the -30 to -100°C range, this Arrhenius plot showed a marked maximum near -70°C for polymers prepared with AlEt2Cl-HCl catalyst systems. Features of this polymerization reaction are discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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