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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 695-706 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A comparative study was undertaken of the cationic oligomerization/polymerization of the natural propenylbenzene derivatives, anethole, isoeugenol, and isosafrole, together with synthetic o-methoxypropenylbenzene and N,N-dimethyl-p-propenylaniline using boron trifluoride diethyletherate as catalyst. Two (optimum) reaction temperatures were employed, -12 and -45°C, and only the (E) isomers of the monomers were studied. The order of reactivity of the monomers was found to be anethole 〉 isoeugenol 〉 isosafrole 〉 o-methoxypronylbenzene as measured by following the rate of loss of monomer by proton magnetic resonance spectrometry at -12°C. N,N-dimethyl-p-propenylaniline only appeared to form a complex with the catalyst. Low-molecularweight polymeric materials were prepared from anethole, isosafrole, and isoeugenol at -45°C using the same catalyst while o-methoxypropenylbenzene formed oligomers. Isosafrole was recovered unchanged when treated with the boron trifluoride diethyl etherate initiator system at -78°C in an attempt to increase the molecular weight of the polyisosafrole.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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