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  • 1995-1999  (1)
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    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1581-1587 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The range of ADMET polymerization active catalysts has been expanded to include classical catalytic systems. The acyclic diene metathesis (ADMET) polymerization of hydrocarbon dienes has been performed using the aryloxy-tungsten complexes WCl4(O-2,6-C6H3Ph2)2 (4), W(O)Cl2(O-2,6-C6H3Br2)2 (5), and WCl4(O-2,6-C6H3Br2)2 (6) as the precatalytic species in combination with tetrabutyltin, tetramethyltin and tri-n-butyltin hydride as the cocatalytic entities. High molecular weight polyoctenylene and polyheptenylene are obtained under bulk polymerization conditions. The scope of these classical metathesis catalysts in the polymerization of other hydrocarbon as well as functionalized dienes is studied, revealing significant reactivity differences with respect to the previously studied well-defined metathesis catalysts and providing insights into the identification of suitable classical systems for ADMET polymerization.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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