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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2549-2560 
    ISSN: 0887-624X
    Keywords: halfsandwich metallocene ; homogeneous catalysis ; terpolymerization ; ethene ; styrene ; 1-octene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethene was co- and terpolymerized with 1-octene and styrene using the methylalumoxane (MAO) activated halfsandwich metallocene Me2Si(Me4Cp)(N-t.-butyl)TiCl2(Cp = cyclopentadienyl, Me = methyl) as catalyst. At temperatures of 40 and 60°C styrene concentration was varied in order to investigate the influence of the comonomers. Despite decreasing the overall activity with respect to ethene/1-octene copolymerization, polymerization activity was found to exibit a relative maximum with increasing styrene concentration. An explanation is given taking two different comonomer effects into account. Low styrene concentration promoted higher 1-octene incorporation compared to ethene/1-octene copolymerization but significantly lowered the molecular weight of the terpolymers. With constant ethene and 1-octene concentration it was possible to produce ethene/1-octene/styrene terpolymers with styrene content varying from 0 to 25 mol % and 1-octene content varying from 8 to 21 mol %. All terpolymers were amorphous. With constant ethene content it was found possible to vary their glass transition temperature with 1-octene/styrene molar ratio incorporated in the terpolymer. 13C-NMR spectroscopic microstructure analysis showed that no styrene/1-octene sequences were found in the terpolymer backbone. Furthermore terpolymerizations were conducted successfully incorporating norbornene, 1,5-hexadiene and propene as monomers in terpolymertization with ethene and styrene. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2549-2560, 1997
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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