E. P. Talzi, D. E. Babushkin, N. V. Semikolenova, V. N. Zudin, and V. A. Zakharov
Boreskov Institute of Catalysis, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090 Russia
Received August 22, 2000
AbstractThe structures of intermediates generated by the activation of 2,6-bis[1-(2,6-dimethylphe-
nylimino)ethyl]pyridineiron(II) chloride (1) with various cocatalysts, methylalumoxane (MAO), trimethylalu-
minum (TMA), and TMA in combination with B(C6F5)3 and Ph3CB(C6F5)4, is studied by 1H and 2H NMR spec-
troscopy. The 1/AlMe3 system exhibits a higher catalytic activity in ethylene polymerization than the 1/MAO
system. The activity of the latter decreases sharply with a decrease in the amount of AlMe3 in MAO. Neutral Fe(II)
complexes rather than cationic intermediates are suggested to be active components in both catalytic systems.
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