Abstract
The compound Cp*TiMe3 can be activated with a variety of Lewis and Brønsted acids to generate precursors of the cationic species [Cp*TiMe2]+. The latter can serve as an initiator for (a) the polymerization of ethylene and α -olefins via η2 coordination and a Ziegler–Natta process, (b) the ring opening metathesis polymerization of norbornene and the cyclopolymerization of 1,5-hexadiene, and (c) the polymerization of styrene, vinyl ethers, N-vinyl carbazole and isobutylene via η1carbocationic process. In addition, an as yet undefined product of decomposition of [Cp*TiMe2]+ catalyzes the polymerization of styrene to highly stereoregular syndiotactic polystyrene.
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Ewart, S.W., Baird, M.C. Olefin polymerization by pentamethylcyclopentadienyl trimethyltitanium, Cp*TiMe3 . Topics in Catalysis 7, 1–8 (1999). https://doi.org/10.1023/A:1019107632144
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DOI: https://doi.org/10.1023/A:1019107632144