4.6 Article

Transition metal-catalyzed polymerization of polar allyl and diallyl monomers

Journal

MRS BULLETIN
Volume 38, Issue 3, Pages 252-259

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1557/mrs.2013.51

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Funding

  1. Grants-in-Aid for Scientific Research [22685012, 25109517] Funding Source: KAKEN

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Recent advances in polymerization of allyl and diallyl monomers catalyzed by homogeneous Ziegler-Natta catalysts are reviewed. Zirconocene catalysts are effective for copolymerization of ethylene or propylene with Al-masked allyl monomers, as well as homopolymerization of allylsilanes. Phosphine-sulfonate Pd complexes promote the copolymerization of ethylene with various polar allyl monomers, in the absence of a masking agent. Late transition metal catalysts promote stereoselective cyclopolymerization of diallyl monomers having various polar functional groups. The cyclopolymerization of alkyl-substituted diallyl monomers by Pd diimine complexes affords the polymer having alternating oligomethylene and trans-1,2-cyclopentene groups.

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