4.4 Article

Novel Controlled Polymerization of Cyclo-olefins, Dienes, and Trienes by Utilizing Reaction Properties of Late Transition Metals

Journal

MACROMOLECULAR CHEMISTRY AND PHYSICS
Volume 212, Issue 15, Pages 1545-1551

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/macp.201100182

Keywords

cyclo-olefins; isomerization polymerization; late transition metal catalysts; non-conjugated dienes; stereoselective polymerization

Funding

  1. Ministry of Education, Science, Sports and Culture, Japan [22685012]
  2. Grants-in-Aid for Scientific Research [22685012] Funding Source: KAKEN

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Pd complexes with diimine ligands promote polymerization of cyclopentenes, 1,6-dienes, and 1,6,11-trienes to afford polymers having 1,2- or 1,3-five-membered ring in every repeating unit. The Pd complexes with C-2 symmetrical structure catalyze the polymerization reactions to produce polymers with high stereoselectivity. Some of the obtained polymers show characteristic properties such as thermoreversible gelation and liquid crystal formation. Ni complexes bring about the cyclopolymerization of the dienes to afford polymers containing five- and/or six-membered rings in controlled stereochemistry.

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