CYCLOPOLYMERIZATION OF 2,6-DICARBOMETHOXY-1,6-HEPTADIENE BY GROUP-TRANSFER POLYMERIZATION

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dc.contributor.authorKIM, YBko
dc.contributor.authorCHOI, WJko
dc.contributor.authorChoi, Byong-Seokko
dc.contributor.authorCHOI, SKko
dc.date.accessioned2013-02-25T05:44:51Z-
dc.date.available2013-02-25T05:44:51Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1991-09-
dc.identifier.citationMACROMOLECULES, v.24, no.18, pp.5006 - 5008-
dc.identifier.issn0024-9297-
dc.identifier.urihttp://hdl.handle.net/10203/60355-
dc.description.abstractA difunctional methacrylate monomer, 2,6-dicarbomethoxy-1,6-heptadiene (DCHD), was cyclopolymerized by group-transfer polymerization (GTP). The polymerization could be initiated by silyl enol ether in the presence of bifluoride or bibenzoate salt as a catalyst. "Living" cyclopolymerization was achieved to give a linear polymer of a cyclohexane repeat unit without any network structure. The polydispersity of poly(DCHD) was in the range of 1.23-1.28. The structure of the resulting polymer was characterized by C-13 NMR, H-1 NMR, and IR spectroscopy. Block copolymers with controlled sequence lengths were prepared from methyl methacrylate and n-butyl methacrylate.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleCYCLOPOLYMERIZATION OF 2,6-DICARBOMETHOXY-1,6-HEPTADIENE BY GROUP-TRANSFER POLYMERIZATION-
dc.typeArticle-
dc.identifier.wosidA1991GD71400005-
dc.identifier.scopusid2-s2.0-0026414024-
dc.type.rimsART-
dc.citation.volume24-
dc.citation.issue18-
dc.citation.beginningpage5006-
dc.citation.endingpage5008-
dc.citation.publicationnameMACROMOLECULES-
dc.contributor.localauthorChoi, Byong-Seok-
dc.contributor.nonIdAuthorKIM, YB-
dc.contributor.nonIdAuthorCHOI, WJ-
dc.type.journalArticleArticle-
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