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BielawskiChristopher W

Bielawski, Christopher W.
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dc.citation.endPage 881 -
dc.citation.number 4 -
dc.citation.startPage 874 -
dc.citation.title POLYMER CHEMISTRY -
dc.citation.volume 3 -
dc.contributor.author Wu, Zong-Quan -
dc.contributor.author Radcliffe, Jonathan D. -
dc.contributor.author Ono, Robert J. -
dc.contributor.author Chen, Zheng -
dc.contributor.author Li, Zicheng -
dc.contributor.author Bielawski, Christopher W. -
dc.date.accessioned 2023-12-22T05:37:56Z -
dc.date.available 2023-12-22T05:37:56Z -
dc.date.created 2020-07-10 -
dc.date.issued 2012 -
dc.description.abstract Block copolymers comprised of poly(3-hexylthiophene) and three different poly(isocyanide)s were synthesized in a single pot via the sequential addition of 2-bromo-3-hexyl-5-chloromagnesiothiophene followed by 2-(2-methoxyethoxy) ethyl 4-isocyanobenzoate, tert-butyl 4-isocyanobenzoate, or 1-isocyanohexadecane to a solution of 1,3-bis(diphenylphosphino) propane dichloronickel. Similarly, block copolymers of poly(1-dodecylpyrrole) along with poly(2,5-bis(hexyloxy) phenylene) and a poly(arylisocyanide) were also prepared using an analogous methodology. The respective mechanistically distinct polymerizations proceeded in a controlled fashion, were mediated by a common catalyst, and afforded well-defined block copolymers with tunable molecular weights and compositions. Selected block copolymers exhibited higher-order structures in solution and microphase separation characteristics in the solid state. -
dc.identifier.bibliographicCitation POLYMER CHEMISTRY, v.3, no.4, pp.874 - 881 -
dc.identifier.doi 10.1039/c2py00566b -
dc.identifier.issn 1759-9954 -
dc.identifier.scopusid 2-s2.0-84863269980 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/33167 -
dc.identifier.url https://pubs.rsc.org/en/content/articlelanding/2012/PY/c2py00566b#!divAbstract -
dc.identifier.wosid 000301199600009 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Synthesis of conjugated diblock copolymers: two mechanistically distinct, sequential living polymerizations using a single catalyst -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Polymer Science -
dc.relation.journalResearchArea Polymer Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus CHAIN-GROWTH POLYMERIZATIONS -
dc.subject.keywordPlus GRIGNARD METATHESIS METHOD -
dc.subject.keywordPlus BLOCK-COPOLYMERS -
dc.subject.keywordPlus TRANSFER POLYCONDENSATION -
dc.subject.keywordPlus LOW POLYDISPERSITY -
dc.subject.keywordPlus MOLECULAR-WEIGHT -
dc.subject.keywordPlus PHASE-SEPARATION -
dc.subject.keywordPlus SOLAR-CELLS -
dc.subject.keywordPlus SIDE-CHAIN -
dc.subject.keywordPlus POLYTHIOPHENE -

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