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Cited 19 time in webofscience Cited 22 time in scopus
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dc.contributor.authorToshifumi Satoh-
dc.contributor.authorNaoki Nishikawa-
dc.contributor.authorDaisuke Kawato-
dc.contributor.authorDaichi Suemasa-
dc.contributor.authorSungmin Jung-
dc.contributor.authorYoung Yong Kim-
dc.contributor.authorRee, M-
dc.contributor.authorToyoji Kakuchi-
dc.date.accessioned2015-06-25T03:26:17Z-
dc.date.available2015-06-25T03:26:17Z-
dc.date.created2013-12-20-
dc.date.issued2014-01-
dc.identifier.issn1759-9954-
dc.identifier.other2015-OAK-0000028512en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/12716-
dc.description.abstractWell-defined hydroxyl end-functionalized poly(n-hexyl isocyanate), PHIC-(OH)(2) and PHIC-(OH)(3), as rod-type macroinitiators were synthesized by the Cu-catalyzed azide-alkyne cycloaddition reactions of azido end-functionalized PHIC with ethynyl alcohol derivatives. The PHIC-(OH)(2) and PHIC-(OH) 3 were suitable macroinitiators for the ring-opening polymerization of L-LA and epsilon-CL leading to the synthesis of novel rod-coil type miktoarm star copolymers, PHIC-b-PLLA(2), PHIC-b-PLLA(3), PHIC-b-PCL2, and PHIC-b-PCL3, with controlled molecular weights, narrow polydispersities, and controlled arm numbers. Additionally, the thermal and solution properties of the obtained miktoarm star copolymers along with the corresponding block copolymers, PHIC-b-PLLA and PHIC-b-PCL, were characterized by TGA, DSC, and DLS analyses.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherRSC-
dc.relation.isPartOfPolymer Chemistry-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titlePrecise synthesis of a rod-coil type miktoarm star copolymer containing poly(n-hexyl isocyanate) and aliphatic polyester-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/C3PY00985H-
dc.author.googleSatoh T., Nishikawa N., Kawato D., Suemasa D., Jung S., Kim Y.Y., Ree M., Kakuchi T.en_US
dc.relation.volume5en_US
dc.relation.issue2en_US
dc.relation.startpage588en_US
dc.relation.lastpage599en_US
dc.contributor.id10115761en_US
dc.relation.journalPolymer Chemistryen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIEen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationPolymer Chemistry, v.5, no.2, pp.588 - 599-
dc.identifier.wosid000328647200039-
dc.date.tcdate2019-01-01-
dc.citation.endPage599-
dc.citation.number2-
dc.citation.startPage588-
dc.citation.titlePolymer Chemistry-
dc.citation.volume5-
dc.contributor.affiliatedAuthorRee, M-
dc.identifier.scopusid2-s2.0-84890469189-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc14-
dc.description.scptc15*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusLIVING ANIONIC-POLYMERIZATION-
dc.subject.keywordPlusRING-OPENING POLYMERIZATION-
dc.subject.keywordPlusTRANSFER RADICAL POLYMERIZATION-
dc.subject.keywordPlusHYDROPHILIC BLOCK-COPOLYMERS-
dc.subject.keywordPlusBENZYL BROMIDE MOIETIES-
dc.subject.keywordPlusBRANCHED POLYMERS-
dc.subject.keywordPlusSUCCESSIVE SYNTHESIS-
dc.subject.keywordPlus1,1-DIPHENYLETHYLENE DERIVATIVES-
dc.subject.keywordPlusFUNCTIONALIZED POLYSTYRENES-
dc.subject.keywordPlusMORPHOLOGICAL BEHAVIOR-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-

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