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dc.contributor.authorChen, Ya-Joen_US
dc.contributor.authorWu, Bing-Jyunen_US
dc.contributor.authorWang, Fu-Shengen_US
dc.contributor.authorChi, Mu-Huanen_US
dc.contributor.authorChen, Jiun-Taien_US
dc.contributor.authorPeng, Chi-Howen_US
dc.date.accessioned2015-12-02T02:59:40Z-
dc.date.available2015-12-02T02:59:40Z-
dc.date.issued2015-10-13en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.macromol.5b01101en_US
dc.identifier.urihttp://hdl.handle.net/11536/128416-
dc.description.abstractCobalt-mediated radical polymerization (CMRP) was used to prepare well-defined poly(vinyl acetate) (PVAc) as the macroinitiator in the reverse atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) and styrene (Sty) for the synthesis of block copolymers of PVAc-b-PMMA and PVAc-b-PSty with linearly increased molecular weight and smoothly shifted gel permeation chromatography (GPC) traces. The chain extension from PVAc to PMMA or PSty via the hybridization of CMRP and ATRP required neither a difunctional initiator nor further chain-end modification and was as simple as regular chain extension in the reverse ATRP process. Because the cobalt complex bonded to the chain end of PVAc was dissociated during the ATRP process, this method also efficiently solved the issue of metal removal in the CMRP process.en_US
dc.language.isoen_USen_US
dc.titleHybridization of CMRP and ATRP: A Direct Living Chain Extension from Poly(vinyl acetate) to Poly(methyl methacrylate) and Polystyreneen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.macromol.5b01101en_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume48en_US
dc.citation.issue19en_US
dc.citation.spage6832en_US
dc.citation.epage6838en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000362921500009en_US
dc.citation.woscount0en_US
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