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dc.contributor.authorHuang, CFen_US
dc.contributor.authorLee, HFen_US
dc.contributor.authorKuo, SWen_US
dc.contributor.authorXu, HYen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:39:26Z-
dc.date.available2014-12-08T15:39:26Z-
dc.date.issued2004-03-29en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.polymer.2004.01.051en_US
dc.identifier.urihttp://hdl.handle.net/11536/26929-
dc.description.abstractA series of novel multifunctional initiators derived from adamantane-based derivatives have been used in the syntheses of various styrenic and (meth)acrylic star polymers by atom transfer radical polymerization (ATRP). Conditions were identified in each system to produce star polymers with nearly monomodal molecular distributions. These synthesized star polymers have glass transition temperatures similar to those known for high-molecular-weight linear polymers. We obtained a series of adamantane-contained star polymers covering a wide range of molecular weights by adjusting the monomer-to-initiator ratio and the solvent polarity. Because of reaction heterogeneity and inevitable termination processes, the occurrence of star-star coupling led to a lower than predicted molecular weight polydispersity. When hydrolyzed from their cores by NaOH, the values of Mw of the arms of the PMMA star polymer did not change with reaction time, at least for the first 48 h of the reaction, which implies that no significant PMMA hydrolysis occurs within this interval of time. (C) 2004 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectadamantaneen_US
dc.subjectatom transfer radical polymerizationen_US
dc.subjectPMMAen_US
dc.titleStar polymers via atom transfer radical polymerization from adamantane-based coresen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.polymer.2004.01.051en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume45en_US
dc.citation.issue7en_US
dc.citation.spage2261en_US
dc.citation.epage2269en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000220268300022-
dc.citation.woscount46-
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