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dc.contributor.authorHuang, CFen_US
dc.contributor.authorWang, SKen_US
dc.contributor.authorKuo, SWen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:39:11Z-
dc.date.available2014-12-08T15:39:11Z-
dc.date.issued2004-05-05en_US
dc.identifier.issn0021-8995en_US
dc.identifier.urihttp://dx.doi.org/10.1002/app.20151en_US
dc.identifier.urihttp://hdl.handle.net/11536/26785-
dc.description.abstractThe homopolymerization and copolymerization of tert-butyl methacrylate (tBMA) and norbornene (NB) with nickel(II) acetylacetonate in combination with methylaluminoxane were systematically investigated. This catalytic system showed high activity toward the homopolymerization of both NB and tBMA. For these copolymerizations, activity was gradually lost with an addition of tBMA to NB or of NB to tBMA. This result was qualitatively explained with the trigger coordination mechanism. Furthermore, the determination of the reactivity ratios indicated a significantly whigher reactivity for NB than for tBMA (r(NB) = 4.14 and r(tBMA) = 0.097), and this was interpreted by the coordination mechanism. The synthesized acrylate/NB copolymers exhibited glass-transition temperatures of 100-250degreesC. The absence of crystallinity and the homogeneous repartition of the monomer units along the main chain yielded products with high transparency and high stability. (C) 2004 Wiley Periodicals, Inc.en_US
dc.language.isoen_USen_US
dc.subjectpolynorborneneen_US
dc.subjectmetalloceneen_US
dc.subjectmethylaluminoxane (MAO)en_US
dc.titleHomopolymerization and copolymerization of tert-butyl methacrylate and norbornene with nickel-based methylaluminoxane catalystsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/app.20151en_US
dc.identifier.journalJOURNAL OF APPLIED POLYMER SCIENCEen_US
dc.citation.volume92en_US
dc.citation.issue3en_US
dc.citation.spage1824en_US
dc.citation.epage1833en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000220435000061-
dc.citation.woscount12-
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