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dc.contributor.authorChu, PPen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorChang, FCen_US
dc.contributor.authorFan, SYen_US
dc.date.accessioned2014-12-08T15:45:49Z-
dc.date.available2014-12-08T15:45:49Z-
dc.date.issued2000-01-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0032-3861(99)00450-4en_US
dc.identifier.urihttp://hdl.handle.net/11536/30821-
dc.description.abstractPolynorbornene (PNB) or cycle olefin copolymer (COC) can undergo conformational conversion into the more stable T(T)G conformer from T(T)T and G(T)G. The conversion constitutes the nascent stage for the reordering process of the COG. Interconversion between two major chain conformers leads to two groups of C-13 NMR resonances corresponding to the CH carbon in the norbornene chain at 53 ppm (T(T)T + G(T)G) and 49 ppm (T(T)G). Chain reordering following the conversion leads to the condensation of the COC bulk and raises its T-g, substantially. The presence of random PE segment not only improves its segmental motion but also facilitates the conversion into the most stable T(T)G conformation. (C) 1999 Elsevier Science Ltd. Ail rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectcycle olefin copolymeren_US
dc.subjectconformeren_US
dc.subjectsolid state NMRen_US
dc.titleConformational conversion and chain ordering in cycle olefin copolymer (COC)en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0032-3861(99)00450-4en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume41en_US
dc.citation.issue1en_US
dc.citation.spage401en_US
dc.citation.epage404en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000083372700042-
dc.citation.woscount22-
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