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dc.contributor.authorHuang, WJen_US
dc.contributor.authorChang, FCen_US
dc.contributor.authorChu, PPJen_US
dc.date.accessioned2014-12-08T15:45:05Z-
dc.date.available2014-12-08T15:45:05Z-
dc.date.issued2000-07-01en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0032-3861(99)00842-3en_US
dc.identifier.urihttp://hdl.handle.net/11536/30405-
dc.description.abstractIn this paper, we report two simple and effective bromination methods to brominate the cycle olefin copolymer (COC). A suitable metallic catalyst can accomplish functionalization and chromophorization of the brominated COG. A 2nd NLO dye, Disperse Orange 3(DO3) containing the -NH2 functional group, has been grafted onto either the norbornene unit or the PE segment of the COC backbone successfully, by the palladium catalyst, Pd-2(dba)(2)(Bis[dibenzylideneacetone] dipalladium). The observed low dye grafting content can be attributed to the higher hindrance of the norbornene ring. Based on UV results, the NLO-COC, having dye grafted onto the norbornene unit shows more red shift than that grafted onto the PE unit, probably due to greater shielding on the chromorphor. (C) 2000 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectcyclo olefin copolymer (COC)en_US
dc.subjectbrominationen_US
dc.subject2nd nonlinear optical polymeren_US
dc.titleFunctionalization and chemical modification of cyclo olefin copolymers (COC)en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0032-3861(99)00842-3en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume41en_US
dc.citation.issue16en_US
dc.citation.spage6095en_US
dc.citation.epage6101en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000087123900009-
dc.citation.woscount25-
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