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dc.contributor.authorLi, MSen_US
dc.contributor.authorMa, CCMen_US
dc.contributor.authorChen, JLen_US
dc.contributor.authorLin, MLen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:02:54Z-
dc.date.available2014-12-08T15:02:54Z-
dc.date.issued1996-01-15en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma950978uen_US
dc.identifier.urihttp://hdl.handle.net/11536/1501-
dc.description.abstractIn the Bisphenol A base polycarbonate-Bisphenol A base epoxy blend system, the carbonate group can react with epoxide in the presence of a tertiary amine. The transesterification reactions convert the original aromatic/aromatic carbonate of PC to aromatic/aliphatic and aliphatic/aliphatic carbonates. IR spectroscopy shows an unknown major structure formed during the later stages of the transesterification reaction. The unknown structure was investigated by a model reaction using diphenyl carbonate and phenyl glycidyl ether leading to the formation of 4-(phenoxymethyl)-1,3-dioxolan-2-one (PMD), which has been identified by IR, UV, H-1 NMR, C-13 NMR, and mass spectroscopy. The mechanism of forming the cyclic carbonate is proposed to proceed through a zwitterion and a nucleophile attack of the aromatic/aliphatic or the aliphatic/aliphatic carbonate group.en_US
dc.language.isoen_USen_US
dc.titleEpoxy-polycarbonate blends catalyzed by a tertiary amine .1. Mechanism of transesterification and cyclizationen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma950978uen_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume29en_US
dc.citation.issue2en_US
dc.citation.spage499en_US
dc.citation.epage506en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1996TQ37900001-
dc.citation.woscount30-
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