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dc.contributor.authorSu, YCen_US
dc.contributor.authorChen, WCen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:19:43Z-
dc.date.available2014-12-08T15:19:43Z-
dc.date.issued2005-02-14en_US
dc.identifier.issn0032-3861en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.polymer.2004.09.059en_US
dc.identifier.urihttp://hdl.handle.net/11536/14005-
dc.description.abstractP-Cyclodextrin (P-CD) forms inclusion complexes (ICs) with adamantane-modified benzoxazines (2 benzoxazine and 3 benzoxazine). These benzoxazines can readily penetrate into the CD's hydrophobic cavity, causing turbidity of their solutions, from which fine crystalline powders are obtained. We characterized these complexes by powder X-ray diffraction, C-13 and C-13 CP/MAS NMR spectroscopies, DSC, and TGA. The X-ray diffraction and solid-state C-13 CP/MAS NMR spectroscopy indicate that the IC domains of the polypseudorotaxanes maintain their channel-type structures after the ring-opening curing reactions have occurred. Furthermore, DSC measurements indicate that complexing the adamantane-modified benzoxazine units with beta-CDs result in stiffer main chains and, thus, higher glass transition temperature. TGA also indicates that the inclusion complexes have enhanced its thermal stability. (C) 2004 Published by Elsevier Ltd.en_US
dc.language.isoen_USen_US
dc.subjectcyclodextrinen_US
dc.subjectbenzoxazineen_US
dc.subjectpolypseudorotaxaneen_US
dc.titlePreparation and characterization of poly seudorotaxanes based on adamantane-modified polybenzoxazines and beta-cyclodextrinen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.polymer.2004.09.059en_US
dc.identifier.journalPOLYMERen_US
dc.citation.volume46en_US
dc.citation.issue5en_US
dc.citation.spage1617en_US
dc.citation.epage1623en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000226995500022-
dc.citation.woscount15-
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