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dc.contributor.authorYang, Sheng-Hsiungen_US
dc.contributor.authorHuang, Chun-Haoen_US
dc.contributor.authorChen, Chiu-Hsiangen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.date.accessioned2014-12-08T15:10:09Z-
dc.date.available2014-12-08T15:10:09Z-
dc.date.issued2009-01-02en_US
dc.identifier.issn1022-1352en_US
dc.identifier.urihttp://dx.doi.org/10.1002/macp.200800467en_US
dc.identifier.urihttp://hdl.handle.net/11536/7758-
dc.description.abstractA new series of disubstituted polyacetylene derivatives that contain multi-fluorine atoms on the pendent phenyl ring have been synthesized and characterized. The results reveal a greater red-shift in UV-vis absorption and PL emission upon incorporating more fluorine atoms on the pendent phenyl ring. Among them, disubstituted polyacetylene with a difluorophenyl group (PDPA-2F) showed the highest luminescent efficiency. The F device performance can be promoted by blending a hole-transporting material TM-TPD into PDPA-2F as the active layer or by using a light-emitting copolymer in which PDPA-2F was copolymerized with a carbazole group (PDPA-2Fcab). A light-emitting diode of ITO/PEDOT/PDPA-2Fcab/Ca/Al revealed a maximum luminescence of 4230 cd . m(-2) at 14 V and a maximum current efficiency of 3.37 cd . A(-1) at 7 V.en_US
dc.language.isoen_USen_US
dc.subjectconjugated polymersen_US
dc.subjectlight-emitting diodesen_US
dc.subjectmetathesisen_US
dc.subjectpolyacetylenesen_US
dc.titleSynthesis and Electroluminescent Properties of Disubstituted Polyacetylene Derivatives Containing Multi-Fluorophenyl and Cyclohexylphenyl Side Groupsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/macp.200800467en_US
dc.identifier.journalMACROMOLECULAR CHEMISTRY AND PHYSICSen_US
dc.citation.volume210en_US
dc.citation.issue1en_US
dc.citation.spage37en_US
dc.citation.epage47en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000262599700004-
dc.citation.woscount16-
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