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dc.contributor.authorChen, CHen_US
dc.contributor.authorShu, CFen_US
dc.date.accessioned2014-12-08T15:38:51Z-
dc.date.available2014-12-08T15:38:51Z-
dc.date.issued2004-07-01en_US
dc.identifier.issn0887-624Xen_US
dc.identifier.urihttp://dx.doi.org/10.1002/pola.20179en_US
dc.identifier.urihttp://hdl.handle.net/11536/26601-
dc.description.abstractWe have synthesized aromatic polyquinolines containing both spirobifluorene and cardofluorene moieties in the main chain by applying acid-catalyzed Friedlander quinoline synthesis. The incorporation of these rigid nonplanar structures into the polymer backbone, which restricts segmental mobility, significantly increases both the glass-transition temperature and thermal stability, while providing enhanced solubility as a result of a decrease in the degree of molecular packing and crystallinity. We have also examined the optical and electrochemical properties of these polyquinolines. The low-lying lowest unoccupied molecular orbital energy level and quasireversible electrochemical reduction of these polyquinolines suggest their potential for use as electron-injecting/transporting materials in polymer light-emitting diodes. (C) 2004 Wiley Periodicals, Inc.en_US
dc.language.isoen_USen_US
dc.subjectelectrochemistryen_US
dc.subjectfluorescenceen_US
dc.subjectlight-emitting diodes (LED)en_US
dc.subjectpolyquinolines solution propertiesen_US
dc.subjectthermal propertiesen_US
dc.titlePolyquinolines containing both spirobifluorene and cardofluorene units: Synthesis and characterizationen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/pola.20179en_US
dc.identifier.journalJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRYen_US
dc.citation.volume42en_US
dc.citation.issue13en_US
dc.citation.spage3314en_US
dc.citation.epage3322en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000222124600020-
dc.citation.woscount13-
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