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dc.contributor.authorWu, FIen_US
dc.contributor.authorShu, CFen_US
dc.contributor.authorChien, CHen_US
dc.contributor.authorTao, YTen_US
dc.date.accessioned2014-12-08T15:35:38Z-
dc.date.available2014-12-08T15:35:38Z-
dc.date.issued2005-01-31en_US
dc.identifier.issn0379-6779en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.synthmet.2004.09.029en_US
dc.identifier.urihttp://hdl.handle.net/11536/24053-
dc.description.abstractWe have synthesized and characterized a series of fluorene-based oxadiazole derivatives, in each of which two identical oxadiazole moieties are linked to a fluorene unit via an sp(3)-hybridized carbon atom (C-9) to form a rigid, nonplanar structure. This structural feature leads to a reduction in the tendency to crystallize and an increase in the glass transition temperature. Electrochemical studies revealed that these materials undergo reversible reductions and have high electron affinities. Each fluorene-based oxadiazole exhibited reasonably good performance when it was used as the electron-transporting layer in a multi-layer organic EL device. (C) 2004 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectoxadiazoleen_US
dc.subjectfluoreneen_US
dc.subjectelectron-transporting materialen_US
dc.subjectOLEDen_US
dc.titleFluorene-based oxadiazoles: thermally stable electron-transporting materials for light-emitting devicesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.synthmet.2004.09.029en_US
dc.identifier.journalSYNTHETIC METALSen_US
dc.citation.volume148en_US
dc.citation.issue2en_US
dc.citation.spage133en_US
dc.citation.epage139en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000226261900006-
dc.citation.woscount22-
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