完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHuang, THen_US
dc.contributor.authorWhang, WTen_US
dc.contributor.authorZheng, HGen_US
dc.contributor.authorLin, JTSen_US
dc.date.accessioned2014-12-08T15:17:30Z-
dc.date.available2014-12-08T15:17:30Z-
dc.date.issued2006-02-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/12688-
dc.description.abstractDipolar compounds (abbreviated as QuPy) featuring quinoxaline acceptors and diarylamine or triarylamine donors were prepared via palladium-catalyzed C-N or C-C bond formation in good yields. They possess high thermal stability with a high decomposition temperature (T-d > 400 degrees C) and exhibit no crystalline character. The emission colors of the materials vary from green to orange red and are dependent on the nature of the electron-withdrawing segments and solvents. Two types of double-layer organic light-emitting diodes (OLEDs) were constructed using these dipolar compounds as hole-transporting/emitting layers and TPBI or Alq(3) as an electron-transporting layer: (I) ITO/QuPy/Alq(3)/Mg:Ag and (II) ITO/QuPy/TPBI/Mg:Ag (TPBI = 1,3,5-tris(N-phenylbenzimidazol-2-yl)-benzen; Alq(3) = 1,3,5-tris(N-phenyl-benzimidazol-2-yl)-benzene). The recombination zone in most of those devices were confined in the quinoxaline layers, The green to orange colors in these devices correspond well with the film PL of the material used. The relation between the energy levels of the compounds and the performance of the light-emitting diode are discussed.en_US
dc.language.isoen_USen_US
dc.subjectquinoxalineen_US
dc.subjecttriarylamineen_US
dc.subjectelectroluminescent materialsen_US
dc.subjectdipolar compoundsen_US
dc.titleQuinoxalines incorporating triarylamines: Dipolar electroluminescent materials with tunable emission characteristicsen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume53en_US
dc.citation.issue1en_US
dc.citation.spage233en_US
dc.citation.epage242en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000235896500028-
dc.citation.woscount4-
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