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dc.contributor.authorChen, CHen_US
dc.contributor.authorTang, CWen_US
dc.date.accessioned2014-12-08T15:43:12Z-
dc.date.available2014-12-08T15:43:12Z-
dc.date.issued2001-11-26en_US
dc.identifier.issn0003-6951en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1420583en_US
dc.identifier.urihttp://hdl.handle.net/11536/29240-
dc.description.abstractWe have discovered two stericly hindered green coumarin derivatives which showed significantly better thermal stability and overall electroluminescence (EL) performance than those of the corresponding 3-(2-benzothiazolyl)-7-(diethylamino)-2H-1-benzopyran-2-one (C-6) and 10-(2-benzothiazolyl)-1,1,7,7-tetramethyl- 2,3,6,7-tetrahydro-1H,5H,11H-benzo[l]pyrano[6,7, 8-ij] quinolizin-11-one (C-545T). The strategic incorporation of bulky spacer t-butyl groups in these dopants considerably delays the onset of concentration quenching. In particular, 10-[2(5,7-di-t-butyl)benzothiazolyl]-1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H,11H-benzo-[l]pyrano[6,7,8-ij]quinolizin-11-one (C-545TB) with its superb thermal stability (T-g=142 degreesC; T-d=327 degreesC), high luminance efficiency (similar to 13 cd/A), good Commission Interationale d'Eclairage (CIE) coordinates (x=0.30; y=0.64) and a nearly flat EL efficiency dependence on drive current stands out as one of the best choice of green dopants for use in the passive-matrix organic light-emitting diode displays. (C) 2001 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleEfficient green organic light-emitting diodes with stericly hindered coumarin dopantsen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1420583en_US
dc.identifier.journalAPPLIED PHYSICS LETTERSen_US
dc.citation.volume79en_US
dc.citation.issue22en_US
dc.citation.spage3711en_US
dc.citation.epage3713en_US
dc.contributor.department友訊交大聯合研發中心zh_TW
dc.contributor.departmentD Link NCTU Joint Res Ctren_US
dc.identifier.wosnumberWOS:000172204400051-
dc.citation.woscount90-
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