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dc.contributor.authorMalinauskas, Tadasen_US
dc.contributor.authorDaskeviciene, Maryteen_US
dc.contributor.authorKazlauskas, Karolisen_US
dc.contributor.authorSu, Hai-Chingen_US
dc.contributor.authorGrazulevicius, Juozas Vidasen_US
dc.contributor.authorJursenas, Sauliusen_US
dc.contributor.authorWu, Chung-Chihen_US
dc.contributor.authorGetautis, Vytautasen_US
dc.date.accessioned2014-12-08T15:11:55Z-
dc.date.available2014-12-08T15:11:55Z-
dc.date.issued2011-03-11en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tet.2011.01.026en_US
dc.identifier.urihttp://hdl.handle.net/11536/9151-
dc.description.abstractMultifunctional phosphorescent bis-cyclometallated iridium(III) complexes based on the 2-phenyl-1,2,3-benzotriazole moiety and bearing branched hole-transporting carbazole fragments were synthesized. The isolated compounds were found to be amorphous and expressed very good solubility. Introduction of flexible aliphatic chains of various lengths into the iridium complexes enabled manipulation of their glass transition temperature. The iridium complexes exhibited red phosphorescence emission at 650 nm with the lifetime of 5.7 mu s and phosphorescence quantum yields of 0.22 and 0.17 in solution and solid state, respectively, at room temperature. The shielding effect of the carbazolyl moieties on the concentration quenching of phosphorescence of the iridium centers was found to result in the increased excited state lifetime and quantum yield due to the suppressed exciton migration. Non-optimized OLED devices, based on the phosphorescent bis-cyclometallated iridium(III) complex without host material were fabricated and their electroluminescence properties were evaluated. (C) 2011 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectCarbazoleen_US
dc.subjectIridium complexen_US
dc.subjectPhosphorescenceen_US
dc.subjectTriazoleen_US
dc.titleMultifunctional red phosphorescent bis-cyclometallated iridium complexes based on 2-phenyl-1,2,3-benzotriazole ligand and carbazolyl moietiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tet.2011.01.026en_US
dc.identifier.journalTETRAHEDRONen_US
dc.citation.volume67en_US
dc.citation.issue10en_US
dc.citation.spage1852en_US
dc.citation.epage1861en_US
dc.contributor.department照明與能源光電研究所zh_TW
dc.contributor.departmentInstitute of Lighting and Energy Photonicsen_US
dc.identifier.wosnumberWOS:000288188600014-
dc.citation.woscount21-
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