Deep Red Phosphorescence of Cyclometalated Iridium Complexes by o-Carborane Substitution

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dc.contributor.authorBae, Hye Jinko
dc.contributor.authorChung, Jinko
dc.contributor.authorKim, Hyungjunko
dc.contributor.authorPark, Jihyunko
dc.contributor.authorLee, Kang-Munko
dc.contributor.authorKoh, Tae-Wookko
dc.contributor.authorLee, Yoon Supko
dc.contributor.authorYoo, Seunghyupko
dc.contributor.authorDo, Youngkyuko
dc.contributor.authorLee, Min Hyungko
dc.date.accessioned2014-08-29T02:12:25Z-
dc.date.available2014-08-29T02:12:25Z-
dc.date.created2014-02-10-
dc.date.created2014-02-10-
dc.date.issued2014-01-
dc.identifier.citationINORGANIC CHEMISTRY, v.53, no.1, pp.128 - 138-
dc.identifier.issn0020-1669-
dc.identifier.urihttp://hdl.handle.net/10203/188998-
dc.description.abstractHeteroleptic (C<^>N)(2)Ir(acac) (C<^>N = 5-MeCBbtp (5a); 4-BuCBbtp (5b); 5-BuCBbtp (5c); 5-(R)CBbtp = 2-(2'-benzothienyl)-5-(2-R-ortho-carboran-1-yl)-pyridinato-C-2,N, R = Me and n-Bu; 4-BuCBbtp = 2-(2'-benzothienyl)-4-(2-n-Bu-ortho-carboran-1-yl)-pyridinato-C-2,N, acac = acetylacetonate) complexes supported by o-carborane substituted C<^>N-chelating ligand were prepared, and the crystal structures of 5a and 5b were determined by X-ray diffraction. While 5a and 5c exhibit a deep red phosphorescence band centered at 644 nm, which is substantially red-shifted compared to that of unsubstituted (btp)(2)Ir(acac) (6) (lambda(em) = 612 nm), 5b is nonemissive in THF solution at room temperature. In contrast, all complexes are emissive at 77 K and in the solid state. Electrochemical and theoretical studies suggest that the carborane substitution leads to the lowering of both the HOMO and LUMO levels, but has higher impact on the LUMO stabilization than the HOMO, resulting in the reduction of the triplet excited state energy. In particular, the LUMO stabilization in the 4-substituted 5b is more contributed by carborane than that in the 5-substituted 5a. The solution-processed electroluminescent device incorporating 5a as an emitter displayed deep red phosphorescence (CIE coordinate: 0.693, 0.290) with moderate performance (max eta(EQE) = 3.8%) whereas the device incorporating 5b showed poor performance, as well as weak luminance.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectLIGHT-EMITTING-DIODES-
dc.subjectAGGREGATION-INDUCED EMISSION-
dc.subjectDENSITY-FUNCTIONAL THEORY-
dc.subjectMOLECULAR-ORBITAL METHODS-
dc.subjectEXCITED-STATE PROPERTIES-
dc.subjectC-C DISTANCE-
dc.subjectIR(III) COMPLEXES-
dc.subjectELECTROPHOSPHORESCENT DEVICES-
dc.subjectPHOTOPHYSICAL PROPERTIES-
dc.subjectELECTRONIC-PROPERTIES-
dc.titleDeep Red Phosphorescence of Cyclometalated Iridium Complexes by o-Carborane Substitution-
dc.typeArticle-
dc.identifier.wosid000329529800022-
dc.identifier.scopusid2-s2.0-84891816686-
dc.type.rimsART-
dc.citation.volume53-
dc.citation.issue1-
dc.citation.beginningpage128-
dc.citation.endingpage138-
dc.citation.publicationnameINORGANIC CHEMISTRY-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorLee, Yoon Sup-
dc.contributor.localauthorYoo, Seunghyup-
dc.contributor.localauthorDo, Youngkyu-
dc.contributor.nonIdAuthorPark, Jihyun-
dc.contributor.nonIdAuthorLee, Min Hyung-
dc.type.journalArticleArticle-
dc.subject.keywordPlusLIGHT-EMITTING-DIODES-
dc.subject.keywordPlusAGGREGATION-INDUCED EMISSION-
dc.subject.keywordPlusDENSITY-FUNCTIONAL THEORY-
dc.subject.keywordPlusMOLECULAR-ORBITAL METHODS-
dc.subject.keywordPlusEXCITED-STATE PROPERTIES-
dc.subject.keywordPlusC-C DISTANCE-
dc.subject.keywordPlusIR(III) COMPLEXES-
dc.subject.keywordPlusELECTROPHOSPHORESCENT DEVICES-
dc.subject.keywordPlusPHOTOPHYSICAL PROPERTIES-
dc.subject.keywordPlusELECTRONIC-PROPERTIES-
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