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The study of the sublimable six-coordinated aluminum quinolate with sulfonamide substitutents

dc.citation.epage305en_US
dc.citation.issue4-6en_US
dc.citation.spage302en_US
dc.citation.volume397en_US
dc.citation.woscount3
dc.contributor.authorCheng, JAen_US
dc.contributor.authorChen, CHen_US
dc.contributor.authorYang, HLen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department友訊交大聯合研發中心zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentD Link NCTU Joint Res Ctren_US
dc.date.accessioned2014-12-08T15:37:26Z
dc.date.available2014-12-08T15:37:26Z
dc.date.issued2004-10-21en_US
dc.description.abstractA sublimationable blue-green host materials based on tris(8-hydroxyquinolato)aluminum, meridional tris(5-N-ethylanilinesulfonamide-8-quinolato) aluminum, mer-Al(Saq)(3), was investigated and characterized by thermogravimetric analysis (TGA) and H-1 nuclear magnetic resonance (NMR). Via molecular engineering, the sublimation enthalpy of mer-Al(Saq)(3) can be adjusted by introducing the N-ethylanilinesulfonamide substitutent. Its electroluminescence (EL) was also characterized by the device architecture of glass/ITO (200 nm)/CuPc (15 nm)/NPB (60 nm)/mer-Al(Saq)(3) (55 nm)/LiF (1 nm)/Al (200 nm). It shows a blue-green spectrum with blue-green of 1931 CIEx,y(0.25, 0.39). Our experiments revealed that the Al-N bond order might not be the major issue in sublimation process. (C) 2004 Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.cplett.2004.08.132en_US
dc.identifier.issn0009-2614en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2004.08.132en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/25745
dc.identifier.wosnumberWOS:000224541000003
dc.language.isoen_USen_US
dc.titleThe study of the sublimable six-coordinated aluminum quinolate with sulfonamide substitutentsen_US
dc.typeArticleen_US

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