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Introduction of new ancillary ligands to the iridium complexes having 2,3-diphenylquinolinato ligands for OLED

Authors
Lee, Hyun ShinAhn, So YounHuh, Hyun SueHa, Yunkyoung
Issue Date
15-Sep-2009
Publisher
ELSEVIER SCIENCE SA
Keywords
Pyrazolone-based ancillary ligands; (przl-R series); Iridium complex; 2,3-Diphenylquinolinato ligand; Red phosphorescence; OLED
Citation
JOURNAL OF ORGANOMETALLIC CHEMISTRY, v.694, no.20, pp.3325 - 3330
Journal Title
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume
694
Number
20
Start Page
3325
End Page
3330
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/21798
DOI
10.1016/j.jorganchem.2009.06.003
ISSN
0022-328X
Abstract
We investigated the effect of an ancillary ligand (AL) on the emission color and luminous efficiencies of its complex, Ir(4-Me-2,3-dpq)(2)(AL),where 4-Me-2,3-dpq represents 4-methyl-2,3-diphenylquinolinato ligand. We expected that ancillary ligand modi. cation by introduction of the bulky substituent to the complexes might allow luminous efficiency increase by reduction of T -T annihilation. Furthermore, some ancillary ligands may contribute to. ne-tuning of their complex emission colors by influencing the energy level of Ir d-orbitals upon the orbital mixing. As new ancillary ligands substituting for acac which is a typical AL in the iridium complexes, pyrazolone-based ligands, 4-R-5-methyl-2-phenyl-2,4-dihydropyrazol3- one series (przl-R), were prepared, where R represents C6H5, C6H4CH3 and C6H4Cl. These ligands were chelated to the iridium center to yield a new series of the iridium complexes, Ir(4-Me-2,3- dpq)(2)(przl-R). The X-ray crystal structure of Ir(4-Me-2,3-dpq)(2)(przl-C6H4Cl) was determined. The electrochemical and luminescence properties of the iridium complexes were investigated. The effect of the przl-substituents on the emission colors of the complexes was not significant. On the other hand, the luminous efficiencies of Ir(4-Me-2,3-dpq) 2(przl-C6H5) and Ir(4-Me-2,3-dpq)(2)(przl-C6H4CH3) were higher than that of Ir(4-Me-2,3-dpq)(2)(acac). (C) 2009 Elsevier B.V. All rights reserved.
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