Synthesis and photophysics of a new deep red soluble phosphorescent iridium(III) complex based on chlorine-methyl-substituted 2,4 diphenyl quinoline

被引:8
作者
Dahule, H. K. [2 ]
Dhoble, S. J. [3 ]
Ahn, J. -S. [1 ]
Pode, Ramchandra [1 ]
机构
[1] Kyung Hee Univ, Dept Phys, Seoul 130701, South Korea
[2] Shivaji Sci Coll, Dept Phys, Nagpur 440012, Maharashtra, India
[3] Rashatrasant Tukadoji Maharaj Nagpur Univ, Dept Phys, Nagpur 440033, Maharashtra, India
关键词
Iridium complex; Chlorinated quinoline; X-ray diffraction; Thermogravimetric analysis (TGA); Photoluminescence; Deep red emitter; LIGHT-EMITTING-DIODES; HIGHLY EFFICIENT; DEVICES; EMITTERS; LIGANDS; REGION; HOST;
D O I
10.1016/j.jpcs.2011.09.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new iridium complex with a chlorine-methyl-substituted 2,4 diphenyl quinoline, (Cl-MDPQ) ligand has been synthesized. The synthesized iridium metal complex, Ir(Cl-MDPQ)(2)(acac) where Cl-MDPQ=chlorinemethyl substituted, 2,4 diphenyl quinoline, acac=acetyl acetone is characterized by employing different techniques such as mass spectrometry, H-1 NMR, DTA/TGA, XRD, and FTIR. The molecular structures of Cl-MDPQ and Ir(Cl-MDPQ)(2)(acac) complexes are confirmed by the FTIR spectra. Strong singlet metal-to-ligand charge-transfer ((MLCT)-M-1) and triplet metal-to-ligand charge-transfer ((MLCT)-M-3) absorption peaks at 353 and 437 rim in tetrahydrofuran (THF) are reported in the synthesized complex, respectively. A deep red emitting Ir(Cl-MDPQ)(2)(acac) complex at 662 nm is promising for flexible organic devices. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1524 / 1528
页数:5
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