Blue Phosphorescent Mono-cyclometalated Iridium(III) Complexes

被引:2
|
作者
Ham, Ho Wan [1 ]
Yang, Yoon A. [1 ]
Kim, Young Sik [1 ,2 ]
机构
[1] Hongik Univ, Dept Informat Display, Seoul 121791, South Korea
[2] Hongik Univ, Dept Sci, Seoul 121791, South Korea
关键词
Phosphorescence; OLED materials; Iridium complex; Mixed ancillary ligands; LIGANDS; GREEN;
D O I
10.3938/jkps.57.1695
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
New deep blue phosphorescent iridium(III) complexes comprised of one cyclometalate, two phosphines trans to each other and two cis-ancillary ligands, such as Ir(F(2)Meppy)(PPh2Me)(2)(H)(Cl), Ir(F(2)Meppy)(PPh2Me)(2)(H)(NCMe)(+), and Ir(F(2)Meppy)(PPh2Me)(2)(H)(CN), [F(2)Meppy = 2-(2', 4'-difluorophenyl)-4-methyl-pyridine] were synthesized and studied to tune the phosphorescence wavelength to the deep blue region and to enhance the luminescence efficiencies. We investigated the strong field effects of ancillary ligands to gain insight into the factors responsible for the emission color change and the different luminescence efficiency. Reducing the molecular weight of the phosphine ligand with PPh2Me leads to more efficient deep-blue organic light-emitting devices (OLED) by thermal processing instead of through solution processing. The electron-withdrawing difluoro group substituted on the phenyl ring, the electron-donating methyl group on the pyridyl ring, and the cyano strong field ancillary ligand increased the HOMO-LUMO gap and achieved a hypsochromic shift in the emission color. As a result, the maximum emission spectra of Ir(F(2)Meppy)(PPh2Me)(2)-(H)(Cl), Ir(F(2)Meppy)(PPh2Me)(2)(H)(NCMe)(+), and Ir(F(2)Meppy)(PPh2Me)(2)-(H)(CN) were in the ranges of 440.5, 437, 436 nm, respectively.
引用
收藏
页码:1695 / 1698
页数:4
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