Takao Takiguchi
Canon Inc.
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Dalton Transactions | 2005
Shinjiro Okada; Keiji Okinaka; Hironobu Iwawaki; Manabu Furugori; Masashi Hashimoto; Taihei Mukaide; Jun Kamatani; Satoshi Igawa; Akira Tsuboyama; Takao Takiguchi; Kazunori Ueno
This study reports substituent effects of iridium complexes with 1-phenylisoquinoline ligands. The emission spectra and phosphorescence quantum yields of the complexes differ from that of tris(1-phenylisoquinolinato-C2,N)iridium(iii)(Irpiq) depending on the substituents. The maximum emission peak, quantum yield and lifetime of those complexes ranged from 598-635 nm, 0.17-0.32 and 1.07-2.34 micros, respectively. This indicates the nature of the substituents has a significant influence on the kinetics of the excited-state decay. The substituents attached to phenyl ring have an influence on a stability of the HOMO. Furthermore, those substituents have effect on the contribution to a mixing between 3pi-pi* and (3)MLCT for the lowest excited states. Some of the complexes display the larger quantum yield than Irpiq, which has the quantum yield of 0.22. The organic light emitting diode (OLED) device based on tris [1-(4-fluoro-5-methylphenyl)isoquinolinato-C2,N]iridium(iii)(Ir4F5Mpiq) yielded high external quantum efficiency of 15.5% and a power efficiency of 12.4 lm W(-1) at a luminance of 218 cd m(-2). An emission color of the device was close to an NTSC specification with CIE chromaticity characteristics of (0.66, 0.34).
SID Symposium Digest of Technical Papers | 2002
Shinjiro Okada; Hironobu Iwawaki; Manabu Furugori; Jun Kamatani; Satoru Igawa; Takashi Moriyama; Seishi Miura; Akira Tsuboyama; Takao Takiguchi; Hidemasa Mizutani
We studied red emissive materials of Ir-complex. We demonstrate high efficiency red OLED devices employing phosphorescent dopant. Ir(piq)3 [Iridium(III)tris(1-phenyl-isoquinolinato-N, C2)] shows maximum emission peak of 623nm and excellent Q.Y with 0.66 compared to Ir(ppy)3 as a unit. Efficiency of the EL device is 8.0 lm/W, 9.3 cd/A at 100cd/m2, 623 lm/W, 8.4 cd/A at 300cd/m2. CIE- coordinate is (0.68,0.33) and it meets NTSC specification.
Journal of the American Chemical Society | 2003
Akira Tsuboyama; Hironobu Iwawaki; Manabu Furugori; Taihei Mukaide; Jun Kamatani; Satoshi Igawa; Takashi Moriyama; Seishi Miura; Takao Takiguchi; Shinjiro Okada; Mikio Hoshino; Kazunori Ueno
Archive | 2002
Jun Kamatani; Shinjiro Okada; Akira Tsuboyama; Takao Takiguchi; Seishi Miura; Koji Noguchi; Takashi Moriyama; Satoshi Igawa; Manabu Furugori
Archive | 2002
Takao Takiguchi; Shinjiro Okada; Akira Tsuboyama; Seishi Miura; Takashi Moriyama; Jun Kamatani; Manabu Furugori
Archive | 2001
Takao Takiguchi; Hidemasa Mizutani; Shinjiro Okada; Akira Tsuboyama; Seishi Miura; Takashi Moriyama; Satoshi Igawa; Jun Kamatani; Manabu Furugori
Archive | 2001
Akira Tsuboyama; Hidemasa Mizutani; Shinjiro Okada; Takao Takiguchi; Takashi Moriyama; Jun Kamatani
Archive | 2001
Jun Kamatani; Shinjiro Okada; Akira Tsuboyama; Takao Takiguchi; Seishi Miura; Koji Noguchi; Takashi Moriyama; Satoshi Igawa; Manabu Furugori
Archive | 2002
Jun Kamatani; Shinjiro Okada; Akira Tsuboyama; Takao Takiguchi; Satoshi Igawa
Archive | 2002
Akira Tsuboyama; Hidemasa Mizutani; Shinjiro Okada; Takao Takiguchi; Seishi Miura; Takashi Moriyama; Satoshi Igawa; Jun Kamatani; Manabu Furugori