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624744-81-6

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624744-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 624744-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,4,7,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 624744-81:
(8*6)+(7*2)+(6*4)+(5*7)+(4*4)+(3*4)+(2*8)+(1*1)=166
166 % 10 = 6
So 624744-81-6 is a valid CAS Registry Number.

624744-81-6Downstream Products

624744-81-6Relevant articles and documents

Homoleptic Cyclometalated Iridium Complexes with Highly Efficient Red Phosphorescence and Application to Organic Light-Emitting Diode

Tsuboyama, Akira,Iwawaki, Hironobu,Furugori, Manabu,Mukaide, Taihei,Kamatani, Jun,Igawa, Satoshi,Moriyama, Takashi,Miura, Seishi,Takiguchi, Takao,Okada, Shinjiro,Hoshino, Mikio,Ueno, Kazunori

, p. 12971 - 12979 (2007/10/03)

Phosphorescence studies of a series of facial homoleptic cyclometalated iridium(III) complexes have been carried out. The complexes studied have the general structure Ir(III)(C-N)3, where (C-N) is a monoanionic cyclometalating ligand: 2-(5-methylthiophen-2-yl)pyridinato, 2-(thiophen-2-yl)-5-trifluoromethylpyridinato, 2,5-di(thiophen-2-yl)pyridinato, 2,5-di(5-methylthiophen-2-yl)pyridinato, 2-(benzo[b]thiophen-2-yl)pyridinato, 2-(9,9-dimethyl-9H-fluoren-2-yl)pyridinato, 1-phenylisoquinolinato, 1-(thiophen-2yl)isoquinolinato, or 1-(9,9-dimethyl-9H-fluoren-2-yl)isoquinolinato. Luminescence properties of all the complexes at 298 K in toluene are as follows: quantum yields of phosphorescence φp = 0.08-0.29, emission peaks λ max = 558-652 nm, and emission lifetimes τ = 0.74-4.7 μs. Bathochromic shifts of the Ir(thpy)3 family [the complexes with 2-(thiophen-2-yl)pyridine derivatives] are observed by introducing appropriate substituents, e.g., methyl, trifluoromethyl, or thiophen-2-yl. However, φp of the red emissive complexes (λmax > 600 nm) becomes small, caused by a significant decrease of the radiative rate constant, kr. In contrast, the complexes with the 1-arylisoquinoline ligands are found to have marked red shifts of λmax and very high φp (0.19-0.26). These complexes are found to possess dominantly 3MLCT (metal-to-ligand charge transfer) excited states and have kr values approximately 1 order of magnitude larger than those of the Ir(thpy)3 family. An organic light-emitting diode (OLED) device that uses Ir(1-phenylisoquinolinato)3 as a phosphorescent dopant produces very high efficiency (external quantum efficiency ηex = 10.3% and power efficiency 8.0 Im/W at 100 cd/m2) and pure-red emission with 1931 CIE (Commission Internationale de L'Eclairage) chromaticity coordinates (x = 0.68, y = 0.32).

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