574750-94-0Relevant articles and documents
Tertiary amine derivatives and organic electroluminescent device including the same
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Paragraph 0137; 0138; 0141; 0142, (2021/06/01)
A UV-region high-energy external light source is effectively absorbed to minimize damage to organic materials in the organic electroluminescent device. 1 Is a cross-sectional view of an organic electroluminescence device according to the present invention. O-2 electrode 1 Or more organic material layers disposed between the (2) and (1) th electrodes. A capping layer is included. The organic material layer and/or the capping layer may include the 1 st amine derivative represented by Formula 3. Chemical Formula 1. Wherein each substituent in Formula 1 is as defined in the description of the invention.
Arylation of aryllithiums with: S-arylphenothiazinium ions for biaryl synthesis
Morofuji, Tatsuya,Yoshida, Tatsuki,Tsutsumi, Ryosuke,Yamanaka, Masahiro,Kano, Naokazu
, p. 13995 - 13998 (2020/11/21)
Aryllithiums are one of the most common and important aryl nucleophiles; nevertheless, methods for arylation of aryllithums to produce biaryls have been limited. Herein, we report arylation of aryllithiums with S-arylphenothiazinium ions through selective
NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DIVICE INCLUDING THE SAME
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Paragraph 0132-0135, (2019/03/12)
The present invention relates to a novel compound and an organic light emitting device including the same. The compound of the present invention is represented by chemical formula 1, wherein Ar_1 is a substituted or unsubstituted C_6 to C_35 aryl group or a substituted or unsubstituted C_5 to C_25 heteroaryl group; R_1, R_2, and R_3 are each independently hydrogen, deuterium, a substituted or unsubstituted C_1 to C_30 alkyl group, a substituted or unsubstituted C_6 to C_30 aryl group, or a substituted or unsubstituted C_5 to C_30 heteroaryl group; and L_1 and L_2 are each independently a direct bond or phenylene. According to the present invention, high efficiency, long lifetime, low driving voltage, and driving stability of an organic light emitting device can be secured.COPYRIGHT KIPO 2019