6782-77-0Relevant academic research and scientific papers
Compound, application thereof and organic electroluminescence device
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Paragraph 0063-0065, (2019/04/06)
The invention relates to a compound shown as a general formula (I), wherein Ar is selected from substituted or unsubstituted aromatic hydrocarbon group of C6-C30, substituted or unsubstituted polycyclic aromatic hydrocarbon group of C1-C30, substituted or unsubstituted heterocyclic aromatic hydrocarbon group of C4-C30, substituted or unsubstituted fused heterocyclic aromatic hydrocarbon group of C8-C30 and substituted or unsubstituted aromatic-ammonia group of C6-C30, and R1 to R10 are independently selected from C6-C20, substituted or unsubstituted polycyclic aromatic hydrocarbon group of C1-C20, substituted or unsubstituted heterocyclic aromatic hydrocarbon group of C4-C20, substituted or unsubstituted fused heterocyclic aromatic hydrocarbon group of C8-C20 and substituted or unsubstituted aromatic-ammonia group of C6-C20 respectively. The invention further relates to an organic electroluminescence device.
Compound and its use and the organic electroluminescent light-emitting device (by machine translation)
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Paragraph 0059; 0060; 0061, (2019/04/10)
The invention of the formula (1) shown in the fused heterocyclic compounds and organic electroluminescent device in the application, the compounds of this invention with high triplet energy level, at the same time having a high current carrier transmissio
Addition Products of Hydrazine Derivatives to Azo-Alkenes, Part V: The Reaction of α-(1-Phenylhydrazino)alkanone Phenylhydrazones with Acids and Acid Derivatives
Schantl, J. G.,Prean, M.
, p. 299 - 308 (2007/10/02)
The bifunctional title compounds 2 react with acylating, carbamoylating and sulfonylating reagents mostly at the primary amino group of the hydrazine function.Both functional groups of 2 are attacked by N,N'-carbonyldiimidazole converting it into 1H-1,2,4
