25288-76-0Relevant academic research and scientific papers
Preparation method of tertiary amine compound
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, (2020/03/29)
The invention provides a preparation method of a tertiary amine compound, and belongs to the technical field of organic chemistry. The preparation method of the tertiary amine compound comprises the following steps: performing a carbon-nitrogen coupling reaction on a compound of chemical formula 2 and a compound of chemical formula 3 to obtain a compound of chemical formula 4; and carrying out thecarbon-nitrogen coupling reaction on the compound of chemical formula 4 and a compound of chemical formula 5 to obtain the compound of chemical formula 1, wherein the chemical formula 1, the chemicalformula 2, the chemical formula 3, the chemical formula 4 and the chemical formula 5 are shown in the description.
NOVEL TRIAZINE COMPOUND, AND ORGANIC ELECTRONIC ELEMENT AND PLANT-GROWING LIGHTING THAT USE THE SAME
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, (2018/07/28)
PROBLEM TO BE SOLVED: To provide a triazine compound which has a high triplet energy level and excellent heat resistance, and can be used as an organic electronic element material realizing an element with high efficiency, low voltage and a long life. SOLUTION: In the triazine compound, as represented by the general formula [1] in the figure, a triazine backbone moiety is linked to a dibenzofuran or dibenzothiophene backbone moiety via a biphenyl backbone moiety, where X is an oxygen atom or sulfur atom. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT
Triarylated amine derivative and organic electroluminescence device with same
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, (2018/09/08)
The invention discloses a triarylated amine derivative and an organic electroluminescence device with the same, and relates to the technical field of organic photoelectric materials. The triarylated amine derivative has a large conjugated system, thereby having high hole mobility and presenting good hole transmissibility; in addition, the triarylated amine derivative has high thermal stability anddissolubility and is beneficial for material film forming. The organic electroluminescence device comprises a cathode, an anode and one or more organic matter layers. The organic matter layers are located between the cathode and the anode. At least one of the organic matter layers contains the triarylated amine derivative. The organic electroluminescence device has low driving voltages, high light-emitting efficiency, light-emitting luminance and long service life.
COMPOUND FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME
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, (2017/12/01)
This invention provides a compound for an organic electroluminescent device and an organic electroluminescent device including the same. This invention provides a compound for an organic EL device, which may have high thermal stability, improved light emission efficiency and lifetime and hole transport capability. Further, when this compound is used as a hole transport layer material in contact with a light emitting layer, thereby increasing a triplet energy, ultimately improving efficiency of the organic EL device and lifetime.
PHOSPHORESCENT EMITTERS
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, (2011/09/16)
Compounds including a ligand with a dibenzo-fused 5-membered ring substituent are provided. In particular, the compounds may be iridium complexes including imidazole coordinated to the dibenzo-substituted ligand. The dibenzo-fused 5-membered ring moiety of the ligand may be twisted or minimally twisted out of plane with respect to the rest of the ligand structure. The compound may be used in organic light emitting devices, particularly as emitting dopants in blue devices. Devices comprising the compounds may demonstrate improved stability while maintaining excellent color.
Synthesis of Monoamino and Monohydroxydibenzothiophenes
Kudo, Hirotaka,Castle, Raymond N.,Lee, Milton L.
, p. 215 - 218 (2007/10/02)
The synthesis of the four monoaminodibenzothiophenes and the four monohydroxydibenzothiophenes is described.
Preparation of esters of phosphorus acids
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, (2008/06/13)
Esters of phosphorus acids are prepared by an improved process whereby aromatic alcohols and phosphorus halides are reacted at specified temperatures in the presence of amine catalysts thereby providing high yields of substantially pure esters and allowing preparation of selected halogen-containing mono- and di-esters of phosphorus acids wherein halogen is directly bonded to phosphorus having substantially no side reactant contamination. The phosphorus esters are useful as intermediates in the preparation of plasticizers, oil additives and functional fluids.
