Organic iridium metal complex and preparation method and application thereof
An iridium metal complex, organic technology, applied in indium organic compounds, platinum group organic compounds, organic chemistry, etc., can solve the problems of low blue light color purity and luminous efficiency, and achieve the effects of high yield and easy reaction
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[0038] Correspondingly, the embodiment of the present invention also provides a method that can be used to prepare the organic iridium metal complex of the general molecular structure formula (I), the preparation method flow is as follows figure 1 shown. The preparation method of the organic iridium metal complex comprises the following steps:
[0039] S01. Provide the compound A of the general formula of the following structural formula;
[0040]
[0041]S02. Using compound A to prepare chlorine bridge dimer B: in an oxygen-free environment, the compound A provided in step S01 is subjected to heat reflux reaction with iridium trichloride hydrate or sodium chloroiridite hydrate in a reaction solvent, Generate the chlorine bridge dimer B of following structural formula general formula:
[0042]
[0043] S03. Ligand exchange reaction between chlorine bridge dimer B and 3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole to prepare organic compound with general molecular stru...
Embodiment 1
[0084] Bis(2-(4',6'-difluoro-5'-cyanophenyl)-5-phenylpyrimidine-N,C 2 ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium metal complex and its synthesis method:
[0085] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-5-phenylpyrimidine:
[0086] The specific steps are: under nitrogen protection, mix 2.35g (10mmol) 2-bromo-5-phenylpyrimidine, 2.20g (12mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.58g (0.5mmol) Tetrakis(triphenylphosphine)palladium (ie palladium catalyst) was dissolved in 50mL of toluene, and then 25mL of an aqueous solution containing 2.76g (20mmol) of potassium carbonate was added dropwise to the reaction system. Stir the reaction under heating to 100°C for 10 h. After the reaction solution was cooled to room temperature, it was extracted with dichloromethane, separated, washed with water until neutral, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was distilled off the solvent under reduced pressure to obtain ...
Embodiment 2
[0098] Bis(2-(4',6'-difluoro-5'-cyanophenyl)-4-(fluoren-9'-yl)pyrimidine-N,C 2 ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium metal complex and its synthesis method:
[0099] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-4-(fluoren-9'-yl)pyrimidine:
[0100] The specific steps are: under nitrogen protection, mix 3.23g (10mmol) 2-bromo-4-(fluoren-9'-yl)pyrimidine, 1.83g (10mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.21g (0.3mmol) dichlorobis(triphenylphosphine) palladium was dissolved in 60mL N,N-dimethylformamide solution (ie DMF), then 30mL containing 1.59g (15mmol) carbonic acid was added dropwise to the reaction system Aqueous solution of sodium. Stir the reaction under heating to 90°C for 12h. After the reaction solution was cooled to room temperature, it was extracted with dichloromethane, separated, washed with water until neutral, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was distilled off the solvent under r...
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