Blue phosphorescence iridium complexes, preparing method thereof and organic electroluminescent device
An iridium metal complex, blue phosphorescence technology, applied in luminescent materials, electro-solid devices, organic chemistry, etc., can solve the problems of poor luminescence performance and development lag of light-emitting devices, reduce interaction force, increase solubility, reduce The effect of self-quenching
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[0040] see figure 1 , the preparation method of the blue phosphorescence iridium metal complex of an embodiment, comprises the steps:
[0041] Step S110: In a protective gas atmosphere, dissolve compound F and 2,4-bis(trifluoromethyl)phenylboronic acid in a molar ratio of 1:1 to 1.5 in the first solvent, and add an organopalladium catalyst and carbonic acid The aqueous solution of salt is subjected to Suzuki coupling reaction for 10 to 15 hours, and compound A is obtained after separation and purification, and the structural formula of compound F is , the structural formula of compound A is , wherein R is an alkoxy group having 1 to 20 carbon atoms.
[0042] The protective gas is argon, helium or neon.
[0043] The first solvent is toluene or N,N-dimethylformamide (DMF). The amount of the first solvent is suitable for fully dissolving compound F and 2,4-bis(trifluoromethyl)phenylboronic acid. Preferably, the concentration of compound F in the first solvent is 0.07-0.11 ...
Embodiment 1
[0072] Blue Phosphorescent Bis(2-(4',6'-bis(trifluoromethyl)phenyl)-5-methoxypyrimidine-N,C 2 Synthesis of ')(5-(2'-pyridyl)-1,2,3,4-tetrazole)iridium complexes
[0073] Blue Phosphorescent Bis(2-(4',6'-bis(trifluoromethyl)phenyl)-5-methoxypyrimidine-N,C 2 ')(5-(2'-pyridyl)-1,2,3,4-tetrazole) iridium complex has the following structural formula:
[0074]
[0075] (1) Synthesis of 2-(2',4'-bis(trifluoromethyl)phenyl)-5-methoxypyrimidine
[0076]
[0077] Under nitrogen protection, 0.94g (5mmol) 2-bromo-5-methoxypyrimidine, 1.55g (6mmol) 2,4-bis(trifluoromethyl)phenylboronic acid and 0.29g (0.25mmol) tetrakis(triphenyl) Phosphorus) palladium was dissolved in 30mL of DMF, and then 15mL of an aqueous solution containing 1.27g (12mmol) of sodium carbonate was added dropwise to the reaction system. Heated and stirred under reflux for 10h. After the reaction solution was cooled to room temperature, it was extracted with dichloromethane, separated, washed with water until ne...
Embodiment 2
[0099] Blue Phosphorescent Bis(2-(4',6'-bis(trifluoromethyl)phenyl)-4-hexyloxypyrimidine-N,C 2 Synthesis of ')(5-(2'-pyridyl)-1,2,3,4-tetrazole)iridium complexes
[0100] Blue Phosphorescent Bis(2-(4',6'-bis(trifluoromethyl)phenyl)-4-hexyloxypyrimidine-N,C 2 ')(5-(2'-pyridyl)-1,2,3,4-tetrazole) iridium complex has the following structural formula:
[0101]
[0102] (1) Synthesis of 2-(2',4'-bis(trifluoromethyl)phenyl)-4-hexyloxypyrimidine
[0103]
[0104] Under nitrogen protection, 1.30g (5mmol) 2-bromo-4-hexyloxypyrimidine, 1.93g (7.5mmol) 2,4-bis(trifluoromethyl)phenylboronic acid and 0.21g (0.3mmol) dichlorobis( Triphenylphosphine)palladium was dissolved in 30mL of toluene, and then 15mL of an aqueous solution containing 1.38g (10mmol) of potassium carbonate was added dropwise to the reaction system. Heated and stirred under reflux for 12h. After the reaction solution was cooled to room temperature, it was extracted with dichloromethane, separated, washed with wa...
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