Organic electro-phosphorescent material and preparation method thereof, and organic electroluminescent device
A phosphorescent material, electromechanical technology, applied in the field of phosphorescent materials, can solve the problems of the luminous color purity of blue phosphorescent materials, the efficiency attenuation bottleneck of luminous efficiency devices, etc.
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[0038] The preparation process of the organic electrophosphorescent material (P) of the present invention is roughly divided into the following steps:
[0039] (1) Synthesize compound C through Suzuki coupling reaction of compound E and compound F; wherein, compound F is 2,4-difluoro-3-cyanophenylboronic acid, and the structural formulas of compound E and compound C are as follows:
[0040] Compound E is Compound C is Among them, R is C 1 ~C 20 straight-chain or branched-chain alkoxy groups.
[0041] (2) Reaction of compound C prepared in step (1) with compound D to generate a chlorine-bridged dimer, namely compound A. Wherein, compound D is trihydrate iridium trichloride IrCl 3 ·3H 2 O. The structural formula of compound A is as follows:
[0042]
[0043] (3) Compound A prepared in step (2) is used as the main structure of the ring metal ligand, and 3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole (ie Compound B) is used as an auxiliary ligand source to react com...
Embodiment 1
[0049] The organic electrophosphorescent material (P) disclosed in this example is the complex bis(2-(4',6'-difluoro-5'-cyanophenyl)-5-methoxypyrimidine-N,C 2' )(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium, its structural formula is as follows:
[0050]
[0051] It is prepared by the following steps:
[0052] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-5-methoxypyrimidine
[0053] The synthetic reaction formula of 2-(2',4'-difluoro-3'-cyanophenyl)-5-methoxypyrimidine is as follows:
[0054]
[0055] The specific steps are: under nitrogen protection, mix 1.89g (10mmol) 2-bromo-5-methoxypyrimidine, 2.20g (12mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.58g (0.5mmol ) Tetrakis(triphenylphosphine)palladium was dissolved in 35mL of toluene solution, and then 15mL of potassium carbonate solution containing 2.76g (20mmol) was added dropwise to the reaction system. Heat to 100°C and stir the reaction for 6h. After the reaction solution was cooled to ...
Embodiment 2
[0070] The organic electrophosphorescent material disclosed in this example is the complex bis(2-(4',6'-difluoro-5'-cyanophenyl)-4-hexyloxypyrimidine-N,C 2 ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium, its structural formula is as follows:
[0071]
[0072] It is prepared by the following steps:
[0073] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-4-hexyloxypyrimidine
[0074] The reaction formula for the synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-4-hexyloxypyrimidine is as follows:
[0075]
[0076] The specific steps are: under the protection of nitrogen, mix 2.59g (10mmol) 2-bromo-4-hexyloxypyrimidine, 1.83g (10mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.21g (0.3mmol ) dichlorobis(triphenylphosphine)palladium was dissolved in 40mL of N,N-dimethylformamide solution (ie DMF), and then 20mL of sodium carbonate solution containing 1.06g (10mmol) was added dropwise to the reaction system. Stir the reaction under heating to 80°C for 10h. ...
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