Blue light organic electrophosphorescent material iridium metal complex, preparation method thereof, and organic electroluminescent device
A technology of iridium metal complexes and phosphorescent materials, applied in the field of organic electroluminescent materials, can solve problems such as poor blue light color purity, achieve the effects of reducing self-quenching, high blue light emission wavelength, and increasing solubility
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[0042] see figure 1 , the preparation method of the above-mentioned blue light organic electrophosphorescent material iridium metal complex, comprising the following steps:
[0043] S1, under the protection of inert gas, the structural formula is The compound A and the structural formula are The compound B is dissolved in the first organic solvent containing catalyst and alkali to obtain a reaction solution, which is subjected to Suzuki coupling reaction at a temperature of 80-90° C. for 10-15 hours. After the reaction is stopped, the reaction solution is separated and purified, get the structural formula as ring metal ligand; wherein, the molar ratio of compound A to compound B is 1:1~1:1.5; wherein, R is C 1 ~C 20 The alkoxy group; the reaction formula is:
[0044]
[0045] S2. Under the protection of an inert gas, the cyclometal ligand and iridium trichloride trihydrate are dissolved in a mixed solvent formed by 2-ethoxyethanol and water at a molar ratio of 2:1 t...
Embodiment 1
[0073] Example 1: Complex bis(2-(2′,6′-difluoropyridin-3′-yl)-5-methoxypyrimidine-N,C 4 Synthesis of ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole)iridium
[0074] (1) Synthesis of 2-(2′,6′-difluoropyridin-3′-yl)-5-methoxypyrimidine
[0075]
[0076] Under nitrogen protection, 1.89g (10mmol) 2-bromo-5-methoxypyrimidine (compound A1), 1.91g (12mmol) 2,6-difluoropyridine-3-boronic acid (compound B) and 0.58g (0.5 mmol) Tetrakis(triphenylphosphine)palladium was dissolved in 35mL of toluene, then 15mL of aqueous solution containing 2.76g (20mmol) of potassium carbonate was added dropwise to the reaction system to form a reaction solution. The reaction solution was heated and stirred at 90° 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 t...
Embodiment 2
[0095] Example 2: Complex bis(2-(2′,6′-difluoropyridin-3′-yl)-4-hexyloxypyrimidine-N,C 4 Synthesis of ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole)iridium
[0096] (1) Synthesis of 2-(2′,6′-difluoropyridin-3′-yl)-4-hexyloxypyrimidine
[0097]
[0098] Under nitrogen protection, 1.30g (5mmol) 2-bromo-4-hexyloxypyrimidine (compound A2), 0.79g (5mmol) compound B and 0.14g (0.2mmol) dichlorobis (triphenylphosphine) palladium Dissolve in 35mL of DMF, and then dropwise add 15mL of an aqueous solution containing 2.07g (15mmol) of potassium carbonate to the reaction system to form a reaction solution. The reaction solution was heated to 80° C. and stirred for 12 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 the crude product. A mixture of...
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