Iridium metal complex, preparation method thereof and organic electroluminescent device
An iridium metal complex, selected technology, applied in electric solid devices, electrical components, luminescent materials, etc., can solve the problems of easy environmental pollution, high synthesis cost, and high purification requirements
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Embodiment 1
[0088] Example 1 Preparation of compound numbered L001
[0089]
[0090] Step 1. Under the nitrogen protection system, weigh A-001 (64.5mmol, 10.00g), IrC1 3 ·3H 2 Put O (24.8mmo1, 8.75g) into the reaction system, add a mixed solution of 300mL ethylene glycol ether and 100mL purified water, reflux for 24 hours under nitrogen protection, and then cool to room temperature, where a precipitate precipitates. The precipitate is filtered off with water , Anhydrous ethanol and petroleum ether were washed and dried in sequence to obtain a yellow powder bridging ligand B-001 (7.05 g, yield 53%).
[0091] Step 2. Weigh intermediate B-001 (4.67mmol, 5.00g), add silver trifluoromethanesulfonate (14mmol, 3.58g), then add 100mL of dichloromethane to the system, add 40mL of methanol, and under nitrogen protection, After refluxing for 24 hours, cooling to room temperature, the column chromatography (short column) filtrate was concentrated until a solid precipitated to obtain the iridium complex in...
Embodiment 2
[0098] Example 2 Preparation of compound numbered L091
[0099]
[0100] Step 1. Under the nitrogen protection system, weigh A-091 (64.5mmol, 16.85g), IrC1 3 ·3H 2 Put O (24.8mmo1, 8.75g) into the reaction system, add a mixed solution of 300mL ethylene glycol ether and 100mL purified water, reflux for 24 hours under nitrogen protection, and then cool to room temperature, where a precipitate precipitates. The precipitate is filtered off with water , Anhydrous ethanol, and petroleum ether followed by washing and drying to obtain a yellow powder bridging ligand B-091 (9.65 g, yield 52%).
[0101] Step 2. Weigh intermediate B-091 (4.67mmol, 6.99g), add silver trifluoromethanesulfonate (14.00mmol, 3.58g), then add 100mL of dichloromethane to the system, add 40mL of methanol, and under nitrogen protection Reflux for 24 hours, cool to room temperature, and concentrate the filtrate by column chromatography (short column) until a solid precipitates to obtain the iridium complex intermediate...
Embodiment 3
[0108] Example 3 Preparation of compound numbered L126
[0109]
[0110] Step 1. Under the nitrogen protection system, weigh A-126 (64.5mmol, 16.84g), IrC1 3 ·3H 2 Put O (24.8mmo1, 8.75g) into the reaction system, add a mixed solution of 300mL ethylene glycol ether and 100mL purified water, reflux for 24 hours under nitrogen protection, and then cool to room temperature, where a precipitate precipitates. The precipitate is filtered off with water , Anhydrous ethanol, and petroleum ether followed by washing and drying to obtain a yellow powder bridging ligand B-126 (10.20 g, yield 55%).
[0111] Step 2. Weigh intermediate B-126 (4.67mmol, 6.99g), add silver trifluoromethanesulfonate (14mmol, 3.58g), then add 100mL of dichloromethane to the system, add 40mL of methanol, and under nitrogen protection, It was refluxed for 24 hours, cooled to room temperature, and the column chromatography (short column) filtrate was concentrated until a solid precipitated to obtain the iridium complex ...
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