Phosphorescent iridium complex and preparation method thereof, and electroluminescent device
A technology of phosphorescent iridium complexes and bridging ligands is applied in the field of novel high-efficiency phosphorescent iridium complexes and their preparation, and electroluminescent devices, which can solve the problems of low brightness, poor quality, and easy breakdown of devices, and achieve Effects of prolongation of phosphorescence lifetime, reduction of driving voltage, and improvement of luminous efficiency
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Embodiment 1
[0050] Embodiment 1: Preparation G-001
[0051]
[0052] The first step: under the nitrogen protection system, weigh the formula A-001 (64.5mmol, 10.00g), IrC1 3 ·3H 2 O (21.5mmol, 7.58g) was put into the reaction system, a mixed solution of 300m1 ethylene glycol ether and 100m1 pure water was added, refluxed for 24 hours under the protection of nitrogen, and then cooled to room temperature, a precipitate was precipitated, the precipitate was suction filtered, and water , absolute ethanol, and petroleum ether were washed and dried in sequence. The bridging ligand B-001 (5.20 g, 46.8% yield) was obtained as a yellow powder.
[0053] The second step: Weigh the bridging ligand B-001 (4.66mmol, 5.00g), add silver trifluoromethanesulfonate (10.25mmol, 2.69g), then add 100ml of dichloromethane to the system, add 40ml of methanol, Under the protection of nitrogen, it was refluxed for 24 hours, cooled to room temperature, and the column chromatography (short column) filtrate was...
Embodiment 2
[0060] Embodiment 2: preparation G-014
[0061]
[0062] The first step: under the nitrogen protection system, weigh A-014 (64.5mmol, 10.00g), IrC1 3 ·3H 2 O (21.5mmol, 7.58g) was put into the reaction system, a mixed solution of 300m1 ethylene glycol ether and 100m1 pure water was added, refluxed for 24 hours under the protection of nitrogen, and then cooled to room temperature, a precipitate was precipitated, the precipitate was suction filtered, and water , absolute ethanol, and petroleum ether were washed and dried in sequence. The bridging ligand B-014 was obtained as a yellow powder (5.8 g, yield 50.3%).
[0063] The second step: Weigh the bridging ligand B-014 (4.66mmol, 5.00g), add silver trifluoromethanesulfonate (10.25mmol, 2.69g), then add 100ml of dichloromethane to the system, add 40ml of methanol, Under the protection of nitrogen, it was refluxed for 24 hours, cooled to room temperature, and the column chromatography (short column) filtrate was concentrated...
Embodiment 3
[0070] Embodiment 3: preparation G-022
[0071]
[0072] The first step: under the nitrogen protection system, weigh the formula A-022 (33mmol, 10.00g), IrC1 3 ·3H 2 O (11mmol, 3.87g) was put into the reaction system, a mixed solution of 300m1 ethylene glycol ether and 100m1 pure water was added, refluxed for 24 hours under the protection of nitrogen, and then cooled to room temperature, a precipitate was precipitated, the precipitate was suction filtered, water, Rinse with absolute ethanol and petroleum ether in sequence, and dry. The bridging ligand B-022 was obtained as a yellow powder (5.31 g, yield 57%).
[0073] The second step: Weigh the bridging ligand B-022 (2.96mmol, 5.00g), add silver trifluoromethanesulfonate (6.51mmol, 1.71g), then add 100ml of dichloromethane to the system, add 40ml of methanol, Under the protection of nitrogen, it was refluxed for 24 hours, cooled to room temperature, and the column chromatography (short column) filtrate was concentrated u...
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