Metal organic light-emitting material and application thereof in OLED (organic light-emitting diode) device
A luminescent material, a metal-organic technology, applied in luminescent materials, organic chemistry, electric solid-state devices, etc., can solve the problems of low phosphorescence efficiency, poor stability and life, and obstacles to commercialization
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Embodiment 1
[0129] Embodiment 1: the synthesis of compound I-1
[0130]
[0131] The synthesis path is as follows:
[0132]
[0133] In a 500mL three-necked flask equipped with mechanical stirring, reflux condensing device and nitrogen protection device, M1 (14.2g, 0.01mol) and H1 (3.4g, 0.01mol) were added in turn, and then 200ml of ethanol was added, and the mixture was heated to reflux for 24 After 1 hour, the reactant was cooled to room temperature, and the resulting yellow solid was filtered, dissolved in dichloromethane, and separated by column chromatography to obtain 4.36 g of a bright yellow solid with a yield of 52%.
[0134] Elemental analysis (C46H27D5IrN3O): theoretical C, 65.77; H, 4.44; Ir, 22.88; N, 5.00; O, 1.90; found C, 65.71, H, 4.38, N, 5.02.
Embodiment 2
[0135] Embodiment 2: the synthesis of compound 1-19
[0136]
[0137] The synthesis path is as follows:
[0138]
[0139] H4 was used to replace H1, an appropriate material ratio was selected, other raw materials and steps were the same as in Example 1, and 5.45 g of product I-19 was obtained with a yield of 61%.
[0140] Elemental analysis (C49H30D13IrN3O): theoretical C, 65.74; H, 6.30; Ir, 21.47; N, 4.69; O, 1.79; found C, 65.77, H, 6.32, N, 4.66.
Embodiment 3
[0141] Embodiment 3: the synthesis of compound I-21
[0142]
[0143] The synthesis path is as follows:
[0144]
[0145] Replace M1 with M2, replace H1 with H2, select the appropriate material ratio, and other raw materials and steps are the same as in Example 1 to obtain 4.88g of product I-21 with a yield of 55%.
[0146] Elemental analysis (C48H27D13FIrN3O): theoretical value C, 64.12; H, 5.94; F, 2.11; Ir, 21.38; N, 4.67;
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