Dendritic main body material and organic electroluminescence device prepared from the same
A technology of electroluminescent devices and main materials, which is applied in the direction of electroluminescent light sources, electric light sources, electrical components, etc., and can solve problems such as device efficiency reduction
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Embodiment 1
[0057] Embodiment 1: the synthesis of the compound of chemical formula (2)
[0058] Reaction 1:
[0059]
[0060] Under nitrogen protection, compound 3.1g (5.0mmol) of chemical formula (8), peripheral branch D 1 4.6g (16.5mmol), potassium carbonate 4.2g (30.0mmol), cuprous iodide 300mg (1.5mmol), 18-crown-6 211mg (0.8mmol) and 1,3-dimethyl-3,4,5 , a mixture of 2 mL of 6-tetrahydro-2-pyrimidinone (DMPU) was heated to 170 ° C, reacted for 24 hours, neutralized the remaining potassium carbonate with dilute hydrochloric acid, extracted with dichloromethane, washed with ammonia water to remove copper ions, and washed with saturated saline until medium properties, dried over anhydrous sodium sulfate, and the solvent was evaporated by rotary evaporation under reduced pressure, followed by column separation to obtain 4.4 g of the compound of chemical formula (2), with a yield of 82%.
Embodiment 2
[0061] Embodiment 2: the synthesis of the compound of chemical formula (3)
[0062] Reaction 2:
[0063]
[0064] Under nitrogen protection, the compound 1.6g (2.5mmol) of chemical formula (8), the peripheral branch D 2 5.9g (8.2mmol), potassium carbonate 2.1g (15.0mmol), cuprous iodide 150mg (0.75mmol), 18-crown-6 106mg (0.4mmol) and 1,3-dimethyl-3,4,5 , a mixture of 5 mL of 6-tetrahydro-2-pyrimidinone (DMPU) was heated to 190°C, reacted for 48 hours, neutralized the remaining potassium carbonate with dilute hydrochloric acid, extracted with dichloromethane, washed with ammonia water to remove copper ions, and washed with saturated saline until medium properties, dried over anhydrous sodium sulfate, and the solvent was evaporated by rotary evaporation under reduced pressure, followed by column separation to obtain 3.3 g of the compound of chemical formula (3), with a yield of 55%.
Embodiment 3
[0065] Embodiment 3: the synthesis of the compound of chemical formula (4)
[0066] Reaction 3:
[0067]
[0068] Under the protection of nitrogen, the compound 3.3g (5.0mmol) of chemical formula (9), the peripheral branch D 1 4.6g (16.5mmol), potassium carbonate 4.2g (30.0mmol), cuprous iodide 300mg (1.5mmol), 18-crown-6 211mg (0.8mmol) and 1,3-dimethyl-3,4,5 , a mixture of 2 mL of 6-tetrahydro-2-pyrimidinone (DMPU) was heated to 170 ° C, reacted for 24 hours, neutralized the remaining potassium carbonate with dilute hydrochloric acid, extracted with dichloromethane, washed with ammonia water to remove copper ions, and washed with saturated saline until medium properties, dried over anhydrous sodium sulfate, and the solvent was evaporated by rotary evaporation under reduced pressure, followed by column separation to obtain 3.4 g of the compound of chemical formula (4), with a yield of 61%.
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