A kind of high-efficiency organic light-emitting material and its preparation and application
An electroluminescent material and organic technology, applied in the direction of luminescent materials, preparation of organic compounds, organic chemistry, etc., can solve the problems of complex synthesis methods, low brightness, low efficiency, and inability to fully satisfy full-color display, and achieve high luminescence efficiency effect
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Embodiment 1
[0023] Embodiment 1: the synthesis of compound 001
[0024] The specific synthetic route is shown in the following formula:
[0025]
[0026] (1) Weigh 37.8g of tetrabenzotriphenyl, dissolve it in 200mL of dichloromethane, add 39.16g of NBS, raise the temperature to 40°C, stir and react for 24 hours, spin dry the organic solvent, and put the obtained crude product into the column layer Analysis (petroleum ether / dichloromethane=1:1) resulted in 41.83 g of light yellow solid 6,13-dibromotetrabenzotriphenyl.
[0027] (2) Under the condition of nitrogen protection, add 30ml of anhydrous tetrahydrofuran solution, 3.74g of magnesium bars, and 2 pieces of iodine into the three-necked flask. After the Grignard reagent triggers, add 41.83g of 6,13-dibromotetrabenzotriphenyl 100ml of anhydrous tetrahydrofuran solution, reacted for 3 hours under ice-water bath conditions, added dropwise 12ml of anhydrous N,N-dimethylformamide to the reaction solution, then slowly raised to room tempe...
Embodiment 2
[0030] Embodiment 2: the synthesis of compound 002
[0031] The specific synthetic route is shown in the following formula:
[0032]
[0033] (1) Weigh 37.8g of tetrabenzotriphenyl, dissolve it in 200mL of dichloromethane, add 39.16g of NBS, raise the temperature to 40°C, stir and react for 24 hours, spin dry the organic solvent, and put the obtained crude product into the column layer Analysis (petroleum ether / dichloromethane=1:1) resulted in 41.83 g of light yellow solid 6,13-dibromotetrabenzotriphenyl.
[0034] (2) Under the condition of nitrogen protection, add 30ml of anhydrous tetrahydrofuran solution, 3.74g of magnesium bars, and 2 pieces of iodine into the three-necked flask. After the Grignard reagent triggers, add 41.83g of 6,13-dibromotetrabenzotriphenyl 100ml of anhydrous tetrahydrofuran solution, reacted for 3 hours under ice-water bath conditions, added dropwise 12ml of anhydrous N,N-dimethylformamide to the reaction solution, then slowly raised to room tempe...
Embodiment 3
[0037] Embodiment 3: the synthesis of compound 003
[0038] The specific synthetic route is shown in the following formula:
[0039]
[0040] (1) Weigh 37.8g of tetrabenzotriphenyl, dissolve it in 200mL of dichloromethane, add 39.16g of NBS, raise the temperature to 40°C, stir and react for 24 hours, spin dry the organic solvent, and put the obtained crude product into the column layer Analysis (petroleum ether / dichloromethane=1:1) resulted in 41.83 g of light yellow solid 6,13-dibromotetrabenzotriphenyl.
[0041] (2) Under the condition of nitrogen protection, add 30ml of anhydrous tetrahydrofuran solution, 3.74g of magnesium bars, and 2 pieces of iodine into the three-necked flask. After the Grignard reagent triggers, add 41.83g of 6,13-dibromotetrabenzotriphenyl 100ml of anhydrous tetrahydrofuran solution, reacted for 3 hours under ice-water bath conditions, added dropwise 12ml of anhydrous N,N-dimethylformamide to the reaction solution, then slowly raised to room tempe...
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