Benzanthracene organic luminescent material, and preparation method and application thereof
A light-emitting material, a technology of benzanthracene, which is applied in the preparation of light-emitting materials, organic compounds, organic chemistry, etc., can solve the problem that anthracene light-emitting materials cannot meet the requirements of OLED use, and meet the needs of industrial development, high purity, The effect of improving solubility
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Embodiment 1
[0029] Embodiment 1: the synthesis of compound 001
[0030] The specific synthetic route is shown in the following formula:
[0031]
[0032] Under the condition of nitrogen protection, add 10.81g of phenylenediamine, 47.10g of bromobenzene, 0.75g of tris(dibenzylideneacetone)dipalladium, 2,2,-bis(diphenylphosphine)-1,1 into a 300ml single-necked bottle ,-binaphthyl (BINAP) 1.05g, potassium tert-butoxide 10.5g, dehydrated toluene 200ml, react at 85°C for 6 hours. After cooling, the reaction solution was filtered, and the obtained crude product was purified by silica gel chromatography, and dried under reduced pressure to obtain 24.73 g of a white solid intermediate.
[0033] Weigh 92.11g of benzanthracene bromine substitutes, 24.73g of white solid intermediate, 12.32g of potassium tert-butoxide, 0.56g of palladium (II) acetate, 0.51g of tri-tert-butylphosphine, add 250ml of dehydrated toluene, at 85℃ Reaction for 7 hours. The reaction solution was filtered, the crude pro...
Embodiment 2
[0034] Embodiment 2: the synthesis of compound 002
[0035] The specific synthetic route is shown in the following formula:
[0036] Under the condition of nitrogen protection, add 18.40g of phenylenediamine, 47.10g of bromobenzene, 1.50g of tris(dibenzylideneacetone)dipalladium, 2,2,-bis(diphenylphosphine)-1, 2.1 g of 1,-binaphthyl (BINAP), 21.1 g of potassium tert-butoxide, and 200 ml of dehydrated toluene were reacted at 86° C. for 7 hours. After cooling, the reaction solution was filtered, and the obtained crude product was purified by silica gel chromatography, and dried under reduced pressure to obtain 30.27 g of a white intermediate.
[0037] Weigh 92.11g of benzanthracene bromine substitute, 30.27g of white intermediate, 12.32g of potassium tert-butoxide, 0.56g of palladium(II) acetate, 0.51g of tri-tert-butylphosphine, add 250ml of dehydrated toluene, and react at 86°C 8 hours. The reaction solution was filtered, the crude product obtained was purified by silica ...
Embodiment 3
[0038] Embodiment 3: the synthesis of compound 003
[0039] The specific synthetic route is shown in the following formula:
[0040]
[0041]Under the condition of nitrogen protection, add 15.82g of naphthalene diamine, 47.10g of bromobenzene, 1.50g of tris(dibenzylideneacetone)dipalladium, 2,2,-bis(diphenylphosphine)-1,1 into a 300ml one-port bottle 2.1 g of -binaphthyl (BINAP), 21.1 g of potassium tert-butoxide, and 200 ml of dehydrated toluene were reacted at 86°C for 6 hours. After cooling, the reaction solution was filtered, and the obtained crude product was purified by silica gel chromatography, and dried under reduced pressure to obtain 28.56 g of a white intermediate.
[0042] Weigh 92.11g of benzanthracene bromine substitute, 28.56g of white intermediate, 12.32g of potassium tert-butoxide, 0.56g of palladium(II) acetate, 0.51g of tri-tert-butylphosphine, add 250ml of dehydrated toluene, and react at 87°C 7 hours. The reaction solution was filtered, the crude pr...
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