Organic electroluminescent compound and organic electroluminescent device comprising the same
A luminescent and compound technology, applied in the field of organic electroluminescent compounds, can solve the problems of reduced quantum efficiency, reduced device service life, quantum efficiency and service life deterioration, and achieves high luminous efficiency, long service life, and low drive. The effect of voltage
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example 1
[0091] Example 1: Preparation of Compound C-4
[0092]
[0093] 10g of compound a-1 (31mmol), 11.2g of compound b-1 (31mmol), 1.42g of three (dibenzylideneacetone) dipalladium (0) (1.6mmol), 1.6mL of tri-tert-butyl Phosphine (3.1 mmol, 50% solution in toluene), 5.9 g of sodium tert-butoxide (62 mmol), and 154 mL of toluene were introduced into the reaction vessel, and the mixture was refluxed for 4 hours. The reaction solution was cooled to room temperature, and then the solvent was removed by a rotary evaporator. The residue was purified by column chromatography to obtain 8.3 g of Compound C-4 (yield: 44%).
example 2
[0094] Example 2: Preparation of Compound C-5
[0095]
[0096] 7.0g of compound a-1 (22mmol), 8.6g of compound b-2 (24mmol), 0.60g of three (dibenzylideneacetone) dipalladium (0) (0.66mmol), 0.6mL of tri-tert-butyl Phosphine (1.32 mmol, 50% solution in toluene), 3.1 g of sodium tert-butoxide (32 mmol), and 110 mL of toluene were introduced into the reaction vessel, and the mixture was refluxed for 2 hours. The reaction solution was cooled to room temperature, and then the solvent was removed by a rotary evaporator. The residue was purified by column chromatography to obtain 0.9 g of Compound C-5 (yield: 7%).
example 3
[0097] Example 3: Preparation of Compound C-6
[0098]
[0099] 7.4g of compound a-1 (23mmol), 10.0g of compound b-3 (23mmol), 1.0g of three (dibenzylideneacetone) dipalladium (0) (1.2mmol), 1.1mL of tri-tert-butyl Phosphine (2.3 mmol, 50% solution in toluene), 4.4 g of sodium tert-butoxide (46 mmol), and 114 mL of toluene were introduced into the reaction vessel, and the mixture was refluxed for 5 hours. The reaction solution was cooled to room temperature, and then the solvent was removed by a rotary evaporator. The residue was purified by column chromatography to obtain 4.9 g of Compound C-6 (yield: 31%).
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