Organic light-emitting material and application thereof
An electroluminescent material, organic technology, applied in the direction of luminescent materials, organic chemistry, silicon organic compounds, etc., can solve the problems of different, difficult to achieve full-color RGB, efficiency, insufficient life, etc., to achieve the degree of crystallization inhibition, good industrialization The effect of foreground and color purity improvement
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Embodiment 1
[0056] Example 1 (compound 06)
[0057] The concrete synthetic route of this compound is provided now:
[0058]
[0059] 250ml four-necked bottle, under the protection of nitrogen, add 0.01mol intermediate A, 0.011mol diphenylamine, 0.03mol sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol tri-tert-butylphosphine, 150ml toluene, heated to reflux for 20 hours, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, passed through a silica gel column, beaten with a mixed solvent of toluene:ethanol=1:2 (volume ratio), and recrystallized White solid, purity (HPLC) 98.1%, yield 62.2%.
[0060] Elemental analysis structure (molecular formula C 52 h 37 N): theoretical value C, 92.41; H, 5.52; N, 2.07
[0061] Test value: C, 92.39; H, 5.57; N, 2.04
Embodiment 2
[0062] Example 2 (compound 11)
[0063] The concrete synthetic route of this compound is provided now:
[0064]
[0065] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol of intermediate B, 0.011mol of bis(4-tert-butylphenyl)amine, 0.03mol of sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol tri-tert-butylphosphine, 150ml toluene, heated to reflux for 20 hours, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, passed through a silica gel column, beaten with a mixed solvent of toluene:ethanol=1:3 (volume ratio), and recrystallized White solid, purity (HPLC) 97.8%, yield 60.4%.
[0066] Elemental analysis structure (molecular formula C 50 h 51 N): theoretical value C, 90.18; H, 7.72; N, 2.10
[0067] Test value: C, 89.94; H, 7.76; N, 2.30
Embodiment 3
[0068] Example 3 (compound 15)
[0069] The concrete synthetic route of this compound is provided now:
[0070]
[0071] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol of intermediate C, 0.025mol of bis(4-tert-butylphenyl)amine, 0.03mol of sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol tri-tert-butylphosphine, 150ml toluene, heated to reflux for 20 hours, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, passed through a silica gel column, beaten with a mixed solvent of toluene:ethanol=1:2.5 (volume ratio), and recrystallized White solid, purity (HPLC) 98.3%, yield 53.1%.
[0072] Elemental analysis structure (molecular formula C 69 h 55 N 2 O): theoretical value C, 89.19; H, 6.07; N, 3.01; O, 1.72
[0073] Test value: C, 89.24; H, 6.10; N, 2.98; O, 1.68
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