A kind of organic luminescent material and its application on oled
An organic and electroluminescent technology, applied in the field of semiconductors, can solve the problems of insufficient efficiency, lifespan, difficult to achieve full-color RGB, very different, etc., to achieve the effect of improving color purity, good industrialization prospects, and inhibiting the degree of crystallization
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Embodiment 1
[0057] Example 1 (Compound 04)
[0058] The concrete synthetic route of this compound is provided now:
[0059]
[0060] 250ml four-necked bottle, under the protection of nitrogen, add 0.01mol intermediate A, 0.025mol 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=1:3 (volume ratio), and recrystallized White solid, purity (HPLC) 98.3%, yield 62.2%.
[0061] Elemental analysis structure (molecular formula C 53 h 38 N 2 o 2 ): Theoretical value C,86.62; H,5.21; N,3.81; O,4.35 Test value: C,86.67; H,5.16; N,3.80; O,4.37
Embodiment 2
[0062] Example 2 (Compound 08)
[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 A, 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=1:2 (volume ratio), and recrystallized White solid, purity (HPLC) 98.6%, yield 54.1%.
[0066] Elemental analysis structure (molecular formula C 62 h 55 NO): Theoretical value C,89.71; H,6.68; N,1.69; O,1.93 Test value: C,89.68; H,6.71; N,1.71; O,1.92
Embodiment 3
[0067] Example 3 (compound 14)
[0068] The concrete synthetic route of this compound is provided now:
[0069]
[0070] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol of intermediate A, 0.025mol of bis(3,4-dimethylphenyl)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 57.8%.
[0071] Elemental analysis structure (molecular formula C 71 h 56 N 2 o 2 ): Theoretical value C,87.98; H,5.82; N,2.89; O,3.30 Test value: C,87.89; H,5.84; N,2.80; O,3.47
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