Organic light emission diode device and application thereof
An electroluminescent device and electroluminescent technology, applied in the fields of electro-solid devices, electrical components, organic chemistry, etc., can solve the problem of efficiency roll-off, difficult and high exciton utilization rate, high fluorescence radiation efficiency, and low S1 state radiation transition rate and other problems, to achieve the effect of efficiency and life improvement, high efficiency
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Embodiment 1
[0067] Example 1 Compound 1
[0068] The concrete synthetic route of this compound is provided now:
[0069]
[0070] Add 0.01mol 3,6-dibromo-1,8-diaza-9-fluorenone, 0.025mol 10H-phenoxazine, 0.03mol sodium tert-butoxide to a 250ml four-necked flask under nitrogen atmosphere , 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol of tri-tert-butylphosphine, 150ml of toluene, heated to reflux for 24 hours, sampling plate, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, and passed through a silica gel column to obtain the target product with a purity of 99.2% and a yield of 75.00%.
[0071] Elemental analysis structure (molecular formula C 35 h 20 N 4 o 3 ): theoretical value C, 77.20; H, 3.70; N, 10.29; O, 8.81; test value: C, 77.29;
[0072] HPLC-MS: The molecular weight of the material is 544.15, and the measured molecular weight is 544.62.
Embodiment 2
[0073] Example 2 Compound 4
[0074]
[0075] The preparation method of compound 4 is the same as that of Example 1, except that the raw material 9,10-dihydro-9,9-dimethylacridine is used instead of 10H-phenoxazine.
Embodiment 3
[0076] Example 3 Compound 7
[0077] The concrete synthetic route of this compound is provided now:
[0078]
[0079] In a 250ml four-necked flask, add 0.01mol 3,6-bis-(4-bromophenyl)-1,8-diaza-9-fluorenone, 0.025mol 5-phenyl -10-hydrophenazine, 0.03mol sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol of tri-tert-butylphosphine, 150ml of toluene, heated to reflux for 24 hours, sampled and plated, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, and passed through a silica gel column to obtain the target product with a purity of 99.5% and a yield of 72.00%.
[0080] Elemental analysis structure (molecular formula C 59 h 38 N 6 O): theoretical value C, 83.67; H, 4.52; N, 9.92; O, 1.89; tested value: C, 83.73; H, 4.39; N, 9.90;
[0081] HPLC-MS: The molecular weight of the material is 846.31, and the measured molecular weight is 846.40.
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