Organic compound containing dimethylanthracene and application thereof in OLED
A technology of organic compounds, dimethyl anthracene, applied in the field of organic optoelectronic materials, which can solve problems such as disparity
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[0071] Example 1: Synthesis of Compound 2:
[0072] synthetic route:
[0073]
[0074] In a 250ml three-necked flask, under the protection of nitrogen, add 0.01mol of raw material A1, 0.012mol of raw material B1, 0.03mol of sodium tert-butoxide, 5×10 -5 molpd 2 (dba) 3 , 5×10 -5 mol tri-tert-butylphosphorus, 150 ml of toluene, heated to reflux for 24 hours, sampling point plate, the reaction was complete; natural cooling, filtration, rotary evaporation of the filtrate, column chromatography to obtain the target product, HPLC purity 99.1%, yield 67.3%;
[0075] Elemental analysis structure (molecular formula C 67 H 55 N 3 ): Theoretical C, 89.20; H, 6.14; N, 4.66; Tested: C, 89.20; H, 6.15; N, 4.65.
[0076] HPLC-MS: The molecular weight of the material is 902.17, and the measured molecular weight is 902.57.
Example Embodiment
[0077] Example 2: Synthesis of Compound 3:
[0078] synthetic route:
[0079]
[0080] In a 250ml three-necked flask, under the protection of nitrogen, add 0.01mol of raw material A1, 0.012mol of raw material B2, 0.03mol of sodium tert-butoxide, 5×10 -5 mol pd 2 (dba) 3 , 5×10 -5 mol tri-tert-butylphosphorus, 150 ml of toluene, heated to reflux for 24 hours, sampling point plate, the reaction was complete; natural cooling, filtration, rotary evaporation of the filtrate, column chromatography to obtain the target product, HPLC purity 99.3%, yield 62.7%;
[0081] Elemental analysis structure (molecular formula C 64 H 49 N 3 O): theoretical C, 87.74; H, 5.64; N, 4.80; O, 1.83; found: C, 87.74; H, 5.62; N, 4.82; O, 1.82.
[0082] HPLC-MS: The molecular weight of the material is 876.09, and the measured molecular weight is 876.51.
Example Embodiment
[0083] Example 3: Synthesis of Compound 9:
[0084] synthetic route:
[0085]
[0086] In a 250ml three-necked flask, under the protection of nitrogen, add 0.01mol of raw material A1, 0.012mol of raw material B3, 0.03mol of sodium tert-butoxide, 5×10 -5 mol pd 2 (dba) 3 , 5×10 -5 mol tri-tert-butylphosphorus, 150 ml of toluene, heated to reflux for 24 hours, sampling point plate, the reaction was complete; natural cooling, filtration, rotary evaporation of the filtrate, column chromatography to obtain the target product, HPLC purity 99.4%, yield 71.2%;
[0087] Elemental analysis structure (molecular formula C 64 H 45 N 3 O): Theoretical C, 88.15; H, 5.20; N, 4.82; O, 1.83; Tested: C, 88.14; H, 5.21; N, 4.83; O, 1.82.
[0088] HPLC-MS: The molecular weight of the material is 872.06, and the measured molecular weight is 872.48.
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