Organic compound with xanthene as core and use thereof
An organic compound, xanthene technology, applied in the field of organic optoelectronic materials, can solve problems such as disparity, and achieve the effects of avoiding aggregation, improving current efficiency and lifetime, improving exciton utilization and high fluorescence radiation efficiency.
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Embodiment 1
[0062] Embodiment 1: the synthesis of compound 1:
[0063] synthetic route:
[0064]
[0065] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material A1, 0.024mol raw material B1, 0.04mol sodium tert-butoxide, 1×10 -4 molpd 2 (dba) 3 , 1×10 -4 mol of tri-tert-butylphosphine, 250ml of toluene, heated to reflux for 24 hours, sampling point plate, the reaction was complete; natural cooling, filtration, filtrate rotary evaporation, column chromatography to obtain the target product, HPLC purity 99.2%, yield 69.1%;
[0066] Elemental analysis structure (molecular formula C 65 h 64 N 2 O): theoretical value C, 87.80; H, 7.25; N, 3.15; O, 1.80; tested value: C, 87.79; H, 7.24; N, 3.16;
[0067] HPLC-MS: The molecular weight of the material is 889.22, and the measured molecular weight is 889.58.
Embodiment 2
[0068] Embodiment 2: the synthesis of compound 3:
[0069] synthetic route:
[0070]
[0071] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material A2, 0.012mol raw material B2, 0.03mol sodium tert-butoxide, 5×10 -5 mol pd 2 (dba) 3 , 5×10 -5 mol of tri-tert-butylphosphine, 150ml of toluene, heated to reflux for 24 hours, sampling point plate, the reaction was complete; natural cooling, filtration, filtrate rotary evaporation, column chromatography to obtain the target product, HPLC purity 99.3%, yield 71.3%;
[0072] Elemental analysis structure (molecular formula C 55 h 38 N 2 O): theoretical value C, 88.92; H, 5.16; N, 3.77; O, 2.15; tested value: C, 88.93; H, 5.15; N, 3.78;
[0073] HPLC-MS: The molecular weight of the material is 742.90, and the measured molecular weight is 743.27.
Embodiment 3
[0074] Embodiment 3: the synthesis of compound 7:
[0075] synthetic route:
[0076]
[0077] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material A3, 0.012mol raw material B3, 0.03mol sodium tert-butoxide, 5×10 -5 mol pd 2 (dba) 3 , 5×10 -5 mol of tri-tert-butylphosphine, 150ml 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 99.7%, yield 75.4%;
[0078] Elemental analysis structure (molecular formula C 55 h 38 N 2 O): theoretical value C, 88.92; H, 5.16; N, 3.77; O, 2.15; tested value: C, 88.95; H, 5.15; N, 3.76;
[0079] HPLC-MS: The molecular weight of the material is 742.90, and the measured molecular weight is 743.31.
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