Compound, display panel and display device
A display panel and compound technology, applied in silicon organic compounds, compounds of group 5/15 elements of the periodic table, compounds of group 4/14 elements of the periodic table, etc.
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Embodiment 1
[0102] Synthesis of Compound P7
[0103]
[0104]S1 (5.0mmol), 9,9-dimethyl-9,10-dihydroacridine S2 (10.4mmol), (dibenzylideneacetone) dipalladium (0) (0.2mmol), sodium tert-butoxide (14.0mmol), 4,5-bisdiphenylphosphine-9,9-dimethylxanthene (0.2mmol) were put into a 250mL three-necked flask, and while stirring, the degassing and nitrogen replacement were repeated three times rapidly, and passed Add 50 mL of toluene to the syringe. The mixture was heated to reflux for 3 hours under nitrogen flow. After the reaction, water was added to the reaction solution left to cool to room temperature, extracted with dichloromethane, and washed with saturated brine. After drying the organic layer with anhydrous sodium sulfate, the solvent was distilled off and purified by column chromatography to obtain P7 (3.4 mmol, 68%).
[0105] MALDI-TOFMS: m / z calculated value: C 42 h 28 N 6 S 2 : 680.2; measured value: 680.5.
[0106] Elemental Analysis Calculated: C, 74.09; H, 4.15; N, 12....
Embodiment 2
[0108] Synthesis of compound P23
[0109]
[0110] Under nitrogen protection, weigh compound S3 (7.5mmol), S4 (15.5mmol), [Pd 2 (dba) 3 ]·CHCl 3 (0.3mmol) and HP(tBu) 3 ·BF 4 (0.6mmol), was added to a 250mL two-necked flask. Inject 100mL of toluene into the two-necked flask (pass N in advance 2 15min to remove oxygen), and then add 12mL of K with a concentration of 1M dropwise 2 CO 3 Aqueous solution (pass N in advance 2 15min to remove oxygen), and stirred overnight at room temperature. After the reaction was completed, 100 mL of deionized water was added, and then 2 mL of 2M HCl was added dropwise. Extract with dichloromethane, collect the organic phase, and wash with anhydrous Na 2 SO 4 Dry processing. The dried solution was filtered, and the solvent was removed by a rotary evaporator to obtain a crude product. The crude product was purified by silica gel column chromatography, and the final purification gave solid S5 (5.6 mmol, 75%).
[0111] MALDI-TOFMS: ...
Embodiment 3
[0117] Synthesis of Compound P29
[0118]
[0119] S7 (2.7mmol), 9,9-dimethyl-9,10-dihydroacridine S2 (5.7mmol), (dibenzylideneacetone) dipalladium (0) (0.35mmol), sodium tert-butoxide (10.0mmol) and tri-tert-butylphosphine tetrafluoroborate (0.7mmol) were put into a 500mL three-necked flask, and while stirring, degassing and nitrogen replacement were repeated three times rapidly, and 200mL toluene was added through a syringe. The mixture was heated to reflux for 3 hours under nitrogen flow. After the reaction, water was added to the reaction solution left to cool to room temperature, extracted with dichloromethane, and washed with saturated brine. After drying the organic layer with anhydrous sodium sulfate, the solvent was distilled off and purified by column chromatography to obtain P23 (1.60 mmol, 59%).
[0120] MALDI-TOFMS: m / z calculated: C38H30Br2N2S2: 736.0; measured: 736.2
[0121]
[0122] In a 250ml three-necked flask, first mix S9 (7.5mmol), pinacol dibora...
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