Platinum complex, application thereof and organic photoelectric device comprising the platinum complex
A technology of organic photoelectric devices and platinum complexes, which is applied in the fields of platinum group organic compounds, platinum organic compounds, organic chemistry, etc., can solve the problems of limited types and difficulties of organic photoelectric devices, and achieve high stability and luminous efficiency, good Stability and the effect of improving luminous efficiency
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Synthetic example 1
[0078] Synthesis of Platinum Complex 226
[0079] (1) Synthesis of 1-1:
[0080]
[0081] Preparation process: Add 2-bromocarbazole (3.69g, 15mmol), 2-bromo-4-methylpyridine 0002 (1.42mL, 15mmol), cuprous iodide (0.3 mmoL, 0.02equiv), 1-methylimidazole (0.3mmol, 0.2equiv), t-BuOLi (18mmol, 1.2equiv) and toluene (50mL), the resulting mixture was heated to 120°C and stirred for 8 minutes after bubbling nitrogen gas for 10 minutes. Hour. Cool to room temperature, add water to quench the reaction, extract with ethyl acetate, combine the organic phases, wash with an appropriate amount of saturated aqueous sodium chloride solution and dry over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained crude product was separated and purified by silica gel column chromatography, the eluent was petroleum ether:ethyl acetate=25:1, and a white solid was obtained with a yield of 93%.
[0082] (2) Synthesis of 1-2:
[0083]
[0084] Preparat...
Synthetic example 2
[0106] Synthesis of Platinum Complex 16
[0107] (1) Synthesis of 2-1:
[0108]
[0109] Preparation process: Add 2-bromocarbazole (3.69g, 15mmol), 2-bromopyridine 0002 (1.42mL, 15mmol), cuprous iodide (0.3mmoL, 0.02equiv) to a 48mL sealed tube with a magnetic rotor in sequence , 1-methylimidazole (0.3mmol, 0.2equiv), t-BuOLi (18mmol, 1.2equiv) and toluene (50mL), the resulting mixture was bubbled with nitrogen for 10 minutes and then heated to 120°C and stirred for 8 hours. Cool to room temperature, add water to quench the reaction, extract with ethyl acetate, combine the organic phases, wash with an appropriate amount of saturated aqueous sodium chloride solution, and dry over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained crude product was separated and purified by silica gel column chromatography, the eluent was petroleum ether: ethyl acetate = 25:1, and the product 2-1 was obtained with a yield of 95%.
[0110] (2) Synt...
Synthetic example 3
[0125] Synthesis of Platinum Complex 63
[0126] (1) Synthesis of 3-1:
[0127]
[0128] Preparation process: Add intermediate 1-1 (1equiv), 3-amino-phenol (1.2equiv), cuprous iodide (10%), L-proline (L-Pro, 20 %), cesium carbonate (2equiv) and dimethylsulfoxide (0.5M). The resulting mixture was bubbled with nitrogen for 10 minutes and stirred at 120°C for 3 days. After cooling, water and ethyl acetate (EA) were added, and the mixture was filtered. The aqueous phase was extracted with ethyl acetate, and the organic phases were combined, washed with brine, and the organic phase was washed with anhydrous Na 2 SO 4 dry. Using PE:EA=8:1 as eluent, the obtained solution was purified by silica gel chromatography to obtain product 3-1 (brown viscous liquid, yield 69%).
[0129] (2) Synthesis of 3-2:
[0130]
[0131] Preparation process: 15ml of acetone and 25ml of acetic acid were added to a solution of 8g of 2-chloro-3-amino-4,6-lutidine in 20ml of dichloromethane. 6 ...
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Abstract
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