A kind of iridium-containing polymer red light material and its synthesis method
A synthesis method and polymer technology, applied in the direction of luminescent materials, chemical instruments and methods, etc., can solve the problems of not designing narrow bandgap metal complexes, etc., and achieve the effects of good mechanical properties, good film-forming performance, and good solubility
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Embodiment 1
[0015] Measure 10mL of toluene (10min ultrasonic vibration with nitrogen gas) and add it into a 25mL three-neck flask, weigh bis-[(4-bromo-thiophene)-phenylpyridine]-β-heptanedione iridium complex monomer (0.0036g , 0.00358mmol), 9,9-dioctyl-2,7-dibromofluorene (0.0962g, 0.175mmol), 9,9-dioctylfluorene-2,7-diboronic acid bis(1,3- Propylene glycol) ester (0.1g, 0.179mmol), Pd(PPh 3 ) 4 (0.0062g, 0.00537mmol) into a three-necked flask, after removing the air in the system, add 1mL tetraethylammonium hydroxide solution, under the protection of nitrogen, react at 100°C in the dark for 72h, add 9,9-dioctylfluorene -2,7-diboronic acid bis(1,3-propanediol) ester (0.005g, 0.00895mmol) (dissolved in 1.5mL toluene) was continued for 12h, and 2mL of bromobenzene was added to continue the reaction for 12h. After the reaction, the palladium catalyst in the reaction was removed by filtration, and most of the solvent was evaporated with a rotary evaporator, the remaining solution was settl...
Embodiment 2
[0017] Measure 10mL of toluene (10min ultrasonic vibration with nitrogen) and add it into a 25mL three-neck flask, weigh bis-[(4-bromo-thiophene)-phenylpyridine]-β-heptanedione iridium complex monomer (0.0072g , 0.00716mmol), 9,9-dioctyl-2,7-dibromofluorene (0.0942g, 0.172mmol), weighed 9,9-dioctylfluorene-2,7-diboronic acid bis(1, 3-propanediol) ester (0.1g, 0.179mmol), Pd(PPh 3 ) 4 (0.0062g, 0.00537mmol) into a three-necked flask, after removing the air in the system, add 1mL tetraethylammonium hydroxide solution, under the protection of nitrogen, react at 90°C in the dark for 60h, add 9,9-dioctylfluorene-2 , 7-diboronic acid bis(1,3-propanediol) ester (0.005g, 0.00895mmol) (dissolved in 1.5mL toluene) was continued for 6h, and 2mL of bromobenzene was added to continue the reaction for 6h. After the reaction, the palladium catalyst in the reaction was removed by filtration, and most of the solvent was evaporated with a rotary evaporator, the remaining solution was settled ...
Embodiment 3
[0019] Measure 10mL of xylene (10min ultrasonic vibration with nitrogen gas) into a 25mL three-necked flask, weigh bis-[(4-bromo-thiophene)-phenylpyridine]-β-heptanedione iridium complex monomer (0.0180 g, 0.0179mmol), 9,9-dioctyl-2,7-dibromofluorene (0.0889g, 0.162mmol), weighed 9,9-dioctylfluorene-2,7-diboronic acid bis(1 , 3-propanediol) ester (0.1g, 0.179mmol), Pd(PPh 3 ) 4 (0.0062g, 0.00537mmol) into the bottle, remove the air in the system, add 1mL tetraethylammonium hydroxide solution, under the protection of nitrogen, react at 105°C in the dark for 64h, add 9,9-dioctylfluorene-2 , 7-diboronic acid bis(1,3-propanediol) ester (0.005g, 0.00895mmol) (dissolved in 1.5mL toluene) was continued for 12h, and 2mL of bromobenzene was added to continue the reaction for 12h. After the reaction, the palladium catalyst in the reaction was removed by filtration, and most of the solvent was evaporated with a rotary evaporator, the remaining solution was settled in methanol, the drie...
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