Preparation method of zinc oxide quantum dot modified polyfluorene blue polymer luminescent material
A technology of luminescent materials and quantum dots, which is applied in the direction of luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc., and can solve the problems of limited application in the field of PLED, poor processability, and fluorescence of excimer associations
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Embodiment 1
[0023] 1) Synthesis of 1,4-di-n-butoxybenzene
[0024] Add a mixture of hydroquinone (0.1 mol), n-bromobutane (0.2 mol) and sodium hydroxide (0.2 mol) at a molar ratio of 1:2:2 into a 250 mL three-necked flask, add 60 mL of ethanol solvent and Filled with nitrogen protection. After stirring at 70 °C for 24 h, the solution turned from yellow to grayish brown. After the reaction, the solution was poured into deionized water, stirred for 1 h, and then left to precipitate a precipitate. After suction filtration, washing, and drying, it was recrystallized with ethanol, and after vacuum drying, a white flaky crystal product was obtained with a yield of 85%.
[0025] 2) Synthesis of 1,4-dibutoxy-2,5-bisbromomethylbenzene
[0026] Add a mixture of 1,4-di-n-butoxybenzene (50 mmol), paraformaldehyde (100 mmol) and hydrobromic acid (100 mmol) at a molar ratio of 1:2:2 into a 250 mL three-neck flask, 60 mL of glacial acetic acid and 12 mL of phosphoric acid were filled with nitrogen pr...
Embodiment 2
[0039] 1) Synthesis of 1,4-di-n-butoxybenzene
[0040] Add a mixture of hydroquinone (0.1 mol), n-bromobutane (0.2 mol) and sodium hydroxide (0.2 mol) at a molar ratio of 1:2:2 into a 250 mL three-necked flask, add 60 mL of ethanol solvent and Filled with nitrogen protection. After stirring at 78 °C for 24 h, the solution turned from yellow to grayish brown. After the reaction, the solution was poured into deionized water, stirred for 1 h, and then left to precipitate a precipitate. After suction filtration, washing, and drying, it was recrystallized with ethanol, and after vacuum drying, a white flaky crystal product was obtained with a yield of 85%.
[0041] 2) Synthesis of 1,4-dibutoxy-2,5-bisbromomethylbenzene
[0042] Add a mixture of 1,4-di-n-butoxybenzene (50 mmol), paraformaldehyde (125 mmol) and hydrobromic acid (150 mmol) at a molar ratio of 1:2.5:3 into a 250 mL three-neck flask, 60 mL of glacial acetic acid and 12 mL of phosphoric acid were filled with nitrogen ...
Embodiment 3
[0055] 1) Synthesis of 1,4-di-n-butoxybenzene
[0056] Add a mixture of hydroquinone (0.1 mol), n-bromobutane (0.2 mol) and sodium hydroxide (0.2 mol) at a molar ratio of 1:2:2 into a 250 mL three-necked flask, add 60 mL of ethanol solvent and Filled with nitrogen protection. After stirring at 78 °C for 24 h, the solution turned from yellow to grayish brown. After the reaction, the solution was poured into deionized water, stirred for 1 h, and then left to precipitate a precipitate. After suction filtration, washing, and drying, it was recrystallized with ethanol, and after vacuum drying, a white flaky crystal product was obtained with a yield of 85%.
[0057] 2) Synthesis of 1,4-dibutoxy-2,5-bisbromomethylbenzene
[0058] Add a mixture of 1,4-di-n-butoxybenzene (50 mmol), paraformaldehyde (100 mmol) and hydrobromic acid (150 mmol) at a molar ratio of 1:2:3 into a 250 mL three-neck flask, 60 mL of glacial acetic acid and 12 mL of phosphoric acid were filled with nitrogen pr...
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