Novel poly-p-phenylene vinylene electroluminescent materials and method for preparing same
An electroluminescent material, polyphenylene vinylene technology, applied in the direction of light-emitting materials, chemical instruments and methods, etc., can solve the problems of carrier injection rate mismatch, affecting the efficiency of light-emitting devices, obvious interfaces, microcavities, etc., to achieve The reaction conditions are easy to control, not easy to fail, and have good anti-aging performance
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Embodiment 1
[0036] Example 1: Preparation of oxadiazole derivatives
[0037] In a 250mL three-necked flask equipped with a stirrer, a reflux condenser and a drying tube, add 28.0g of benzoyl hydrazide, 20.3g of isophthaloyl chloride, 100mL of tetrahydrofuran and 18mL of anhydrous pyridine, heat to 65°C, reflux and stir. After 8 hours, cool to room temperature, pour the reaction solution into 1000 mL of ice-water mixture, stir well, let stand and filter, repeatedly wash with ice water and cold ethanol, and vacuum dry to obtain white powder dibenzoyl isophthalic hydrazide 25.3 g.
[0038] Add 20.1g of dibenzoyl isophthalic hydrazide and 50mL of phosphorus oxychloride into a 250mL three-necked flask equipped with a stirrer, reflux condenser and drying tube, heat to 105°C, reflux and stir for 5 hours, and cool to room temperature , Pour the reaction solution into 1000 mL of ice-water mixture, stir well, stand still and filter, wash with distilled deionized water and ethanol in turn, and then recr...
Embodiment 2
[0039] Example 2: Preparation of PPV
[0040] Dissolve 0.02mol of 1,3-bis(5-phenyl)-1,3,4-oxadiazole benzene in dioxane, add 0.025mol of formaldehyde, 0.025mol of paraformaldehyde and 100mL of formaldehyde at room temperature. Concentrated hydrochloric acid, stirred and refluxed for 6h, distilled under reduced pressure to remove the solvent, cooled, filtered and washed with ethanol, and recrystallized to obtain a chloromethylated oxadiazole derivative.
[0041] Dissolve 0.02 mol of the chloromethylated oxadiazole derivative in 180 mL of anhydrous tetrahydrofuran, add an appropriate amount of potassium tert-butoxide in anhydrous tetrahydrofuran solution with stirring until it reaches 2.5 times the molar amount of the monomer, and stir at room temperature After 6 hours, 100 mL of a mixture of methanol and water with a volume ratio of 1:1 was added, filtered, and a red precipitate was separated. After being washed 3 times with ethanol, the PPV was obtained by vacuum drying with a num...
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