A compound, oled display panel and electronic device
A display panel and compound technology, which is applied in the field of OLED display panels, can solve the problems of device electron and hole mobility imbalance, device efficiency and life decline, and electron transport performance degradation, etc., and achieves low driving voltage and high glass transition temperature. and thermal decomposition temperature, the effect of excellent film stability and uniformity
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preparation example 1
[0128] Preparation of Compound HB03
[0129]
[0130] The preparation method is as follows:
[0131] (1) Preparation of compound HB03-1:
[0132] In a 250 mL round bottom flask, 2,6-dibromo-4-iodo-pyridine (10 mmol), 2,4-diphenyl-6-boronate-pyrimidine (12 mmol) and Pd(PPh 3 )4 (0.3mmol) was added to a mixture of toluene (30mL) / ethanol (20mL) and potassium carbonate (12mmol) aqueous solution (10mL), and refluxed under nitrogen atmosphere for 12h. The resulting mixture was cooled to room temperature, added to water, and filtered through a pad of celite. The filtrate was extracted with dichloromethane, washed with water, and dried over anhydrous magnesium sulfate. After filtration and evaporation, the crude product was purified by silica gel column chromatography The final product HB03-1 was obtained.
[0133] (2) Preparation of compound HB03:
[0134] In a 250 mL round bottom flask, the intermediate product HB03-1, copper iodide (15 mmol), potassium tert-butoxide (65 mmol...
preparation example 2
[0137] Preparation of compound HB11
[0138]
[0139] The preparation method is as follows:
[0140] (1) Preparation of compound HB11-1:
[0141] In a 250 mL round bottom flask, 2,6-dibromo-4-iodo-benzene (10 mmol), 2,6-dinaphthyl-4-boronate-pyridine (12 mmol) and Pd(PPh 3 ) 4 (0.3mmol) was added to a mixture of toluene (30mL) / ethanol (20mL) and potassium carbonate (12mmol) aqueous solution (10mL), and the reaction was refluxed under nitrogen atmosphere for 12h. The resulting mixture was cooled to room temperature, added to water, and filtered through a pad of celite. The filtrate was extracted with dichloromethane, washed with water, and dried over anhydrous magnesium sulfate. After filtration and evaporation, the crude product was purified by silica gel column chromatography The final product HB11-1 was obtained.
[0142] (2) Preparation of compound HB11:
[0143] In a 250 mL round bottom flask, the intermediate product HB11-1, copper iodide (15 mmol), potassium tert...
preparation example 3
[0146] Preparation of compound HB35
[0147]
[0148] The preparation method is as follows:
[0149] (1) Preparation of compound HB35-1:
[0150] In a 250 mL round bottom flask, 2,6-dibromo-4-iodo-benzene (10 mmol), 2,6-diphenyl-4-boronate-pyridine (12 mmol) and Pd(PPh 3 ) 4 (0.3mmol) was added to a mixture of toluene (30mL) / ethanol (20mL) and potassium carbonate (12mmol) aqueous solution (10mL), and the reaction was refluxed under nitrogen atmosphere for 12h. The resulting mixture was cooled to room temperature, added to water, and filtered through a pad of celite. The filtrate was extracted with dichloromethane, washed with water, and dried over anhydrous magnesium sulfate. After filtration and evaporation, the crude product was purified by silica gel column chromatography The final product HB35-1 was obtained.
[0151] (2) Preparation of compound HB35:
[0152] In a 250 mL round bottom flask, the intermediate product HB35-1 (10 mmol), 2-(4-boronate) benzene-carbazol...
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