Organic electroluminescent material containing triphenylamine structure and organic electroluminescent device using organic electroluminescent material
A technology of electroluminescent materials and electroluminescent devices, which is applied in the directions of luminescent materials, electro-solid devices, electrical components, etc., can solve the problems of high starting voltage, short service life, low luminous efficiency, etc., and achieves improved efficiency and service life, The effect of prolonging life and improving light output
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Embodiment 1
[0050]
[0051] The synthetic method of organic electroluminescent material (1) is as follows:
[0052]
[0053]Compound 1-a (2g, 731.13g / mol, 2.74mmol), compound 1-b (3.1eq, 1.38g, 163.04g / mol, 8.49mmol) and sodium carbonate (6eq, 1.74g, 105.99g / mol, 16.44mmol) into ethylene glycol diamine ether (40g, 20 times the quality of compound 1-a) and water (40g, 20 times the quality of compound 1-a), stir and mix and then add three (o-toluene Base) phosphine (5%eq, 0.042g, 304.37g / mol, 0.14mmol) and palladium (II) acetate (1%eq, 0.006g, 224.51g / mol, 0.027mmol), after warming up to reflux for 15h, the The organic phase was separated, washed with water, and concentrated under reduced pressure to obtain a crude product, which was then subjected to column chromatography to obtain an organic electroluminescent material (1) (1.71g, yield 73.6%), MS (EI): 848 (M + ).
Embodiment 2
[0055]
[0056] The synthetic method of organic electroluminescent material (2) is as follows:
[0057]
[0058] Compound 2-a (2g, 478.85g / mol, 4.18mmol), compound 2-b (3.1eq, 2.76g, 213.06 / mol, 12.95mmol) and sodium carbonate (6eq, 2.66g, 105.99g / mol, 25.06 mmol) into ethylene glycol diamine ether (40g, 20 times the mass of compound 2-a) and water (40g, 20 times the mass of compound 2-a), stir and mix and then add three (o-tolyl) ) phosphine (5%eq, 0.064g, 304.37g / mol, 0.21mmol) and palladium (II) acetate (1%eq, 0.009g, 224.51g / mol, 0.042mmol), after warming up to reflux reaction for 15h, the organic The phases were separated, washed with water, and concentrated under reduced pressure to obtain a crude product, which was then subjected to column chromatography to obtain an organic electroluminescent material (2) (2.28g, yield 73.2%), MS (EI): 746 (M + ).
Embodiment 3
[0060]
[0061] The synthetic method of organic electroluminescent material (4) is as follows:
[0062]
[0063] Compound 3-a (2g, 478.85g / mol, 4.18mmol), compound 3-b (3.1eq, 3.41g, 263.08 / mol, 12.95mmol) and sodium carbonate (6eq, 2.66g, 105.99g / mol, 25.06 mmol) into ethylene glycol diamine ether (40g, 20 times the quality of compound 3-a) and water (40g, 20 times the quality of compound 3-a), stir and mix and then add three (o-tolyl) ) phosphine (5%eq, 0.064g, 304.37g / mol, 0.21mmol) and palladium (II) acetate (1%eq, 0.009g, 224.51g / mol, 0.042mmol), after warming up to reflux reaction for 15h, the organic The phases were separated, washed with water, and concentrated under reduced pressure to obtain a crude product, which was then subjected to column chromatography to obtain an organic electroluminescent material (4) (2.24g, yield 71.8%), MS (EI): 746 (M + ).
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