Blue fluorescence doped material with high efficiency and long service life, application thereof and organic electroluminescent device
A technology of blue fluorescence and doping materials, applied in the field of organic electroluminescence, can solve the problems of poor electronic orbital energy level matching, reduced material working stability, difficulty in light-emitting devices, etc. Stable performance and improved luminous efficiency
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Embodiment 1
[0041]
[0042] The preparation method of the blue fluorescent doped material (1) is as follows:
[0043]
[0044]Under nitrogen protection, compound 1-a (1.0g, 172.11g / mol, 5.81mmol), compound 1-b (1eq, 2.35g, 404.99g / mol, 5.81mmol), sodium tert-butoxide (1.1eq, 0.61 g, 96.1g / mol, 6.39mmol), tris(dibenzylideneacetone)dipalladium (0.05eq, 0.27g, 915g / mol, 0.29mmol), tri-tert-butylphosphine (0.05eq, 0.059g, 202.32g / mol, 0.29mol), toluene (10ml) were added in the reaction flask, and after the addition was completed, the temperature was raised to reflux for 5 hours. The organic phase was obtained by liquid separation, and the organic phase was dried with anhydrous magnesium sulfate and then spin-dried, and purified by column chromatography to obtain compound 1-c (2.03g, yield 70.4%), MS (EI): 497 (M + ).
[0045]
[0046] Under nitrogen protection, compound 1-c (1.8g, 497.17g / mol, 3.62mmol) was added into tert-butylbenzene (18ml), stirred and cooled to -40°C, and the ...
Embodiment 2
[0048]
[0049] The preparation method of the blue fluorescent doped material (6) is as follows:
[0050]
[0051] Under nitrogen protection, compound 2-a (1.0g, 169.09g / mol, 5.91mmol), compound 2-b (1eq, 2.4g, 404.99g / mol, 5.91mmol), sodium tert-butoxide (1.1eq, 0.62 g, 96.1g / mol, 6.5mmol), tris(dibenzylideneacetone)dipalladium (0.05eq, 0.27g, 915g / mol, 0.3mmol), tri-tert-butylphosphine (0.05eq, 0.06g, 202.32g / mol, 0.3mol), toluene (10ml) into the reaction flask, after the addition, the temperature was raised to reflux reaction for 10h, after the reaction was completed, it was lowered to room temperature, then added 10ml of water and stirred for 30min to obtain the filtrate, which was filtered through diatomaceous earth The organic phase was obtained by liquid separation, and the organic phase was dried with anhydrous magnesium sulfate and then spin-dried, and purified by column chromatography to obtain compound 2-c (2.13g, yield 72.8%), MS (EI): 494 (M + ).
[0052]...
Embodiment 3
[0055]
[0056] The preparation method of the blue fluorescent doped material (12) is as follows:
[0057]
[0058] Under nitrogen protection, compound 3-a (1.0g, 253.18g / mol, 3.95mmol), compound 3-b (1eq, 1.6g, 404.99g / mol, 3.95mmol), sodium tert-butoxide (1.1eq, 0.42 g, 96.1g / mol, 4.34mmol), tris(dibenzylideneacetone)dipalladium (0.05eq, 0.18g, 915g / mol, 0.2mmol), tri-tert-butylphosphine (0.05eq, 0.04g, 202.32g / mol, 0.2mol), toluene (10ml) were added in the reaction flask, after the addition was completed, the temperature was raised to reflux for 5 hours, after the reaction was completed, the temperature was lowered to room temperature, and 10ml of water was added and stirred for 15 minutes to obtain the filtrate, which was filtered through diatomaceous earth The organic phase was obtained by liquid separation, and the organic phase was dried with anhydrous magnesium sulfate and then spin-dried, and purified by column chromatography to obtain compound 3-c (1.65g, yiel...
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