Blue fluorescence doped material with good thermal stability and high efficiency and organic electroluminescent device
A technology with thermal stability and blue fluorescence, which is applied in luminescent materials, electric solid-state devices, organic chemistry, etc., can solve the problems of light-emitting devices, poor matching of electron orbital energy levels and energy levels, and reduce the working stability of materials, etc., to achieve Improve luminous efficiency, good conjugation effect, improve thermal stability and luminous efficiency
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Embodiment 1
[0037]
[0038] The synthetic method of blue fluorescent dopant material (1) is as follows:
[0039] (1)
[0040]
[0041] Under nitrogen protection, compound 1-a (5.0g, 438.95g / mol, 11.39mmol), compound 1-b (1eq, 2.32g, 203.94g / mol, 11.39mmol), sodium tert-butoxide (1.1eq, 1.2 g, 96.1g / mol, 12.53mmol), tris(dibenzylideneacetone)dipalladium (0.05eq, 0.52g, 915g / mol, 0.57mmol), tri-tert-butylphosphine (0.05eq, 0.12g, 202.32g / mol, 0.57mol), toluene (50ml) 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, it was cooled to room temperature, and then 50ml 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 1-c (4.72g, ...
Embodiment 2
[0049]
[0050] The synthetic method of blue fluorescent dopant material (6) is as follows:
[0051] Step (1) is identical with embodiment 1
[0052] (2)
[0053]
[0054] Under nitrogen protection, compound 2-a (2g, 514.98g / mol, 3.88mmol), compound 2-b (1eq, 0.87g, 225.15g / mol, 3.88mmol), sodium tert-butoxide (1.1eq, 0.41g , 96.1g / mol, 4.27mmol), tris(dibenzylideneacetone) dipalladium (0.05eq, 0.178g, 915g / mol, 0.19mmol), tri-tert-butylphosphine (0.05eq, 0.039g, 202.32g / mol, 0.19mol), toluene (20ml) was added to the reaction flask, after the addition was completed, the temperature was raised to reflux for 5 hours, after the reaction was completed, the room temperature was lowered to room temperature, and 20ml of water was added to stir for 15 minutes, and then filtered to obtain the filtrate, which was filtered through diatomaceous earth. The organic phase was obtained from the liquid, and the organic phase was dried with anhydrous magnesium sulfate and then spin-dri...
Embodiment 3
[0058]
[0059] The synthetic method of blue fluorescent dopant material (11) is as follows:
[0060] Step (1) is identical with embodiment 1
[0061] (2)
[0062]
[0063] Under nitrogen protection, compound 3-a (2g, 514.98g / mol, 3.88mmol), compound 3-b (1eq, 1.54g, 397.18g / mol, 3.88mmol), sodium tert-butoxide (1.1eq, 0.41g , 96.1g / mol, 4.27mmol), tris(dibenzylideneacetone) dipalladium (0.05eq, 0.178g, 915g / mol, 0.19mmol), tri-tert-butylphosphine (0.05eq, 0.039g, 202.32g / mol, 0.19mol), toluene (20ml) was added to the reaction flask, after the addition was completed, the temperature was raised to reflux for 5 hours, after the reaction was completed, the room temperature was lowered to room temperature, and 20ml of water was added to stir for 15 minutes, and then filtered to obtain the filtrate, which was filtered through diatomaceous earth. The organic phase was obtained from the liquid, and the organic phase was dried with anhydrous magnesium sulfate and then spin-dr...
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