Organic luminescent material, preparation method thereof and organic electroluminescence device containing organic luminescent material
A luminescent material and organic technology, applied in luminescent materials, electrical solid devices, electrical components, etc., can solve the problems of color purity, efficiency and thermal stability, difficult material application display, blue color purity is not high enough, etc., to achieve excellent Effect of electroluminescent properties, proper color coordinates, long device lifetime
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preparation example Construction
[0064] Step 1, the preparation of intermediate 1
[0065] Add compound 1, N-bromosuccinimide and dichloromethane solvent into the reaction vessel, stir the mixture at room temperature, when the reaction is complete, add water to it, extract the mixture with dichloromethane, and filter the extract under reduced pressure , the obtained compound is recrystallized from ethanol to obtain intermediate 1;
[0066] Step 2, the preparation of intermediate 2
[0067] Intermediate 1, Pd 2 (dba) 3 , biboronic acid pinacol ester and potassium acetate were dissolved in 1,4-dioxane, and in a nitrogen atmosphere, the reactants were refluxed and stirred for reaction. The extracted product was dried with magnesium sulfate and filtered, then the filtered product was concentrated under reduced pressure, and the concentrated product was purified by silica gel column chromatography to obtain intermediate 2;
[0068] Step 3, the preparation of intermediate 3
[0069] Add intermediate 2, compoun...
preparation example 1
[0079] [Preparation Example 1] Preparation of Compound 1
[0080]
[0081] Preparation of Compound A-1
[0082] 2,3-Dibromoanthracene (15.0g 44.64mmol), phenylboronic acid (13.6g 111.6mmol), potassium carbonate (30.8g 223.2mmol) were added to 500mL of toluene / ethanol / water (volume ratio 3:1:1) in a mixed solvent. Replace the air with nitrogen three times, add tetrakis(triphenylphosphine)palladium (2.58g 0.22mmol), replace the air with nitrogen three times again, and heat to 90°C under the protection of nitrogen. TLC monitoring. After the reaction was completed, it was cooled to room temperature under the protection of nitrogen. Use a separatory funnel to separate the liquid and keep the organic phase. The catalyst was removed using celite and the celite was washed with DCM until free of product. Concentrate the filtrate to a small amount, mix the sample with silica gel, and separate using a silica gel funnel to obtain intermediate A-1 (12.8 g, yield = 87%).
[0083] P...
preparation example 2
[0093] [Preparation Example 2] Preparation of Compound 18
[0094] According to the method of preparation example 1, the replace with Will replace with Will replace with Compound 18 was prepared, and its mass spectral value was 955.40.
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