Anthracene-containing compound, synthesis method thereof, and organic electroluminescent device
A technology of electroluminescent devices and compounds, which is applied in the fields of electro-solid devices, silicon organic compounds, chemical instruments and methods, etc., can solve the problem of low electron and hole recombination efficiency, low luminous efficiency of light-emitting devices, and inability to effectively balance current carrying It can improve the recombination rate of carriers, enhance the direction of charge migration, and not easy to crystallize.
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Embodiment 1
[0057] [Example 1] Synthesis of compound 3
[0058]
[0059] Step1: Under the protection of nitrogen, add 2-bromoanthracene (2.16g, 8.4mmol), 9-acridineboronic acid (2.05g, 9.2mmol), tetrakistriphenylphosphine palladium (0.09g, 0.08mmol), carbonic acid into the reaction vessel Potassium (3.48g, 25.2mmol), 60mL toluene, 20mL ethanol and 20mL distilled water, stirred at 120°C for 3h. After the reaction, distilled water to stop the reaction, ethyl acetate extraction, organic layer with MgSO 4 After drying, the solvent was distilled off under reduced pressure, and then purified by silica gel column chromatography to obtain Intermediate 3-1 (1.94 g, 65%).
[0060] Step2: Add 3-1 (3.55g, 10.0mmol), 60mL of DMF solution, 60mL of glacial acetic acid, and 50mL of chloroform to the reactor under the condition of nitrogen and no light, add NBS (2.22g, 12.5mmol), and stir for 2h at room temperature. The crude product was precipitated, filtered and washed with methanol to obtain Intermediate 3...
Embodiment 2
[0064] [Example 2] Synthesis of compound 4
[0065] According to the synthesis method of compound 3, compound 4 (4.28 g, 67%) was obtained.
[0066]
Embodiment 3
[0067] [Example 3] Synthesis of compound 5
[0068] According to the synthesis method of compound 3, compound 5 (3.56 g, 62%) was obtained.
[0069]
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