Organic electroluminescent compound and application thereof
A compound and electroluminescence technology, applied in the field of compounds, can solve the problems of low luminous efficiency and insufficient carrier transmission efficiency, and achieve the effects of improving luminous efficiency, improving carrier transmission efficiency and low power consumption
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[0049] In addition, the present invention provides a method for preparing the above-mentioned OLED device, comprising the following steps:
[0050] 1) Ultrasonic cleaning of the transparent anode electrode ITO substrate in isopropanol for 5-10 minutes, and exposure to ultraviolet light for 20-30 minutes, followed by plasma treatment for 5-10 minutes;
[0051]2) Put the processed ITO substrate into the evaporation equipment, and first evaporate the hole transport layer material as the hole transport layer;
[0052] 3) Then evaporate the light-emitting layer, mix and evaporate the material of the light-emitting layer, and 5--10% Ir(ppy)3;
[0053] 4) Then use the electron transport layer material to vapor-deposit an electron transport layer, then vapor-deposit 0.5-2nm LiF, and then vapor-deposit 100-200nm metal Al;
[0054] Wherein, one of the hole transport layer material, light emitting layer material and electron transport layer material is a compound represented by general ...
Embodiment 1
[0061] The preparation method of compound 1
[0062]
[0063] Dissolve 100mmol compound 1-a and 120mmol bromobenzene in 1000ml toluene, add potassium carbonate 200mmol and 1mmol catalyst Pd[P(C 6 h 5 ) 3 ] 4 , reflux reaction under nitrogen protection for 24 hours, after the completion of the reaction, add 500ml of distilled water, cool and filter, extract with dichloromethane, wash with salt water, separate the organic layer, remove the organic solvent by rotary evaporation, pass the crude product through the column, and then use dichloromethane and Purified by ethanol recrystallization and dried in vacuum to obtain 86 mmol of product compound 1.
[0064] Molecular weight characterization MS 475.14;
[0065] 1 H-NMR: 7.98(2H), 7.82(2H), 7.74(2H), 7.72(2H), 7.73(2H), 7.54(2H), 7.69(2H), 7.86(2H), 7.64(2H), 7.61 (2H), 7.44(1H).
Embodiment 2
[0067] The preparation method of compound 2
[0068]
[0069] Dissolve 100mmol compound 2-a and 120mmol bromobenzene in 1000ml toluene, add potassium carbonate 200mmol and 1mmol catalyst Pd[P(C 6 h 5 ) 3 ] 4 , reflux reaction under nitrogen protection for 24 hours, after the completion of the reaction, add 500ml of distilled water, cool and filter, extract with dichloromethane, wash with salt water, separate the organic layer, remove the organic solvent by rotary evaporation, pass the crude product through the column, and then use dichloromethane and Purified by ethanol recrystallization and dried in vacuum to obtain 88 mmol of product compound 2.
[0070] Molecular weight characterization MS 475.14;
[0071] 1 H-NMR: 7.98(2H), 7.82(2H), 7.74(2H), 7.72(2H), 7.73(2H), 7.54(2H), 7.69(2H), 7.86(2H), 7.64(1H), 7.63 (1H), 7.61(2H), 7.63(1H), 7.44(1H).
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