Triarylamine organic compound and organic light-emitting device thereof
An organic compound and triarylamine technology, which is applied in the field of triarylamine organic compounds and their organic light-emitting devices, can solve problems such as electron/hole migration mismatch, achieve enhanced electron donating ability, reduce total reflection loss and waveguide loss, Effect of excellent hole transport performance
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[0159] The preparation and formation methods of each layer in the organic light-emitting device are not particularly limited, and vacuum evaporation method, spin coating method, vapor deposition method, blade coating method, laser thermal transfer method, electrospray coating method, slit coating method can be used. Either of the cloth method and the dip coating method, the method of vacuum vapor deposition is preferably used in the present invention.
[0160] The organic light-emitting device of the present invention can be widely used in the fields of panel display, lighting source, flexible OLED, electronic paper, organic solar cell, organic photoreceptor or organic thin film transistor, signboard, signal lamp and the like.
Embodiment 1
[0167] [Example 1] Synthesis of Compound 1
[0168]
[0169] Synthesis of Intermediate A-1
[0170] Under the protection of nitrogen, toluene (600mL), a-1 (8.83g, 60mmol), b-1 (23.84g, 60mmol), palladium acetate (0.20g, 0.90mmol), tert-butanol were added successively to the 1L reaction flask Sodium (11.53 g, 120 mmol) and tri-tert-butylphosphine (8 mL in toluene). And react under the condition of reflux for 2 hours. After the reaction stopped, the mixture was cooled to room temperature, filtered with diatomaceous earth, the filtrate was concentrated, recrystallized with methanol, filtered with suction and rinsed with methanol to obtain a recrystallized solid to obtain intermediate A-1 (21.70 g, yield 78%) , HPLC detection solid purity ≧ 99.7%.
[0171] Synthetic compound 1
[0172] Under nitrogen protection, toluene solvent (600mL), c-1 (9.83g, 36mmol), intermediate A-1 (16.69g, 36mmol), Pd 2 (dba) 3 (0.33g, 0.36mmol), BINAP (0.67g, 1.08mmol) and sodium tert-butoxide ...
Embodiment 2
[0174] [Example 2] Synthesis of Compound 9
[0175]
[0176] Using the same method as in Synthesis Example 1, replacing c-1 with equimolar c-9, compound 9 (17.26 g) was synthesized, and the solid purity was detected by HPLC > 99.8%. Mass Spectrum m / z: 705.3361 (Theoretical: 705.3396). Theoretical element content (%)C 54 h 43 N: C, 91.88; H, 6.14; N, 1.98. Measured element content (%): C, 91.93H, 6.10; N, 2.03.
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