An organic light emitting device
A technology of organic light-emitting devices and organic substances, which is applied in the manufacture of electric solid-state devices, semiconductor devices, semiconductor/solid-state devices, etc. Luminous efficiency and driving voltage, and the effect of improving luminous efficiency
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[0142] 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.
[0143] 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.
[0144] The second hole transport layer made of the material of formula (I) and the covering layer made of the material of formula (IV), the corresponding compounds can be obtained by the following methods:
[0145] The triarylamine compound represent...
Embodiment 1
[0154] [Example 1] Synthesis of Compound 1-1
[0155]
[0156] Step1: Synthesis of intermediate A-1
[0157] Under nitrogen protection, toluene (600mL), a-1 (20.00g, 0.06mol), b-1 (23.83g, 0.06mol), palladium acetate (0.21g, 0.93mmol), tert- Sodium butoxide (11.3 g, 0.117 mol) 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 (30.41g, yield 78%) , HPLC detection solid purity ≧ 99.7%.
[0158] Step2: Synthesis of compound 1-1
[0159] Under nitrogen protection, toluene solvent (600ml), c-1 (5.83g, 36mmol), intermediate A-1 (23.39g, 36mmol), Pd 2 (dba) 3 (330mg, 0.36mmol), BINAP (0.67g, 1.08mmol) and sodium tert-butoxide (3.23g, 33.6mmol), stirred and ...
Embodiment 2
[0161] [Example 2] Synthesis of Compound 1-22
[0162] Compound 1-22 (17.66 g) was synthesized by the method of compound 1-1 above, and the purity of the solid was detected by HPLC ≧99.7%. Mass Spectrum m / z: 730.3419 (Theoretical: 730.3396). Theoretical element content (%)C 56 h 34 D. 5 N: C, 92.02; H, 6.07; N, 1.92 Measured element content (%): C, 92.02; H, 6.07; N, 1.95.
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