Aromatic amine compound, material containing same and organic electroluminescence device
A technology of compounds and aromatic amines, which is applied in the field of organic electroluminescent devices and materials, can solve the problems of complex manufacturing process and affecting the distribution of OLED radiation spectrum
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Embodiment 1
[0072] Embodiment 1, the preparation of compound ONA-101
[0073] Step 1: Preparation of Intermediate Int.-1
[0074]
[0075] 15.0g (59.2mmol) of 3,3'-dichlorobenzidine (CAS: 91-94-1) was dissolved in 100ml of dry toluene, and 69.0g (0.29mol) of 4-bromobiphenyl was added under nitrogen protection and 28.5g of sodium tert-butoxide, then add 0.61g of Pd 2 (dba) 3 CHCl 3 And 0.3ml of 10% tri-tert-butylphosphonium toluene solution, heated to 100°C and stirred for 24 hours, cooled to room temperature, added 100ml of water, stirred and filtered, washed the filter cake with water and ethanol to obtain 33.7g of white solid, collected rate of 66%.
[0076] The second step: the preparation of compound ONA-101
[0077]
[0078] 10g (11.6mmol) of the intermediate Int.-1 prepared in the first step and 5.9g (34.8mmol) of diphenylamine were mixed, and 80ml of toluene, 3.4g of sodium tert-butoxide and 20mg of Pd were added 2 (dba) 3 , under the protection of nitrogen, add 0.05ml o...
Embodiment 2
[0079] Embodiment 2, the preparation of compound formula ONA-100, ONA-102~ONA-209
[0080] With reference to the preparation method of Example 1, the compound formula ONA- 100. ONA-102-ONA-209.
Embodiment 3
[0081] Embodiment 3, the preparation of compound formula ONA-211
[0082] The first step: preparation of intermediate Int.-2
[0083]
[0084] 15.0g (59.2mmol) of 3,3'-dichlorobenzidine SM-0 was dissolved in 100ml of dry toluene, and under nitrogen protection, 38.8g (0.12mol) of 2,2'-dibromobiphenyl and 28.5 g of sodium tert-butoxide, then add 0.61 g of Pd 2 (dba) 3 CHCl 3 And 0.3ml of 10% tri-tert-butylphosphonium toluene solution, heated to 100°C and stirred for 24 hours, cooled to room temperature, diluted with 100ml of water, extracted with dichloromethane, collected organic phase, dried, filtered, and the filtrate was decompressed After concentrating to dryness, the obtained brown solid was mixed with ethanol and heated to boiling, filtered while hot, and the filter cake was washed with ethanol to obtain 23.6 g of white solid with a yield of 72%.
[0085] The second step: the preparation of compound ONA-211
[0086]
[0087] 10.0g (18.0mmol) of the intermediate...
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