Organic light-emitting device
An electroluminescent device, an organic technology, applied in the direction of electric solid state devices, electrical components, semiconductor devices, etc., can solve the problems of large energy level difference, low device efficiency, and poor life.
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Synthetic example 1
[0065] Synthesis of Compound P1
[0066]
[0067] M (30mmol), 7H-benzocarbazole (30mmol), sodium tert-butoxide (40mmol), tris(dibenzylideneacetone) dipalladium (1%), tri-tert-butylphosphine (2%), toluene 200ml was added to the reaction flask, heated to 120°C for 6 hours, TLC monitored the completion of the reaction, after cooling down, water and dichloromethane were added for extraction, the organic phase was concentrated and recrystallized from toluene to obtain compound P1.
Synthetic example 2
[0069] Synthesis of Compound P2
[0070] Add M (0.1mol), p-chlorophenylboronic acid (0.12mol), potassium carbonate (0.2mol), dioxane (150ml), tetrakis(triphenylphosphine)palladium (1%), and water 30ml into the reaction flask , heated to 80° C. for 5 h, and TLC monitored the completion of the reaction. After cooling down, a large amount of solids precipitated, filtered, and the filter cake was washed with ethanol and dried to obtain intermediate M2.
[0071] M2 (30mmol), 7H-benzocarbazole (30mmol), sodium tert-butoxide (40mmol), tris(dibenzylideneacetone) dipalladium (1%), tri-tert-butylphosphine (2%), toluene 200ml was added to the reaction flask, heated to 120°C for 6 hours, TLC monitored the completion of the reaction, after cooling down, water and dichloromethane were added for extraction, the organic phase was concentrated and recrystallized from toluene to obtain compound P2.
Synthetic example 3
[0073] Synthesis of Compound P11
[0074] The method is the same as that in Synthesis Example 2, except that 7H benzocarbazole is replaced by an equivalent amount of carbazole to obtain compound P11.
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