A nitrogen-doped material and its application
A heteroaryl, selected technology, applied in the application field of organic electroluminescent devices, can solve the problems of electron and hole mismatch, efficiency roll-off, and shortened life of the light-emitting layer, and achieve voltage and efficiency improvement and increase The effect of life, good thermal stability
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Synthetic example 1
[0036] Synthesis Example 1: Synthesis of Compound M1
[0037]
[0038] In the reaction flask, add 1-bromo-5-iodonnaphthalene 33g (100mmol), o-nitrophenylboronic acid 18.4g (110mmol), Pd 2 (PPh3) 4 0.9g, toluene 500mL, potassium carbonate 43.3g (314mmol), water 100Ml, 100°C for 3.5h. After the reaction is complete, stop the reaction. After cooling to room temperature and filtering, the obtained solid was purified by recrystallization from toluene to obtain white powder M1-1.
[0039]In the reaction flask, add M1-116.3g (100mmol), triphenylphosphine 26.2g (100mmol), o-dichlorobenzene 500ml, and react at 140°C for 10h. After the reaction is complete, stop the reaction. After cooling to room temperature and filtering, the obtained solid was purified by recrystallization from toluene to obtain white powder M1-2.
[0040] In the reaction bottle, add 29.5g (100mmol) of M1-2, 2g of CuI-ZMS5, 10g of S, 12g of KOH, and 300mL of DMF to react for 24h. After the reaction is comple...
Synthetic example 2
[0042] Synthesis Example 2: Synthesis of Compound M2
[0043] In the same way, by replacing the chloropyridine boronic acid in different positions, we can get the following
[0044]
Synthetic example 3
[0045] Synthesis Example 3: Synthesis of Compound M3
[0046] In the same way, o-nitrophenylboronic acid is replaced by o-nitropyridineboronic acid in the reaction scheme, and chloropyridineboronic acid is replaced by chlorophenylboronic acid in the reaction formula to obtain
[0047]
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