Organic electroluminescent device
An electroluminescent device and luminescent technology, applied in the OLED field, can solve the problems of large band gap, high driving voltage, and inability to fully use energy effectively, and achieve good stability, high photoluminescence efficiency, and low price Effect
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Embodiment 1
[0093] Synthesis of C1. Under a nitrogen atmosphere, dissolve 1 mol of potassium tert-butoxide into 20 ml of DML and stir for 1 hour, then add 1 mol of carbazole in the DML solution dropwise, and stir for 1 hour after all the addition is complete. Then, a DMF solution in which 0.2 mol of 2,3,4,5,6-pentafluorobenzonitrile was dissolved was added dropwise and stirred for 5 hours. Then the reaction solution was poured into water and filtered to obtain a solid. Separation with a chromatographic column. C1 was obtained with a yield of 90%.
[0094] Mass spectrum: 929.
[0095] Elemental analysis: C: 86.60, H: 4.35, N: 9.05.
Embodiment 2
[0097] Synthesis of C2. The reactant carbazole was replaced by tert-butyl carbazole, and C2 was obtained through the same synthesis method as in Example 1, with a yield of 91%.
[0098] Mass spectrum: 1490.
[0099] Elemental analysis: C: 86.20, H: 8.16, N: 5.64.
Embodiment 3
[0101] Synthesis of C3. The reactant carbazole was replaced by phenylcarbazole, and C3 was obtained through the same synthesis method as in Example 1, with a yield of 91%.
[0102] Mass spectrum: 1689.
[0103] Elemental analysis: C: 90.20 H: 4.83 N: 4.97.
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