An organic small molecule high-efficiency room temperature phosphorescent material based on aroimide and its preparation and application
A reaction and substituent technology, applied in the field of organic luminescence and its anti-counterfeiting, can solve the problems of difficult mass production, long synthesis steps, and few molecular types, etc., and achieve the effect of cheap raw materials, simple synthesis method, and high luminous efficiency
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Embodiment 1
[0036] The reaction equation is as follows:
[0037]
[0038] The specific steps of the reaction are as follows:
[0039] A mixture of compound formula A-1 and compound formula B-1 in glacial acetic acid was refluxed for 4 hours. The solid was separated from the mixture (the reaction liquid was cooled to room temperature, and the precipitate was filtered), and the product formula I-1 was obtained.
[0040] The H NMR spectrum of the compound shown in formula Ⅰ-1 is as follows: figure 1 As shown, the characterization data are as follows:
[0041] 1 H NMR (300MHz, Chloroform-d) δ7.98 (d, J=7.7Hz, 2H), 7.70–7.51 (m, 8H), 7.36–7.23 (m, 4H), 7.20–7.12 (m, 2H), HR-MS(APCI)m / z calcd for C 26 h 16 N 2 o 2 [M+H] + 389.12, found 389.13.
[0042] From the above detection results, it can be seen that the structure of the compound represented by formula I-1 is correct.
Embodiment 2
[0044] The reaction equation is as follows:
[0045]
[0046] The specific steps of the reaction are as follows:
[0047] A mixture of compound formula A-1 and compound formula B-1 in glacial acetic acid was refluxed for 4 hours. The solid was separated from the mixture (the reaction liquid was cooled to room temperature, and the precipitate was filtered), and the product formula I-2 was obtained.
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