Benzotriazole boron nitrogen derivative small molecular material and application thereof in organic electronic device
A technology for benzotriazole boron nitrogen and organic electronic devices, which is applied to small molecule materials of benzotriazole boron nitrogen derivatives and its application in organic electronic devices, can solve the problem of low HOMO/LUMO energy level and realize the Market barriers, affecting device efficiency and other issues, to achieve the effect of improving battery efficiency, wide absorption range, and long device life
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Embodiment 1
[0028] Embodiment 1: the synthesis of compound 1
[0029]
[0030] Add 1-1 (6.44g, 6mmol), 1-2 (3.86g, 20mmol) and 5mL pyridine into a 500mL two-necked flask, then pump argon three times, add 250mL chloroform under the protection of argon, and react at 65°C 24 hours. Cool to room temperature, extract three times with dichloromethane, combine the organic phases, dry filter and spin dry with silica gel, separate and purify by column chromatography (n-hexane: dichloromethane = 3:1) to obtain 3.84 g of purple powder, yield 45% . MS(EI)m / z:[M]+:1423.56.
Embodiment 2
[0031] Embodiment 2: the synthesis of compound 2
[0032]
[0033] Add 1-1 (5.37g, 5mmol), 1-3 (3.91g, 16mmol) and 5mL pyridine into a 500mL two-necked flask, then pump argon three times, add 300mL chloroform under the protection of argon, and react at 65°C for 24 hours . Cool to room temperature, extract three times with dichloromethane, combine the organic phases, dry filter and add silica gel to spin dry, separate and purify by column chromatography (n-hexane:dichloromethane=3:1) to obtain 2.98g of purple powder, yield 39% . MS(EI)m / z:[M]+:1526.62.
Embodiment 3
[0034] Embodiment 3: the synthesis of compound 3
[0035]
[0036] Add 1-1 (6.44g, 6mmol), 1-4 (4.57g, 20mmol) and 5mL pyridine into a 500mL two-neck flask, then pump argon three times, add 300mL chloroform under the protection of argon, and react at 65°C for 24 hours . Cool to room temperature, extract three times with dichloromethane, combine the organic phases, dry filter and add silica gel to spin dry, separate and purify by column chromatography (n-hexane:dichloromethane=3:1) to obtain 3.32 g of purple powder, yield 37% . MS(EI)m / z:[M]+:1493.56.
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