Compound having D-pi-A structure as well as preparation method and application of compound
A technology of compounds and synthesis methods, applied in the field of preparation of organic second-order nonlinear chromophores, can solve problems such as electronic bridges that have not been reported and used, and achieve convenient deviceization process, high thermal decomposition temperature and glass transition temperature, and good orientation. The effect of stability
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Embodiment 1
[0084] An organic second-order nonlinear chromophore with D-π-A structure based on indacene derivatives was synthesized as shown below:
[0085]
[0086] The synthetic route is as follows:
[0087]
[0088] 1) Synthesis of Compound 2
[0089] 44 mg of phosphine salt (0.092 mmol) and 100 mg of indacene derivative (compound 1, 0.093 mmol) were dissolved in 1,2-dichloroethane solvent, and 10 mg of sodium hydride (0.42 mmol) was slowly added at 0°C. Stir at room temperature for 24 hours, pour the reaction product into water, separate the layers, extract the aqueous phase with dichloromethane, combine the organic phases, dry the organic phase with anhydrous magnesium sulfate, filter, and remove the dichloromethane by rotary evaporation to obtain a crude product. Column chromatography (stationary phase is 200-300 mesh silica gel, mobile phase is a mixture of petroleum ether and ethyl acetate, petroleum ether: ethyl acetate = 3:1) to obtain 70 mg of yellow powder with a yield ...
Embodiment 2
[0097] An organic second-order nonlinear chromophore with D-π-A structure based on indacene derivatives was synthesized as shown below:
[0098]
[0099] The synthetic route is as follows:
[0100] 1) Synthesis of compound 2-2
[0101] 63 mg of phosphine salt (0.103 mmol) and 100 mg of indacene derivative (compound 1-2, 0.104 mmol) were dissolved in 1,2-dichloroethane solvent, and 11 mg of sodium hydride (0.46 mmol) was slowly added at 0°C. Stir at room temperature for 24 hours, pour the reaction product into water, separate the layers, extract the aqueous phase with dichloromethane, combine the organic phases, dry the organic phase with anhydrous magnesium sulfate, filter, and remove the dichloromethane by rotary evaporation to obtain a crude product. Column chromatography (stationary phase is 200~300 mesh silica gel, mobile phase is a mixture of petroleum ether and ethyl acetate, petroleum ether: ethyl acetate = 3:1), and 85 mg of powdery compound 3 is obtained with a ...
Embodiment 3
[0107] An organic second-order nonlinear chromophore with D-π-A structure based on indacene derivatives was synthesized as shown below:
[0108]
[0109] The synthetic route is as follows:
[0110]
[0111] 1) Synthesis of compound 2-3
[0112] 55 mg of phosphine salt (0.083 mmol) and 100 mg of indacene derivative (compound 1-3, 0.084 mmol) were dissolved in 1,2-dichloroethane solvent, and 9 mg of sodium hydride (0.375 mmol) was slowly added at 0°C. Stir at room temperature for 24 hours, pour the reaction product into water, separate the layers, extract the aqueous phase with dichloromethane, combine the organic phases, dry the organic phase with anhydrous magnesium sulfate, filter, and remove the dichloromethane by rotary evaporation to obtain a crude product. Column chromatography (stationary phase is 200-300 mesh silica gel, mobile phase is a mixture of petroleum ether and ethyl acetate, petroleum ether: ethyl acetate = 3:1) to obtain 76 mg of yellow powder with a yiel...
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