A kind of d-a-d' asymmetric structure polymer membrane pswt and its preparation method and application
An asymmetric structure, D-A-D technology, applied in nonlinear optics, instruments, optics, etc., can solve the problems of general optical contrast, single color display, single oxidation potential, etc., to achieve uniform film morphology, easy control structure, and preparation The effect of low energy consumption
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Embodiment 1
[0057] (1) Preparation of monomer SWT
[0058]First, 2,7-dibromo-9 fluorenone (3mmol, 1.044g), 2-thiophene boronic acid (1.5mmol, 0.4335g), potassium carbonate (2mmol, 0.2764g) and tetrakis (three) phenyl phosphopalladium ( 0.0025mmol, 0.0311g) was dissolved in a mixed solution of tetrahydrofuran (20ML) and toluene (30ML) under the condition of nitrogen protection, and 2ml of deionized water was added, and refluxed for 8 hours. and dichloromethane mixed reagent extraction, the obtained organic phase was dried by adding anhydrous magnesium sulfate, and then the sample was mixed by rotary evaporation, and the corresponding mobile phase was selected for column chromatography, and finally 2-thiophene-7-bromo-9-fluorenone mono After that, the obtained 2-thiophene-7-bromo-9-fluorenone monomer (3mmol, 1.022g), 4-(diphenylamino)phenylboronic acid (3mmol, 0.876g), potassium carbonate ( 2mmol, 0.2815g) and tetrakis(tri)phenylphosphopalladium (0.025mmol, 0.031g) were dissolved in a mixe...
Embodiment 2
[0066] (1) Preparation of monomer SWT
[0067] First, 2,7-dibromo-9 fluorenone (3mmol, 1.044g), 2-thiophene boronic acid (1.5mmol, 0.4335g), potassium carbonate (2mmol, 0.2764g) and tetrakis (three) phenyl phosphopalladium ( 0.0025mmol, 0.0311g) was dissolved in a mixed solution of tetrahydrofuran (20ML) and toluene (30ML) under the condition of nitrogen protection, and 2ml of deionized water was added, and refluxed for 8 hours. and dichloromethane mixed reagent extraction, the obtained organic phase was dried by adding anhydrous magnesium sulfate, and then the sample was mixed by rotary evaporation, and the corresponding mobile phase was selected for column chromatography, and finally 2-thiophene-7-bromo-9-fluorenone mono After that, the obtained 2-thiophene-7-bromo-9-fluorenone monomer (3mmol, 1.022g), 4-(diphenylamino)phenylboronic acid (3mmol, 0.876g), potassium carbonate ( 2mmol, 0.2815g) and tetrakis(tri)phenylphosphopalladium (0.025mmol, 0.031g) were dissolved in a mix...
Embodiment 3
[0073] (1) Preparation of monomer SWT
[0074] First, 2,7-dibromo-9 fluorenone (3mmol, 1.044g), 2-thiophene boronic acid (1.5mmol, 0.4335g), potassium carbonate (2mmol, 0.2764g) and tetrakis (three) phenyl phosphopalladium ( 0.0025mmol, 0.0311g) was dissolved in a mixed solution of tetrahydrofuran (20ML) and toluene (30ML) under the condition of nitrogen protection, and 2ml of deionized water was added, and refluxed for 8 hours. and dichloromethane mixed reagent extraction, the obtained organic phase was dried by adding anhydrous magnesium sulfate, and then the sample was mixed by rotary evaporation, and the corresponding mobile phase was selected for column chromatography, and finally 2-thiophene-7-bromo-9-fluorenone mono After that, the obtained 2-thiophene-7-bromo-9-fluorenone monomer (3mmol, 1.022g), 4-(diphenylamino)phenylboronic acid (3mmol, 0.876g), potassium carbonate ( 2mmol, 0.2815g) and tetrakis(tri)phenylphosphopalladium (0.025mmol, 0.031g) were dissolved in a mix...
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