Amplified conjugated fluorescent porous polymer, fluorescent sensing film and its preparation method and application
A porous polymer, fluorescent sensing technology, applied in the field of fluorescent sensing materials, can solve the problem that the fluorescent sensor cannot further meet the requirements of fast, sensitive, and high selectivity, and achieves the problem of inhibiting fluorescence quenching, high selection, and transmission. Sensitivity-enhancing effect
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Embodiment 1
[0057] This embodiment provides an intermediate 2-4, the synthesis route of which is as follows:
[0058] ;
[0059] The preparation method of monomer 2-4 specifically comprises the following steps:
[0060] 1) Synthesis of compound 2-1
[0061] ;
[0062] Put anthracene (3.55 g, 20.0 mmol), 1,4-benzoquinone (1.30 g, 12.0 mmol), 2,3,5,6-tetrachlorobenzoquinone (4.90 g, 20.0 mmol) into the reaction flask, add Glacial acetic acid (125 mL), heated to reflux and stirred for 16 h. After the reaction was completed, return to room temperature, and use a Buchner funnel to filter under vacuum to obtain a solid filter cake. Wash the solid with glacial acetic acid, methanol, and ether to obtain a crude product. The crude product was separated and purified by column chromatography, and the eluent used was a mixed solvent of dichloromethane and ethyl acetate at a volume ratio of 50: 1 to obtain yellow solid 2-1 (3.10 g, 68%). The H NMR spectrum of compound 2-1 is as follows figure...
Embodiment 2
[0074] This example provides an amplified conjugated fluorescent porous polymer (polymer 1), and the synthetic route of polymer 1 is as follows:
[0075] ;
[0076] The preparation method of polymer 1 specifically comprises the following steps:
[0077] Under argon atmosphere, the compound pentadecene 2-4 (0.478 g, 1 mmol), 1,6-dibromopyrene (0.360 g, 1 mmol), catalyst Pd(PPh 3 ) 4 (0.058 g, 0.05 mmol) and cuprous iodide CuI (0.010 g, 0.05 mmol) were put into the reaction flask, and the nitrogen gas was exhausted three times with a double-row tube, and ultra-dry toluene (12 mL) treated with potassium-sodium alloy was added and isopropylamine ( i -Pr 2 NH) (6 mL), heated to 130 o C stirred and reacted for two days. After the reaction was completed, the reaction mixture cooled to room temperature was poured into deionized water, extracted five times with dichloromethane, and the combined organic layers were dried with anhydrous sodium sulfate and concentrated under vacuum...
Embodiment 3
[0079] This example provides an amplified conjugated fluorescent porous polymer (polymer 2), and the synthesis route of polymer 2 is as follows:
[0080] ;
[0081] The preparation method of polymer 2 specifically comprises the following steps:
[0082] Under argon atmosphere, the compound pentadecene 2-4 (0.478 g, 1 mmol), 9,9-dioctyl-2,7-dibromofluorene (0.760 g, 1 mmol), catalyst Pd(PPh 3 ) 4 (0.058 g, 0.05 mmol) and cuprous iodide CuI (0.010 g, 0.05 mmol) were put into the reaction flask, and the nitrogen gas was exhausted three times with a double-row tube, and ultra-dry toluene (12 mL) treated with potassium-sodium alloy was added and Isopropylamine (i -Pr 2 NH) (6 mL), heated to 130 o C stirred and reacted for two days. After the reaction was completed, the reaction mixture cooled to room temperature was poured into deionized water, extracted five times with dichloromethane, and the combined organic layers were dried with anhydrous sodium sulfate and concentrated ...
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