Chloride ion fluorescent probe and preparation method and application thereof
A fluorescent probe and chloride ion technology, applied in the field of chemical analysis ion detection, can solve the problems of limiting anion species and fluorescence response sensitivity, and achieve the effects of convenient identification, good ion selectivity and high sensitivity
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[0036] Preparation formula of the present invention:
[0037]
Embodiment 1
[0039]Under nitrogen protection, 100mg (0.24mmol) 2,7-dibromo-9-cycloheptatrienylfluorene, 106mg (0.53mmol) 2-biphenylboronic acid, 0.47g (3.4mmol) potassium carbonate, then add the mixed solvent of toluene (8ml), ethanol (8ml), water (8ml) in the ratio of 1:1:1 with the volume ratio, and add the tetrakis (triphenylene) of catalytic amount Phosphine) palladium, heated to reflux, reacted for 6 hours, cooled, extracted the reaction solution with dichloromethane, combined the organic layers, washed with saturated brine, dried the organic phase over magnesium sulfate, filtered, evaporated the solvent, and separated by column chromatography to obtain 2 , 7-bis(biphenyl-2-yl)-9-cycloheptatrienylene fluorene 42 mg, yield 31%.
Embodiment 2
[0041] Under nitrogen protection, 100mg (0.24mmol) 2,7-dibromo-9-cycloheptatrienylfluorene, 144mg (0.73mmol) 2-biphenylboronic acid, 0.47g (3.4mmol) potassium carbonate, then add the mixed solvent of toluene (8ml), ethanol (8ml), water (8ml) in the ratio of 1:1:1 with the volume ratio, and add the tetrakis (triphenylene) of catalytic amount Phosphine) palladium, heated to reflux, reacted for 12 hours, cooled, extracted the reaction solution with dichloromethane, combined the organic layers, washed with saturated brine, dried the organic phase with magnesium sulfate, filtered, evaporated the solvent, and separated by column chromatography to obtain 2 , 55 mg of 7-bis(biphenyl-2-yl)-9-cycloheptatrienylene fluorene, yield 41%.
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