Cross-linked polymer based on copolymerization fluorenol and preparation method and usage of cross-linked polymer
A technology of cross-linked polymers and copolyfluorene alcohols, which is applied in the field of cross-linked polymer materials of copolyfluorene alcohols and its preparation, can solve the problems of few studies on the photoelectric properties of super-crosslinked polymers, and achieve low cost and wide application Foreground, easy-to-operate effects
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[0025] The preparation method of the above-mentioned cross-linked polymer based on copolymerized fluorenyl alcohol is as follows: using the fluorenyl tertiary alcohol copolymer as a reaction substrate, Friedel-Crafts reaction occurs in the presence of an acid catalyst to form a corresponding fluorenyl cross-linked polymer, Its reaction route is:
[0026]
[0027] The specific steps are: add the fluorenyl tertiary alcohol copolymer as the reaction substrate into the reaction container, then add the solvent to dissolve it, finally add the acid catalyst, and react for at least 3 hours. After the reaction is completed, add water to quench the reaction. First extraction, drying over anhydrous sodium sulfate, and rotary evaporation under reduced pressure to remove the solvent until a viscous reaction solution remains, then settle with methanol, filter, and extract the filter residue with acetone in a Soxhlet extractor to finally obtain the target product .
Embodiment 1
[0030] The structural formula of the cross-linked polymer based on copolymerized fluorenol of the present embodiment is:
[0031]
[0032] Its synthetic route is:
[0033]
[0034] The specific steps are:
[0035] (1) Preparation of compound a
[0036] Weigh carbazole (3g, 17.94mmol), potassium hydroxide (2.01, 35.88mmol) in a 100mL three-necked reaction flask, seal the device at the same time, and inject hexyl bromide (2.44, 16.14mmol) and 40mL of acetone into the flask middle. The reaction temperature is 80°C, and the reaction time is 24h. After the reaction is completed, when the temperature drops to room temperature, add water (15mL) to quench, extract with dichloromethane, combine organic phases, dry over anhydrous magnesium sulfate, and extract with dichloromethane and water , and dried with anhydrous sodium sulfate, concentrated by rotary evaporation, wet loading, passed through the column with pure petroleum ether, and rotary evaporated to obtain 2.3 g of whit...
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