Selenium or tellurium functionalized covalent organic framework material as well as preparation method and application thereof
A covalent organic framework, functionalized technology, applied in chemical instruments and methods, organic active ingredients, medical preparations of non-active ingredients, etc. Advantages and other issues, to achieve the effect of simple operation, easy control and high sensitivity
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Embodiment 1
[0041] Example 1: Preparation of covalent organic framework materials bridged by selenium bonds
[0042] The reaction equation for preparing selenium bond-functionalized COF is shown in the following formula. Add 4,4'-diaminodiphenylselenide (792mg, 3mmol) and trimesaldehyde (324mg, 2mmol) to the reaction tube, and then add Add 10mL of a mixed solution of dioxane and mesitylene (the volume ratio of dioxane and mesitylene is 1:3), and after fully dissolving, add the catalyst aqueous solution of acetic acid (6mL, 5mmol / mL) dropwise to the above in solution. Finally, the samples in the reaction tube were subjected to liquid nitrogen cold cutting-vacuumizing-thawing treatment to achieve anaerobic high vacuum conditions, and finally placed in an oil bath at 80°C for 72 hours in the dark. After the reaction was completed, when the temperature of the system dropped to room temperature, precipitation appeared, and the solid product was separated by centrifugation, and washed repeated...
Embodiment 2
[0044] Example 2: Preparation of covalent organic framework materials bridged by diselenide bonds
[0045] The reaction equation for preparing diselenide functionalized COF is shown in the following formula. Add 4,4'-diaminodiphenyl diselenide (516mg, 1.5mmol) and trimesaldehyde (162mg, 1.0mmol) into the reaction tube, Subsequently, a mixed solution of 10 mL of dioxane and mesitylene (the volume ratio of dioxane and mesitylene is 1:1) was added to the reaction tube. After fully dissolving, the catalyst aqueous acetic acid solution (3 mL, 1 mmol / mL) Add dropwise to the above solution. Finally, the samples in the reaction tube were subjected to liquid nitrogen cold cutting-vacuumizing-thawing treatment to achieve anaerobic high vacuum conditions, and finally placed in an oil bath at 150°C for 24 hours to avoid light. After the reaction was completed, when the temperature of the system dropped to room temperature, precipitation appeared, and the solid product was separated by ce...
Embodiment 3
[0052] Example 3: Preparation of covalent organic framework materials bridged by selenium bonds
[0053]The reaction equation for preparing selenium-bonded functionalized COF is shown in the following formula. Add 4,4'-dialdehyde diphenylselenide (868 mg, 3 mmol) and 1,3,5-triaminobenzene (246 mg, 2 mmol) into the reaction tube ), then add a mixed solution of 10mL dioxane and mesitylene (dioxane and mesitylene volume ratio is 3:5) to the reaction tube, after fully dissolving, the catalyst aqueous acetic acid solution (1mL, 10mmol / mL) was added dropwise to the above solution. Finally, the samples in the reaction tube were subjected to liquid nitrogen cold cutting-vacuumizing-thawing treatment to achieve anaerobic high vacuum conditions, and finally placed in a 120°C oil bath for 48 hours to avoid light. After the reaction was completed, when the temperature of the system dropped to room temperature, precipitation appeared, and the solid product was separated by centrifugation...
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