Preparation method of cage type n-propyl oligomeric silsesquioxane
A technology of polysilsesquioxane and propyltrimethoxysilane, applied in the direction of organic silicon compounds, etc., can solve the problems of difficult reaction control, complicated treatment process, a large amount of waste acid, etc., and achieves short preparation period and high yield. High and pollution-reducing effect
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Embodiment 1
[0030] In a 1L grinding bottle, add 0.6L of ethanol, 56.0mL of concentrated hydrochloric acid (38wt%), and 50.0mL of n-propyltriethoxysilane in sequence, mix well, and seal the bottle. Control the temperature of the reaction solution at 0-5°C, let the system hydrolyze and condense for 96 hours under stirring conditions, remove the reaction solution by filtration to obtain a white powder solid, wash with methanol three times, and dry in a vacuum oven for 5.0 hours to obtain 15.1997 g products. The yield was 73.9%. Structure Characterization: 29 Si-NMR, -66.93ppm (CDCl 3 ); 1 H-NMR, 0.63ppm (t, Si-CH 2 -, 2H), 0.98ppm (t, -CH 3 , 3H) and 1.47ppm (m, -CH 2 -,2H)(CDCl 3 ); 13 C-NMR, 14.40ppm, 16.33ppm and 17.33ppm (CDCl 3 ); FTIR, 1114cm -1 (νSi-O-Si), 1220cm -1 (νSi-C), 2958cm -1 , 2930cm -1 and 2872cm -1 (ν C-H), 1464cm -1 and 1378cm -1 (δC-H); MS, [M] + =762.5925; single crystal diffraction, C 24 h 56 Si 8 o 12 , M=761.88, triclinic, space group P -1 , ...
Embodiment 2
[0032] In a 3L round bottom flask, add 1.6L of methanol, 200.0mL of concentrated hydrochloric acid (37%), and 150.0mL of n-propyltriethoxysilane in sequence, mix well, and seal the bottle. Control the temperature of the reaction solution at 0-5°C, let the system hydrolyze and condense for 120 hours under stirring conditions, and use the filtered reaction solution for later use to obtain a white powder solid, wash it with methanol three times, and dry it in a vacuum oven for 5 hours to obtain 43.9950g product. The yield was 71.3%, and the structural characterization of the product was as in Example 1.
Embodiment 3
[0034] In a 500mL ground-mouth Erlenmeyer flask, add 200mL of ethanol and 80.0mL of the filtered mother liquor in Example 1, 20.0mL of concentrated hydrochloric acid (36.5wt%), and 21.0mL of n-propyltrimethoxysilane, mix well, and seal bottle mouth. Control the temperature of the reaction solution at 0-5°C, let the system hydrolyze and condense for 80 hours under stirring conditions, remove the reaction solution by filtration to obtain a white powder solid, wash with methanol three times, and dry in a vacuum oven for 5 hours to obtain 9.4327g product. The yield was 83.2%, and the structural characterization of the product was as in Example 1.
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