Reactive fluorosilicone resin as well as preparation method and application thereof
A fluorosilicone resin, reactive technology, used in epoxy resin coatings, chemical instruments and methods, coatings, etc., can solve the problem of low dielectric constant dielectric loss, organic pollutants without self-cleaning performance, glass transition temperature Low problems such as reducing dielectric loss and dielectric constant, excellent self-cleaning performance, and increasing adhesion performance
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Embodiment 1
[0055] This embodiment provides a reactive fluorosilicone resin, the structure of which is shown in Formula 2:
[0056]
[0057] The preparation method of the compound shown in Formula 2 is: dissolve 1 mol of diphenyldimethoxysilane in 100 mL of NMP, add 1 mol of perfluorododecanol and 0.01 mol of dibutyltin oxide, react at 100 ° C for 2.5 h, and distill After the solvent was separated, 1 mol of epichlorohydrin was added to the obtained product, and reacted at 80° C. for 2 hours. After the reaction, the product was purified to obtain the compound shown in formula 2.
[0058] 1 H NMR (CDCl 3 ,500MHz): δ7.60~7.52(m, 2H, Ar-H), 7.48~7.40(m, 4H, Ar-H), 7.36~7.27(m, 4H, Ar-H), 4.19~4.11(s ,2H,CH 2 ), 4.10~4.02 (d, H, CH 2 ), 3.77~3.71 (d, H, CH 2 ), 2.69~2.62 (m, H, CH 2 ), 2.69~2.62(m, H, CH), 2.36~2.58(m, H, CH 2 ).
Embodiment 2
[0060] This embodiment provides a reactive fluorosilicone resin, the structure of which is shown in formula 3:
[0061]
[0062] The preparation method of the compound shown in formula 3 is: dissolve 1 mol of dimethylvinylmethoxysilane in 100 mL of NMP, add 1 mol of perfluorobutanol and 0.01 mol of dibutyltin oxide, react at 100 ° C for 2 h, and distill After the solvent is separated, the product is purified to obtain the compound shown in formula 3.
[0063] 1 H NMR (CDCl 3 ,500MHz): δ5.43~5.36(t, H, CH=C H 2 ), 5.35~5.29(t, H, C H =CH 2 ), 5.19~5.11 (t, H, CH=C H 2 ), 4.15~4.08 (s, 2H, CH 2 ), 0.22~0.15 (s, 6H, CH 3 ).
Embodiment 3
[0065] This embodiment provides a reactive fluorosilicone resin, the structure of which is shown in Formula 4:
[0066]
[0067] The preparation method of the compound shown in formula 4 is: dissolve 1 mol of chloromethyldimethoxysilane in 100 mL of NMP, add 1 mol of perfluorooctyl alcohol and 0.01 mol of dibutyltin oxide, react at 135 °C for 4.5 h, and distill After the solvent was separated, the product was mixed with 1 mol glycine and 0.01 mol dibutyltin oxide, reacted at 80° C. for 2 h, and the product was purified to obtain the compound shown in formula 4.
[0068] 1 H NMR (CDCl 3 ,500MHz): δ4.15~4.08(s, 2H, CH 2 ), 3.83~3.75(t, 2H, CH 2 ), 3.58~3.51 (s, 3H, CH 3 ), 2.67~2.59 (s, H, CH 2 ), 1.55~1.47(t, 2H, NH 2 ), 0.25~0.17 (s, 3H, CH 3 ).
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