Unsaturated fluorocarbon, preparation method and application thereof
A fluorocarbon and compound technology, applied in the field of polymer materials, can solve problems such as low glass transition temperature, poor multi-layering ability, and 5G communication terminal obstruction, and achieve excellent mechanical properties and dielectric properties, good heat resistance. Performance and mechanical properties, effect of excellent dielectric properties
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Embodiment 1
[0040] The present invention provides a kind of unsaturated fluorocarbon compound, its structure is as shown in formula I:
[0041]
[0042] The preparation method of the compound shown in formula I is: mix 1 mol perfluorododecanoic acid with 1.2 mol 4-vinyl-benzyl alcohol, add 100 mL of 0.1 mol / L sodium hydroxide solution, heat the reaction at 80 ° C for 2 h with mechanical stirring, and cool to room temperature, washed 5 times with 500 mL of water, separated, added anhydrous sodium sulfate, allowed to stand for 2 hours, and filtered to obtain the compound represented by formula I.
[0043] 1 H NMR (CDCl 3 ,500MHz): δ7.67~7.61(m, 2H, Ar-H), 7.35~7.27(m, 2H, Ar-H), 6.66~6.60(m, H, CH 2 =C H ), 5.63~5.57(t, H, C H 2 =CH), 5.25~5.19(s, 2H, CH 2 ), 5.21~5.16(t, H, C H 2 =CH).
Embodiment 2
[0045] The present invention provides a kind of unsaturated fluorocarbon compound, its structure is as shown in formula II:
[0046]
[0047] The preparation method of the compound shown in formula II is: mix 1mol perfluorobutyric acid with 1.2mol 2-methyl-1,4-dihydrobenzyl alcohol, add 100mL of 0.1mol / L sodium hydroxide solution, mechanically stir at 80°C Heat the reaction for 2.5 h, cool to room temperature, wash 5 times with 500 mL of water, separate the liquid, add anhydrous sodium sulfate, let stand for 2 h, and filter to obtain the compound shown in formula II.
[0048] 1 H NMR (CDCl 3 ,500MHz): δ5.88~5.82(m, H, CH=C H ), 5.41~5.35 (m, H, C H =CH), 5.22~5.18(t, H, C H =C), 4.28~4.22(s, 2H, CH 2 ), 3.48~3.42(d, H, CH), 2.69~2.60(t, 2H, CH 2 ), 1.85~1.80 (t, 3H, CH 3 ).
Embodiment 3
[0050] The present invention provides an unsaturated fluorocarbon compound, the structure of which is shown in formula X:
[0051]
[0052] The preparation method of the compound shown in formula III is as follows: 1.2 mol of perfluorooctanoic acid and 1 mol of methallyl alcohol are mixed, 20 mL of concentrated sulfuric acid is added, mechanically stirred and heated to reflux for 2.5 hours, cooled to room temperature, washed 5 times with 500 mL of water, separated, added without Sodium sulfate water, let stand for 2h, and filter to obtain the compound represented by formula III.
[0053] 1 H NMR (CDCl 3 ,500MHz): δ5.35~5.30(s, H, CH 2 =C), 5.21~5.15(s, H, CH 2 =C), 4.78~4.72(s, 2H, CH 2 ), 1.85~1.79 (s, 3H, CH 3 ).
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Abstract
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