Novel perfluoropolyether-based silane compound and surface composition thereof
A technology of perfluoropolyether silane and perfluoropolyether, which is applied in the field of new perfluoropolyether-based silane compounds and their surface compositions, can solve the problem of limited application range and space, high baking temperature and baking temperature of surface compositions. baking time etc.
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Embodiment 1
[0065] Example 1 Synthesis of novel perfluoropolyether-based compound key intermediates (perfluoropolyether-based alkenes)
[0066] Step1 Ammonolysis reaction: Preparing perfluoropolyether-based amides from acyl fluoride ethers
[0067] Under nitrogen protection, in the 5.0L three-neck flask equipped with dropping funnel, reflux condenser and thermometer, charge 800g1,3-bis(trifluoromethyl)benzene and 800g tetrahydrofuran, then 1600g (0.2mol) by Chemical formula F-(CF 2 CF 2 O) j (CF 2 O) k -CF 2 -COF means ether fluoride compound (average molecular weight: 4000) was added under nitrogen protection, and the temperature was lowered to below -20°C, ammonia gas was slowly introduced for about 1 hour (about 34g), and it was raised to room temperature for 4 hours. Low boilers were removed under reduced pressure and the fluorine phase was washed 2 x 200 g methanol. The fluorine phase was vacuum-dried by an oil pump for 2 hours to obtain 1520g (96% yield) of perfluoropolyether...
Embodiment 2
[0075] Embodiment 2 Novel perfluoropolyether-based silane preparation (A)
[0076] Into a 1L airtight autoclave, add 200g (0.046mol) F-(CF 2 CF 2 O) j (CF 2 O) k -CF 2 -CH 2 N(CH 2 CH=CH 2 ) 2 compound, 200 g perfluorooctane, triacetoxymethylsilane, l,3-divinyl 1,1,3,3-tetramethyldisiloxane complexed Pt gold catalyst and 16.8 g trimethoxy Silane (0.14mol), reacted at 100°C for 6 hours, evaporated the solvent in a dry environment to obtain 200g of liquid, and used 1 H NMR spectral analysis, showing the corresponding CH 2 =CHCH 2 The peak of the hydrogen atom on the O double bond functional group disappears completely, confirming that the F-(CF 2 CF 2 O) j (CF 2 O) k -CF 2 -CH 2 N(CH 2 CH 2 CH 2 Si(OCH 3 ) 3 ) 2 (A) Generated.
[0077] The product compound (A) synthesized above was dissolved in Novec HFE 7200 hydrofluoroether (manufactured by 3M Company) to prepare a product with a solid content of 20% for sale.
Embodiment 3
[0078] Embodiment 3 Novel perfluoropolyether-based silane preparation (B)
[0079] With the method of embodiment 2, use triethoxysilane to replace trimethoxysilane, make 200g F-(CF 2 CF 2 O) j (CF 2 O) k -CF 2 -CH 2 N(CH 2 CH 2 CH 2 Si(OCH 2 CH 3 ) 3 ) 2 (B). And use Novec HFE 7200 hydrofluoroether (manufactured by 3M company) to dissolve and prepare the product with 20% solid content for sale.
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