Antibacterial composite coating as well as preparation method and product thereof
A composite coating, antibacterial coating technology, applied in coatings, pharmaceutical formulations, catheters, etc., to achieve good lubricity, reduce the development of bacterial resistance, and good firmness.
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[0131] These antibacterial molecule or functional group mainly by esterification, transesterification, amidation reaction, the reaction click, protonation reaction, ionic reaction, ring opening reactions, addition reactions, elimination reactions, aldol reactions, initiation introduction of the polymerization reaction or the like. For example, adamantane and PHMG chloride (polyhexamethylene guanidine hydrochloride) introducing a substituted guanidinium group occurs; 6-bromo-β- cyclodextrin and quaternary aminoethanol ammonium reactions introducing a quaternary ammonium group; bovine serum albumin and allyl bromide click reaction introducing serum proteins and the like. In some embodiments of the invention, the functions of the guest molecule and / or the main body of the molecule as a functional molecule, more preferably a modified cyclodextrin guanidine salts and / or quaternary ammonium modified cyclodextrin, cyclodextrins generally contain 6 to 12 D- glucopyranose units, typica...
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[0140] Preparation Example 1: Preparation of hydroxyethyl methacrylate
[0141] In a 250 mL three-flavor equipped with mechanical stirring, 26.0 g of hydroxyethyl methacrylate (0.2 mol), 100 ml of dried dichloromethane and 25.3 g of triethylamine (0.25 mol) were added, and slow drops with constant pressure drip funnel Add 21.7 g of acryloyl chloride (0.24 mol), at 0 ° C for 0.5 hours, the temperature above 28 ° C for 10 hours, the crude product was filtered, and the crude product was separated from the column chromatography, dried 30.2 g of yellow sheet crystal, methyl methacrylate Ethyl acrylate, such as structural formula, yield 82%. 1 H NMR (CDCL 3 ) δ: 6.44 (m, 1h, ch 2 = CH), 6.10 (m, 2H, CH 2 = CH, CH = CH), 5.84 (M, 1H, CH 2 = CH), 5.58 (M, 1H, CH = CH), 4.38 (M, 4H, COOCH 2 CH 2 OCO), 1.94 (S, 3H, CH 3 .
[0142]
Example Embodiment
[0143] Preparation 2: Preparation of Benzophenone-2-aminopropylthyl methacrylate (IIA)
[0144] 18.4 g (0.1 mol) Preparation Example 1 made of methyl methacrylate hydroxyethyl acrylate was added to a 250 ml of three flasks, 100 mL of ethanol was added, and stirred, 19.7 g (0.1 mol) 4-amino group was added. Benzophenone, temperature rise to 60 ° C for 14 hours. The reaction liquid was dried, and the crystallization of ethanol and ethyl acetate was recrystallized to give 34 g of pale yellow solid, and the yield was 90%. 1 HNMR (CDCL 3 ) δ: 7.32-7.87 (M, 9H, benzene ring), 6.42-6.48 (m, 2H, CH 2 = CH), 4.78 (S, 2H, -CH 2 -CH 2 -O), 4.32 (S, 2H, -CH 2 -CH 2 -O), 3.62 (m, 2H, NH-CH 2 -CH 2 -), 2.58 (m, 2H, NH-CH 2 -CH 2 -), 2.01 (s, 3h, ch 3 ), Specifically, see figure 1 .
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