Dendritic macromolecular quaternary ammonium salt compound, preparation method and application thereof
A technology of quaternary ammonium salts and macromolecules, applied in botany equipment and methods, chemical instruments and methods, applications, etc., can solve the problems of poor biocidal properties and low penetration, and achieve low cost, easy operation, and low cost. cytotoxic effect
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Embodiment 1
[0049] Embodiment 1: the synthesis of the dendrimer surface quaternary ammonium compound of terminal amino group
[0050] 4.76 g of amino-terminated dendrimers G1.0 (NH 2 ) 3 (1equiv, 10mmol) was dissolved in 500mL of anhydrous toluene solution, under ice bath conditions, 3.30g of 2-chloroethyl isocyanate (1.02equiv, 30.6mmol) was added dropwise, and the reaction was stirred 12 hours. Then add 7.67g of N,N-dimethyldodecylamine (1.2equiv, 36mmol), 100mL of N,N-dimethylacetamide, and 100mL of toluene, slowly heat to 80°C, and react at constant temperature for 72 hours, then The solution was concentrated to about 100 mL, and the concentrate was precipitated in acetone. The mixture was filtered and dried in vacuo at 60 °C to obtain a yellow solid material (70% yield).
[0051] IR(KBr,cm -1 ): C-H saturated 2930.4cm -1 ,C=O 1639.9cm -1 ,N-H bend1562.3cm -1 , and N-H stretch 3297.9cm -1 . 1 H NMR (CDCl 3 , δ / ppm): 0.89, 1.25-1.73, 1.82-1.87, 2.54, 3.20, 3.36, 3.51, 3.67, 3...
Embodiment 2
[0052] Embodiment 2: the synthesis of the dendrimer surface quaternary ammonium salt functional compound of terminal acrylate group
[0053] Add 6.55g of acrylate-terminated dendrimer G1.0(acrylate)8 (5.26mmol), 4.43g of diethanolamine (42.2mmol) and 9.49g of methanol into a 100mL three-necked flask in sequence, and stir at 25°C The reaction was carried out for 24 hours. After the reaction, the methanol was distilled off under reduced pressure to obtain 11.0 g (5.28 mmol) of G1.0(OH)16 as a colorless viscous product with a purity of 94.6%.
[0054] Weigh 6.25g (3.00mmol) G1.0(OH)16 into a 100mL three-neck round bottom flask, add 10mL of chloroform, stir to dissolve, slowly add SOCl 2 The acid-binding agent pyridine of the amount of equal substance, then add dropwise 6.55g (0.055mol) SOCl 2 After the dropwise addition was completed, the oil bath was heated to raise the temperature, magnetically stirred at 85° C., and refluxed for 6 hours. After the reaction is over, wait for ...
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