Preparation method of temperature and pH sensitive organic/inorganic hybrid material POSS/PDMAEMA-b-PNIPAM
A hybrid material and sensitive technology, applied in the field of chemical industry and new materials, can solve the problems of poor product dispersion, complicated preparation process, and low monomer selectivity, and achieve high production yield, no pollution to the environment, and stereoselectivity strong effect
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Embodiment 1
[0028]The first step of synthesis: take 5.56 g of dimethylaminoethyl methacrylate monomer in a 25 mL single-necked round bottom flask. Take 100 mg of 4-cyano-4-(thiobenzoyl)valeric acid and 20.42 mg of azobisisobutyronitrile powder in a 50 mL beaker, add 10 mL of dioxane to dissolve. Then the two were mixed, and the one-necked flask was evacuated at 0°C through the "T-shaped" tee, and nitrogen gas was introduced. Under the protection of nitrogen, it was placed in an oil bath at 90 °C for 12 h, and stirred uniformly by magnetic force. After the reaction was completed, the flask was cooled to room temperature and vented to the atmosphere, and the cooled solution was rotated at 45° C. to remove the solvent. Dissolve the sample in 10 mL of dichloromethane, add it dropwise to 300 mL of ice petroleum ether, let it stand for 4 hours, remove the upper liquid, and obtain a viscous sample at the bottom. The above steps were repeated twice, and finally the samples were vacuum-dried at ...
Embodiment 2
[0034] Same as Example 1, but the amount of dimethylaminoethyl methacrylate in the first step of synthesis becomes 19.46g, and the monomer (dimethylaminoethyl methacrylate) and chain transfer agent (4-cyano) in the system -4-(thiobenzoyl)valeric acid) and initiator (azobisisobutyronitrile) molar ratio was changed to 350:1:0.3.
Embodiment 3
[0036] Same as Example 1, but the amount of dimethylaminoethyl methacrylate in the first step of synthesis is changed to 11.12g, and the monomer (dimethylaminoethyl methacrylate) and chain transfer agent (4-cyano) in the system -4-(thiobenzoyl)valeric acid) and the initiator (azobisisobutyronitrile) in a molar ratio of 200:1:0.3.
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