A method for synthesizing glucose-containing block copolymers by raft method
A technology of block copolymer and glucose, applied in the field of synthesizing glucose-containing block copolymer by RAFT method, can solve the problems of uncontrollable reaction and free radical termination reaction, and achieve the effect of low dispersion width and low toxicity
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Embodiment 1
[0026] (1) Dissolve 12g of divinyl adipate and 4g of glucose in 100mL of anhydrous pyridine, add 0.5g of alkaline protease, and react in a constant temperature water bath at 50°C and 210rpm for 4 days to synthesize vinyl adipate glucose ester ( OVAG), the yield was 67%.
[0027] (2) Dissolve 0.58g of synthesized OVAG and 1.78g of N-isopropylacrylamide (NIPAm) in 2mL of DMF, add 1.5mg of AIBN as an initiator, add 63mg of a chain transfer agent, and react for 12h under the protection of nitrogen in an oil bath at 70°C. The reaction was terminated in an ice-water bath, and the ether precipitate was dissolved with methanol, and this was repeated three times. After purification, P(NIPAm-OVAG) was obtained with a yield of 82%.
[0028] (3) Dissolve 0.3g of synthesized P(NIPAm-OVAG) and 0.216g of N-isopropylacrylamide (NIPAm) in 1mL of DMF, add 0.25mg of AIBN as an initiator, and react for 7h under the protection of nitrogen in an oil bath at 70°C. Liquid nitrogen was used to stop t...
Embodiment 2
[0030] (1) Dissolve 12g of divinyl adipate and 6g of glucose in 100mL of anhydrous pyridine, add 0.5g of alkaline protease, and react in a constant temperature water bath at 50°C and 200rpm for 4 days to synthesize vinyl adipate glucose ester ( OVAG), the yield was 61%.
[0031] (2) Dissolve 0.58g of synthesized OVAG and 0.80g of N-isopropylacrylamide (NIPAm) in 2mL of DMF, add 0.75mg of AIBN as an initiator, add 32mg of a chain transfer agent, and react for 12h under the protection of nitrogen in an oil bath at 70°C. The reaction was terminated in an ice-water bath, and the ether precipitate was dissolved with methanol, and this was repeated three times. After purification, P(NIPAm-OVAG) was obtained with a yield of 80%.
[0032] (3) Dissolve 0.3g of synthesized P(NIPAm-OVAG) and 0.19g of N-isopropylacrylamide (NIPAm) in 1mL of DMF, add 0.23mg of AIBN as an initiator, and react for 6h under the protection of nitrogen in an oil bath at 70°C. Liquid nitrogen was used to termin...
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