Hydrogel with self-repairing function and preparation method of hydrogel
A hydrogel, self-healing technology, applied in organic chemistry and other directions, can solve the problems of reduced hydrogel strength, water retention and spatial limitation of strength, etc., to achieve improved water retention, good shape memory function, and rich selection of raw materials. Effect
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Embodiment 1
[0033] Step 1, the synthesis of compound A
[0034] First, 10 g of PEG and 2.2 g of triethylamine were added into a 100 mL round bottom flask, dissolved in 60 mL of dichloromethane, and cooled to 0 °C in an ice bath. Then slowly add 3.68g of 2-bromoisobutyryl bromide diluted with 5mL of dichloromethane dropwise into the round bottom flask, stir, and react at room temperature for 24h after the dropwise addition is completed. Triethylamine hydrochloride, repeated twice, and then precipitated with ether 2 to 3 times, then dried under vacuum at 40°C for 12 hours after suction filtration, and the product was a brown solid. The molecular weight of PEG used in this example is 2000 g / mol.
[0035] The NMR hydrogen of compound A ( 1 HNMR) spectrogram such as figure 1 As shown, δ~3.75ppm is the peak of methylene group on PEG, and δ~1.45ppm is the peak of methyl group on isobutyryl group.
[0036] Step 2, the synthesis of compound B
[0037] Add 1.5g MIC to a 100mL round bottom flas...
Embodiment 2
[0042] Step 1, the synthesis of compound A was synthesized with reference to Example 1, wherein the molecular weight of PEG was 4000 g / mol.
[0043] Step 2, the synthesis of compound B is the same as in Example 1.
[0044] Step 3, Synthesis of Compound C Referring to Example 1, the amount of Compound A used is 0.4 g.
Embodiment 3
[0046] Step 1, the synthesis of compound A was synthesized with reference to Example 1, wherein the molecular weight of PEG was 6000 g / mol.
[0047] Step 2, the synthesis of compound B is the same as in Example 1.
[0048] Step 3, Synthesis of Compound C Referring to Example 1, the amount of Compound A used is 0.62 g.
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