Temperature sensitive type water-soluble polymers based on D-pi-A structure as well as preparation method and application of water-soluble polymers
A water-soluble polymer, temperature-sensitive technology, applied in the direction of organic chemistry, can solve the problems of short life of active oxygen species, unfavorable synthesis and preparation, limited migration distance, etc., to achieve high singlet oxygen yield, high efficiency singlet oxygen Yield, effects of good biocompatibility
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Embodiment 1
[0038] Embodiment 1: Preparation of polymerized monomer containing D-π-A structure
[0039]
[0040] Preparation of compound 2: Under the catalysis of copper powder (7mmol), 1 (30mmol) and p-bromobenzaldehyde (10mmol)), anhydrous potassium carbonate (40mmol) were stirred and reacted for 24 hours under a nitrogen atmosphere at 180°C , distilled under reduced pressure to remove nitrobenzene, filtered to remove potassium carbonate and copper powder, then extracted three times with water and dichloromethane to collect the organic phase, dried and removed water, and then rotary evaporated to remove the organic solvent, and the obtained oily mixture was purified through a column. 2 was obtained as a yellow solid. Yield: 43%.
[0041] 1 H NMR (400MHz, CDCl 3 )δ=10.12(s,1H),8.19–8.09(m,4H),7.85–7.76(m,2H),7.54–7.48(m,2H),7.44(ddd,J=8.3,7.1,1.2Hz, 2H), 7.34 (ddd, J=8.3, 8.0, 1.2Hz, 2H).
[0042] Preparation of compound 3: N-bromosuccinimide (20mmol) was dissolved in dichloromet...
Embodiment 2
[0056] Embodiment 2: the preparation of polymer PM-1, PM-2
[0057] The preparation of polymer PM-1: compound 11 (0.08mmol), [3-(acrylamido) propyl] trimethylammonium chloride (0.1 mmol) and n-propylacrylamide (3.8mmol), azobis Add isobutyronitrile (0.004mmol) into the polymerization tube and seal it, add redistilled tetrahydrofuran solvent, stir and react at 80°C under nitrogen atmosphere for 24 hours, cool down to room temperature, then slowly add the reaction solution dropwise into diethyl ether, settle and filter, and then use The yellow floc product PM-1 was obtained by extraction with toluene.
[0058]
[0059] Among them, x=2, y=2.5, z=95.5.
[0060] Preparation of Polymer PM-2: The experimental procedure is the same as the preparation of Polymer PM-1 above.
[0061]
[0062] Wherein, x=2, y=8, z=90.
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