A kind of preparation method of cellulose nanopaper with circularly polarized fluorescence emission
A fluorescence emission, cellulose technology, applied in chemical instruments and methods, luminescent materials, etc., can solve problems such as non-ideal brittleness, affecting the mechanical properties of nanoparticles, fragmentation, etc.
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[0032] A kind of preparation method of the cellulose nano paper of circularly polarized fluorescence emission of the present invention, specifically comprises the following steps:
[0033] Step 1, synthesizing 4-(4-vinylbenzyl)acetophenone (VBAP). Specifically: add 4-vinylbenzyl chloride (2-200mmol), 4-hydroxyacetophenone (4-400mmol), potassium hydroxide (4-400mmol) and N,N-dimethyl formamide (2-200mL) to obtain a mixed solution A, then stirred at 45°C for 12h under nitrogen, after the reaction, cooled the mixed solution A to room temperature, and used deionized water (20-2000mL) to precipitate the mixed solution A, It was then washed with deionized water, filtered, and dried in a vacuum oven at 45°C to obtain 4-(4-vinylbenzyl)acetophenone (VBAP) crude oil, which was recrystallized with ether to purify VBAP.
[0034] Step 2, synthesis of 1-(4-(4-vinylbenzyl)phenyl)-trifluorobutane-1,3-dione (VBTF);
[0035] Dissolve ethyl trifluoroacetate (1-100mmol) and sodium hydride (1-10...
Embodiment 1
[0044] Step 1, synthesizing 4-(4-vinylbenzyl)acetophenone (VBAP). Specifically: add 4-vinylbenzyl chloride (2mmol), 4-hydroxyacetophenone (4mmol), potassium hydroxide (4mmol) and N,N-dimethylformamide (2mL) to the reflux device respectively, The mixed solution A was obtained, and then stirred at 45° C. for 12 h under nitrogen. After the reaction, the mixed solution A was cooled to room temperature, and the mixed solution A was precipitated with deionized water (20 mL), then washed with deionized water, and filtered. The crude oil of 4-(4-vinylbenzyl)acetophenone (VBAP) was obtained by drying in a vacuum oven at 45° C., and the VBAP was purified by recrystallization with ether, with a yield of 93.2%.
[0045] Step 2, synthesis of 1-(4-(4-vinylbenzyl) phenyl)-trifluorobutane-1,3-dione (VBTF); ethyl trifluoroacetate (1mmol) and sodium hydride ( 1mmol) was dissolved in tetrahydrofuran (3mL), and stirred at room temperature for 10min to obtain a mixed solution B. The VBAP (0.5mmol...
Embodiment 2
[0053] Step 1, synthesizing 4-(4-vinylbenzyl)acetophenone (VBAP). Specifically: add 4-vinylbenzyl chloride (2mmol), 4-hydroxyacetophenone (4mmol), potassium hydroxide (4mmol) and N,N-dimethylformamide (2mL) to the reflux device respectively, The mixed solution A was obtained, and then stirred at 45° C. for 12 h under nitrogen. After the reaction, the mixed solution A was cooled to room temperature, and the mixed solution A was precipitated with deionized water (20 mL), then washed with deionized water, and filtered. The crude oil of 4-(4-vinylbenzyl)acetophenone (VBAP) was obtained by drying in a vacuum oven at 45° C., and the VBAP was purified by recrystallization with ether, with a yield of 93.2%.
[0054] Step 2, synthesis of 1-(4-(4-vinylbenzyl) phenyl)-trifluorobutane-1,3-dione (VBTF); ethyl trifluoroacetate (1mmol) and sodium hydride ( 1mmol) was dissolved in tetrahydrofuran (3mL), and stirred at room temperature for 10min to obtain a mixed solution B. The VBAP (0.5mmol...
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