Polymerizable electrolyte and preparation method and application thereof
A polymer electrolyte and electrolyte technology, applied in the field of polymerizable electrolyte and its preparation, can solve the problems of high energy density, long cycle intrinsic safety, etc., achieve excellent electrochemical performance, increase discharge specific capacity, and widen the electrochemical window Effect
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Embodiment 1
[0090] raw material
[0091] Preparation method: Under a nitrogen atmosphere, mix the raw material (0.88g, 0.01mol) and lithium hydroxide (0.24g, 0.01mol) with 10ml of methanol solution, and react at 15°C for 8 hours. The resulting mixed solution was dried under reduced pressure at 30° C. and a vacuum of about −0.1 MPa to remove the solvent to obtain an intermediate. Add boron trifluoride diethyl ether complex (1.45g, 0.01mol) and 15ml THF (tetrahydrofuran) to the intermediate, stir and react at 40°C for 6 hours, and place the resulting mixture at 30°C and a vacuum of about -0.1MPa Drying under reduced pressure, the obtained crude product was filtered and dried with dichloromethane to obtain the product A1. The yield was 86%, NMR such as figure 1 shown.
Embodiment 2
[0093] raw material
[0094] Preparation method: Under nitrogen atmosphere, mix the raw material (0.90g, 0.01mol) and boron trifluoride tetrahydrofuran complex (1.40g, 0.01mol) in 15ml of ethylene glycol dimethyl ether, and react at room temperature for 10 hours. The obtained mixed solution was dried under reduced pressure at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Dissolve lithium ethoxide (0.52g, 0.01mol) in 10ml of ethanol and slowly add it to the intermediate, stir and react at 45°C for 8 hours, and dry the resulting mixture under reduced pressure at 45°C and vacuum degree of about -0.1MPa , The obtained solid was washed three times with n-butyl ether, filtered and dried to obtain the product A2. The yield was 80%, NMR such as figure 2 shown.
Embodiment 3
[0096] raw material
[0097] Preparation method: Under argon atmosphere, mix the raw material (1.15g, 0.01mol) and boron trifluoride etherate complex (1.49g, 0.0105mol) in 15mlTHF (tetrahydrofuran), and react at room temperature for 12 hours. The resulting mixed solution was dried under reduced pressure at 30° C. and a vacuum of about −0.1 MPa to remove the solvent to obtain an intermediate. Add 6.25ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 7 hours, and dry the resulting mixture under reduced pressure at 30°C and vacuum degree of about -0.1MPa , the obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product A3. The yield was 89%, NMR such as image 3 shown.
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