Multi-element sulfenyl boron trifluoride salt electrolyte as well as preparation method and application thereof
A boron trifluoride and electrolyte technology, applied in organic electrolytes, non-aqueous electrolytes, chemical instruments and methods, etc., to achieve the effects of widening the electrochemical window, increasing the discharge specific capacity, and improving electrochemical performance
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Embodiment 1
[0157] raw material Among them, Q means
[0158] Preparation method: under nitrogen atmosphere, mix 0.01mol of the raw material and boron trifluoride tetrahydrofuran complex (5.6g, 0.04mol) in 15ml of ethylene glycol dimethyl ether, and react at room temperature for 12 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 (2.08g, 0.04mol) 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 M1 with a yield of 94%. figure 1 shown.
Embodiment 2
[0160] raw material Among them, Q means
[0161] Preparation method: under argon atmosphere, mix 0.01mol of the raw material and boron trifluoride etherate complex (5.68g, 0.04mol) in 15ml of THF (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 25ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 6 hours, and dry the resulting mixture under reduced pressure at 40°C and a vacuum of about -0.1MPa. The obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product M2 with a yield of 90%. figure 2 shown.
Embodiment 3
[0163] raw material Among them, Q means
[0164] Preparation method: Under a nitrogen atmosphere, take 0.01mol of the raw material and lithium methoxide (1.52g, 0.04mol), mix well with 20ml of methanol, and react at room temperature for 8 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. Boron trifluoride tetrahydrofuran complex (5.58g, 0.04mol) and 15ml THF (tetrahydrofuran) were added to the intermediate, and the reaction was stirred at room temperature for 16 hours. Drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain the product M3 with a yield of 87%.
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