Electrolyte containing sulfenyl boron trifluoride salt and preparation method and application thereof
A technology of sulfur-based boron trifluoride and boron trifluoride, which is applied in the field of electrolytes containing sulfur-based boron trifluoride salts and its preparation, can solve problems such as correlation or deducibility uncertainty, and achieve electrochemical Effects of performance improvement, widening electrochemical window, and improving cycle performance
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Embodiment 1
[0075] Embodiment 2: raw material
[0076] Preparation method: under argon atmosphere, mix 0.01mol of the raw material and boron trifluoride etherate complex (2.98g, 0.021mol) in 15ml of THF, 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 14ml 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, Q being -S-BF 3 Li. The yield was 82%, NMR such as figure 2 shown.
Embodiment 2
[0077] Embodiment 3: raw material
[0078] Preparation method: Under a nitrogen atmosphere, take 0.01mol of the raw material and lithium methoxide (0.76g, 0.02mol), mix well with 20ml of methanol, and react at room temperature for 13 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. Add boron trifluoride tetrahydrofuran complex (3.07g, 0.022mol) and 15ml THF to the intermediate, stir and react at room temperature for 12 hours, and depressurize the resulting mixture at 30°C and a vacuum of about -0.1MPa After drying, the resulting solid was washed three times with isopropyl ether, filtered, and dried to give the product M3, Q being -S-BF 3 Li. Yield 84%, NMR as image 3 shown.
Embodiment 3
[0079] Embodiment 4: raw material
[0080] Preparation method: under an argon atmosphere, mix 0.01 mol of raw materials and boron trifluoride tetrahydrofuran complex (3.07 g, 0.022 mol) in 15 ml of THF, 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 14ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 12 hours, 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 M4, Q being -S-BF 3 Li. The yield was 84%, NMR as Figure 4 shown.
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