Sulfur-based boron trifluoride salt electrolyte containing unsaturated heterocyclic ring as well as preparation method and application of sulfur-based boron trifluoride salt electrolyte
A boron trifluoride and unsaturated technology, which is applied in the field of sulfur-based boron trifluoride salt electrolytes and its preparation, can solve problems such as correlation or deducibility uncertainty, achieve electrochemical performance improvement, and broaden the electrochemical performance. Effect of chemical window, high ionic conductivity
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Embodiment 1
[0077] Example 1: Raw materials
[0078] Preparation method: under nitrogen atmosphere, mix 0.01 mol of raw material and boron trifluoride tetrahydrofuran complex (2.8 g, 0.02 mol) in 15 ml of ethylene glycol dimethyl ether, and react at room temperature for 12 hours. The obtained mixed solution was dried under reduced pressure under the conditions of 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Lithium ethoxide (1.04g, 0.02mol) was dissolved in 10ml of ethanol and slowly added to the intermediate. The reaction was stirred at room temperature for 8 hours, and the resulting mixture was dried under reduced pressure at 40°C and a vacuum of about -0.1MPa. , the obtained solid was washed three times with n-butyl ether, filtered and dried to obtain product M1, and Q was -S-BF 3 Li. The yield was 77%, NMR as figure 1 shown.
Embodiment 2
[0079] Example 2: Raw materials
[0080] Preparation method: under argon atmosphere, mix 0.01 mol of raw material and boron trifluoride ether complex (2.98 g, 0.021 mol) in 15 ml of THF, and react at room temperature for 12 hours. The obtained mixed solution was dried under reduced pressure under the conditions of 30° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. 14ml of butyllithium in hexane solution (c=1.6mol / L) was added to the intermediate, the reaction was stirred at room temperature for 6 hours, and the resulting mixed solution was dried under reduced pressure at 40°C and a vacuum degree of about -0.1MPa, The obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product M2, and Q was -S-BF 3 Li. The yield was 85%, NMR as figure 2 shown.
Embodiment 3
[0081] Example 3: Raw materials
[0082] Preparation method: under nitrogen atmosphere, take 0.01 mol of raw material and lithium methoxide (0.76 g, 0.02 mol), mix well with 20 ml of methanol, and react at room temperature for 18 hours. The obtained mixed solution was dried under reduced pressure under the conditions of 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. The boron trifluoride tetrahydrofuran complex (3.07 g, 0.022 mol) was added to the intermediate, and the reaction was stirred at room temperature for 12 hours, and the obtained mixed solution was dried under reduced pressure at 40 ° C and a vacuum degree of about -0.1 MPa to obtain The solid was washed three times with isopropyl ether, filtered and dried to obtain the product M3, and Q was -S-BF 3 Li. Yield 84%, NMR as image 3 shown.
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