Electrolyte containing saturated carbocyclic sulfenyl organic salt as well as preparation method and application of electrolyte
A technology for electrolytes and organic salts, which is applied in the field of electrolytes containing saturated carbocyclic sulfur-like organic salts and its preparation, can solve problems such as not much research results and no industrial application results, and achieve excellent electrochemical performance. Effects of improved chemical properties and high ionic conductivity
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Embodiment 1
[0070] Example 1: Raw materials
[0071] 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 45°C for 8 hours, and the resulting mixture was dried under reduced pressure at 45°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 79%, NMR as figure 1 shown.
Embodiment 2
[0072] Example 2: Raw materials
[0073] Preparation method: under argon atmosphere, mix 0.01mol of raw material and boron trifluoride ether complex (2.98g, 0.021mol) in 15ml of THF (tetrahydrofuran), and react at room temperature for 12 hours. Under the condition of vacuum degree of about -0.1MPa, the solvent is removed by drying under reduced pressure 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, where Q was -S-BF 3 Li. The yield was 87%, NMR as figure 2 shown.
Embodiment 3
[0074] Example 3: Raw materials
[0075] 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 8 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 (3.07g, 0.022mol) and 15ml of THF (tetrahydrofuran) were added to the intermediate, and the reaction was stirred at room temperature for 12 hours. Drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain product M3, Q is -S-BF 3 Li. Yield 86%, NMR as image 3 shown.
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