Ternary oxygen-based electrolyte and preparation and application thereof
An electrolyte and hydrocarbon-based technology, applied in the preparation of sugar derivatives, circuits, electrical components, etc., can solve the problems of no great achievements, no reference source, increased resistance, etc., to improve electrochemical performance, widen the electrochemical window, The effect of improving the discharge specific capacity
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Embodiment 1
[0093] Example 1: Raw materials M1
[0094] Preparation method: under nitrogen atmosphere, mix 0.01 mol of raw material and boron trifluoride tetrahydrofuran complex (4.19 g, 0.03 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 (1.56g, 0.03mol) was dissolved in 10ml of ethanol and slowly added to the intermediate, 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, wherein Q is OBF 3 Li. The yield was 87%, NMR as figure 1 shown.
Embodiment 2
[0095] Example 2: Raw materials M2
[0096] Preparation method: under argon atmosphere, metal lithium sheet (0.21 g, 0.03 mol) was slowly added to 0.01 mol of raw material, reacted at room temperature for 1 hour, and then heated to 50° C. until the lithium sheet reacted completely to obtain an intermediate. Boron trifluoride butyl ether complex (5.94g, 0.03mol) was added to the intermediate, and the reaction was stirred at 50°C for 6 hours, and the obtained mixed solution was dried under reduced pressure at 50°C and a vacuum degree of about -0.1MPa. , the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain product M2, wherein Q is OBF 3 Li. Yield was 89%.
Embodiment 3
[0097] Example 3: Raw materials M3
[0098] Preparation method: under nitrogen atmosphere, take 0.01 mol of raw material and lithium methoxide (1.14 g, 0.03 mol), mix 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 (4.19g, 0.03mol) and 15ml THF (tetrahydrofuran) were added to the intermediate, and the reaction was stirred at room temperature for 6 hours. Drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain product M3, wherein Q is OBF 3 Li. Yield 85%.
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