Ternary electrolyte containing unsaturated heterocyclic ring and preparation method and application thereof
An unsaturated, electrolyte technology, applied in the battery field, can solve problems such as correlation or deducibility uncertainty, and achieve the effects of improving electrochemical performance, inhibiting decomposition, and increasing discharge specific capacity
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Embodiment 1
[0071] Example 1: Raw materials M1
[0072] 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, and the reaction was stirred at room temperature for 8 hours, and the resulting mixed solution 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, wherein Q is OBF 3 Li. The yield was 86%.
Embodiment 2
[0073] Example 2: Raw materials M2
[0074] Preparation method: under argon atmosphere, mix 0.01 mol of raw material and boron trifluoride ether complex (4.26 g, 0.03 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. 18.75ml 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 three times with cyclohexane, filtered and dried to obtain product M2, wherein Q is OBF 3Li. The yield was 88%.
Embodiment 3
[0075] Example 3: Raw materials M3
[0076] 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 (4.19 g, 0.03 mol) was added to the intermediate, and the reaction was stirred at room temperature for 7 hours. 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 product M3, wherein Q is OBF 3 Li. Yield 87%, NMR as figure 1 shown.
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