Saturated heterochain ternary electrolyte as well as preparation method and application thereof
A technology of electrolytes and heterochains, applied in the field of saturated heterochain ternary electrolytes and their preparation, can solve problems such as correlation or deducibility uncertainty, achieve improved electrochemical performance, widen the electrochemical window, and improve cycle performance effect
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Embodiment 1
[0057] Example 1: Raw materials
[0058] Preparation method: under argon atmosphere, mix 0.01 mol of raw material and boron trifluoride diethyl ether complex (4.26 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 30° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. 18.90ml of butyllithium in hexane solution (c=1.6mol / L) was added to the intermediate, and the reaction was stirred at room temperature for 6 hours, and dried under reduced pressure at 40°C and vacuum degree of about -0.1MPa to obtain a crude The product was washed three times with cyclohexane, filtered and dried to obtain product M1, wherein Q is OBF 3 Li. The yield was 87%, NMR as figure 1 shown.
Embodiment 2
[0059] Example 2: Raw materials
[0060] 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 6 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 product M2, wherein Q is OBF 3 Li. Yield 78%, NMR as figure 2 shown.
Embodiment 3
[0061] Example 3: Raw materials
[0062] Preparation method: 0.01 mol of raw material and boron trifluoride ether complex (4.26 g, 0.03 mol) were mixed uniformly in 15 ml of THF in a glove box, and the reaction was carried out at room temperature for 12 hours. The obtained mixed solution is dried under reduced pressure under the conditions of room temperature and vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Lithium ethoxide (1.56 g, 0.03 mol) was dissolved in 10 ml of ethanol and added to the intermediate, and 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 -0.1 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. The yield was 85%, NMR as image 3 shown.
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