Ternary electrolyte containing aromatic ring structure and preparation and application thereof
An electrolyte and aromatic ring technology, which is applied in the fields of compounds containing elements of group 3/13 of the periodic table, circuits, organic chemistry, etc., can solve the problems of no -OBF3M group research publication, no industrial application results, time cost and economy High cost and other issues, to achieve excellent electrochemical performance, improved electrochemical performance, and improved discharge specific capacity
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Embodiment 1
[0065] Example 1: Raw materials
[0066] 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 the product M1. The yield was 79%, NMR as figure 1 shown.
Embodiment 2
[0067] Example 2: Raw materials
[0068] Preparation method: under argon atmosphere, mix 0.01 mol of raw material and boron trifluoride ether complex (4.26 g, 0.03 mol) evenly, and react at room temperature for 12 hours 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 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. The yield was 88%, NMR as figure 2 shown.
Embodiment 3
[0069] Example 3: Raw materials
[0070]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. After drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain the product M3. Yield 81%, NMR as image 3 shown.
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