Electrolyte containing saturated carbocyclic structure and preparation method and application thereof
A carbon ring structure, electrolyte technology, applied in organic electrolytes, non-aqueous electrolytes, chemical instruments and methods, etc., to achieve high ionic conductivity, improved electrochemical performance, and simple reactions.
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Embodiment 1
[0078] raw material
[0079] Preparation method: Under nitrogen atmosphere, mix the raw material (0.01mol) and boron trifluoride tetrahydrofuran complex (1.4g, 0.01mol) in 15ml of ethylene glycol dimethyl ether, and react at room temperature for 12 hours. The obtained mixed solution was dried under reduced pressure at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Dissolve lithium ethoxide (0.52g, 0.01mol) in 10ml of ethanol and slowly add it to the intermediate, stir and react at 45°C for 8 hours, and dry the resulting mixture under reduced pressure at 45°C and vacuum degree of about -0.1MPa , The obtained solid was washed three times with n-butyl ether, filtered and dried to obtain the product P1. The yield of product P1 was 81%.
Embodiment 2
[0081] raw material
[0082] Preparation method: Under argon atmosphere, mix the raw material (0.01mol) and boron trifluoride etherate complex (1.42g, 0.01mol) in 15ml THF (tetrahydrofuran), and react at room temperature for 12 hours. The resulting mixed solution was dried under reduced pressure at 30° C. and a vacuum of about −0.1 MPa to remove the solvent to obtain an intermediate. Add 6.30ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 10 hours, and dry the resulting mixture under reduced pressure at 40°C and vacuum degree of about -0.1MPa , the obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product P2. The yield of product P2 is 84%, and the proton nuclear magnetic spectrum is as figure 1 shown.
Embodiment 3
[0084] raw material
[0085] Preparation method: under a nitrogen atmosphere, take a certain amount of raw materials (0.01mol) and lithium methoxide (0.38g, 0.01mol), mix them with 20ml of methanol, and react at room temperature for 8 hours. The obtained mixed solution was dried under reduced pressure at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Boron trifluoride tetrahydrofuran complex (1.47g, 0.0105mol) and 15ml THF (tetrahydrofuran) were added to the intermediate, and the reaction was stirred at room temperature for 18 hours. Drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain the product P3. The yield of product P3 was 79%.
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