Polycyclic electrolyte and preparation and application thereof
An electrolyte and ring technology, applied in circuits, electrical components, secondary batteries, etc., can solve problems such as uncertainty in correlation or inference, and achieve inhibition of electrolyte decomposition, high ionic conductivity, and electrochemical performance improvement. Effect
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Embodiment 1
[0074] Embodiment 1: raw material M1
[0075] Preparation method: under a nitrogen atmosphere, mix 0.01 mol of raw materials and boron trifluoride tetrahydrofuran complex (2.8 g, 0.02 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 at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Dissolve lithium ethoxide (1.04g, 0.02mol) 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 M1. Yield was 74%, NMR as figure 1 shown.
Embodiment 2
[0076] Embodiment 2: raw material M2
[0077] Preparation method: Under argon atmosphere, the raw material 4-hydroxy-3-nitro-5,6,7,8-tetrahydro-1H-quinoline-2-hydroxyl (2.10g, 0.01mol) and boron trifluoride Diethyl ether complex (2.98g, 0.021mol) was mixed uniformly in 15ml of ethylene glycol dimethyl ether, and reacted 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 14ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 6 hours, wash the resulting mixed solution with xylene for 3 times, and store at 40°C under a vacuum of about -0.1MPa Drying under reduced pressure under the conditions above, the obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product M2. The yield was 83%, NMR such as figure 2 shown.
Embodiment 3
[0078] Embodiment 3: raw material M3
[0079] Preparation method: Under a nitrogen atmosphere, take 0.01mol of the raw material and lithium methoxide (0.76g, 0.02mol), mix well 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 (3.07g, 0.022mol) was added to the intermediate, stirred at room temperature for 6 hours, and the resulting mixture was dried under reduced pressure at 40°C and a vacuum of about -0.1MPa to obtain The solid was washed three times with isopropyl ether, filtered and dried to give the product M3. Yield 76%, NMR as image 3 shown.
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