Electrolyte for lithium secondary battery and lithium secondary battery comprising same
A lithium secondary battery and electrolyte technology, applied in non-aqueous electrolyte storage batteries, secondary batteries, lithium storage batteries, etc., can solve the problems of low reliability of non-aqueous electrolytes and reduced durability of lithium secondary batteries, and achieve excellent reliability , the effect of excellent life characteristics and high output performance
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Synthetic example 1
[0180] After dissolving 1 equivalent of sodium monofluorophosphate in a dimethylformamide solvent, 2 equivalents of trimethylchlorosilane was added dropwise at 0°C, and the reaction was carried out at room temperature for 2 hours. After the reaction, diethyl ether was added to perform an extraction process, the solvent of the diethyl ether layer was removed, and the remaining volatile substances were removed by vacuum drying, whereby the compound represented by Chemical Formula 2 was synthesized.
[0181] [Chemical formula 2]
[0182]
[0183] The synthesized compounds show 1 H NMR CDCl 3 δ0.3ppm, P-NMR CDCl 3 δ-26ppm, F-NMR CDCl 3 delta-72ppm.
Synthetic example 2
[0185] After dissolving 1 equivalent of the compound represented by Chemical Formula 2 in dimethyl carbonate, adding 1 equivalent of lithium hydroxide, and reacting for 24 hours, the compound represented by Chemical Formula 3 was synthesized.
[0186] [Chemical formula 3]
[0187]
[0188] The synthesized compounds show 1 H NMR CDCl 3 δ0.3ppm, P-NMR CDCl 3 δ-26ppm, F-NMR CDCl 3 δ-72 ppm, ICP-MS Li:P:Si ratio 1:0.9:0.9 (calculated 1:1:1).
Synthetic example 3
[0190] After adding 1 equivalent of the compound represented by chemical formula 2 to 0.6 equivalent of phosphorus pentachloride, when PCl 5 When completely dissolved, the volatile substances are removed by a vacuum pump, and then the compound represented by Chemical Formula 4 is synthesized by distillation and purification.
[0191] [Chemical formula 4]
[0192]
[0193] The synthesized compounds show 1 H NMR CDCl 3 δ0.3ppm, P-NMR CDCl 3 δ-32ppm, F-NMR CDCl 3 delta-71ppm.
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Abstract
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