Production method for lithium sulfamate, and novel lithium sulfamate
US-2021087059-A1 · Mar 25, 2021 · US
US11916195B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11916195-B2 |
| Application number | US-201917041721-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 11, 2019 |
| Priority date | Mar 27, 2018 |
| Publication date | Feb 27, 2024 |
| Grant date | Feb 27, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An electrolyte solution containing a compound (1) represented by the formula (1), (wherein R101 and R102 are each individually a substituent such as a C1-C7 alkyl group, and the substituent optionally contains at least one divalent to hexavalent hetero atom in a structure or optionally has a structure obtained by replacing at least one hydrogen atom by a fluorine atom or a C0-C7 functional group) and at least one compound (11) selected from compounds such as a compound represented by formula (11-1) (wherein R111 and R112 are the same as or different from each other and are each a hydrogen atom or the like, and R113 is an alkyl group free from a fluorine atom or the like):
Opening claim text (preview).
The invention claimed is: 1. An electrolyte solution comprising a compound (1) represented by the following formula (1) and at least one compound (11) selected from the group consisting of compounds represented by the following formulas (11-1) to (11-5), the formula (1) being wherein R 101 and R 102 are each individually a substituent represented by —H, —F, a group represented by the formula: —O p101 —(SiR 103 2 O) n101 —SiR 104 3 , wherein R 103 and R 104 are each individually an alkyl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom, an alkenyl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom, an alkynyl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom, or an aryl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom; n101 is an integer of 0 or greater; and p101 is 0 or 1, a C1-C7 alkyl group, a C2-C7 alkenyl group, a C2-C7 alkynyl group, a C6-C15 aryl group, —SO 2 X 101 , wherein X 101 is —H, —F, or an alkyl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom, —SO 3 X 102 , wherein X 102 is —H, —F, or an alkyl group obtained by optionally replacing at least one hydrogen atom by a fluorine atom, or a C2-C7 hydrocarbon group that forms a cyclic structure by bonding of R 101 and R 102 , the cyclic structure optionally containing a multiple bond, and the substituent optionally contains at least one divalent to hexavalent hetero atom in a structure or optionally has a structure obtained by replacing at least one hydrogen atom by a fluorine atom or a C1-C7 functional group, the formula (11-1) being wherein R 111 and R 112 are the same as or different from each other and are each a hydrogen atom, a fluorine atom, or an alkyl group optionally containing a fluorine atom, and R 113 is an alkyl group free from a fluorine atom or an organic group containing an unsaturated carbon-carbon bond, the formula (11-2) being wherein R 121 is an optionally fluorinated C1-C7 alkyl group, an optionally fluorinated C2-C8 alkenyl group, an optionally fluorinated C2-C9 alkynyl group, or an optionally fluorinated C6-C12 aryl group, and optionally contains at least one selected from the group consisting of O, Si, S, and N in a structure, the formula (11-3) being wherein R 131 and R 132 are (i) each individually H, F, an optionally fluorinated C1-C7 alkyl group, an optionally fluorinated C2-C7 alkenyl group, an optionally fluorinated C2-C9 alkynyl group, or an optionally fluorinated C5-C12 aryl group, or (ii) hydrocarbon groups binding to each other to form a 5- or 6-membered hetero ring with a nitrogen atom, and R 131 and R 132 each optionally contain at least one selected from the group consisting of O, S, and N in a structure, the formula (11-4) being wherein Rf 141 is CF 3 —, CF 2 H—, or CFH 2 —, and R 141 is an optionally fluorinated C2-C5 alkenyl group or an optionally fluorinated C2-C8 alkynyl group and optionally contains Si in a structure, the formula (11-5) being CH 3 CFX 151 COOR 151 wherein R 151 is a C1-C4 alkyl group, and X 151 is H or F. 2. An electrochemical device comprising the electrolyte solution according to claim 1 . 3. A lithium ion secondary battery comprising the electrolyte solution according to claim 1 . 4. A module comprising the electrochemical device according to claim 2 . 5. A module comprising the lithium ion secondary battery according to claim 3 .
characterised by the additives · CPC title
characterised by additives · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
characterised by the solute, e.g. salts, anions or cations therein · CPC title
Mixture of solvents · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.