BAX agonist, compositions, and methods related thereto
US-9402850-B2 · Aug 2, 2016 · US
US2016137597A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016137597-A1 |
| Application number | US-201414778487-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 18, 2014 |
| Priority date | Mar 20, 2013 |
| Publication date | May 19, 2016 |
| Grant date | — |
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The invention relates to sulfonate compounds with the following formula (I): in which: R 2 represents an ethyl group, an n-propyl group or an isopropyl group; when R 2 is an ethyl group, R 1 is an ethyl group, an n-propyl group or an n-butyl group; when R 2 is an n-propyl group, R 1 is a methyl group, an ethyl group, an n-propyl group or an n-butyl group; or when R 2 is an isopropyl group, R 1 is a methyl group, an ethyl group, an n-propyl group or an n-butyl group. Use of these compounds as electrolyte solvent for lithium batteries.
Opening claim text (preview).
1 . A sulfonate compound of formula (I): wherein R 2 is an ethyl group, an n-propyl group or an isopropyl group, wherein: when R 2 is an ethyl group, le is an ethyl group, an n-propyl group or an n-butyl group; when R 2 is an n-propyl group, R 1 is a methyl group, an ethyl group, an n-propyl group or an n-butyl group; and when R 2 is an isopropyl group, R 1 is a methyl group, an ethyl group, an n-propyl group or an n-butyl group. 2 . The compound according to claim 1 , wherein R 2 is an n-propyl group and R 1 is a methyl group. 3 . The compound according to claim 1 , wherein R 2 is an n-propyl group and R 1 is an ethyl group. 4 . The compound according to claim 1 , wherein R 2 is an ethyl group and R 1 is an ethyl group. 5 . A method for preparation of a sulfonate compound of formula (I) according to claim 1 , comprising reacting a hydroxyether compound of formula R 1 —O—CH 2 —CH 2 —OH, R 1 being as defined in claim 1 with an X—SO 2 —R 2 compound, where X is a halogen atom and R 2 being as defined in claim 1 , in a medium comprising a base and one organic solvent. 6 . The compound according to claim 1 , wherein the compound is an organic solvent of a lithium salt. 7 . A composition, comprising a compound according to claim 1 and a lithium salt. 8 . The composition according to claim 7 , wherein the lithium salt is at least one selected from the group consisting of LiPF 6 , LiClO 4 , LiBF 4 , LiAsF 6 , LiCF 3 SO 3 , LiN(CF 3 SO 2 ) 3 , LiN(C 2 F 5 SO 2 ), lithium bistrifluoromethylsulfonylimide LiN[SO 2 CF 3 ] 2 and mixtures thereof. 9 . The composition according to claim 7 , wherein the composition is a lithium ion conducting electrolyte. 10 . A lithium battery comprising an electrochemical cell comprising the composition according to claim 9 which is an electrolyte, located between a positive electrode and a negative electrode. 11 . The lithium battery according to claim 10 , wherein the negative electrode is a material comprising a lithium titanium oxide. 12 . The lithium battery according to claim 10 , wherein the positive electrode is a material comprising a material of formula LiMn 2-z Ni z O 4 , where 0<z<2.
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
Negative electrodes · CPC title
characterised by the solvents · CPC title
of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title
of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy (H01M4/505, H01M4/525 take precedence) · CPC title
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