23590-03-6Relevant articles and documents
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Nash,C.P.,Schaefer,W.P.
, p. 1319 - 1324 (1969)
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An ionic compound, and an electrolyte solution and a secondary battery comprising an ionic compound
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Paragraph 0108; 0113; 0115; 0126; 0129-0130, (2020/04/17)
An electrolyte for a secondary, battery and Si an electrolytic solution for a secondary battery and 1 a 2 secondary battery comprising the same are provided to improve the stability of a secondary battery by using an ionic compound having a structure represented by the following Chemical Formula I, No.No. STR84No.No. wherein X is an ionic compound having a structure represented by Structural Formula (I). No.No. STR84No.No. The compound of formula ( Claim The compound of formula ( Claim (by machine translation)
SULFONYLIMIDE SALT AND METHOD FOR PRODUCING THE SAME
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Page/Page column 12, (2011/02/26)
The present invention provides a method for producing fluorosulfonylimides more safely, rapidly and efficiently, which enables suppression of production of by-products, and fluorosulfonylimides. The method for producing a fluorosulfonylimide salt of the present invention includes a step of reacting a fluoride compound containing at least one element selected from the group consisting of elements of Group 11 to Group 15 and Period 4 to Period 6 (excluding arsenic and antimony) with a compound represented by the following general formula (I) to give a fluorosulfonylimide salt represented by the general formula (II): wherein R1 denotes at least one element selected from the group consisting of elements of Group 11 to Group 15 and Period 4 to Period 6 (excluding arsenic and antimony); R3 denotes fluorine, chlorine or a fluorinated alkyl group having 1 to 6 carbon atoms; R4 denotes fluorine or a fluorinated alkyl group having 1 to 6 carbon atoms; and m denotes an integer of 2 or 3.
Diphenylboron Chelates of α-(Dialkylamino)carboxylic Acids and their N-Oxides
Kliegel, Wolfgang,Graumann, Juergen
, p. 950 - 961 (2007/10/02)
α-(Dialkylamino)carboxylic acids and their N-oxides react with oxybis(diphenylborane) or similar diphenylborane derivatives to give five- or six-membered diphenylboron chelate rings, respectively, the structure of which is supported by spectroscopic evidence.