Bistriflimide

The anion is widely used in ionic liquids (such as trioctylmethylammonium bis(trifluoromethylsulfonyl)imide), since it is less toxic and more stable than more "traditional" counterions such as tetrafluoroborate. This anion is also of importance in lithium-ion and lithium metal batteries (LiTFSI) because of its high dissociation and conductivity. It has the added advantage of suppressing crystallinity in poly(ethylene oxide), which increases the conductivity of that polymer below its melting point at 50 °C. ==Bistriflimidic acid==

The conjugate acid of bistriflimide, which is frequently referred to by the trivial name bistriflimidic acid (sometimes shortened to triflimidic acid; CAS: 82113-65-3), is a commercially available superacid. It is a crystalline compound, but is hygroscopic to the point of being deliquescent. Owing to its very high acidity and good compatibility with organic solvents it has been employed as a catalyst in a wide range of chemical reactions. Its pKa value in water cannot be accurately determined but in acetonitrile it has been estimated as −0.10 and in 1,2-dichloroethane −12.3 (relative to the pKa value of 2,4,6-trinitrophenol (picric acid), anchored to zero to crudely approximate the aqueous pKa scale), making it more acidic than triflic acid (pKaMeCN = 0.70, pKaDCE(relative to picric acid) = −11.4). ==Naming==

Developing an IUPAC name for bistriflimide that indicates the structure and reactivity is challenging, and changes to current names have been proposed. The main difficulty arises from the ambiguous use of the word amide to mean an acylated (including sulfonylated) amine or the anionic form of an amine. Likewise, imide can refer to a bisacylated amine or a twice deprotonated amine. Thus, depending on the system used, there is ambiguity as to whether amide or imide is being used to refer to the parent acid or the anion. (The anion has been referred to as an amidate or imidate in an attempt to distinguish it from the acid.) The complications in naming these compounds was highlighted in an article by the IUPAC.{{cite journal The name 1,1,1-trifluoro-N-((trifluoromethyl)sulfonyl)methanesulfonamide is also an unambiguous IUPAC-acceptable name, though the symmetry of the molecule is not apparent from this construction. ==See also==