Bistriflimide, also known variously as bis(trifluoromethane)sulfonimide, bis(trifluoromethanesulfonyl)imide, bis(trifluoromethanesulfonyl)imidate (and variations thereof), informally and somewhat inaccurately as triflimide or triflimidate , or by the abbreviations TFSI or NTf2, is a non-coordinating anion with the chemical formula (−. Its salts are typically referred to as being metal triflimidates.
Applications
The anion is widely used in (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 (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 p Ka 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 p Ka value of 2,4,6-trinitrophenol (picric acid), anchored to zero to crudely approximate the aqueous p Ka scale[Absolute p Ka values in dichloroethane are about 45 units higher, making their values very large for all but the strongest superacids (see: J. Phys. Chem. A 2015, 119, 735).]), making it more acidic than triflic acid (p KaMeCN = 0.70, p KaDCE(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 Imide or Inorganic imide. 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.
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
