Category
page 1Superacids
perchloric acid
chemical compound
fluoroantimonic acid
chemical compound
superacid
In chemistry, a superacid (according to the original definition) is an acid with an acidity greater than that of 100% pure sulfuric acid (), which has a Hammett acidity function (H0) of −12. According to the modern definition, a superacid is a medium in which the chemical potential of the proton is higher than in pure sulfuric acid. Commercially available superacids include trifluoromethanesulfonic acid (), also known as triflic acid, and fluorosulfuric acid (), both of which are about a thousand times stronger (i.e. have more negative H0 values) than sulfuric acid. Most strong superacids are
fluorosulfonic acid
chemical compound
chlorosulfonic acid
chemical compound
antimony pentafluoride
chemical compound
triflic acid
chemical compound
hydridohelium(1+)
onium ion of helium; protonated helium
magic acid
superacid system prepared from a Brønsted and a Lewis superacid
Hammett acidity function
measure of acidity used for extremely acidic solutions

carborane
thumb|right|Ball-and-stick model of o-carborane
<!-- thumb|right|Ball-and-stick model of the [[carborane acid anion (acidic proton not displayed)
carborane acid
chemical compound
methanium
In chemistry, methanium is a complex positive ion with formula (metastable transitional form, a carbon atom covalently bonded to five hydrogen atoms) or (fluxional form, namely a molecule with one carbon atom covalently bonded to three hydrogen atoms and one dihydrogen molecule), bearing a +1 electric charge. It is a superacid and one of the onium ions, indeed the simplest carbonium ion.
triflidic acid
chemical compound
pentacyanocyclopentadiene
Pentacyanocyclopentadiene is a derivative of cyclopentadiene with five cyano groups with the molecular formula C5H(CN)5. The corresponding anion, pentacyanocyclopentadienide, is a ligand with the molecular formula . In contrast to other anions based on a C5 ring unit it binds to metals through the pendant cyano groups rather than the C5 ring. The anion was first synthesised by Webster in the 1960s and its conjugate acid much later on. More recently Wright has discovered its extensive coordination chemistry. By virtue of a combination of mesomeric and aromatic stabilization of its anion, pentac
bistriflimide
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 [(CF3SO2)2N]−. Its salts are typically referred to as being metal triflimidates.