Fluoroantimonic acid

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Fluoroantimonic acid
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Names
IUPAC name
Fluoroantimonic acid
Systematic IUPAC name
Fluoranium hexafluorostibanuide
Fluoranium hexafluoridoantimonate(1−)
Identifiers
16950-06-4 N
ChemSpider 32741664 N
EC Number 241-023-8
Jmol 3D model Interactive image
  • InChI=1S/FH2.6FH.Sb/h1H2;6*1H;/q+1;;;;;;;+5/p-6 N
    Key: HBGBSIVYTBPVEU-UHFFFAOYSA-H N
  • [FH2+].F[Sb-](F)(F)(F)(F)F
Properties
H
2
SbF
7
Molar mass 256.765
Appearance Colorless liquid
Density 2.885 g/cm3
Solubility SO2ClF, SO2
Acidity (pKa) −25
Basicity (pKb) 39
Vapor pressure {{{value}}}
Related compounds
Related acids
Antimony pentafluoride

Hydrogen fluoride
Magic acid

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Fluoroantimonic acid (systematically named fluoranium hexafluorostibanuide and fluoranium hexafluoridoantimonate(1−)) is an inorganic compound with the chemical formula H
2
FSbF
6
(also written H
2
F[SbF
6
]
, 2HF•SbF5, or simply HF-SbF5). It is an ionic liquid created by reacting hydrogen fluoride (HF) with antimony pentafluoride (SbF5) in a stoichiometric ratio of 2:1. It is the strongest known superacid, which has been demonstrated to protonate even hydrocarbons to afford carbocations and H2.[1] Similar acids can be created by using excess antimony pentafluoride.[2]

The reaction to produce fluoroantimonic acid is:

2 HF \rightleftharpoons H2F+ + F
SbF5 + F → SbF6

The overall reaction is:

SbF5 + 2 HF → SbF6 + H2F+

The second reaction is not in equilibrium, therefore the overall reaction is not in equilibrium. The reaction is exothermic.

The F, produced by autoionization of hydrogen fluoride, reacts with SbF5 to yield the adduct SbF6 In the fluoronium ion, hydrogen fluoride is coordinated to the hydrogen ion. The anion is classified as noncoordinating and is both a very weak nucleophile and a very weak base.

The acid is often said to contain "naked protons", but the "free" protons are, in fact, always bonded to hydrogen fluoride molecules to make the fluoronium cations (similar to the hydronium cation in aqueous solution).[3] It is the fluoronium ion that accounts for fluoroantomonic acid's extreme acidity. Fluoroantimonic acid is 1016 (10 quadrillion) times stronger than 100% sulfuric acid.[4] The protons easily migrate through the solution, moving from H2F+ to HF, when present, by the Grotthuss mechanism:

H2F+ + HF \rightleftharpoons HF + H2F+

Fluoroantimonic acid thermally decomposes at higher temperatures, generating hydrogen fluoride gas.

Structure

Two related products have been crystallised from HF-SbF5 mixtures, and both have been analyzed by single crystal X-ray crystallography. These salts have the formulas [H2F+][Sb2F11] and [H3F2+][Sb2F11]. In both salts, the anion is Sb2F11.[5] As mentioned above, SbF6 is weakly basic; the larger anion Sb2F11 is expected to be still weaker.

The following values[citation needed] are based upon the Hammett acidity function. Increased acidity is indicated by smaller (in this case, more negative) values of H0.

Applications

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This extraordinarily strong acid protonates nearly all organic compounds. In 1967, Bickel and Hogeveen showed that 2HF•SbF5 will remove H2 from isobutane and methane from neopentane to form carbenium ions:[6][7]

(CH3)3CH + H+ → (CH3)3C+ + H2
(CH3)4C + H+ → (CH3)3C+ + CH4

Materials compatible with fluoroantimonic acid as a solvent include SO2ClF, and sulfur dioxide; some chlorofluorocarbons have also been used. Containers for HF-SbF5 are made of PTFE.

Safety

HF-SbF5 is extremely corrosive, toxic, and moisture sensitive.[2] Like most strong acids, fluoroantimonic acid can react violently with water, owing to the exothermic hydration. Consequently, it cannot be used in aqueous solution, only in hydrofluoric solution.

See also

References

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