Fluorosulfuric acid

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Fluorosulfuric acid
Skeletal formula of fluorosulfuric acid Fluorosulfuric-acid-2D.png
Skeletal formula of fluorosulfuric acid
Spacefill model of fluorosulfuric acid Fluorosulfuric-acid-3D-vdW.png
Spacefill model of fluorosulfuric acid
Fluorosulphuric acid.jpg
Names
IUPAC name
Sulfurofluoridic acid
Systematic IUPAC name
Fluorosulfuric acid[ citation needed ]
Other names
Fluorosulfonic acid,
Fluorosulphonic acid,
Fluorinesulfonic acid,
Fluorinesulphonic acid,
Fluoridosulfonic acid,
Fluoridosulphonic acid,
Sulfuric fluorohydrin,
Epoxysulfonyl fluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.029.227 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 232-149-4
MeSH Fluorosulfonic+acid
PubChem CID
RTECS number
  • LP0715000
UNII
UN number 1777
  • InChI=1S/FHO3S/c1-5(2,3)4/h(H,2,3,4) Yes check.svgY
    Key: UQSQSQZYBQSBJZ-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/FHO3S/c1-5(2,3)4/h(H,2,3,4)
    Key: UQSQSQZYBQSBJZ-UHFFFAOYAW
  • OS(F)(=O)=O
  • FS(=O)(=O)O
Properties
FHO3S
Molar mass 100.06 g·mol−1
AppearanceColorless liquid
Density 1.726 g cm−3
Melting point −87.5 °C; −125.4 °F; 185.7 K
Boiling point 165.4 °C; 329.6 °F; 438.5 K
Acidity (pKa)-10
Conjugate base Fluorosulfate
Structure
Tetragonal at S
Tetrahedral at S
Hazards
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-acid.svg
Danger
H314, H332 [1]
P280, P305+P351+P338, P310 [1]
NFPA 704 (fire diamond)
4
0
3
W
OX
Safety data sheet (SDS) ICSC 0996
Related compounds
Related compounds
Antimony pentafluoride
Trifluoromethanesulfonic acid
Hydrofluoric acid
Sulfurous acid
Sulfuric acid
Sulfur hexafluoride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Fluorosulfuric acid (IUPAC name: sulfurofluoridic acid) is the inorganic compound with the chemical formula HSO3F. It is one of the strongest acids commercially available. It is a tetrahedral molecule and is closely related to sulfuric acid, H2SO4, substituting a fluorine atom for one of the hydroxyl groups. It is a colourless liquid, although commercial samples are often yellow. [2]

Contents

Properties

Fluorosulfuric acid is a free-flowing colorless liquid. It is soluble in polar organic solvents (e.g. nitrobenzene, acetic acid, and ethyl acetate), but poorly soluble in nonpolar solvents such as alkanes.

HSO3F is one of the strongest known simple Brønsted acids. [3] It has an H0 value of −15.1 compared to 12 for sulfuric acid. The combination of HSO3F and the Lewis acid antimony pentafluoride produces "Magic acid", which is a far stronger protonating agent. These acids are categorized as "superacids", acids stronger than 100% sulfuric acid.

Reflecting its strong acidity, HSO3F dissolves almost all organic compounds that are even weak proton acceptors. [4] HSO3F hydrolyzes slowly to hydrogen fluoride (HF) and sulfuric acid. The related triflic acid (CF3SO3H) retains the high acidity of HSO3F but is more hydrolytically stable. The self-ionization of fluorosulfonic acid also occurs:

2 HSO3F ⇌ [H2SO3F]+ + [SO3F]    K = 4.0 × 10−8 (at 298 K)

HSO3F isomerizes alkanes and catalyzes the alkylation of hydrocarbons with alkenes, [5] although it is unclear if such applications are of commercial importance. It can also be used as a laboratory fluorinating agent. [6]

Production

Fluorosulfuric acid is prepared by the reaction of HF and sulfur trioxide: [2]

SO3 + HF → HSO3F

Alternatively, KHF2 or CaF2 can be treated with oleum at 250 °C. Once freed from HF by sweeping with an inert gas, HSO3F can be distilled in a glass apparatus. [6]

Safety

Fluorosulfuric acid is considered to be highly toxic and extremely corrosive. It hydrolyzes to release HF. Addition of water to HSO3F can be violent, similar to the addition of water to sulfuric acid but much more violent.

See also

Related Research Articles

<span class="mw-page-title-main">Acid</span> Chemical compound giving a proton or accepting an electron pair

An acid is a molecule or ion capable of either donating a proton (i.e. hydrogen ion, H+), known as a Brønsted–Lowry acid, or forming a covalent bond with an electron pair, known as a Lewis acid.

<span class="mw-page-title-main">Hydrofluoric acid</span> Solution of hydrogen fluoride in water

Hydrofluoric acid is a solution of hydrogen fluoride (HF) in water. Solutions of HF are colorless, acidic and highly corrosive. It is used to make most fluorine-containing compounds; examples include the commonly used pharmaceutical antidepressant medication fluoxetine (Prozac) and the material PTFE (Teflon). Elemental fluorine is produced from it. It is commonly used to etch glass and silicon wafers.

In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair. Because electrophiles accept electrons, they are Lewis acids. Most electrophiles are positively charged, have an atom that carries a partial positive charge, or have an atom that does not have an octet of electrons.

In chemistry, a superacid (according to the original definition) is an acid with an acidity greater than that of 100% pure sulfuric acid (H2SO4), 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 (CF3SO3H), also known as triflic acid, and fluorosulfuric acid (HSO3F), both of which are about a thousand times stronger (i.e. have more negative H0 values) than sulfuric acid. Most strong superacids are prepared by the combination of a strong Lewis acid and a strong Brønsted acid. A strong superacid of this kind is fluoroantimonic acid. Another group of superacids, the carborane acid group, contains some of the strongest known acids. Finally, when treated with anhydrous acid, zeolites (microporous aluminosilicate minerals) will contain superacidic sites within their pores. These materials are used on massive scale by the petrochemical industry in the upgrading of hydrocarbons to make fuels.

<span class="mw-page-title-main">Sulfonic acid</span> Organic compounds with the structure R−S(=O)2−OH

In organic chemistry, sulfonic acid refers to a member of the class of organosulfur compounds with the general formula R−S(=O)2−OH, where R is an organic alkyl or aryl group and the S(=O)2(OH) group a sulfonyl hydroxide. As a substituent, it is known as a sulfo group. A sulfonic acid can be thought of as sulfuric acid with one hydroxyl group replaced by an organic substituent. The parent compound is the parent sulfonic acid, HS(=O)2(OH), a tautomer of sulfurous acid, S(=O)(OH)2. Salts or esters of sulfonic acids are called sulfonates.

A mineral acid is an acid derived from one or more inorganic compounds, as opposed to organic acids which are acidic, organic compounds. All mineral acids form hydrogen ions and the conjugate base when dissolved in water.

<span class="mw-page-title-main">Magic acid</span> Chemical compound

Magic acid (FSO3H·SbF5) is a superacid consisting of a mixture, most commonly in a 1:1 molar ratio, of fluorosulfuric acid (HSO3F) and antimony pentafluoride (SbF5). This conjugate Brønsted–Lewis superacid system was developed in the 1960s by the George Olah lab at Case Western Reserve University, and has been used to stabilize carbocations and hypercoordinated carbonium ions in liquid media. Magic acid and other superacids are also used to catalyze isomerization of saturated hydrocarbons, and have been shown to protonate even weak bases, including methane, xenon, halogens, and molecular hydrogen.

An inorganic nonaqueous solvent is a solvent other than water, that is not an organic compound. These solvents are used in chemical research and industry for reactions that cannot occur in aqueous solutions or require a special environment. Inorganic nonaqueous solvents can be classified into two groups, protic solvents and aprotic solvents. Early studies on inorganic nonaqueous solvents evaluated ammonia, hydrogen fluoride, sulfuric acid, as well as more specialized solvents, hydrazine, and selenium oxychloride.

Antimony pentafluoride is the inorganic compound with the formula SbF5. This colourless, viscous liquid is a strong Lewis acid and a component of the superacid fluoroantimonic acid, formed upon mixing liquid HF with liquid SbF5 in 1:1 ratio. It is notable for its strong Lewis acidity and the ability to react with almost all known compounds.

<span class="mw-page-title-main">Hydrogen fluoride</span> Chemical compound

Hydrogen fluoride (fluorane) is an inorganic compound with chemical formula HF. It is a very poisonous, colorless gas or liquid that dissolves in water to yield an aqueous solution termed hydrofluoric acid. It is the principal industrial source of fluorine, often in the form of hydrofluoric acid, and is an important feedstock in the preparation of many important compounds including pharmaceuticals and polymers, e.g. polytetrafluoroethylene (PTFE). HF is also widely used in the petrochemical industry as a component of superacids. Due to strong and extensive hydrogen bonding, it boils at near room temperature, much higher than other hydrogen halides.

<span class="mw-page-title-main">Fluoroantimonic acid</span> Chemical compound

Fluoroantimonic acid is a mixture of hydrogen fluoride and antimony penta­fluoride, containing various cations and anions. This mixture is a superacid that, in some sense, is over a billion times stronger than 100% sulfuric acid in terms of its protonating ability measured by Hammett function. It even protonates some hydro­carbons to afford pentacoordinate carbo­cations. Fluoro­antimonic acid is corrosive. Like its precursor hydrogen fluoride, it attacks glass, but can be stored in containers lined with PTFE (Teflon) or PFA.

<span class="mw-page-title-main">Triflic acid</span> Chemical compound

Triflic acid, the short name for trifluoromethanesulfonic acid, TFMS, TFSA, HOTf or TfOH, is a sulfonic acid with the chemical formula CF3SO3H. It is one of the strongest known acids. Triflic acid is mainly used in research as a catalyst for esterification. It is a hygroscopic, colorless, slightly viscous liquid and is soluble in polar solvents.

<span class="mw-page-title-main">Sulfur tetrafluoride</span> Chemical compound

Sulfur tetrafluoride is the chemical compound with the formula SF4. It is a colorless corrosive gas that releases dangerous HF upon exposure to water or moisture. Despite these unwelcome characteristics, this compound is a useful reagent for the preparation of organofluorine compounds, some of which are important in the pharmaceutical and specialty chemical industries.

<span class="mw-page-title-main">Tantalum pentafluoride</span> Chemical compound

Tantalum(V) fluoride is the inorganic compound with the formula TaF5. It is one of the principal molecular compounds of tantalum. Characteristic of some other pentafluorides, the compound is volatile but exists as an oligomer in the solid state.

<span class="mw-page-title-main">Leveling effect</span> Effect of solvents on properties of acids and bases

Leveling effect or solvent leveling refers to the effect of solvent on the properties of acids and bases. The strength of a strong acid is limited ("leveled") by the basicity of the solvent. Similarly the strength of a strong base is leveled by the acidity of the solvent. When a strong acid is dissolved in water, it reacts with it to form hydronium ion (H3O+). An example of this would be the following reaction, where "HA" is the strong acid:

The Hammett acidity function (H0) is a measure of acidity that is used for very concentrated solutions of strong acids, including superacids. It was proposed by the physical organic chemist Louis Plack Hammett and is the best-known acidity function used to extend the measure of Brønsted–Lowry acidity beyond the dilute aqueous solutions for which the pH scale is useful.

<span class="mw-page-title-main">Fluoroboric acid</span> Chemical compound

Fluoroboric acid or tetrafluoroboric acid is an inorganic compound with the simplified chemical formula H+[BF4]. Unlike other strong acids like H2SO4 or HClO4, the pure tetrafluoroboric acid does not exist. The term "fluoroboric acid" refers to a range of chemical compounds, depending on the solvent. The H+ in the simplified formula of fluoroboric acid represents the solvated proton. The solvent can be any suitable Lewis base. For instance, if the solvent is water, fluoroboric acid can be represented by the formula [H3O]+[BF4], although more realistically, several water molecules solvate the proton: [H(H2O)n]+[BF4]. The ethyl ether solvate is also commercially available, where the fluoroboric acid can be represented by the formula [H( 2O)n]+[BF4], where n is most likely 2.

Acid strength is the tendency of an acid, symbolised by the chemical formula , to dissociate into a proton, , and an anion, . The dissociation of a strong acid in solution is effectively complete, except in its most concentrated solutions.

Fluorine forms a great variety of chemical compounds, within which it always adopts an oxidation state of −1. With other atoms, fluorine forms either polar covalent bonds or ionic bonds. Most frequently, covalent bonds involving fluorine atoms are single bonds, although at least two examples of a higher order bond exist. Fluoride may act as a bridging ligand between two metals in some complex molecules. Molecules containing fluorine may also exhibit hydrogen bonding. Fluorine's chemistry includes inorganic compounds formed with hydrogen, metals, nonmetals, and even noble gases; as well as a diverse set of organic compounds. For many elements the highest known oxidation state can be achieved in a fluoride. For some elements this is achieved exclusively in a fluoride, for others exclusively in an oxide; and for still others the highest oxidation states of oxides and fluorides are always equal.

<span class="mw-page-title-main">Carborane acid</span> Class of chemical compounds

Carborane acidsH(CXB
11
Y
5
Z
6
)
(X, Y, Z = H, Alk, F, Cl, Br, CF3) are a class of superacids, some of which are estimated to be at least one million times stronger than 100% pure sulfuric acid in terms of their Hammett acidity function values (H0 ≤ –18) and possess computed pKa values well below –20, establishing them as some of the strongest known Brønsted acids. The best-studied example is the highly chlorinated derivative H(CHB
11
Cl
11
)
. The acidity of H(CHB
11
Cl
11
)
was found to vastly exceed that of triflic acid, CF
3
SO
3
H
, and bistriflimide, (CF
3
SO
2
)
2
NH
, compounds previously regarded as the strongest isolable acids.

References

  1. 1 2 Sigma-Aldrich Co., Phosphoric acid. Retrieved on 2014-05-09.
  2. 1 2 Erhardt Tabel, Eberhard Zirngiebl, Joachim Maas "Fluorosulfuric Acid" in "Ullmann's Encyclopedia of Industrial Chemistry" 2005, Wiley-VCH, Weinheim. doi : 10.1002/14356007.a11_431
  3. Christopher A. Reed "Myths about the Proton. The Nature of H+ in Condensed Media" Acc. Chem. Res., 2013, 46 (11), pp 2567–2575. doi : 10.1021/ar400064q
  4. Olah, G. A.; Prakash, G. K.; Wang, Q.; Li, X.-Y. (2001). "Fluorosulfuric Acid". Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Synthesis. John Wiley & Sons. doi:10.1002/047084289X.rf014. ISBN   0471936235.
  5. Olah, G.; Farooq, O.; Husain, A.; Ding, N.; Trivedi, N.; Olah, J. (1991). "Superacid HSO3F/HF-Catalyzed Butane Isomerisation". Catalysis Letters. 10 (3–4): 239–247. doi:10.1007/BF00772077. S2CID   94408218.
  6. 1 2 Cotton, F. A.; Wilkinson, G. (1980). Advanced Inorganic Chemistry (4th ed.). New York: Wiley. p. 246. ISBN   0-471-02775-8.