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Antimony pentafluoride

 
Sci-Tech Dictionary: antimony pentafluoride
(′an·tə′mō·nē ′pent·ə′flu̇r′īd)

(inorganic chemistry) SbF5 A corrosive, hygroscopic, moderately viscous fluid; reacts violently with water; forms a clear solution with glacial acetic acid; used in the fluorination of organic compounds.


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Antimony pentafluoride
Antimony pentafluoride
Antimony pentafluoride
IUPAC name
Other names antimony pentafluoride
pentafluoridoantimony
Identifiers
CAS number 7783-70-2 Yes check.svgY
UN number 1732
RTECS number CC5800000
SMILES
InChI
InChI key CCIMPPQYTRNALI-RNQIAQHSAI
ChemSpider ID 21172742
Properties
Molecular formula SbF5
Molar mass 216.74 g/mol
Appearance colorless oily liquid
hygroscopic
Density 2.99 g/cm3 [1]
Melting point

8.3 °C, 281 K, 47 °F

Boiling point

149.5 °C, 423 K, 301 °F

Solubility in water Reacts with water
Solubility soluble in KF
Hazards
MSDS ICSC 0220
EU Index 051-003-00-9
EU classification Harmful (Xn)
Dangerous for the environment (N)
R-phrases R20/22, R51/53
S-phrases (S2), S61
NFPA 704
NFPA 704.svg
0
3
1
W
Related compounds
Other anions Antimony pentachloride
Other cations Phosphorus pentafluoride
Arsenic pentafluoride
Bismuth pentafluoride
Related compounds Antimony trifluoride
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Antimony pentafluoride is the chemical compound with the formula SbF5. This colourless, viscous liquid is a valuable Lewis acid and a component of the superacid fluoroantimonic acid, the strongest known acid. Some features that give the compound scientific interest are its Lewis acidity and that it also reacts with almost all known compounds.[2]

Contents

Preparation

Antimony pentafluoride is prepared by the reaction of antimony pentachloride with anhydrous hydrogen fluoride:

SbCl5 + 5 HF → SbF5 + 5 HCl

It may also be prepared from antimony trifluoride and fluorine, or by treating antimony pentoxide with aqueous hydrofluoric acid and evaporing water.

Structure and chemical reactions

In the gas phase, SbF5 adopts a trigonal bipyramidal structure of D3h point group symmetry (see picture). The structure is more complex in the liquid and solid state. The liquid contains polymers wherein each Sb is octahedral, the structure being described with the formula [SbF4(μ-F)2]n. The crystalline material is tetrameric, i.e. it has the formula [SbF4(μ-F)]4. The Sb-F bonds are 2.02 Å within the eight-membered Sb4F4 ring; the remaining fluoride ligands radiating from the four Sb centers are shorter at 1.82 Å.[3] The related species PF5 and AsF5 are monomeric in the solid and liquid states, probably due to the smaller sizes of the central atom, which limits their coordination number. BiF5 is a polymer.[4]

SbF5 is a strong Lewis acid, exceptionally so toward sources of F to give the very stable anion [SbF6]. The latter reacts with additional SbF5 to give [Sb2F11].

In the same way that SbF5 enhances the Brønsted acidity of HF, it enhances the oxidizing power of F2. This effect is illustrated by the oxidation of oxygen:[5]

2 SbF5 + F2 + 2 O2 → 2 [O2]+[SbF6]

Antimony pentafluoride has also been used in the first discovered chemical reaction that produces fluorine gas from fluoride compounds:

4 SbF5 + 2 K2MnF6 → 4 KSbF6 + 2 MnF3 + F2

The driving force for this reaction is the high affinity of SbF5 for F, which is the same property which recommends the use of SbF5 to generate superacids.

Safety

SbF5 reacts violently with many compounds, often releasing dangerous hydrogen fluoride. It is also corrosive to the skin.

References

  1. ^ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0070494398
  2. ^ Olah, G. A.; Prakash, G. K. S.; Wang, Q.; Li, X.-y."Antimony(V) Fluoride" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. DOI: 10.1002/047084289.
  3. ^ Edwards, A. J.; Taylor, P. "Crystal structure of Antimony Pentafluoride" Journal of the Chemical Society, Chemical Communications 1971, pp. 1376-7.doi:10.1039/C29710001376
  4. ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
  5. ^ Shamir, J.; Binenboym, J. "Dioxygenyl Salts" Inorganic Syntheses, 1973, XIV, 109-122. ISSN 0073-8077

External links


 
 
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