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Disulfur decafluoride
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| align="center" style="background:lime;" | Ball-and-stick model of disulfur decafluoride Space-filling model of disulfur decafluoride
Names
Preferred IUPAC name
Disulfur decafluoride
Systematic IUPAC name
Decafluoro-1λ6,2λ6-disulfane
Identifiers
CAS Number
5714-22-7
ChemSpider 56348 X markN
EC Number 227-204-4
Jmol 3D model Interactive image
MeSH Disulfur+decafluoride
PubChem 62586
Properties
Appearance colorless liquid
Melting point
Boiling point
Solubility in water
insoluble[1]
Hazards
Main hazards Poisonous
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasoline)Health code 4: Very short exposure could cause death or major residual injury. E.g., VX gasReactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g., phosphorusSpecial hazards (white): no codeNFPA 704 four-colored diamond
3
4
2
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Disulfur decafluoride (S2F10) is a gas discovered in 1934 by Denbigh and Whytlaw-Gray.[2] Each S of the S2F10 molecule is octahedral, and surrounded by 5 fluorines.[3] S2F10 is highly toxic, with toxicity 4 times that of phosgene. It was considered a potential chemical warfare pulmonary agent in World War II because it does not produce lacrimation or skin irritation, thus providing little warning of exposure. It is produced by the electrical decomposition of sulfur hexafluoride (SF6)—an essentially inert insulator used in high voltage systems such as transmission lines, substations and switchgear. S2F10 is also made during the production of SF6, but is distilled out.

Production[]

Disulfur decafluoride is produced primarily by the decomposition of sulfur hexafluoride:

2 SF6 → S2F10 + F2

Properties[]

This compound contains sulfur in the +5 oxidation state.

At temperatures above 150 °C, S
2
F
10
decomposes slowly to SF
6
and SF
4
:

S2F10SF6 + SF4

S
2
F
10
reacts with N
2
F
4
to give SF
5
NF
2
. It reacts with SO
2
to form SF
5
OSO
2
F
in the presence of ultraviolet radiation.

In the presence of excess chlorine gas, S
2
F
10
reacts to form sulfur chloride pentafluoride (SF
5
Cl
):

S
2
F
10
+ Cl
2
→ 2 SF
5
Cl

The analogous reaction with bromine is reversible and yields SF
5
Br
.[4] The reversibility of this reaction can be used to synthesize S
2
F
10
from SF
5
Br
.[5]

Ammonia is oxidised by S
2
F
10
into NSF
3
.[6]

Toxicity[]

S
2
F
10
Sulfur pentafluoride is a colorless gas or liquid with a sulfur-dioxide-like odor.[7] It is about 4 times as poisonous as phosgene. Its toxicity is thought to be caused by its disproportionation in the lungs into SF
6
, which is inert, and SF
4
, which reacts with moisture to form sulfurous acid and hydrofluoric acid.[8] Disulfur decafluoride itself is not toxic due to hydrolysis products, since it is hardly hydrolysed by water and most aqueous solutions.

External links[]

References[]

  1. http://www.chemicalbook.com/ChemicalProductProperty_EN_CB0751782.htm
  2. Denbigh, K. G.; Whytlaw-Gray, R. (1934). "The Preparation and Properties of Disulphur Decafluoride". pp. 1346–1352. Digital object identifier:10.1039/JR9340001346. 
  3. doi: 10.1021/ja01108a015
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  4. doi: 10.1021/ic50034a025
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  5. doi: 10.1016/S0022-1139(97)00096-1
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  6. Mitchell, S. (1996). Biological Interactions of Sulfur Compounds. CRC Press. p. 14. ISBN 0-7484-0245-4. 
  7. "Sulfur Pentaflu". 1988 OSHA PEL Project. CDC NIOSH. http://www.cdc.gov/niosh/pel88/5714-22.html. 
  8. Johnston, H. (2003). A Bridge not Attacked: Chemical Warfare Civilian Research During World War II. World Scientific. pp. 33–36. ISBN 981-238-153-8. 
  • Christophorou, L. G.; Sauers, I. (1991). Gaseous Dielectrics VI. Plenum Press. ISBN 0-306-43894-1. 
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