Disulfur decafluoride

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Template:Chembox Disulfur decafluoride is a chemical compound with the formula Template:Chem2. It was discovered in 1934 by Denbigh and Whytlaw-Gray.[1] Each sulfur atom of the Template:Chem2 molecule is octahedral, and surrounded by five fluorine atoms[2] and one sulfur atom. The two sulfur atoms are connected by a single bond. In the Template:Chem2 molecule, the oxidation state of each sulfur atoms is +5, but their valency is 6 (they are hexavalent). Template:Chem2 is highly toxic, with toxicity four times that of phosgene.

It is a colorless liquid with a burnt match smell similar to sulfur dioxide.[3]

Production

Disulfur decafluoride is produced by photolysis of Template:Chem2:[4]

Template:Chem2

Disulfur decafluoride arises by the decomposition of sulfur hexafluoride. It is produced by the electrical decomposition of sulfur hexafluoride (Template:Chem2)—an essentially inert insulator used in high voltage systems such as transmission lines, substations and switchgear. Template:Chem2 is also made during the production of Template:Chem2.

Properties

The S-S bond dissociation energy is 305 ± 21 kJ/mol, about 80 kJ/mol stronger than the S-S bond in diphenyldisulfide.

At temperatures above 150 °C, Template:Chem/link decomposes slowly (disproportionation) into Template:Chem/link and Template:Chem/link:

S2F10SF6 + SF4

Template:Chem/link reacts with [[Tetrafluorohydrazine|Template:Chem/link]] to give [[Difluoroamino sulfur pentafluoride|Template:Chem/link]]. It reacts with Template:Chem/link to form Template:Chem/link in the presence of ultraviolet radiation.

Template:Chem/link + Template:Chem/link → 2 Template:Chem/link

In the presence of excess chlorine gas, Template:Chem/link reacts to form sulfur chloride pentafluoride (Template:Chem/link):

Template:Chem/link + Template:Chem/link → 2 Template:Chem/link

The analogous reaction with bromine is reversible and yields Template:Chem/link.[5] The reversibility of this reaction can be used to synthesize Template:Chem/link from Template:Chem/link.[6]

Ammonia is oxidised by Template:Chem/link into [[Thiazyl trifluoride|Template:Chem/link]].[7]

Toxicity

Template:Chem/link 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. Disulfur decafluoride is a colorless gas or liquid with a SO2-like odor.[8] It is about four times as poisonous as phosgene. Its toxicity is thought to be caused by its disproportionation in the lungs into Template:Chem/link, which is inert, and Template:Chem/link, which reacts with moisture to form sulfurous acid and hydrofluoric acid.[9]

See also

References

<templatestyles src="Reflist/styles.css" />

  1. Script error: No such module "Citation/CS1".
  2. Script error: No such module "Citation/CS1".
  3. Script error: No such module "citation/CS1".
  4. Script error: No such module "Citation/CS1".
  5. Script error: No such module "Citation/CS1".
  6. Script error: No such module "Citation/CS1".
  7. Script error: No such module "citation/CS1".
  8. Script error: No such module "citation/CS1".
  9. Script error: No such module "citation/CS1".

Script error: No such module "Check for unknown parameters".

  • Script error: No such module "citation/CS1".

External links

  • Script error: No such module "citation/CS1".

Template:Sulfur compounds Script error: No such module "Navbox".