Perxenonic acid

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Structural formula
Structure of perxenonic acid
General
Surname Perxenonic acid
Molecular formula H 4 XeO 6
External identifiers / databases
CAS number 14125-26-9
Wikidata Q2702020
properties
Molar mass 231.32 g mol −1
Physical state

liquid

pK s value
  • <0 (H 4 XeO 6 )
  • 4.29 ± 0.03 (H 3 XeO 6 - )
  • 10.75 ± 0.04 (H 2 XeO 6 2− )
  • > 14 (HXeO 6 3− )
safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Perxenonic acid is an oxygen acid of xenon , which can only exist in an aqueous solution. Their salts are the Perxenate XeO 6 4− .

Extraction and presentation

Perxenonic acid is produced by introducing xenon (VIII) oxide into water.

The perxenate ion XeO 6 4− forms during the disproportionation of the xenonic acid H 2 XeO 4 .

properties

Analogous to xenonic acid , perxenonic acid and perxenate are also strong oxidizing agents . The pH of the solution should be between −0.2 and 13. The binding energy of H 3 XeO 6 - is 25 ° C at 0 ± 5  kJ · mol -1 and the H 2 XeO 6 2 at 3 ± 2  kJ · mol -1 . It has the same structure as telluric acid and is said to share the properties of periodic acid .

Perxenonic acid cannot be isolated as it rapidly decomposes in acidic conditions into xenon (VI) oxide , water and oxygen .

Because of this rapid decomposition, the protonation of H 3 XeO 6 - in H 4 XeO 6 is also not possible.

Salts of perxenonic acid, the perxenates , are already known, such as barium perxenate Ba 2 XeO 6 or sodium perxenate Na 4 XeO 6 . The latter has even been used successfully for the analytical oxidation of Am 3+ to Am 6+ .

literature

  • Walter C. Hamilton, James A. Ibers, Donald R. Mackenzie: Geometry of the Perxenate Ion . Science, Aug. 9, 1963, pp. 532-534 , doi : 10.1126 / science.141.3580.532 .

Individual evidence

  1. a b c d John H. Holloway, Eric G. Hope: Recent Advances in Noble-Gas Chemistry . In: Advances in Inorganic Chemistry . tape 46 . Academic Press, 1998, ISBN 0-08-057895-0 , pp. 51-100 , doi : 10.1016 / S0898-8838 (08) 60149-X .
  2. a b c Ulrik K. Klaening, EH Appelman: Protolytic properties of perxenic acid . October 1988, p. 3760-3762 , doi : 10.1021 / ic00294a018 .
  3. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  4. David W. Oxtoby, Wade A. Freeman, Toby F. Block: Chemistry 4th Edition . ISBN 0-03-033188-9 , chap. 4 , p. 87AP .
  5. ^ Catherine E. Housecroft, AG Sharpe: Inorganic Chemistry . Pearson Education, 2005, ISBN 0-13-039913-2 , pp. 499 .
  6. Bruno Jaselskis, Stanislaus Vas: Xenic Acid Reactions with vic-Diols . J. Am. Chem. Soc, 1964, pp. 2078-2079 , doi : 10.1021 / ja01064a041 .
  7. HP Holcomb: Analytical Oxidation of Americium with Sodium Perxenate . Anal. Chem., March 1965, pp. 415 , doi : 10.1021 / ac60222a002 .