In chemistry, perxenates are salts of the yellow[1] xenon-containing anion XeO4−
6.[2] This anion has octahedral molecular geometry, as determined by Raman spectroscopy, having O–Xe–O bond angles varying between 87° and 93°.[3] The Xe–O bond length was determined by X-ray spectroscopy to be 1.875 Å.[4]
Perxenates are synthesized by the disproportionation of xenon trioxide when dissolved in strong alkali:[5]
- 2 XeO3 (s) + 4 OH− (aq) → Xe (g) + XeO4−
6 (aq) + O2 (g) + 2 H2O (l)
When Ba(OH)2 is used as the alkali, barium perxenate can be crystallized from the resulting solution.[5]
Perxenic acid is the unstable conjugate acid of the perxenate anion, formed by the solution of xenon tetroxide in water. It has not been isolated as a free acid, because under acidic conditions it rapidly decomposes into xenon trioxide and oxygen gas:[6][7]
- 2 HXeO3−
6 + 6 H+ → 2 XeO3 + 4 H2O + O2
Its extrapolated formula, H4XeO6, is inferred from the octahedral geometry of the perxenate ion (XeO4−
6) in its alkali metal salts.[6][4]
The pH of aqueous perxenic acid, (pKH4XeO6), has been indirectly calculated to be < 0, making it a very strong acid. Its first ionization yields H3XeO−
6, which has a pK value of 4.29, still relatively acidic. The twice deprotonated species H2XeO2−
6 has a pK value of 10.81.[8] Due to its rapid decomposition under acidic conditions as described above, however, it is most commonly encountered as perxenate salts, bearing the anion XeO4−
6.[6][2]
Perxenic acid and the anion XeO4−
6 are both strong oxidizing agents,[9] capable of oxidising silver(I) to silver(III), copper(II) to copper(III),[10] and Mn2+ to MnO−
4.[11] The perxenate anion is unstable in acidic solutions,[10] being almost instantaneously reduced to HXeO−
4.[1]
The sodium, potassium, and barium salts are soluble.[12] Barium perxenate solution is used as the starting material for the synthesis of xenon tetroxide (XeO4) by mixing it with concentrated sulfuric acid:[13]
- Ba2XeO6 (s) + 2 H2SO4 (aq) → H4XeO6 (aq) + 2 BaSO4 (s)
Most metal perxenates are stable, except silver perxenate, which decomposes violently.[10]
Sodium perxenate, Na4XeO6, can be used for the analytic separation of trace amounts of americium from curium. The separation involves the oxidation of Am3+ to Am4+ by sodium perxenate in acidic solution in the presence of La3+, followed by treatment with calcium fluoride, which forms insoluble fluorides with Cm3+ and La3+, but retains Am4+ and Pu4+ in solution as soluble fluorides.[9]
- ^ a b Cotton (2007). Advanced Inorganic Chemistry (6th ed.). Wiley-India. p. 593. ISBN 81-265-1338-1.
- ^ a b Egon Wiberg; Nils Wiberg; Arnold Frederick Holleman (2001). Inorganic chemistry. Academic Press. p. 400. ISBN 0-12-352651-5.
- ^ Jeffrey L. Peterson; Howard H. Claassen; Evan H. Appelman (March 1970). "Vibrational spectra and structures of xenate(VI) and perxenate(VIII) ions in aqueous solution". Inorganic Chemistry 9 (3): 619–621. DOI:10.1021/ic50085a037. edit
- ^ a b Hamilton; Ibers, J.; Mackenzie, D. (Aug 1963). "Geometry of the Perxenate Ion". Science 141 (3580): 532–534. Bibcode 1963Sci...141..532H. DOI:10.1126/science.141.3580.532. ISSN 0036-8075. PMID 17738629. edit
- ^ a b Charlie Harding; David Arthur Johnson; Rob Janes (2002). Elements of the p block (volume 9 of Molecular world). Royal Society of Chemistry. p. 93. ISBN 0-85404-690-9.
- ^ a b c Ulrik K. Klaening; E. H. Appelman (October 1988). "Protolytic properties of perxenic acid". Inorganic Chemistry 27 (21): 3760–3762. DOI:10.1021/ic00294a018. edit
- ^ Arnold F. Holleman; Egon Wiberg (2001). Nils Wiberg. ed. Inorganic chemistry. translated by Mary Eagleson, William Brewer. Academic Press. p. 400. ISBN 0-12-352651-5.
- ^ John H. Holloway; Eric G. Hope (1998). A. G. Sykes. ed. Advances in Inorganic Chemistry. 46. Academic Press. p. 67. ISBN 0-12-023646-X.
- ^ a b Holcomb, H. P. (March 1965). "Analytical Oxidation of Americium with Sodium Perxenate". Analytical Chemistry 37 (3): 415. DOI:10.1021/ac60222a002. edit
- ^ a b c Allen J. Bard; Roger Parsons; Joseph Jordan; International Union of Pure and Applied Chemistry (1985). Standard Potentials in Aqueous Solution. CRC Press. p. 778. ISBN 0-8247-7291-1.
- ^ Linus Pauling (1988). General chemistry (3rd ed.). Courier Dover Publications. p. 251. ISBN 0-486-65622-5.
- ^ Thomas Scott; Mary Eagleson (1994). Concise encyclopedia chemistry. Walter de Gruyter. p. 1183. ISBN 3-11-011451-8.
- ^ Charlie Harding; David Arthur Johnson; Rob Janes (2002). Elements of the p block. Great Britain: Royal Society of Chemistry. pp. 92–93. ISBN 0-85404-690-9.
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| Xenon(0) |
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| Xenon(I) |
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| Xenon(II) |
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- XeC6F5F
- XeC6F5C2F3
- XeC6F5CF3
- Xe(C6F5)2
- XeC6F5C6H2F3
- XeC6F5CN
- Xe(CF3)2
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| Xenon(IV) |
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| Xenon(VI) |
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| Xenon(VIII) |
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| Helium compounds |
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| Neon compounds |
- No neon compounds have yet been identified.
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| Argon compounds |
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| Krypton compounds |
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| Xenon compounds |
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Xenon(0)
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Xenon(I)
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Xenon(II)
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Xenon(IV)
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Xenon(VI)
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Xenon(VIII)
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| Radon compounds |
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