Perxenate
Template:Short description In chemistry, perxenates are salts of the yellow<ref name="cotton1" /> xenon-containing anion Template:Chem.<ref name="wiberg">Template:Holleman&Wiberg</ref> This anion has octahedral molecular geometry, as determined by Raman spectroscopy, having O–Xe–O bond angles varying between 87° and 93°.<ref>Template:Cite journal</ref> The Xe–O bond length was determined by X-ray crystallography to be 1.875 Å.<ref name="hamilton1963">Template:Cite journal</ref>
SynthesisEdit
Perxenates are synthesized by the disproportionation of xenon trioxide when dissolved in strong alkali:<ref name="harding2002">Template:Cite book</ref>
- 2 XeO3 (Template:Abbr) + 4 OH− (Template:Abbr) → Xe (Template:Abbr) + Template:Chem (Template:Abbr) + O2 (Template:Abbr) + 2 H2O (Template:Abbr)
When Ba(OH)2 is used as the alkali, barium perxenate can be crystallized from the resulting solution.<ref name="harding2002"/>
Perxenic acidEdit
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:<ref name="klaening">Template:Cite journal</ref><ref>Template:Holleman&Wiberg</ref>
Its extrapolated formula, H4XeO6, is inferred from the octahedral geometry of the perxenate ion (Template:Chem) in its alkali metal salts.<ref name="klaening"/><ref name="hamilton1963"/>
The pKa of aqueous perxenic acid has been indirectly calculated to be below 0, making it an extremely strong acid. Its first ionization yields the anion Template:Chem, which has a pKa value of 4.29, still relatively acidic. The twice deprotonated species Template:Chem has a pKa value of 10.81.<ref>Template:Cite book</ref> Due to its rapid decomposition under acidic conditions as described above, however, it is most commonly known as perxenate salts, bearing the anion Template:Chem.<ref name="klaening" /><ref name="wiberg" />
PropertiesEdit
Perxenic acid and the anion Template:Chem are both strong oxidizing agents,<ref name="holcomb">Template:Cite journal</ref> capable of oxidising silver(I), copper (II) and manganese(II) to (respectively) silver(III), copper(III),<ref name="bard1" /> and permanganate.<ref>Template:Cite book</ref> The perxenate anion is unstable in acidic solutions,<ref name="bard1" /> being almost instantaneously reduced to Template:Chem.<ref name="cotton1">Template:Cotton&Wilkinson6th</ref>
The sodium, potassium, and barium salts are soluble.<ref>Template:Cite book</ref> Barium perxenate solution is used as the starting material for the synthesis of xenon tetroxide (XeO4) by mixing it with concentrated sulfuric acid:<ref>Template:Cite book</ref>
- Ba2XeO6 (s) + 2 H2SO4 (l) → XeO4 (g) + 2 BaSO4 (s) + 2 H2O (l)
Most metal perxenates are stable, except silver perxenate, which decomposes violently.<ref name="bard1">Template:Cite book</ref>
ApplicationsEdit
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.<ref name="holcomb"/>