Ferrate(VI)

Ferrate(VI)

Aromatic skeletal formula of ferrate
Solutions of ferrate (left) and permanganate (right)
Names
IUPAC name Ferrate(VI)
Systematic IUPAC name Tetraoxoironbis(olate)^[citation needed]
Other names [FeO4]^2-
Identifiers
3D model (JSmol)	Interactive image Interactive image
ChEBI	CHEBI:30992^Y
ChemSpider	21865127^Y
Gmelin Reference	2055
PubChem CID	25000034
InChI InChI=1S/Fe.4O/q;;;2*-1^Y Key: XGBDPAYTQGQHEW-UHFFFAOYSA-N^Y InChI=1/Fe.4O/q;;;2*-1/rFeO4/c2-1(3,4)5/q-2 Key: XGBDPAYTQGQHEW-WTZHFVRHAI
SMILES [O-][Fe]([O-])(=O)=O [O-][Fe](=O)(=O)[O-]
Properties
Chemical formula	[FeO4]^2-
Molar mass	119.843 g mol^−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is ^YN ?) Infobox references

Ferrate(VI) is the inorganic anion with the chemical formula [FeO₄]^2−. It is photosensitive, contributes a pale violet colour to compounds and solutions containing it and is one of the strongest water-stable oxidizing species known. Although it is classified as a weak base, concentrated solutions containing ferrate(VI) are corrosive and attack the skin and are only stable at high pH. It is similar to the somewhat more stable permanganate.

Nomenclature

See also: Ferrate

The term ferrate is normally used to mean ferrate(VI), although it can refer to other iron-containing anions, many of which are more commonly encountered than salts of [FeO₄]^2−. These include the highly reduced species disodium tetracarbonylferrate Na₂[Fe(CO)₄], K₂[Fe(CO)₄] and salts of the iron(III) complex tetrachloroferrate [FeCl₄]^− in 1-Butyl-3-methylimidazolium tetrachloroferrate. Although rarely studied, ferrate(V) [FeO₄]^3− and ferrate(IV) [FeO₄]^4− oxyanions of iron also exist. These too are called ferrates.[1]

Synthesis

Ferrate(VI) salts are formed by oxidizing iron in an aqueous medium with strong oxidizing agents under alkaline conditions, or in the solid state by heating a mixture of iron filings and powdered potassium nitrate.[2]

For example, ferrates are produced by heating iron(III) hydroxide with sodium hypochlorite in alkaline solution:[3]

2 Fe(OH)
₃ + 3 OCl^−
+ 4  OH^− → 2 [FeO
₄]^2−
+ 5 H₂O + 3 Cl^−

The anion is typically precipitated as the barium(II) salt, forming barium ferrate.[3]

Properties

Fe(VI) is a strong oxidizing agent over the entire pH range, with a reduction potential (Fe(VI)/Fe(III) couple) varying from +2.2 V to +0.7 V versus SHE in acidic and basic media respectively.

[FeO
₄]^2−
+ 8  H^+ + 3 e^− ⇌ Fe^3+
+ 4 H₂O; E₀ = +2.20 V (acidic medium)

[FeO
₄]^2−
+ 4 H₂O + 3 e^− ⇌ Fe(OH)
₃ + 5 OH^−
; E₀ = +0.72 V (basic medium)

Because of this, the ferrate(VI) anion is unstable at neutral[2] or acidic pH values, decomposing to iron(III):[3] The reduction goes through intermediate species in which iron has oxidation states +5 and +4.[4] These anions are even more reactive than ferrate(VI).[5] In alkaline conditions ferrates are more stable, lasting for about 8 to 9 hours at pH 8 or 9.[5]

Aqueous solutions of ferrates are pink when dilute, and deep red or purple at higher concentrations.[4][6] The ferrate ion is a stronger oxidizing agent than permanganate,[7] and oxidizes ammonia to molecular nitrogen.[8]

The ferrate(VI) ion has two unpaired electrons and is thus paramagnetic. It has a tetrahedral molecular geometry, isostructural with the chromate and permanganate ions.[4]

Applications

Ferrates are excellent disinfectants, and are capable of removing and destroying viruses.[9] They are also of interest as potential as an environmentally friendly water treatment chemical, as the byproduct of ferrate oxidation is the relatively benign iron(III).[10]

Sodium ferrate (Na₂FeO₄) is a useful reagent with good selectivity and is stable in aqueous solution of high pH, remaining soluble in an aqueous solution saturated with sodium hydroxide.^[citation needed]

See also

• High-valent iron
• Potassium ferrate
• Barium ferrate

References

1. Graham Hill; John Holman (2000). Chemistry in context (5th ed.). Nelson Thornes. p. 202. ISBN 0-17-448276-0.
2. R. K. Sharma (2007). Text Book Of Coordination Chemistry. Discovery Publishing House. pp. 124–125. ISBN 978-81-8356-223-2.
3. Gary Wulfsberg (1991). Principles of descriptive inorganic chemistry. University Science Books. pp. 142–143. ISBN 0-935702-66-0.
4. Egon Wiberg; Nils Wiberg; Arnold Frederick Holleman (2001). Inorganic chemistry. Academic Press. pp. 1457–1458. ISBN 0-12-352651-5.
5. Gary M. Brittenham (1994). Raymond J. Bergeron (ed.). The Development of Iron Chelators for Clinical Use. CRC Press. pp. 37–38. ISBN 0-8493-8679-9.
6. John Daintith, ed. (2004). Oxford dictionary of chemistry (5th ed.). Oxford University Press. p. 235. ISBN 0-19-860918-3.
7. Kenneth Malcolm Mackay; Rosemary Ann Mackay; W. Henderson (2002). Introduction to modern inorganic chemistry (6th ed.). CRC Press. pp. 334–335. ISBN 0-7487-6420-8.
8. Karlis Svanks (June 1976). "Oxidation of Ammonia in Water by Ferrates(VI) and (IV)" (PDF). Water Resources Center, Ohio State University. p. 3. Retrieved 2010-05-04.
9. Stanley E. Manahan (2005). Environmental chemistry (8th ed.). CRC Press. p. 234. ISBN 1-56670-633-5.
10. Sharma, Virender K.; Zboril, Radek; Varma, Rajender S. (2015). "Ferrates: Greener Oxidants with Multimodal Action in Water Treatment Technologies". Accounts of Chemical Research. 48 (2): 182–191. doi:10.1021/ar5004219. ISSN 0001-4842. PMID 25668700.