Pervanadyl

Last updated
Pervanadyl
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
1172
  • InChI=1S/2O.V/q;;+1
    Key: UAZIGFGVBWJXOL-UHFFFAOYSA-N
  • O=[V+]=O
Properties
VO+2
Related compounds
Related compounds
 Vanadyl
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Pervanadyl is jargon that has two meanings.

The former are formed by protonation of vanadium(V) oxide in such solutions: [4] [5]

V2O5 + 2 H+ → 2 VO+2 + H2O ( K  = 3.42×10−2)

The ion can form a complex with a single aminopolycarboxylate ligand, [6] or with tridentate Schiff base ligands. [7]

The VO+2/VO2+ redox couple is used at the cathode of the vanadium redox battery. [8] The standard reduction potential of this couple is +1.00 V. [9]

From left to right: VO+2, VO, V, and V in aqueous solution. Vanadium oxidation states.jpg
From left to right: VO+2, VO , V, and V in aqueous solution.

See also

References

  1. ↑ Kustin, Kenneth; Macara, Ian G. (November 1982). "The New Biochemistry of Vanadium". Comments on Inorganic Chemistry. 2 (1–2): 1–22. doi:10.1080/02603598208078107.
  2. ↑ Nucci, L.; Guidelli, R.; Raspi, G. (1973). "Electrochemical behavior of mixtures of pervanadyl ion and hydrogen peroxide in 1M perchloric acid on mercury and platinized platinum". Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases. 69: 82–93. doi:10.1039/f19736900082.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ↑ Campbell, N.J.; Capparelli, M.V.; Griffith, W.P.; Skapski, A.C. (1983). "On the existence of triperoxo vanadium complexes. X-ray crystal structures of K3[VO(O2)2(C2O4]· H2O2 and of (NH4)[VO(O2)2(bipy)·4H2O". Inorganica Chimica Acta. 77: L215 –L216. doi:10.1016/S0020-1693(00)82620-1.
  4. ↑ Bard, Allen J. (1985). Standard potentials in aqueous solution (1st ed.). New York: CRC Press. ISBN   9781351414746.
  5. ↑ LaSalle, M. J.; Cobble, James W. (June 1955). "The Entropy and Structure of the Pervanadyl Ion". The Journal of Physical Chemistry. 59 (6): 519–524. doi:10.1021/j150528a010.
  6. ↑ Yamada, Shinkichi.; Ukei, Yuko.; Tanaka, Motoharu. (April 1976). "Kinetics and mechanism of the complexation reactions of pervanadyl ion with some aminopolycarboxylates". Inorganic Chemistry. 15 (4): 964–967. doi:10.1021/ic50158a048.
  7. ↑ Pal, Satyanarayan; Pal, Samudranil (2000). "A dimeric pervanadyl (VO2+) complex with a tridentate Schiff base ligand". Journal of Chemical Crystallography. 30 (5): 329–333. Bibcode:2000JCCry..30..329P. doi:10.1023/A:1009561224540. S2CID   91300997.
  8. ↑ Jin, Jutao; Fu, Xiaogang; Liu, Qiao; Liu, Yanru; Wei, Zhiyang; Niu, Kexing; Zhang, Junyan (25 June 2013). "Identifying the Active Site in Nitrogen-Doped Graphene for the VO 2+ /VO 2 + Redox Reaction". ACS Nano. 7 (6): 4764–4773. doi:10.1021/nn3046709. PMID   23647240.
  9. ↑ Cotton, F. Albert; Wilkinson, Geoffrey; Murillo, Carlos A.; Bochmann, Manfred (1999), Advanced Inorganic Chemistry (6th ed.), New York: Wiley-Interscience, ISBN   0-471-19957-5
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