Pervanadyl
Appearance
Identifiers | |
---|---|
3D model (JSmol)
|
|
| |
| |
Properties | |
O2V+ | |
Molar mass | 82.939 g·mol−1 |
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 (VO+2) is a pale yellow[1] oxycation of vanadium(V). It is the predominant vanadium(V) species in acidic solutions with pH between 0 and 2, and its salts are formed by protonation of vanadium(V) oxide in such solutions:[2][3]
- V2O5 + 2 H+ → 2 VO+2 + H2O (K = 3.42×10−2)
The ion can form a complex with a single aminopolycarboxylate ligand,[4] or with tridentate Schiff base ligands.[5]
The VO+2/VO2+ redox couple is used at the cathode of the vanadium redox battery.[6] The standard reduction potential of this couple is +1.00 V.[7]
![](http://178.128.105.246/content-http-upload.wikimedia.org/wikipedia/commons/thumb/f/f2/Vanadium_oxidation_states.jpg/300px-Vanadium_oxidation_states.jpg)
See also
[edit]- Vanadate, vanadium(V) oxyanions
References
[edit]- ^ 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.
- ^ Bard, Allen J. (1985). Standard potentials in aqueous solution (1st ed.). New York: CRC Press. ISBN 9781351414746.
- ^ 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.
- ^ 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.
- ^ Pal, Satyanarayan; Pal, Samudranil (2000). "A dimeric pervanadyl (VO2+) complex with a tridentate Schiff base ligand". Journal of Chemical Crystallography. 30 (5): 329–333. doi:10.1023/A:1009561224540. S2CID 91300997.
- ^ 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.
- ^ 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