Chemistry:Pervanadyl
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Short description: Chemical compound
Identifiers | |
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3D model (JSmol)
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Properties | |
O2V+ | |
Molar mass | 82.939 g·mol−1 |
Related compounds | |
Related compounds
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Vanadyl |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
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]
- V
2O
5 + 2 H+
→ 2 VO+
2 + H
2O (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]
See also
- Vanadate, vanadium(V) oxyanions
References
- ↑ 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.
- ↑ 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
Original source: https://en.wikipedia.org/wiki/Pervanadyl.
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