{{short description|Polyatomic ion in chemistry}} {{distinguish||text=the pervanadyl ion, with the formula {{chem|VO|2|+}}}} [[File:Vo(acac)2.png|thumb|right|Structure of vanadyl acetylacetonate]] [[Image:Cavansite.jpg|thumb|right|Cavansite, a mineral containing the vanadyl cation that illustrates its characteristic color]] The '''vanadyl ion''' is an oxovanadium cation, either VO<sup>2+</sup> (called ''oxovanadium(IV)'')<ref name="Bertrand">{{cite journal|last1=Bertrand|first1=Gary L.|last2=Stapleton|first2=George W.|last3=Wulff|first3=Clause A.|last4=Hepler|first4=Loren G.|title=Thermochemistry of Aqueous Pervanadyl and Vanadyl Ions|journal=Inorg. Chem.|date=July 1966|volume=5|issue=7|pages=1283–1284|doi=10.1021/ic50041a048}}</ref> or VO<sup>3+</sup> (called ''oxovanadium(V)''). They are functional groups that are common in the coordination chemistry of vanadium.
Complexes containing oxovanadium(IV) are characteristically blue or purple<ref>{{cite journal|last1=Bellhausen|first1=C.J.|last2=Gray|first2=Harry B.|title=The Electronic Structure of the Vanadyl Ion|journal=Inorganic Chemistry|volume=1|issue=1|year=1962|pages=111-122|doi=10.1021/ic50001a022}}</ref> and paramagnetic.<ref>{{cite journal|last1=Smith|first1=Thomas S. II|last2=LoBrutto|first2=Russell|last3=Pecoraro|first3=Vincent L.|title=Paramagnetic spectroscopy of vanadyl compounds and its applications to biological systems|journal=Coordination Chemistry Reviews|volume=228|issue=1|year=2002|pages=1-18|doi=10.1016/S0010-8545(01)00437-4|url=https://www1.udel.edu/chem/polenova/VHPO/Vanayl_complexes_Paramagn_spectr_CoordChemRev2002.pdf|access-date=12 November 2025|via=University of Delaware}}</ref> A triple bond is proposed to exist between the V<sup>4+</sup> and O<sup>2−</sup> centers.<ref>{{cite journal|author1=Gray, H. B. |author2=Winkler, J. R. |title=Living with Oxygen|journal=Accounts of Chemical Research|year=2018|volume=51|issue=8|pages=1850–1857|doi=10.1021/acs.accounts.8b00245|pmid=30016077|pmc=6106048}}</ref> The description of the bonding in the vanadyl ion was central to the development of modern ligand-field theory.<ref>{{Cite journal|last=Ballhausen|first=C. J.|last2=Gray|first2=Harry B.|date=1962-02-01|title=The Electronic Structure of the Vanadyl Ion|url=https://doi.org/10.1021/ic50001a022|journal=Inorganic Chemistry|volume=1|issue=1|pages=111–122|doi=10.1021/ic50001a022|issn=0020-1669|url-access=subscription}}</ref>
==Natural occurrence== ===Minerals=== Cavansite and pentagonite are vanadyl-containing minerals.{{citation needed|date=November 2025}}
===Water=== VO<sup>2+</sup>, often in an ionic pairing with sodium (NaH<sub>2</sub>VO<sub>4</sub>), is the second most abundant transition metal in seawater, with its concentration only being exceeded by molybdenum.<ref name=Dieter>{{cite book|last1=Rehder|first1=Dieter|title=Bioinorganic Vanadium Chemistry|date=2008|publisher=John Wiley & Sons, Ltd|location=Hamburg, Germany|isbn=9780470065099|pages=5 & 9–10|edition=1st|doi=10.1002/9780470994429|series=Inorganic Chemistry}}</ref> In the ocean the average concentration is 30 nM. Some mineral water springs also contain the ion in high concentrations. For example, springs near Mount Fuji often contain as much as 54 μg per liter.<ref name=Dieter />
==Vanadyl-containing compounds == === Oxovanadium(IV) === * vanadyl acetylacetonate, VO(acac)<sub>2</sub> * vanadyl sulfate, VOSO<sub>4</sub> * vanadyl acetate, VO(CH<sub>3</sub>COO)<sub>2</sub>
=== Oxovanadium(V) === * vanadyl isopropoxide, VO(O-iPr)<sub>3</sub> (iPr denotes isopropyl) * vanadyl nitrate, VO(NO<sub>3</sub>)<sub>3</sub><ref>{{cite journal|last1=Varetti|first1=E.L.|last2=Brandán|first2=S.A.|last3=Ben Altabef|first3=A.|title=Vibrational and electronic spectra of vanadyl nitrate, VO(NO<sub>3</sub>)<sub>3</sub>|journal=Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy|date=April 1995|volume=51|issue=4|pages=669–675|doi=10.1016/0584-8539(94)00154-4|bibcode=1995AcSpA..51..669B}}</ref> * vanadyl perchlorate, {{chem2|VO(ClO4)3}} * vanadyl fluoride, {{chem2|VOF3}} * vanadyl chloride, {{chem2|VOCl3}}
==Related species== * pervanadyl ion, {{chem|VO|2|+}},<ref name="Bertrand" /><ref>{{cite journal|last1=Satyanarayan|first1=Pal|last2=Kasiraman|first2=Rinku Radhika|title=Mononuclear Pervanadyl ({{chem|VO|2|+}}) Complexes with Tridentate Schiff Bases: Self-assembling via C–H…oxo and π-π Interactions|journal=Zeitschrift für Anorganische und Allgemeine Chemie|date=July 2001|volume=627|issue=7|pages=1631–1637|doi=10.1002/1521-3749(200107)627:7<1631::AID-ZAAC1631>3.0.CO;2-H}}</ref> also known as the dioxovanadium(V) ion * metavanadate ion, {{chem|[VO|3|]|''n''|''n''−}} * orthovanadate ion, {{chem|VO|4|3−}} * thiovanadyl ion, VS<sup>2+</sup> * titanyl ion, TiO<sup>2+</sup> * niobyl ion, NbO<sup>2+</sup> * tantalyl ion, TaO<sup>2+</sup>
==References== {{Reflist}}
== General references == {{Commonscat|Vanadyl ion}} * {{Greenwood&Earnshaw}}
{{Vanadium compounds}}
Category:Oxycations Category:Vanadyl compounds