Oxidation states of the first transition series

The positive oxidation states of scandium to zinc, with their d-electron counts, how common they are and a representative species.

33 rows
Sc\ce{Sc}30most stableScX2OX3\ce{Sc2O3}scandium oxide (white)
Ti\ce{Ti}22rareTiO\ce{TiO}titanium monoxide (black)
Ti\ce{Ti}31common[Ti(HX2O)X6]X3+\ce{[Ti(H2O)6]^3+}hexaaquatitanium(III) (violet)
Ti\ce{Ti}40most stableTiOX2\ce{TiO2}titanium dioxide (white pigment)
V\ce{V}23common[V(HX2O)X6]X2+\ce{[V(H2O)6]^2+}vanadium(II) (violet, strong reductant)
V\ce{V}32commonVX3+\ce{V^3+}vanadium(III) (green)
V\ce{V}41most stableVOX2+\ce{VO^2+}vanadyl, oxovanadium(IV) (blue)
V\ce{V}50commonVOX2X+\ce{VO2+}dioxovanadium(V) (yellow); V₂O₅ catalyses the contact process
Cr\ce{Cr}24common[Cr(HX2O)X6]X2+\ce{[Cr(H2O)6]^2+}chromium(II) (sky blue, easily oxidised)
Cr\ce{Cr}33most stable[Cr(HX2O)X6]X3+\ce{[Cr(H2O)6]^3+}chromium(III); Cr₂O₃ is a green pigment
Cr\ce{Cr}42rareCrOX2\ce{CrO2}chromium dioxide (magnetic tape)
Cr\ce{Cr}51rareCrOX4X3−\ce{CrO4^3-}chromate(V) (a few compounds only)
Cr\ce{Cr}60commonCrX2OX7X2−\ce{Cr2O7^2-}dichromate (orange, strong oxidant)
Mn\ce{Mn}25most stable[Mn(HX2O)X6]X2+\ce{[Mn(H2O)6]^2+}manganese(II) (very pale pink)
Mn\ce{Mn}34commonMnX2OX3\ce{Mn2O3}manganese(III) oxide; Mn³⁺ disproportionates in water
Mn\ce{Mn}43commonMnOX2\ce{MnO2}manganese dioxide (black-brown; battery cathodes)
Mn\ce{Mn}52rareMnOX4X3−\ce{MnO4^3-}manganate(V) (blue, very unstable)
Mn\ce{Mn}61commonMnOX4X2−\ce{MnO4^2-}manganate(VI) (green, stable only in base)
Mn\ce{Mn}70commonMnOX4X−\ce{MnO4-}permanganate (purple, strong oxidant)
Fe\ce{Fe}26common[Fe(HX2O)X6]X2+\ce{[Fe(H2O)6]^2+}iron(II) (pale green, oxidised by air)
Fe\ce{Fe}35most stableFeX3+\ce{Fe^3+}iron(III); rust is Fe₂O₃·xH₂O
Fe\ce{Fe}44rare[FeO]X2+\ce{[FeO]^2+}ferryl species (enzyme intermediates)
Fe\ce{Fe}62rareFeOX4X2−\ce{FeO4^2-}ferrate(VI) (red-purple, very strong oxidant)
Co\ce{Co}27most stable[Co(HX2O)X6]X2+\ce{[Co(H2O)6]^2+}cobalt(II) (pink)
Co\ce{Co}36common[Co(NHX3)X6]X3+\ce{[Co(NH3)6]^3+}cobalt(III), stable in complexes (orange-yellow)
Co\ce{Co}45rareCoOX2\ce{CoO2}partly Co(IV) in a charged LiCoO₂ battery cathode
Ni\ce{Ni}28most stable[Ni(HX2O)X6]X2+\ce{[Ni(H2O)6]^2+}nickel(II) (green)
Ni\ce{Ni}37rareNiO(OH)\ce{NiO(OH)}nickel oxyhydroxide (NiMH battery electrode)
Ni\ce{Ni}46rareNiOX2\ce{NiO2}a few compounds only
Cu\ce{Cu}110commonCuX2O\ce{Cu2O}copper(I) oxide (red); Cu⁺ disproportionates in water
Cu\ce{Cu}29most stable[Cu(HX2O)X6]X2+\ce{[Cu(H2O)6]^2+}copper(II) (light blue)
Cu\ce{Cu}38rare[CuFX6]X3−\ce{[CuF6]^3-}a few compounds only
Zn\ce{Zn}210most stable[Zn(HX2O)X6]X2+\ce{[Zn(H2O)6]^2+}zinc ion (colourless)

Only positive states are listed; 0 and negative states occur in carbonyls and similar complexes. “Most stable” means the state most often met in water with air present. d count = group number − oxidation state.

Sources

  1. N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann (1997), ch. 21–29.
  2. C. E. Housecroft, A. G. Sharpe, Inorganic Chemistry, 5th ed., Pearson (2018), ch. 21.

Used in these lessons