water lies below pyridine and cyanide ligand in the spectrochemical series. At fixed metal and dioxolene charges, replacement by water decreases and favours the high-spin limits: Co(II) remains ; Co(III) can become if the splitting falls below the pairing threshold. Replacement by cyanide increases and favours Co(III), , and Co(II), . The two unchanged semiquinonate ligands would then give the Co(II) form a combined independent-spin moment of . The ranking predicts the direction of the change; two substituted donors alone do not guarantee a Co(III) spin crossover, since all six donors determine its splitting. A shift of the valence-tautomer equilibrium is also possible and is separate from this fixed-charge comparison.
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