| Abstract |
The vanadium(IV) N-hydroxyiminodicarboxylate complexes [V(HIDPA)(2)](2-) and [V(HIDA)(2)](2-), close models of the amavadin (a natural product from Amanita fungi lacking the V=O group but exhibiting a rare NO-bound oxyiminate moiety), are shown to be the first recognized complexes of the early transition metals (up to periodic Group 7) that mediate the oxidation of water. The reactions were analyzed by visible spectrophotometry, mass spectrometry, and measurement of evolved dioxygen using Ce4+ as sacrificial oxidant. A mechanism proposed on the basis of DFT calculations involves the reversible oxidation to the mononuclear V-V-\O(N) over dot <\ center, where the redox active oxyimino group plays a key role and metal oxidation state variation is only one unit. The more similar model of the metallobiomolecule, [V(HIDPA)(2)](2-), displays a lower oxidation rate than [V(HIDA)(2)](2-) but does not undergo appreciable degradation, in contrast to the latter. |
