Insight into the mechanism of an iron dioxygenase by resolution of steps following the FeIV=HO species.

Iron oxygenases generate elusive transient oxygen species to catalyze substrate oxygenation in a wide range of metabolic processes. Here we resolve the reaction sequence and structures of such intermediates for the archetypal non-heme Fe(II) and alpha-ketoglutarate-dependent dioxygenase TauD. Time-resolved Raman spectra of the initial species with (16)O(18)O oxygen unequivocally establish the Fe(IV) horizontal lineO structure.

Electron transfer reactions of peroxydisulfate and fluoroxysulfate reactions with the cyanide complexes M(CN)n4- (M=Fe(II), Ru(II), Os(II), Mo(IV), and W(IV)).

The stoichiometry and the kinetics of oxidation of the cyanide complexes M(CN)n4- (M = Fe(II), Ru(II), Os(II), Mo(IV), and W(IV)) by the peroxydisulfate ion, S2O8(2-), and by the much more strongly oxidizing fluoroxysulfate ion, SO4F-, were studied in aqueous solutions containing Li+. Reactions of S2O8(2-) with M(CN)n4- are known to be strongly catalyzed by Li+ and other alkali metal ions, and this applies also to the corresponding reactions of SO4F-. The primary reactions of S2O8(2-) and SO4F- have both been found to be one-electron processes in which the equally strong O-O and O-F bonds are broken.

The intrinsic stability of the second intermediate following the dioxygen-bound form in the O2 reduction by cytochrome c oxidase.

Aeration of a two-electron reduced cytochrome c oxidase provides a species with two Raman bands at 804 and 356 cm(-1), identifying it as the second intermediate following the O2-bound species in the enzymatic O2 reduction process. It degrades directly to the fully oxidized form with a half-life time of 70 min at pH 8.0.