Reversible Carboxylate Shift in a µ-Oxo Diferric Complex in Solution by Acid-/Base-Addition.

ABSTRACT

A reversible carboxylate shift has been observed in a µ-oxo diferric complex in solution by UV-vis-NIR and FTIR spectroscopy triggered by the addition of a base or an acid. A terminal acetate decoordinates upon the addition of a proton, resulting in a shift of the remaining terminal acetato to a µ-η1η1 bridge. The addition of a base restores the original structure containing only terminal acetates. The implications for metalloenzymes with carboxylate-bridged nonheme diiron active sites are discussed.