Tetranuclear Fe Clusters with a Varied Interstitial Ligand: Effects on the Structure, Redox Properties, and Nitric Oxide Activation

A new series of tetranuclear Fe clusters displaying an interstitial μ4-F ligand was prepared for a comparison to previously reported μ4-O analogues. With a single nitric oxide (NO) coordinated as a reporter of small-molecule activation, the μ4-F clusters were characterized in five redox states, from FeII 3{FeNO}8 to FeIII 3{FeNO}7, with NO stretching frequencies ranging from 1680 to 1855 cm–1, respectively. Despite accessing more reduced states with an F– bridge, a two-electron reduction of the distal Fe centers is necessary for the μ4-F clusters to activate NO to the same degree as the μ4-O system; consequently, NO reactivity is observed at more positive potentials with μ4-O than μ4-F. Moreover, the μ4-O ligand better translates redox changes of remote metal centers to diatomic ligand activation. The implication for biological active sites is that the higher-charge bridging ligand is more effective in tuning cluster properties, including the involvement of remote metal centers, for small-molecule activation.