[FeFe] Hydrogenase active site model chemistry in a UiO-66 metal–organic framework

Abstract

The reactivity of [Fe₂(dcbdt)(CO)₆] (1) confined in a UiO-66(Zr) metal–organic framework towards CO ligand substitutions with phosphines of different sizes was investigated. The reaction with smaller phosphines (PX₃, X = Me, Et) is more selective compared to analogous reactions in homogenous solution phase, and two CO ligands at up to 80% of all [FeFe] sites in UiO-66–1 are replaced. The produced [Fe₂(dcbdt)(CO)₄(PX₃)₂] complexes in the UiO-66 matrix behave like typical [FeFe] hydrogenase active site model complexes, are reduced at more cathodic potentials than their hexacarbonyl analogues, and form bridging hydrides under acidic conditions.