Biomimetic [2Fe-2S] clusters with extensively delocalized mixed-valence iron centers.

Abstract A complete series of biomimetic [2Fe-2S] clusters, [(L(Dep) Fe)2 (μ-S)2 ] (3, L(Dep) =CH[CMeN(2,6-Et2 C6 H3 )]2 ), [(L(Dep) Fe)2 (μ-S)2 K] (4), [(L(Dep) Fe)2 (μ-S)2 ][Bu4 N] (5, Bu=n-butyl), and [(L(Dep) Fe)2 (μ-S)2 K2 ] (6), could be synthesized and characterized. The all-ferric [2Fe-2S] cluster 3 is readily accessible through the reaction of [(L(Dep) Fe)2 (μ-H)2 ] (2) with elemental sulfur. The chemical reduction of 3 with one molar equivalent of elemental potassium affords the contact ion pair K(+) [2Fe-2S](-) (4) as a one-dimensional coordination polymer, which in turn reacts with [Bu4 N]Cl to afford the separate ion pair [Bu4 N](+) [2Fe-2S](-) (5). Further reduction of 4 with potassium furnishes the super-reduced all-ferrous [2Fe-2S] cluster 6. Remarkably, complexes 4 and 5 are [2Fe-2S] clusters with extensively delocalized Fe(2+) Fe(3+) pairs as evidenced by (57) Fe Mossbauer, X-ray absorption and emission spectroscopy (XAS, XES) and in accordance with DFT calculations.