S K-edge XAS of CuII, CuI, and ZnII oxidized Dithiolene complexes: Covalent contributions to structure and the Jahn-Teller effect

Reduced dithiolene ligands are bound to high valent Mo centers in the active site of the oxotransferase family of enzymes. Related model complexes have been studied with great insight by Prof. Holm and his colleagues. This study focuses on the other limit of dithiolene chemistry: an investigation of the 2-electron oxidized dithiolene bound to low-valent late transition metal (TM) ions (Zn-II, Cu-I, and Cu-II). The bonding descriptions of the oxidized dithiolene [N,N-dimethyl piperazine 2,3-dithione (Me(2)Dt(0))] complexes are probed using S K-edge X-ray absorption spectroscopy (XAS) and the results are correlated to density functional theory (DFT) calculations. These experimentally supported calculations are then extended to explain the different geometric structures of the three complexes. The Zn-II(Me(2)Dt(0))(2) complex has only ligand-ligand repulsion so it is stabilized at the D-2d symmetry limit. The Cu-I(Me(2)Dt(0))(2) complex has additional weak backbonding thus distorts somewhat from D-2d toward D-2h symmetry. The Cu-II(Me(2)Dt(0))(2) complex has a strong sigma donor bond that leads to both a large Jahn-Teller stabilization to D-2h and an additional covalent contribution to the geometry. The combined strong stabilization results in the square planar, D-2h structure. This study quantifies the competition between the ligand-ligand repulsion and the change in electronic structures in determining the final geometric structures of the oxidized dithiolene complexes, and provides quantitative insights into the Jahn-Teller stabilization energy and its origin.

Automated summary

This study investigates the bonding descriptions and geometric structures of oxidized dithiolene complexes bound to low-valent late transition metal ions, such as Zn-II, Cu-I, and Cu-II, using a combination of S K-edge X-ray absorption spectroscopy and density functional theory calculations. The study quantifies the competition between ligand-ligand repulsion and changes in electronic structures in determining the final geometric structures of the complexes.