Metal-Ligand Exchange Coupling Alters the Open-Shell Ligand Electronic Structure in a Bis(semiquinone) Complex
Abstract
The electronic structure of the bis(dioxolene) bridging ligand -SQ(2) Th-2 - is responsive to metal-ligand magnetic exchange coupling. Comparison of the crystal structure of (NiSQ)(2) Th-2 to that of (ZnSQ)(2) Th-2 indicates an open-shell biradical ground state for the dinuclear Ni(II) complex compared to the closed-shell quinoidal character found in the dinuclear Zn(II) complex. Consistent with a comparison of bond lengths obtained by X-ray diffraction, the analysis of the variable-temperature magnetic susceptibility data for crystalline (NiSQ)(2) Th-2 yields reduced SQ-SQ radical-radical magnetic exchange coupling (J(SQ-SQ) = -203 cm(-1)) compared to that of (ZnSQ)(2) Th-2 (J(SQ-SQ) = -321 cm(-1)). The reduced SQ-SQ exchange coupling in (NiSQ)(2) Th-2 derives from an attenuation of the SQ spin densities, which in turn is derived from the Ni-SQ antiferromagnetic exchange interactions. This reduction in SQ-SQ exchange that we observe for (NiSQ)(2) Th-2 correlates with an effective lengthening of the bridge unit by similar to 2.1 angstrom relative to that of (ZnSQ)(2) Th-2 . This magnitude of the effective increase in the bridge distance is consistent with the (NiSQ)(2) Th-2 J(SQ-SQ) value lying between those of (ZnSQ)(2) Th-2 and (ZnSQ)(2) Th-3 . The ability to modulate spin populations on an organic radical via pairwise Ni-SQ magnetic exchange interactions is a general way to affect electronic coupling in the Th-Th bridge. Our results suggest that metal-radical exchange coupling represents a powerful mechanism for tuning organic molecular electronic structure, with important implications for molecular electronics and molecular electron transport.
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