Stable Mixed-Valent Complexes Formed by Electron Delocalization Across Hydrogen Bonds of Pyrimidinone-Linked Metal Clusters.

Abstract

Electron transfer across a mixed-valent hydrogen-bonded self-dimer of oxo-centered triruthenium clusters bridged by a pair of 4(3 H)-pyrimidinones is reported. Spectroelectrochemical studies in methylene chloride reveal that 1 rapidly self-dimerizes upon one-electron reduction, forming the strongly coupled mixed-valent hydrogen-bonded dimer (12)-. In the mixed-valent state, significantly broadened, partially coalesced ν(CO) bands are observed, allowing estimation of the electron transfer rate ( kET) by an optical Bloch line shape analysis. Simulation of the FTIR line shapes provides an estimate of kET on the order of 1011 s-1, indicating a highly delocalized electronic structure across the hydrogen bonds. These findings are supported by the determination of the formation constant ( KMV) for (12)-, which is found to be on the order of 106 M-1, or nearly 4 orders of magnitude higher than that for the neutral isovalent dimer (12). This represents a stabilization of approximately 5.7 kcal/mol (1980 cm-1) arising from electron exchange across the hydrogen bonds in the mixed-valent state. Significantly, an enormous intensity enhancement of the amide ν(NH) band (3300 cm-1) of (12)- is observed, supporting strong mixing of the bridging ligand vibrational modes with the electronic wave function of the mixed-valent state. These findings demonstrate strong donor-bridge-acceptor coupling and that highly delocalized electronic structures can be attained in hydrogen-bonded systems, which are often considered to be too weakly bound to support strong electronic communication.