Optical Intramolecular Electron Transfer in Opposite Directions through the Same Bridge That Follows Different...

The electrochemical and spectroscopic properties of eight bis(tridentate) cyclometalated Ru^II compounds covalently linked by a phenyl- or xylyl-thiophene bridge to a pendant triphenylamine (TPA) were characterized in fluid solution and immobilized on metal oxide surfaces. Upon surface immobilization, the TPA^+/0 reduction potentials of the phenyl-bridged compounds exhibited large changes, ±100 mV, relative to solution-based values, yet those observed for the xylyl-bridged compounds were relatively unchanged. The highest occupied molecular orbital of the surface-immobilized compounds was associated with either TPA or Ru^II, enabling the study of the electron transfer in opposite directions. Electron transfer in the mixed-valent states of the compounds was found to proceed by different optical pathways for Ru^II → TPA⁺ relative to TPA → Ru^III. Mulliken-Hush analysis of intervalence charge transfer bands for the phenyl-bridged compounds revealed that the electronic coupling matrix element, H_DA, was ∼950 cm^-1 for Ru^II → TPA⁺, while H_DA for TPA → Ru^III appeared to be 2500 cm^-1. In contrast, the xylyl-bridged compounds were weakly coupled. A superexchange analysis, where unoccupied bridge orbitals were taken directly into account, led to a very different conclusion: H_DA did not depend on the charge-transfer direction or path. The results imply that the electron-transfer direction can alter optical charge transfer pathways without influencing the electronic coupling.