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Dinuclear and trinuclear ruthenium complexes, [Ru(trop)(Ctrop)Ru(dppe)Cp] [2b; trop = tropolonato, Ctrop = ethynyltropolonato, dppe = 1,2-bis(diphenylphosphino)ethane] and [Ru(trop){(Ctrop)Ru(dppe)Cp}] (3), were synthesized, and their electronic and electrochemical properties were investigated in comparison with our previously reported complex [Ru(acac)(Ctrop)Ru(dppe)Cp] (2a). The electron-donating Ru(dppe)Cp unit and electron-accepting RuO unit are connected by Ctrop in these complexes. 2a incorporates acetylacetonate as an ancillary ligand, while 2b and 3 incorporate tropolonate as an ancillary ligand. Every complex, 2a, 2b, and 3, exhibits similar UV-vis-near-IR (NIR) absorption spectra, demonstrating the lack of explicit intramolecular electronic communication between the units at least in the neutral state. The weak NIR absorption in 2a further diminished upon electrochemical oxidation, indicating almost no electronic communication between the units. In contrast, 2b and 3 exhibit broad NIR absorptions upon oxidation. Additionally, 3 exhibits four stepwise redox couples in the electrochemical study, which are formally attributed to [Ru(trop)]/[Ru(trop)], two [Ru(dppe)Cp]/[Ru(dppe)Cp], and [Ru(trop)]/[Ru(trop)] couples. Clear separation of the redox couples attributed to the two terminal [Ru(dppe)Cp] units demonstrates the thermodynamic stability of the intermediate oxidation states with respect to disproportionation. Further electrochemical studies using an electrolyte including perfluorinated weakly coordinating anions and density functional theory/time-dependent density functional theory calculations confirmed the effect of ancillary ligands, acetylacetonate and tropolonate. In the case of 2a, electronic delocalization over the whole complex, especially over the [Ru(acac)(trop)] unit, appears to be small. In contrast, the electronic communication between [Ru(dppe)Cp] and [Ru(trop)] units in 3 seems to be enhanced upon oxidation, resulting in the long-range intramolecular electronic communication.

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