The goal of this study was to investigate how the electron-donating capability around the lower valent metal ion and the electron-accepting capability of the higher valent metal ion influence metal to metal charge transfer (MMCT) properties in mixed-valence complexes. A series of trinuclear ruthenium complexes represented as [Ru(ap-4-Me)(CHCOO)NCRuCpMe(dppe)][PF] (CpMe = polymethylcyclopentadienyl, = 0, 1, and 5; and dppe = 1, 2-bis(diphenylphosphino)ethane, ap-4-Me = 2-anilino-4-methylpyridine) and their one-electron oxidized products were synthesized and fully characterized. The UV-vis-NIR spectra confirmed that as the electron donor character of the CpMe(dppe)RuCN fragment enhanced or the electron-accepting capability of the higher valent diruthenium cluster increased, the Ru → RuV2 or RuVI2 Ru MMCT bands shifted to lower energies, which was supported by TDDFT calculations.
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