The (bpy) 2 Ru II and (phen) 2 Ru II moieties were linked to [Ni(OBTTAP)] 1, periphery through coordinate bonds in order to synthesize cationic di-and pentanuclear complexes 2-5 that were obtained as PF 6 -salts. They were characterized by IR, 1 H NMR, UV-vis, and mass spectral data. The electronic absorption, emission and redox data of these bichromophoric systems indicate the presence of a high degree of intercomponent electronic interaction. The position and relative intensities of the Soret and Q bands in these complexes is altered due to peripheral binding of the metal units. The compounds were non-emissive for the Q band excitation but, Soret excitation led to a strong S 2 emission, observed between 400-450 nm. In cyclic voltammetry, the compounds exhibited one Ru centered oxidation together with one or two OBTTAP centered oxidations. The Ru II /Ru III oxidations were observed at significantly lower potentials as compared to the corresponding simple maleonitrilebenzylthioether complexes and has been interpretted in terms of weaker dπ(S)−dπ(Ru) interactions.