Photocatalytic generation of hydrogen from water is an integral part of the next generation clean fuel technologies. The conversion of solar energy into useful chemical energy is of great interest in contemporary investigations. The splitting of water is a multi-electron process involving the breaking and making of chemical bonds which requires multi-component photocatalytic systems. Supramolecular complexes [{(TL)₂Ru(BL)}₂RhX₂](Y)₅ (where TL = terminal ligand, BL = bridging ligand, X = Cl⁻ or Br⁻, and Y = PF₆ ⁻ or Br⁻) have been synthesized and studied for their light absorbing, electrochemical and photocatalytic properties. The supramolecular complexes in this investigation are multi-component systems comprised of two ruthenium based light absorbers connected through bridging ligands to a central rhodium, which acts as an electron collecting center upon excitation. These complexes absorb light throughout the ultraviolet and visible regions of the solar spectrum. The supramolecular complexes possess ruthenium based highest occupied molecular orbitals (HOMO) and a rhodium based lowest unoccupied molecular orbital (LUMO). These molecular devices have been investigated and shown to function as photoinitiated electron collectors at the reactive rhodium metal center, and explored as photocatalysts to generate hydrogen from water in an aqueous solution in the presence of an electron donor.

Many Ru and Os systems display photoactive ³MLCT states. Systems activated by therapeutic window light in the absence of O₂ remain elusive. [(bpy)₂Os(dpp)RhCl₂(phen)]³⁺ photobinds and photocleaves DNA under red light in an oxygen independent manner, due to molecular design involving one Os chromophore coupled to a photoactive cis-Rh^IIICl₂ moiety.