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Irradiation of tris(2,2′-bipyridyl)ruthenium(II) in aqueous solution containing a sacrificial electron acceptor results in formation of bipy3Ru3+, a powerful oxidant which is able, in the presence of a redox catalyst, to oxidise water to O2. Both colloidal RuO2 and simple cobalt(II) ions are effective catalysts for O2 production and, with [Co(NH3)5Cl]2+ as sacrificial electron acceptor, the quantum efficiency for formation of O2 was ca. 12 %. However, when the sacrificial electron acceptor was replaced with Fe3+, which is a reversible redox couple, no O2 was observed upon prolonged irradiation. The absence of O2 in this latter system can be explained by kinetic considerations.
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Harriman et al. (1981) studied this question.
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