Fractional dependence of the free energy of activation on the driving force of charge transfer in the quenching of the excited states of substituted phenanthroline homoleptic ruthenium(ii) complexes in aqueous medium.

The photophysical characteristics of some homoleptic ruthenium(ii) phenanthroline derivatives are investigated in aqueous medium. The lifetimes of the excited MLCT state of the studied complexes were found to be very sensitive to the type of the substituents on the phenanthroline ligand and were found to increase from about 0.96 μs in case of the parent [Ru(Phen)] complex to 2.97 μs in case of [Ru(DPPhen)]. The transient absorption spectra of the current set of complexes were studied also in aqueous medium. Quenching of the excited MLCT states of the studied complexes by molecular oxygen were studied and quenching rate constants were found to be in the range 1.02-4.83 × 10 M s. Values of singlet oxygen quantum yields were found to be in the range 0.01 to 0.25, and the corresponding efficiencies of singlet oxygen thereby produced, , were in the range 0.03-0.52. The mechanism by which the excited MLCT state is quenched by oxygen is discussed in light of the spin statistical factor rate constants and the competition between charge transfer and non-charge transfer quenching pathways. The partial charge transfer parameters, , were obtained and found to be about 0.88 for all complexes except for complexes with values lower than 0.25. The correlation of the activation free energies Δ of the exciplexes formation with the driving force for charge transfer, Δ , gives a charge transfer character of the exciplexes of about 35.0%.