Singlet oxygen quenching by oxygen in tetraphenyl-porphyrin solutions

Time-resolved measurement of singlet oxygen infrared phosphorescence is a powerful tool for determination of quantum yields and kinetics of its photosensitization. This technique was employed to investigate in detail the previously observed effect of singlet oxygen quenching by oxygen. The question whether the singlet oxygen is quenched by oxygen in ground or in excited state was addressed by study of two complementary dependencies of singlet oxygen lifetimes: on dissolved oxygen concentration and on excitation intensity. Oxygen concentration dependence study of meso-tetra(4-sulphonato)phenylpor-phyrin (TPPS4) phosphorescence kinetics showed linearity of the dependence of TPPS4 triplet state rate-constant. Corresponding bimolecular quenching constant of (1.5 +/- 0.1) x 10(9)1/mols was obtained. On the other hand, rate constants of singlet oxygen depopulation exhibit nonlinear dependence on oxygen concentration. Comparison of zero oxygen concentration-extrapolated value of singlet oxygen lifetime of (6.5 +/- 0.4) mu s to (3.7 +/- 0.1)mu s observed under air-saturated conditions indicates importance of the effect of quenching of singlet oxygen by oxygen. Upward-sloping dependencies of singlet oxygen depopulation rate-constant on excitation intensity evidence that singlet oxygen is predominantly quenched by oxygen in excited singlet state. (c) 2006 Elsevier B.V. All rights reserved.