Abstract
Luminescence of singlet oxygen dimols (1O2)2 was studied in aerobic solutions of a nonfluorescent photosensitizer phenalenone in CCl4 and C6F6 using a setup with a mechanical phosphoroscope and relatively low rates of photosensitizer excitation. The luminescence spectrum was found to resemble those reported in our previous papers dealing with dimol luminescence in solutions of porphyrins and other organic dyes. The main maximum was located at 703–706 nm, and two much weaker bands at 640 and 770–780 nm. These data suggest that dimol luminescence arises owing to interaction of two 1O2 molecules and one ground-state pigment molecule. Light is emitted by the dimol-pigment contact complexes, which are formed as a result of 1O2 collisions with metastable, probably triplet, intermediates appearing in 1O2 reaction with pigment molecules. It is proposed that this mechanism of dimol luminescence might be of general importance for photochemical, chemical, and biological systems where singlet oxygen is generated. However, the luminescence of this type dominates at relatively low rates of 1O2 generation. According to the literature data, at high 1O2 generation rates the prevalent type of dimol luminescence has the main maximum at 635–637 nm and is caused by direct collisions of two 1O2 molecules.
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Abbreviations
- DBPQ:
-
2,3,7,8-dibenzopyrene-1,6-quinone
- Pd-TPP:
-
Pd tetraphenylporphyrin
- Pn:
-
phenalenone
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Original Russian Text © A.A. Krasnovsky, K.V. Neverov, 2010, published in Biofizika, 2010, Vol. 55, No. 3, pp. 389–393.
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Krasnovsky, A.A., Neverov, K.V. On the mechanism of photosensitized luminescence of singlet oxygen dimols in air-saturated pigment solutions. BIOPHYSICS 55, 349–352 (2010). https://doi.org/10.1134/S0006350910030012
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DOI: https://doi.org/10.1134/S0006350910030012