Conclusions
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1.
The rate constants of quenching of the triplet state of benzanthrone and phenazine by substituted N,Ndimethylanilines, anilines, and phenols in n-heptane and CH3CN were determined by the method of flash photolysis.
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2.
The capacity of quenching agents to deactivate the triplet state in heptane at the same ionization potential increases as the acidity increases in the order N,N-dimethylanilines > anilines > phenols.
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3.
Total electron transfer is the most probable mechanism of quenching by N,N-dimethylanilines. Quenching by anilines and phenols is due to intercombination conversion in an exciplex with charge transfer and hydrogen bonding.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2009–2014, September, 1982.
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Kuz'min, V.A., Renge, I.V. & Borisevich, Y.E. Flash photolysis study of quenching of triplet states of aromatic compounds by electron donors. Russ Chem Bull 31, 1774–1778 (1982). https://doi.org/10.1007/BF00952374
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DOI: https://doi.org/10.1007/BF00952374