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Flash photolysis study of quenching of triplet states of aromatic compounds by electron donors

  • Physical Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 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.

  2. 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.

  3. 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

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