Conclusions
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1.
Using the methods of laser photolysis and CIDNP the mechanism of the photoreduction of 2,6-diphenyl-1,4-benzoquinone by diphenylamine has been established and the kinetics and spectral characteristics of the short-lived intermediate products formed during the photo-reduction process have been determined.
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2.
Quenching of triplet 2,6-diphenyl-1,4-benzoquinone by diphenylamine occurs by an electron and H-atom transfer mechanism, both processes taking place in an encounter complex and being concurrent with one another.
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3.
The nature of the short-lived intermediate products formed during quenching of the triplet 2,6-diphenyl-1,4-benzoquinone by aromatic amines in a weakly polar medium has been established. When quenching with diphenylamine a nondissociated ion-radical pair is formed, but with triphenylamine a triplet exciplex is formed.
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4.
The predominant role of the triplet mechanism in giving rise to CIDNP in ion-radical reactions which occur in weakly polar media has been confirmed.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2744–2750, December, 1980.
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Levin, P.P., Darmanyan, A.P., Kuz'min, V.A. et al. Investigation of the mechanism of electron and hydrogen-atom transfer during quenching of the triplet state of 2,6-diphenyl-1,4-benzoquinone by aromatic amines using the methods of laser photolysis and CIDNP. Russ Chem Bull 29, 1919–1924 (1980). https://doi.org/10.1007/BF00949657
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DOI: https://doi.org/10.1007/BF00949657