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Deprotonation of short-living radical cations of pyrrolylbenzenes*

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Chemistry of Heterocyclic Compounds Aims and scope

The deprotonation reaction of radical cations of 1-(2-pyrrolyl)-4-(1-vinyl-2-pyrrolyl)benzene has been studied by nanosecond laser photolysis. Bimolecular rate constants have been determined for the transfer of proton to the heterocyclic base. Analysis of the yields has been carried out of the final products of the radical-cation reaction of 1-(2-pyrrolyl)-4-(1-vinyl-2-pyrrolyl)benzene in the presence and absence of bases. Comparison of the results of impulse and stationary photolysis showed that inhibition of the radical cation reaction occurs at the stage of forming the radical cations.

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Authors and Affiliations

  1. A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, 664033, Russia

    I. K. Petrushenko, K. B. Petrushenko, V. I. Smirnov, E. Yu. Shmidt & A. I. Mikhaleva

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  1. I. K. Petrushenko
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  2. K. B. Petrushenko
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  3. V. I. Smirnov
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  4. E. Yu. Shmidt
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  5. A. I. Mikhaleva
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Correspondence to K. B. Petrushenko.

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*Dedicated to Academician B. A. Trofimov on his 70th jubilee.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 705-710, May, 2009.

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Petrushenko, I.K., Petrushenko, K.B., Smirnov, V.I. et al. Deprotonation of short-living radical cations of pyrrolylbenzenes*. Chem Heterocycl Comp 45, 554–559 (2009). https://doi.org/10.1007/s10593-009-0299-2

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  • DOI: https://doi.org/10.1007/s10593-009-0299-2

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