DEPROTONATION OF SHORT-LIVING RADICAL CATIONS OF PYRROLYLBENZENES

Authors

  • И. К. Петрушенко A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033
  • К. Б. Петрушенко A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033
  • В. И. Смирнов A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033
  • Е. Ю. Шмидт A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033
  • А. И. Михалева A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033

DOI:

https://doi.org/10.1007/6721

Keywords:

1-(2-pyrrolyl)-4-(1-vinyl-2-pyrrolyl)benzene, radical-cation, deprotonation, nanosecond laser photolysis

Abstract

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.

How to Cite
Petrushenko, I. K.; Petrushenko, K. B.; Smirnov, V. I.; Shmidt, E. Yu.; Mikhaleva, A. I.  Chem. Heterocycl. Compd. 2009, 45, 554. [Khim. Geterotsikl. Soedin. 2009, 705.]

For this article in the English edition see DOI 10.1007/s10593-009-0299-2

 

Published

2022-04-13

Issue

Section

Original Papers