Regioselectivity of the coupling between radicals and ambident nucleophiles. A theoretical study.

BAUMGARTNER, M. T.; BLANCO, G. A.; PIERINI, A. B.

NEW JOURNAL OF CHEMISTRY

Royal Society of Chemistry

Año: 2008 vol. 32 p. 464 - 471

1144-0546

We here report a theoretical study on the reaction of the anions of phenol, 2-naphthol, the pyrimidine bases (uracil, thymine, cytosine), pyrrole, imidazole and benzimidazole with phenyl and 4-nitrobenzyl radicals with the aim of interpreting the factors that control the regiochemical outcome of these reactions; their main features being C–C bond formation with phenyl radicals and C–heteroatom bond formation with 4-nitrobenzyl radicals. The preferred coupling positions were investigated by evaluation of the frontier molecular orbital theory (FMO) indexes and the potential energy surfaces both at the AM1 and DFT/B3LYP levels. Within the latter methodology, the solvent effect was considered under a continuum model. While FMO predicts the experimental regioselectivity of phenyl radicals with good accuracy, it fails in the nitrobenzyl case. On the other hand, studies of transition state stabilities provide a good prediction of the observed regioselectivity for both types of radicals, mainly when the solvent is taken into account. Trabajo enviado julio 2007; aceptado octubre 2007; publicado en la web noviembre 2007. DOI: 10.1039/b710998a. Publicado en papel en New J. Chem., 2008, 32, 464–471