The ionization potentials of 55 para- and 55 meta-disubstituted benzenes, consisting of all binary combinations of electron-withdrawing groups (-NO2, -CF3, -CHO, -COOH) and electron-donating groups (-Cl, -CH3, -OH, -OCH3, -NH2, and -N(CH3)2) have been calculated using density functional theory with the B3LYP functional and a 6-31G(d) basis set. Relative ionization potentials (ΔIP), referred to benzene, are compared with experimental values and shown to be in good agreement. The disubstituted data were correlated with monosubstituted ΔIP data and shown to require quadratic terms in order to achieve a good fit; the validity of this conclusion was possible due to the low scatter in the calculated data. A simple MO analysis gives a semiquantitative interpretation of the observed trends in substitutent effects, including a discussion of combinations of substituents for which nonadditivity should be expected.

Additional Metadata
Persistent URL dx.doi.org/10.1021/jo991833e
Journal Journal of Organic Chemistry
Citation
DiLabio, G.A. (Gino A.), Pratt, D.A. (Derek A.), & Wright, J.S. (2000). Theoretical calculation of ionization potentials for disubstituted benzenes: Additivity vs non-additivity of substituent effects. Journal of Organic Chemistry, 65(7), 2195–2203. doi:10.1021/jo991833e