Electronic excitation spectra of doublet anion radicals of cyanobenzene and nitrobenzene derivatives: SAC-CI theoretical studies

Abstract

Electronic ground and excited states of anion radicals of cyanobenzene derivatives: 1,3,5-tricyanobenzene, 1,2,4,5-tetracyanobenzene, and tetracyanoquinodimethane (TCNQ) and nitrobenzene derivatives: nitrobenzene, p-nitroaniline, m-nitroaniline, and o-nitroaniline were theoretically investigated by the symmetry adapted cluster-configuration interaction (SAC-CI) method, which is able to produce accurate theoretical electronic excitation spectra even for radical doublet states. For all the target molecules, the present calculations reproduced the positive electron affinities, which were mostly in good agreement with the experimental values, and their features, especially for TCNQ, were characterised by singly occupied molecular orbitals as well as the number of the electron-withdrawing terminal groups. The excitation energies and their oscillator strengths by the SAC-CI method were also in good agreement with the corresponding experimental UV/VIS/NIR spectra observed by one of the authors and other experimental evidences. Except for TCNQ, the present theoretical calculations were successful to first predict the existences of the forbidden (or very low intense) pure valence excited states in near-infrared region. The physical natures of the observed intense spectral bands were clarified and some new assignments to their electronic states were provided. By extending the present work, photo-related molecular designs of new functional electron acceptors may be challenged.