Estimation of Excited-State Geometries of Benzene and Fluorobenzene through Vibronic Analyses of Absorption Spectra

Abstract

The parameters used in theoretical modeling of vibrational patterns within Franck–Condon (FC) approximation can be adjusted to match the vibrationally well-resolved experimental absorption spectrum of molecules. These simulation parameters can then be used to reveal the structural changes occurring between the initial and final states assuming the harmonic oscillator approximation holds for both states. Such a theoretical approach has been applied to benzene and fluorobenzene to disclose the first excited-state geometries of both compounds. The carbon–carbon bond length of benzene in the 1B2u state has been calculated as 1.430 Å, which is in very good agreement with the experimental bond length of 1.432 Å. The FC spectral fit method has been exploited to reveal the 1B2 state of fluorobenzene as well. Commonly employed density functional theory (DFT) and time-dependent DFT methods have been used to calculate the ground- and excited-state geometries of both compounds, respectively. The comparison of geometrical parameters and vibrational frequencies at the relevant states shows that frequently used hybrid functionals perform quite well in the ground state, whereas their performances drop considerably while predicting the excited-state properties. Among the hybrid functionals studied, TD-B3LYP with 6-31+G(d) basis set can be chosen to calculate the excited-state properties of molecules, albeit with much less anticipation of accuracy from the performance that B3LYP usually shows at the ground state.