No abstract

Geometry and vibrational modes of the anthranilic acid molecule in the S(0) and S(1) states were computed using ab initio methods: Hartree-Fock (HF) and configuration interaction of singly excited configurations (CIS) as well as the density functional theory with time-dependent perturbation (TD-DFT). The intensity distribution in the laser-induced fluorescence excitation spectra was modeled in two ways: using displacement parameters for independent modes and using multidimensional Franck-Condon integrals. The change in the molecular geometry upon excitation was calculated from the band intensities within the above two models. Displacement parameters of eight in-plane modes active in the excitation spectrum were optimized to reproduce the experimental intensities of about 40 most intensive and well-separated vibrational bands, while displacement parameters of other in-plane modes were kept frozen at the values resulting from the quantum chemical calculations. The intramolecular hydrogen bond is significantly stronger in the S(1) state than in the ground state. Additionally, bond lengths and angles in the aromatic ring, within the substituents and between the ring and the substituents undergo significant changes and they induce the presence of strong fundamentals in the excitation spectrum.

P and perturber states were described in terms of a set of deperturbed molecular constants, spin-orbit and L-uncoupling interaction parameters, equilibrium constants, 309 term values, as well as isotopologue-independent spin-orbit and rotationelectronic perturbation parameters.