TIME-DEPENDENT DENSITY FUNCTIONAL THEORY STUDY ON DYNAMICS OF HYDROGEN BONDING IN EXCITED STATES OF TRANS-ACETANILIDE IN METHANOL SOLVENT

The hydrogen-bonding dynamics in both singlet and triplet excited states of the trans-acetanilide (AA) in methanol (MeOH) solvent was investigated using the time-dependent density functional theory (TDDFT) method. Geometric optimizations of the hydrogen-bonded AA-MeOH complexes considered here as well as the isolated AA and MeOH molecules were performed using density functional theory (DFT) method. At the same time, the TDDFT method was performed to calculate the electronic transition energies and corresponding oscillation strengths of all the compounds in the low-lying electronically excited states. In this study, only the intermolecular hydrogen bonds C=O center dot center dot center dot H-O and N-H center dot center dot center dot O-H can be formed. A theoretical forecast that changes of hydrogen bonds in the low-lying electronic excited states was proposed. We discussed not only ground-state geometric structures and electronic excitation energies but also frontier molecular orbitals and electron density transition. The intermolecular hydrogen bonds between AA and MeOH molecules play an important role in the geometric structures and electronic excitation energies. Zhao et al. have put forward the relationship between the electronic spectra and hydrogen bonding dynamics for the first time. According to Zhao's rule, a redshift of the relevant electronic spectra will appear if hydrogen bond is strengthened, while the hydrogen bond weakening can make an electronic spectra shift to blue.