A DFT/TD-DFT study of effect of different substituent on ESIPT fluorescence features of 2-(2′-hydroxyphenyl)-4-chloromethylthiazole derivatives

Abstract

Based on density functional theory (DFT) and time-dependent density functional theory (TD-DFT), the effects of substituent on the excited-state intramolecular proton transfer (ESIPT) process and photophysical properties of 2-(2′-hydroxyphenyl)-4-chloromethylthiazole (HCT) are studied. The electron-donating group (CH3, OH) and electron-withdrawing group (CF3, CHO) are introduced to analyze the changes of intramolecular H-bond, the frontier molecular orbitals, the absorption/fluorescence spectra, and the energy barrier of ESIPT process. The calculation results indicate that electron-donating group strengthens the intramolecular H-bond in the S1 state, and leads to an easier ESIPT process. The electron-withdrawing group weakens the corresponding H-bond and makes ESIPT process a little harder. Different substituents also affect the photophysical properties of HCT. The electron-withdrawing group (CF3, CHO) has a little effect on electronic spectra. The electron-donating group (CH3, OH) red-shifts both the absorption and fluorescence emission peaks of HCT, respectively, which causes the Stokes shift to increase.