A theoretical study on the excited state behavior of a series of novel triazole pyrimidine group fluorophores: ESIPT or ICT

Abstract

Fluoropurine analogues are a kind of unnatural bases, which are widely used in chemistry, biological science, pharmacy and other fields. At the same time, fluoropurine analogues of aza-heterocycles play an important role in medicinals research and development. In this work, the excited state behavior of a group of newly developed fluoropurine analogues of aza-heterocycles, triazole pyrimidinyl fluorophores, was comprehensively studied. The reaction energy profiles indicate that excited state intramolecular proton transfer (ESIPT) is difficult to happen, which is further proved by fluorescent spectra results. This work proposed a new and reasonable fluorescence mechanism based on the original experiment, and found that the large Stokes shift of the triazole pyrimidine fluorophore is due to the intramolecular charge transfer (ICT) process of the excited state. Our new discovery is of great significance for the application of this group of fluorescent compounds in other fields and the regulation of fluorescence properties.