Photophysics of Nitro-Substituted Unnatural Nucleic Acid Base

Abstract

The unnatural nucleic acid base (uNAB), 6-amino-3methyl-5-nitropyridin-2(1H)one, often referred to as Z can form a base pair with the uNAB 2-aminoimidazo[1,2-a]-1,3,5-triazin-4(8H)-one (referred to as P) and is analogous to a guanine−cytosine (G-C) pair. However, it is well-known that the nonradiative decay pathway of the P-Z pair is significantly different from that of the G-C pair (Cui et al., Front. Chem. 2020, 8, 605117−605125). In this work, we study the excited state processes in Z using state-of-the-art multireference methods and dynamical techniques to ascertain the predominant nonradiative channels. We find that unlike in the natural NABs, the excited state processes in Z are driven primarily by the −NO 2 group rotation. The electron-withdrawing effect of the −NO 2 substituent plays a crucial role. We further ascertained that ultrafast deactivation channels are possible in Z and identified the stationary point geometries that are responsible for these channels.