# Structure and Optical Properties of New 2-N-Phenylamino-methyl-nitro-pyridine Isomers

## TL;DR

This paper reports the synthesis and analysis of two new isomers of a pyridine compound, revealing how their structure affects optical properties and potential applications.

## Contribution

The novel contribution is the synthesis and detailed characterization of new isomers with distinct methyl positions and their impact on photophysical behavior.

## Key findings

- X-ray diffraction and spectroscopic methods confirmed the structures of the new isomers.
- Methyl substituent positioning modulates structural architecture and optical properties.
- Excitation experiments revealed energy dissipation mechanisms in electronically excited states.

## Abstract

Two new 2-N-phenylamino-(4 or 6)-methyl-3-nitropyridine derivatives were synthesized. Their structures were characterized on the basis of X-ray diffraction, IR, and Raman spectra as well as electron UV-Vis and emission spectra measurements. The experimental results were analyzed in terms of theoretical data in which the quantum chemical DFT and NBO calculations were applied. To elucidate the relaxation pathways of electronically excited states, multiple excitation wavelengths were employed to probe energy dissipation mechanisms in the studied compounds. A systematic analysis was conducted to evaluate how variations in methyl substituent positioning modulate both the structural architecture and photophysical behavior of the isomeric systems. The spectroscopic, structural and theoretical considerations allow us to propose the potential technological applications derived from the unique properties of these isomers.