Structure and Optical Properties of New 2-<i>N</i>-Phenylamino-methyl-nitro-pyridine Isomers.

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 theoreti

SUBMITTER: Godlewska P 

PROVIDER: S-EPMC11989132 | biostudies-literature | 2025 Mar

REPOSITORIES: biostudies-literature