Crystal structure, spectroscopic, and theoretical studies of 2-methylamino-6-methyl-4 nitropyridine N-oxide

The structure and electronic spectra of 2-methylamino-6-methyl-4-nitropyridine N-oxide (2M6M) were investigated. The X-ray structure of 2M6M molecule shows that it crystallizes in the monoclinic system of the P2(1)/n space group and forms internally hydrogen-bonded [N-H center dot center dot center dot O = 2.563(3) angstrom] monomers linked by the same type of intermolecular [2.799(3) angstrom] hydrogen bonds in linear oligomers. Due to weak intermolecular C-H... 0 interactions such oligomers are arranged along the z-axis into a helical-shaped zigzag. The results of quantum chemical DFF/B3LYP/6-31G(d,p) calculations reproduce the absorption spectrum of 2M6M well. The 2M6M molecule shows complex photophysical and photochemical behavior. It exhibits dual fluorescence (with emission maxima at 476 and 536 nm) and decays bi-exponentially (with lifetimes of 2.13 and 0.1 ns). The temperature dependence of the fluorescence intensity in the two bands has a slope of 1450 cm(-1) in the temperature ranges of 200-300 K. These effects are interpreted in terms of excited state intramolecular proton transfer (ESIPT) and creation of tautomeric form of 2M6M. Below 200 K we see the appearance of an emission which can be attributed to a dimeric form. (C) 2008 Elsevier B.V. All rights reserved.