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Synthesis, X-ray and spectroscopic analysis of 2-chloro-4-(methoxymethyl)-6-methyl-5- nitropyridine-3-carbonitrile (CROSBI ID 162603)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Jukić, Marijana ; Cetina, Mario ; Halambek, Jasna ; Ugarković, Ivana Synthesis, X-ray and spectroscopic analysis of 2-chloro-4-(methoxymethyl)-6-methyl-5- nitropyridine-3-carbonitrile // Journal of molecular structure, 979 (2010), 1/3; 108-114. doi: 10.1016/j.molstruc.2010.06.012

Podaci o odgovornosti

Jukić, Marijana ; Cetina, Mario ; Halambek, Jasna ; Ugarković, Ivana

engleski

Synthesis, X-ray and spectroscopic analysis of 2-chloro-4-(methoxymethyl)-6-methyl-5- nitropyridine-3-carbonitrile

Compound 2-chloro-4-(methoxymethyl)-6-methyl-5-nitropyridine-3-carbonitrile (2) has been obtained from 4-(methoxymethyl)-6-methyl-5-nitro-2-oxo-1, 2-dihydropyridine-3-carbonitrile (1) by novel protocol using Vilsmeier-Haack chlorination and its solid state structure was analyzed using Xray analysis. Structural features have been also studied by IR, NMR and electronic spectroscopy, and the optical properties were investigated by UV-vis absorption and fluorescence spectroscopy. Compound 2 crystallizes with two independent molecules in the asymmetric unit with almost identical geometric parameters. One C-H...O hydrogen bond self-assembles one type of independent molecule into chains, while second type is linked by one weak aromatic pi...pi stacking interaction. The absorption and fluorescence maximum of compound 2 were observed at 290 nm and 480 nm, respectively. The effects of solvents were investigated and interpreted on the emission spectra in protic and aprotic solvents in the range 200-600 nm.

substituted pyridine; X-ray diffraction; IR; NMR and UV-vis spectroscopy

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Podaci o izdanju

979 (1/3)

2010.

108-114

objavljeno

0022-2860

10.1016/j.molstruc.2010.06.012

Povezanost rada

Kemija, Biotehnologija

Poveznice
Indeksiranost