Tautomerism of azo dyes in the solid state studied by 15N, 14N, 13C and 1H NMR spectroscopy, X-ray diffraction and quantum-chemical calculations

0523565 - ÚOCHB 2021 RIV GB eng J - Článek v odborném periodiku
Bártová, Kateřina - Císařová, I. - Lyčka, A. - Dračínský, Martin
Tautomerism of azo dyes in the solid state studied by 15N, 14N, 13C and 1H NMR spectroscopy, X-ray diffraction and quantum-chemical calculations.
Dyes and Pigments. Roč. 178, Jul (2020), č. článku 108342. ISSN 0143-7208. E-ISSN 1873-3743
Grant CEP: GA ČR(CZ) GA20-01472S
Institucionální podpora: RVO:61388963
Klíčová slova: azo dyes * tautomerism * NMR spectroscopy * quantum chemistry
Obor OECD: Physical chemistry
Impakt faktor: 4.889, rok: 2020
Způsob publikování: Omezený přístup
https://www.sciencedirect.com/science/article/pii/S0143720820304575?via%3Dihub

The azo–hydrazo tautomerism of four model azo dyes in the solid state is investigated by multinuclear solid-state nuclear magnetic resonance (SS-NMR) spectroscopy, X-ray diffraction and quantum-chemical calculations. The measurement of 15N SS-NMR spectra is the most straightforward way to determine the tautomeric state of solid azo compounds. Unfortunately, the sensitivity of these nuclei for SS-NMR is very low and the acquisition of 15N spectra in a reasonable time may be challenging. It is demonstrated that a natural abundance of almost 100% of another nitrogen isotope, 14N, can be exploited for the investigation of the tautomerism. Indirect detection of 14N nuclei via protons is an elegant approach for the rapid and unequivocal determination of the tautomeric form. Furthermore, a comparison of experimental carbon SS-NMR chemical shifts with those obtained in solution or by quantum-chemical computations can be used for the same purpose.
Trvalý link: http://hdl.handle.net/11104/0307910