Ma Zhiru, Barich Dewey H, Solum Mark S, Pugmire Ronald J
Department of Chemistry and Chemical and Fuels Engineering, University of Utah, Salt Lake City, Utah 84112, USA.
J Agric Food Chem. 2004 Jan 28;52(2):215-21. doi: 10.1021/jf034807x.
Nitrogen-containing compounds are one important class of constituents in tobacco because of various pharmacological and biological properties. Three types of tobacco leaves (burley, bright, and oriental) were studied using solid-state (15)N NMR cross polarization with magic-angle spinning, dipolar dephasing and five pi replicated magic angle turning (FIREMAT) experiments. The results show that burley tobacco leaves contain significantly more pyridinic nitrogen than that of bright or oriental tobacco leaves. The principal values of (15)N chemical shift tensors of nitrogen functional groups were obtained from the FIREMAT data. Possible assignments of solid-state (15)N NMR resonances were made using nitrogen chemical shift tensors in some model compounds or isotropic chemical shift values from liquid NMR results. To the best of our knowledge, this is the first solid-state (15)N NMR study of tobacco plant material.
