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Consumption of H(2)S from Our Daily Diet: Determination by a Simple Chemosensing Method
[Image: see text] A unique method has been developed for comparative analysis of H(2)S produced from food samples from our daily diet, both qualitatively and quantitatively. The selective detection of H(2)S has been executed by introducing a simple chemodosimeter (PN-N(3)) that gives response on the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173501/ https://www.ncbi.nlm.nih.gov/pubmed/30320267 http://dx.doi.org/10.1021/acsomega.8b01751 |
Sumario: | [Image: see text] A unique method has been developed for comparative analysis of H(2)S produced from food samples from our daily diet, both qualitatively and quantitatively. The selective detection of H(2)S has been executed by introducing a simple chemodosimeter (PN-N(3)) that gives response on the basis of intramolecular charge transfer. UV–vis, fluorimetric, and NMR titrations were performed to demonstrate the sensing mechanism and electronic environment of PN-N(3) in the presence of H(2)S. Density functional theory calculations were performed to validate the mechanism of azide (PN-N(3)) reduction to amine (PN-NH(2)) by the strong reducing power of H(2)S. The potentiality of this chemosensing method is that it could be treated as a simple, less-time-consuming, and cost-effective method for determining H(2)S in biological samples in the nanomolar range. |
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