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Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases
Amino acid ionic liquid-supported Schiff bases, derivatives of salicylaldehyde and various amino acids (l-threonine, l-valine, l-leucine, l-isoleucine and l-histidine) have been investigated by means of various spectroscopic techniques (NMR, UV-Vis, IR, MS) and deuterium isotope effects on (13)C-NMR...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269710/ https://www.ncbi.nlm.nih.gov/pubmed/23629755 http://dx.doi.org/10.3390/molecules18054986 |
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author | Ossowicz, Paula Janus, Ewa Schroeder, Grzegorz Rozwadowski, Zbigniew |
author_facet | Ossowicz, Paula Janus, Ewa Schroeder, Grzegorz Rozwadowski, Zbigniew |
author_sort | Ossowicz, Paula |
collection | PubMed |
description | Amino acid ionic liquid-supported Schiff bases, derivatives of salicylaldehyde and various amino acids (l-threonine, l-valine, l-leucine, l-isoleucine and l-histidine) have been investigated by means of various spectroscopic techniques (NMR, UV-Vis, IR, MS) and deuterium isotope effects on (13)C-NMR chemical shifts. The results have shown that in all studied amino acid ionic liquid-supported Schiff bases (except the l-histidine derivative) a proton transfer equilibrium exists and the presence of the COO(−) group stabilizes the proton transferred NH-form. |
format | Online Article Text |
id | pubmed-6269710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62697102018-12-14 Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases Ossowicz, Paula Janus, Ewa Schroeder, Grzegorz Rozwadowski, Zbigniew Molecules Article Amino acid ionic liquid-supported Schiff bases, derivatives of salicylaldehyde and various amino acids (l-threonine, l-valine, l-leucine, l-isoleucine and l-histidine) have been investigated by means of various spectroscopic techniques (NMR, UV-Vis, IR, MS) and deuterium isotope effects on (13)C-NMR chemical shifts. The results have shown that in all studied amino acid ionic liquid-supported Schiff bases (except the l-histidine derivative) a proton transfer equilibrium exists and the presence of the COO(−) group stabilizes the proton transferred NH-form. MDPI 2013-04-29 /pmc/articles/PMC6269710/ /pubmed/23629755 http://dx.doi.org/10.3390/molecules18054986 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ossowicz, Paula Janus, Ewa Schroeder, Grzegorz Rozwadowski, Zbigniew Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title | Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title_full | Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title_fullStr | Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title_full_unstemmed | Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title_short | Spectroscopic Studies of Amino Acid Ionic Liquid-Supported Schiff Bases |
title_sort | spectroscopic studies of amino acid ionic liquid-supported schiff bases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269710/ https://www.ncbi.nlm.nih.gov/pubmed/23629755 http://dx.doi.org/10.3390/molecules18054986 |
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