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Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition

Chromatographic separation of several sets of aromatic position isomers on three cellulose- and one amylose-based chiral stationary phases was performed to evaluate the potential of a polysaccharide-based chiral stationary phase (CSP) in the separation of isomeric or closely similar molecules, and t...

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Detalles Bibliográficos
Autores principales: Shibata, Tohru, Shinkura, Satoshi, Ohnishi, Atsushi, Ueda, Kazuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155686/
https://www.ncbi.nlm.nih.gov/pubmed/28036038
http://dx.doi.org/10.3390/molecules22010038
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author Shibata, Tohru
Shinkura, Satoshi
Ohnishi, Atsushi
Ueda, Kazuyoshi
author_facet Shibata, Tohru
Shinkura, Satoshi
Ohnishi, Atsushi
Ueda, Kazuyoshi
author_sort Shibata, Tohru
collection PubMed
description Chromatographic separation of several sets of aromatic position isomers on three cellulose- and one amylose-based chiral stationary phases was performed to evaluate the potential of a polysaccharide-based chiral stationary phase (CSP) in the separation of isomeric or closely similar molecules, and to understand the interaction mechanism of this type of CSP with analytes. Their ability of molecular recognition was quite outstanding, but the selection rule was particular to each polysaccharide derivative. In the series of analytes, cellulose tris(4-methylbenzoate) and tris(3,5-dimethylphenylcarbamate) exhibited a contrasting selection rule, and the recognition mechanism was considered based on the computer-simulation of the former polymer.
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spelling pubmed-61556862018-11-13 Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition Shibata, Tohru Shinkura, Satoshi Ohnishi, Atsushi Ueda, Kazuyoshi Molecules Article Chromatographic separation of several sets of aromatic position isomers on three cellulose- and one amylose-based chiral stationary phases was performed to evaluate the potential of a polysaccharide-based chiral stationary phase (CSP) in the separation of isomeric or closely similar molecules, and to understand the interaction mechanism of this type of CSP with analytes. Their ability of molecular recognition was quite outstanding, but the selection rule was particular to each polysaccharide derivative. In the series of analytes, cellulose tris(4-methylbenzoate) and tris(3,5-dimethylphenylcarbamate) exhibited a contrasting selection rule, and the recognition mechanism was considered based on the computer-simulation of the former polymer. MDPI 2016-12-28 /pmc/articles/PMC6155686/ /pubmed/28036038 http://dx.doi.org/10.3390/molecules22010038 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shibata, Tohru
Shinkura, Satoshi
Ohnishi, Atsushi
Ueda, Kazuyoshi
Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title_full Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title_fullStr Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title_full_unstemmed Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title_short Achiral Molecular Recognition of Aromatic Position Isomers by Polysaccharide-Based CSPs in Relation to Chiral Recognition
title_sort achiral molecular recognition of aromatic position isomers by polysaccharide-based csps in relation to chiral recognition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155686/
https://www.ncbi.nlm.nih.gov/pubmed/28036038
http://dx.doi.org/10.3390/molecules22010038
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