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Chiroptical Enhancement of Chiral Dicarboxylic Acids from Confinement in a Stereodynamic Supramolecular Cage
[Image: see text] The fundamental implications that chirality has in science and technology require continuous efforts for the development of fast, economic, and reliable quantitative methods for enantiopurity assessment. Among the different analytical approaches, chiroptical techniques in combinati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150167/ https://www.ncbi.nlm.nih.gov/pubmed/35472260 http://dx.doi.org/10.1021/acssensors.2c00038 |
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author | Begato, Federico Penasa, Roberto Licini, Giulia Zonta, Cristiano |
author_facet | Begato, Federico Penasa, Roberto Licini, Giulia Zonta, Cristiano |
author_sort | Begato, Federico |
collection | PubMed |
description | [Image: see text] The fundamental implications that chirality has in science and technology require continuous efforts for the development of fast, economic, and reliable quantitative methods for enantiopurity assessment. Among the different analytical approaches, chiroptical techniques in combination with supramolecular methodologies have shown promising results in terms of both costs and time analysis. In this article, a tris(2-pyridylmethyl)amines (TPMA)-based supramolecular cage is able to amplify the circular dichroism (CD) signal of a series of chiral dicarboxylic acids also in the presence of a complex mixture. This feature has been used to quantify tartaric acid in wines and to discriminate different matrixes using principal component analysis (PCA) of the raw CD data. |
format | Online Article Text |
id | pubmed-9150167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91501672022-05-31 Chiroptical Enhancement of Chiral Dicarboxylic Acids from Confinement in a Stereodynamic Supramolecular Cage Begato, Federico Penasa, Roberto Licini, Giulia Zonta, Cristiano ACS Sens [Image: see text] The fundamental implications that chirality has in science and technology require continuous efforts for the development of fast, economic, and reliable quantitative methods for enantiopurity assessment. Among the different analytical approaches, chiroptical techniques in combination with supramolecular methodologies have shown promising results in terms of both costs and time analysis. In this article, a tris(2-pyridylmethyl)amines (TPMA)-based supramolecular cage is able to amplify the circular dichroism (CD) signal of a series of chiral dicarboxylic acids also in the presence of a complex mixture. This feature has been used to quantify tartaric acid in wines and to discriminate different matrixes using principal component analysis (PCA) of the raw CD data. American Chemical Society 2022-04-26 2022-05-27 /pmc/articles/PMC9150167/ /pubmed/35472260 http://dx.doi.org/10.1021/acssensors.2c00038 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Begato, Federico Penasa, Roberto Licini, Giulia Zonta, Cristiano Chiroptical Enhancement of Chiral Dicarboxylic Acids from Confinement in a Stereodynamic Supramolecular Cage |
title | Chiroptical Enhancement of Chiral Dicarboxylic Acids
from Confinement in a Stereodynamic Supramolecular Cage |
title_full | Chiroptical Enhancement of Chiral Dicarboxylic Acids
from Confinement in a Stereodynamic Supramolecular Cage |
title_fullStr | Chiroptical Enhancement of Chiral Dicarboxylic Acids
from Confinement in a Stereodynamic Supramolecular Cage |
title_full_unstemmed | Chiroptical Enhancement of Chiral Dicarboxylic Acids
from Confinement in a Stereodynamic Supramolecular Cage |
title_short | Chiroptical Enhancement of Chiral Dicarboxylic Acids
from Confinement in a Stereodynamic Supramolecular Cage |
title_sort | chiroptical enhancement of chiral dicarboxylic acids
from confinement in a stereodynamic supramolecular cage |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9150167/ https://www.ncbi.nlm.nih.gov/pubmed/35472260 http://dx.doi.org/10.1021/acssensors.2c00038 |
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