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Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions
In this study, we explorethe synthesis of binaphthyl-based chiral macrocyclic hosts for the first time. They exhibited the selective recognition abilities of iodide anions which can be favored over those of other anions (AcO(−), NO(3)(−), ClO(4)(−), HSO(4)(−), Br(−), PF(6)(−), H(2)PO(4)(−), BF(4)(−)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303813/ https://www.ncbi.nlm.nih.gov/pubmed/37375339 http://dx.doi.org/10.3390/molecules28124784 |
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author | Wang, Zong-Cheng Tan, Ying-Zi Tang, Lin-Li Zeng, Fei |
author_facet | Wang, Zong-Cheng Tan, Ying-Zi Tang, Lin-Li Zeng, Fei |
author_sort | Wang, Zong-Cheng |
collection | PubMed |
description | In this study, we explorethe synthesis of binaphthyl-based chiral macrocyclic hosts for the first time. They exhibited the selective recognition abilities of iodide anions which can be favored over those of other anions (AcO(−), NO(3)(−), ClO(4)(−), HSO(4)(−), Br(−), PF(6)(−), H(2)PO(4)(−), BF(4)(−), and CO(3)F(3)S(−)), as confirmed by UV-vis, HRMS, and (1)H NMR spectroscopy experiments, as well as DFT calculations. Neutral aryl C–H···anion interactions play an important role in the formation complexes. The recognition process can be observed by the naked eye. |
format | Online Article Text |
id | pubmed-10303813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103038132023-06-29 Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions Wang, Zong-Cheng Tan, Ying-Zi Tang, Lin-Li Zeng, Fei Molecules Communication In this study, we explorethe synthesis of binaphthyl-based chiral macrocyclic hosts for the first time. They exhibited the selective recognition abilities of iodide anions which can be favored over those of other anions (AcO(−), NO(3)(−), ClO(4)(−), HSO(4)(−), Br(−), PF(6)(−), H(2)PO(4)(−), BF(4)(−), and CO(3)F(3)S(−)), as confirmed by UV-vis, HRMS, and (1)H NMR spectroscopy experiments, as well as DFT calculations. Neutral aryl C–H···anion interactions play an important role in the formation complexes. The recognition process can be observed by the naked eye. MDPI 2023-06-15 /pmc/articles/PMC10303813/ /pubmed/37375339 http://dx.doi.org/10.3390/molecules28124784 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Wang, Zong-Cheng Tan, Ying-Zi Tang, Lin-Li Zeng, Fei Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title | Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title_full | Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title_fullStr | Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title_full_unstemmed | Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title_short | Binaphthyl-Based Chiral Macrocyclic Hosts for the Selective Recognition of Iodide Anions |
title_sort | binaphthyl-based chiral macrocyclic hosts for the selective recognition of iodide anions |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303813/ https://www.ncbi.nlm.nih.gov/pubmed/37375339 http://dx.doi.org/10.3390/molecules28124784 |
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