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Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt
Combining three features—the high affinity of squaramides toward anions, cooperation in ion pair binding and preorganization of the binding domains in the tripodal platform—led to the effective receptor 2. The lack of at least one of these key elements in the structures of reference receptors 3 and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125518/ https://www.ncbi.nlm.nih.gov/pubmed/34067071 http://dx.doi.org/10.3390/molecules26092751 |
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author | Jagleniec, Damian Wilczek, Marcin Romański, Jan |
author_facet | Jagleniec, Damian Wilczek, Marcin Romański, Jan |
author_sort | Jagleniec, Damian |
collection | PubMed |
description | Combining three features—the high affinity of squaramides toward anions, cooperation in ion pair binding and preorganization of the binding domains in the tripodal platform—led to the effective receptor 2. The lack of at least one of these key elements in the structures of reference receptors 3 and 4 caused a lower affinity towards ion pairs. Receptor 2 was found to form an intramolecular network in wet chloroform, which changed into inorganic–organic associates after contact with ions and allowed salts to be extracted from an aqueous to an organic phase. The disparity in the binding mode of 2 with sulfates and with other monovalent anions led to the selective extraction of extremely hydrated sulfate anions in the presence of more lipophilic salts, thus overcoming the Hofmeister series. |
format | Online Article Text |
id | pubmed-8125518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81255182021-05-17 Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt Jagleniec, Damian Wilczek, Marcin Romański, Jan Molecules Article Combining three features—the high affinity of squaramides toward anions, cooperation in ion pair binding and preorganization of the binding domains in the tripodal platform—led to the effective receptor 2. The lack of at least one of these key elements in the structures of reference receptors 3 and 4 caused a lower affinity towards ion pairs. Receptor 2 was found to form an intramolecular network in wet chloroform, which changed into inorganic–organic associates after contact with ions and allowed salts to be extracted from an aqueous to an organic phase. The disparity in the binding mode of 2 with sulfates and with other monovalent anions led to the selective extraction of extremely hydrated sulfate anions in the presence of more lipophilic salts, thus overcoming the Hofmeister series. MDPI 2021-05-07 /pmc/articles/PMC8125518/ /pubmed/34067071 http://dx.doi.org/10.3390/molecules26092751 Text en © 2021 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 | Article Jagleniec, Damian Wilczek, Marcin Romański, Jan Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title | Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title_full | Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title_fullStr | Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title_full_unstemmed | Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title_short | Tripodal, Squaramide-Based Ion Pair Receptor for Effective Extraction of Sulfate Salt |
title_sort | tripodal, squaramide-based ion pair receptor for effective extraction of sulfate salt |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125518/ https://www.ncbi.nlm.nih.gov/pubmed/34067071 http://dx.doi.org/10.3390/molecules26092751 |
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