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Solvent-Controlled Self-Assembled Oligopyrrolic Receptor †
We report a fully organic pyridine-tetrapyrrolic U-shaped acyclic receptor 10, which prefers a supramolecular pseudo-macrocyclic dimeric structure (10)(2) in a less polar, non-coordinating solvent (e.g., CHCl(3)). Conversely, when it is crystalized from a polar, coordinating solvent (e.g., N,N-dimet...
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/PMC8004224/ https://www.ncbi.nlm.nih.gov/pubmed/33809927 http://dx.doi.org/10.3390/molecules26061771 |
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author | Wang, Fei Liang, Kejiang Larsen, Mads Christian Bähring, Steffen Ishida, Masatoshi Furuta, Hiroyuki Jana, Atanu |
author_facet | Wang, Fei Liang, Kejiang Larsen, Mads Christian Bähring, Steffen Ishida, Masatoshi Furuta, Hiroyuki Jana, Atanu |
author_sort | Wang, Fei |
collection | PubMed |
description | We report a fully organic pyridine-tetrapyrrolic U-shaped acyclic receptor 10, which prefers a supramolecular pseudo-macrocyclic dimeric structure (10)(2) in a less polar, non-coordinating solvent (e.g., CHCl(3)). Conversely, when it is crystalized from a polar, coordinating solvent (e.g., N,N-dimethylformamide, DMF), it exhibited an infinite supramolecular one-dimensional (1D) “zig-zag” polymeric chain, as inferred from the single-crystal X-ray structures. This supramolecular system acts as a potential receptor for strong acids, e.g., p-toluenesulfonic acid (PTSA), methane sulfonic acid (MSA), H(2)SO(4), HNO(3), and HCl, with a prominent colorimetric response from pale yellow to deep red. The receptor can easily be recovered from the organic solution of the host–guest complex by simple aqueous washing. It was observed that relatively stronger acids with pK(a) < −1.92 in water were able to interact with the receptor, as inferred from (1)H NMR titration in tetrahydrofuran-d(8) (THF-d(8)) and ultraviolet–visible (UV–vis) spectroscopic titrations in anhydrous THF at 298 K. Therefore, this new dynamic supramolecular receptor system may have potentiality in materials science research. |
format | Online Article Text |
id | pubmed-8004224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80042242021-03-28 Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † Wang, Fei Liang, Kejiang Larsen, Mads Christian Bähring, Steffen Ishida, Masatoshi Furuta, Hiroyuki Jana, Atanu Molecules Article We report a fully organic pyridine-tetrapyrrolic U-shaped acyclic receptor 10, which prefers a supramolecular pseudo-macrocyclic dimeric structure (10)(2) in a less polar, non-coordinating solvent (e.g., CHCl(3)). Conversely, when it is crystalized from a polar, coordinating solvent (e.g., N,N-dimethylformamide, DMF), it exhibited an infinite supramolecular one-dimensional (1D) “zig-zag” polymeric chain, as inferred from the single-crystal X-ray structures. This supramolecular system acts as a potential receptor for strong acids, e.g., p-toluenesulfonic acid (PTSA), methane sulfonic acid (MSA), H(2)SO(4), HNO(3), and HCl, with a prominent colorimetric response from pale yellow to deep red. The receptor can easily be recovered from the organic solution of the host–guest complex by simple aqueous washing. It was observed that relatively stronger acids with pK(a) < −1.92 in water were able to interact with the receptor, as inferred from (1)H NMR titration in tetrahydrofuran-d(8) (THF-d(8)) and ultraviolet–visible (UV–vis) spectroscopic titrations in anhydrous THF at 298 K. Therefore, this new dynamic supramolecular receptor system may have potentiality in materials science research. MDPI 2021-03-22 /pmc/articles/PMC8004224/ /pubmed/33809927 http://dx.doi.org/10.3390/molecules26061771 Text en © 2021 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 Wang, Fei Liang, Kejiang Larsen, Mads Christian Bähring, Steffen Ishida, Masatoshi Furuta, Hiroyuki Jana, Atanu Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title | Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title_full | Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title_fullStr | Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title_full_unstemmed | Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title_short | Solvent-Controlled Self-Assembled Oligopyrrolic Receptor † |
title_sort | solvent-controlled self-assembled oligopyrrolic receptor † |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004224/ https://www.ncbi.nlm.nih.gov/pubmed/33809927 http://dx.doi.org/10.3390/molecules26061771 |
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