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Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition

The synthesis and characterisation of two novel self‐assembled amphiphiles (SSAs) SQS‐1 and SQS‐2 are reported. Both compounds, based on the squaramide motif, were fully soluble in a range of solvents and were shown to undergo self‐assembly through a range of physical techniques. Self‐assembly was s...

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Autores principales: Kumawat, Lokesh K., Wynne, Conor, Cappello, Emanuele, Fisher, Peter, Brennan, Luke E., Strofaldi, Alessandro, McManus, Jennifer J., Hawes, Chris S., Jolliffe, Katrina A., Gunnlaugsson, Thorfinnur, Elmes, Robert B. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456826/
https://www.ncbi.nlm.nih.gov/pubmed/34351081
http://dx.doi.org/10.1002/cplu.202100275
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author Kumawat, Lokesh K.
Wynne, Conor
Cappello, Emanuele
Fisher, Peter
Brennan, Luke E.
Strofaldi, Alessandro
McManus, Jennifer J.
Hawes, Chris S.
Jolliffe, Katrina A.
Gunnlaugsson, Thorfinnur
Elmes, Robert B. P.
author_facet Kumawat, Lokesh K.
Wynne, Conor
Cappello, Emanuele
Fisher, Peter
Brennan, Luke E.
Strofaldi, Alessandro
McManus, Jennifer J.
Hawes, Chris S.
Jolliffe, Katrina A.
Gunnlaugsson, Thorfinnur
Elmes, Robert B. P.
author_sort Kumawat, Lokesh K.
collection PubMed
description The synthesis and characterisation of two novel self‐assembled amphiphiles (SSAs) SQS‐1 and SQS‐2 are reported. Both compounds, based on the squaramide motif, were fully soluble in a range of solvents and were shown to undergo self‐assembly through a range of physical techniques. Self‐assembly was shown to favour the formation of crystalline domains on the nanoscale but also fibrillar film formation, as suggested by SEM analysis. Moreover, both SQS‐1 and SQS‐2 were capable of anion recognition in DMSO solution as demonstrated using (1)H NMR and UV/Vis absorption spectroscopy, but displayed lower binding affinities for various anions when compared against other squaramide based receptors. In more competitive solvent mixtures SQS‐1 gave rise to a colourimetric response in the presence of HPO(4) (2−) that was clearly visible to the naked eye. We anticipate that the observed response is due to the basic nature of the HPO(4) (2−) anion when compared against other biologically relevant anions.
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spelling pubmed-84568262021-09-27 Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition Kumawat, Lokesh K. Wynne, Conor Cappello, Emanuele Fisher, Peter Brennan, Luke E. Strofaldi, Alessandro McManus, Jennifer J. Hawes, Chris S. Jolliffe, Katrina A. Gunnlaugsson, Thorfinnur Elmes, Robert B. P. Chempluschem Full Papers The synthesis and characterisation of two novel self‐assembled amphiphiles (SSAs) SQS‐1 and SQS‐2 are reported. Both compounds, based on the squaramide motif, were fully soluble in a range of solvents and were shown to undergo self‐assembly through a range of physical techniques. Self‐assembly was shown to favour the formation of crystalline domains on the nanoscale but also fibrillar film formation, as suggested by SEM analysis. Moreover, both SQS‐1 and SQS‐2 were capable of anion recognition in DMSO solution as demonstrated using (1)H NMR and UV/Vis absorption spectroscopy, but displayed lower binding affinities for various anions when compared against other squaramide based receptors. In more competitive solvent mixtures SQS‐1 gave rise to a colourimetric response in the presence of HPO(4) (2−) that was clearly visible to the naked eye. We anticipate that the observed response is due to the basic nature of the HPO(4) (2−) anion when compared against other biologically relevant anions. John Wiley and Sons Inc. 2021-08-05 2021-08 /pmc/articles/PMC8456826/ /pubmed/34351081 http://dx.doi.org/10.1002/cplu.202100275 Text en © 2021 The Authors. ChemPlusChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Kumawat, Lokesh K.
Wynne, Conor
Cappello, Emanuele
Fisher, Peter
Brennan, Luke E.
Strofaldi, Alessandro
McManus, Jennifer J.
Hawes, Chris S.
Jolliffe, Katrina A.
Gunnlaugsson, Thorfinnur
Elmes, Robert B. P.
Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title_full Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title_fullStr Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title_full_unstemmed Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title_short Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition
title_sort squaramide‐based self‐associating amphiphiles for anion recognition
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456826/
https://www.ncbi.nlm.nih.gov/pubmed/34351081
http://dx.doi.org/10.1002/cplu.202100275
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