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Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics

[Image: see text] In biology, polymorphism is a well-known phenomenon by which a discrete biomacromolecule can adopt multiple specific conformations in response to its environment. The controlled incorporation of polymorphism into noncovalent aqueous assemblies of synthetic small molecules is an imp...

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Autores principales: Matsumoto, Nicholas M., Lafleur, René P. M., Lou, Xianwen, Shih, Kuo-Chih, Wijnands, Sjors P. W., Guibert, Clément, van Rosendaal, Johannes W. A. M., Voets, Ilja K., Palmans, Anja R. A., Lin, Yao, Meijer, E. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194755/
https://www.ncbi.nlm.nih.gov/pubmed/30221520
http://dx.doi.org/10.1021/jacs.8b07697
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author Matsumoto, Nicholas M.
Lafleur, René P. M.
Lou, Xianwen
Shih, Kuo-Chih
Wijnands, Sjors P. W.
Guibert, Clément
van Rosendaal, Johannes W. A. M.
Voets, Ilja K.
Palmans, Anja R. A.
Lin, Yao
Meijer, E. W.
author_facet Matsumoto, Nicholas M.
Lafleur, René P. M.
Lou, Xianwen
Shih, Kuo-Chih
Wijnands, Sjors P. W.
Guibert, Clément
van Rosendaal, Johannes W. A. M.
Voets, Ilja K.
Palmans, Anja R. A.
Lin, Yao
Meijer, E. W.
author_sort Matsumoto, Nicholas M.
collection PubMed
description [Image: see text] In biology, polymorphism is a well-known phenomenon by which a discrete biomacromolecule can adopt multiple specific conformations in response to its environment. The controlled incorporation of polymorphism into noncovalent aqueous assemblies of synthetic small molecules is an important step toward the development of bioinspired responsive materials. Herein, we report on a family of carboxylic acid functionalized water-soluble benzene-1,3,5-tricarboxamides (BTAs) that self-assemble in water to form one-dimensional fibers, membranes, and hollow nanotubes. Interestingly, one of the BTAs with the optimized position of the carboxylic group in the hydrophobic domain yields nanotubes that undergo reversible temperature-dependent dynamic reorganizations. SAXS and Cryo-TEM data show the formation of elongated, well-ordered nanotubes at elevated temperatures. At these temperatures, increased dynamics, as measured by hydrogen–deuterium exchange, provide enough flexibility to the system to form well-defined nanotube structures with apparently defect-free tube walls. Without this flexibility, the assemblies are frozen into a variety of structures that are very similar at the supramolecular level, but less defined at the mesoscopic level.
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spelling pubmed-61947552018-10-20 Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics Matsumoto, Nicholas M. Lafleur, René P. M. Lou, Xianwen Shih, Kuo-Chih Wijnands, Sjors P. W. Guibert, Clément van Rosendaal, Johannes W. A. M. Voets, Ilja K. Palmans, Anja R. A. Lin, Yao Meijer, E. W. J Am Chem Soc [Image: see text] In biology, polymorphism is a well-known phenomenon by which a discrete biomacromolecule can adopt multiple specific conformations in response to its environment. The controlled incorporation of polymorphism into noncovalent aqueous assemblies of synthetic small molecules is an important step toward the development of bioinspired responsive materials. Herein, we report on a family of carboxylic acid functionalized water-soluble benzene-1,3,5-tricarboxamides (BTAs) that self-assemble in water to form one-dimensional fibers, membranes, and hollow nanotubes. Interestingly, one of the BTAs with the optimized position of the carboxylic group in the hydrophobic domain yields nanotubes that undergo reversible temperature-dependent dynamic reorganizations. SAXS and Cryo-TEM data show the formation of elongated, well-ordered nanotubes at elevated temperatures. At these temperatures, increased dynamics, as measured by hydrogen–deuterium exchange, provide enough flexibility to the system to form well-defined nanotube structures with apparently defect-free tube walls. Without this flexibility, the assemblies are frozen into a variety of structures that are very similar at the supramolecular level, but less defined at the mesoscopic level. American Chemical Society 2018-09-17 2018-10-17 /pmc/articles/PMC6194755/ /pubmed/30221520 http://dx.doi.org/10.1021/jacs.8b07697 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Matsumoto, Nicholas M.
Lafleur, René P. M.
Lou, Xianwen
Shih, Kuo-Chih
Wijnands, Sjors P. W.
Guibert, Clément
van Rosendaal, Johannes W. A. M.
Voets, Ilja K.
Palmans, Anja R. A.
Lin, Yao
Meijer, E. W.
Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title_full Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title_fullStr Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title_full_unstemmed Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title_short Polymorphism in Benzene-1,3,5-tricarboxamide Supramolecular Assemblies in Water: A Subtle Trade-off between Structure and Dynamics
title_sort polymorphism in benzene-1,3,5-tricarboxamide supramolecular assemblies in water: a subtle trade-off between structure and dynamics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194755/
https://www.ncbi.nlm.nih.gov/pubmed/30221520
http://dx.doi.org/10.1021/jacs.8b07697
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