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Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network
Developing molecular approaches to the creation of robust and water-resistant adhesive materials promotes a fundamental understanding of interfacial adhesion mechanisms as well as future applications of biomedical adhesive materials. Here, we present a simple and robust strategy that combines natura...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042223/ https://www.ncbi.nlm.nih.gov/pubmed/36994382 http://dx.doi.org/10.1093/nsr/nwac139 |
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author | Shi, Chen-Yu He, Dan-Dan Zhang, Qi Tong, Fei Shi, Zhao-Tao Tian, He Qu, Da-Hui |
author_facet | Shi, Chen-Yu He, Dan-Dan Zhang, Qi Tong, Fei Shi, Zhao-Tao Tian, He Qu, Da-Hui |
author_sort | Shi, Chen-Yu |
collection | PubMed |
description | Developing molecular approaches to the creation of robust and water-resistant adhesive materials promotes a fundamental understanding of interfacial adhesion mechanisms as well as future applications of biomedical adhesive materials. Here, we present a simple and robust strategy that combines natural thioctic acid and mussel-inspired iron-catechol complexes to enable ultra-strong adhesive materials that can be used underwater and simultaneously exhibit unprecedentedly high adhesion strength on diverse surfaces. Our experimental results show that the robust crosslinking interaction of the iron-catechol complexes, as well as high-density hydrogen bonding, are responsible for the ultra-high interfacial adhesion strength. The embedding effect of the hydrophobic solvent-free network of poly(disulfides) further enhances the water-resistance. The dynamic covalent poly(disulfides) network also makes the resulting materials reconfigurable, thus enabling reusability via repeated heating and cooling. This molecule-engineering strategy offers a general and versatile solution to the design and construction of dynamic supramolecular adhesive materials. |
format | Online Article Text |
id | pubmed-10042223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100422232023-03-28 Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network Shi, Chen-Yu He, Dan-Dan Zhang, Qi Tong, Fei Shi, Zhao-Tao Tian, He Qu, Da-Hui Natl Sci Rev Research Article Developing molecular approaches to the creation of robust and water-resistant adhesive materials promotes a fundamental understanding of interfacial adhesion mechanisms as well as future applications of biomedical adhesive materials. Here, we present a simple and robust strategy that combines natural thioctic acid and mussel-inspired iron-catechol complexes to enable ultra-strong adhesive materials that can be used underwater and simultaneously exhibit unprecedentedly high adhesion strength on diverse surfaces. Our experimental results show that the robust crosslinking interaction of the iron-catechol complexes, as well as high-density hydrogen bonding, are responsible for the ultra-high interfacial adhesion strength. The embedding effect of the hydrophobic solvent-free network of poly(disulfides) further enhances the water-resistance. The dynamic covalent poly(disulfides) network also makes the resulting materials reconfigurable, thus enabling reusability via repeated heating and cooling. This molecule-engineering strategy offers a general and versatile solution to the design and construction of dynamic supramolecular adhesive materials. Oxford University Press 2022-07-25 /pmc/articles/PMC10042223/ /pubmed/36994382 http://dx.doi.org/10.1093/nsr/nwac139 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shi, Chen-Yu He, Dan-Dan Zhang, Qi Tong, Fei Shi, Zhao-Tao Tian, He Qu, Da-Hui Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title | Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title_full | Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title_fullStr | Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title_full_unstemmed | Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title_short | Robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
title_sort | robust and dynamic underwater adhesives enabled by catechol-functionalized poly(disulfides) network |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042223/ https://www.ncbi.nlm.nih.gov/pubmed/36994382 http://dx.doi.org/10.1093/nsr/nwac139 |
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