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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...

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Autores principales: Shi, Chen-Yu, He, Dan-Dan, Zhang, Qi, Tong, Fei, Shi, Zhao-Tao, Tian, He, Qu, Da-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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