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Dynamic urea bond for the design of reversible and self-healing polymers

Polymers bearing dynamic covalent bonds may exhibit dynamic properties, such as self-healing, shape memory and environmental adaptation. However, most dynamic covalent chemistries developed so far require either catalyst or change of environmental conditions to facilitate bond reversion and dynamic...

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Autores principales: Ying, Hanze, Zhang, Yanfeng, Cheng, Jianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438999/
https://www.ncbi.nlm.nih.gov/pubmed/24492620
http://dx.doi.org/10.1038/ncomms4218
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author Ying, Hanze
Zhang, Yanfeng
Cheng, Jianjun
author_facet Ying, Hanze
Zhang, Yanfeng
Cheng, Jianjun
author_sort Ying, Hanze
collection PubMed
description Polymers bearing dynamic covalent bonds may exhibit dynamic properties, such as self-healing, shape memory and environmental adaptation. However, most dynamic covalent chemistries developed so far require either catalyst or change of environmental conditions to facilitate bond reversion and dynamic property change in bulk materials. Here we report the rational design of hindered urea bonds (urea with bulky substituent attached to its nitrogen) and the use of them to make polyureas and poly(urethane-ureas) capable of catalyst-free dynamic property change and autonomous repairing at low temperature. Given the simplicity of the hindered urea bond chemistry (reaction of a bulky amine with an isocyanate), incorporation of the catalyst-free dynamic covalent urea bonds to conventional polyurea or urea-containing polymers that typically have stable bulk properties may further broaden the scope of applications of these widely used materials.
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spelling pubmed-44389992015-05-20 Dynamic urea bond for the design of reversible and self-healing polymers Ying, Hanze Zhang, Yanfeng Cheng, Jianjun Nat Commun Article Polymers bearing dynamic covalent bonds may exhibit dynamic properties, such as self-healing, shape memory and environmental adaptation. However, most dynamic covalent chemistries developed so far require either catalyst or change of environmental conditions to facilitate bond reversion and dynamic property change in bulk materials. Here we report the rational design of hindered urea bonds (urea with bulky substituent attached to its nitrogen) and the use of them to make polyureas and poly(urethane-ureas) capable of catalyst-free dynamic property change and autonomous repairing at low temperature. Given the simplicity of the hindered urea bond chemistry (reaction of a bulky amine with an isocyanate), incorporation of the catalyst-free dynamic covalent urea bonds to conventional polyurea or urea-containing polymers that typically have stable bulk properties may further broaden the scope of applications of these widely used materials. 2014 /pmc/articles/PMC4438999/ /pubmed/24492620 http://dx.doi.org/10.1038/ncomms4218 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ying, Hanze
Zhang, Yanfeng
Cheng, Jianjun
Dynamic urea bond for the design of reversible and self-healing polymers
title Dynamic urea bond for the design of reversible and self-healing polymers
title_full Dynamic urea bond for the design of reversible and self-healing polymers
title_fullStr Dynamic urea bond for the design of reversible and self-healing polymers
title_full_unstemmed Dynamic urea bond for the design of reversible and self-healing polymers
title_short Dynamic urea bond for the design of reversible and self-healing polymers
title_sort dynamic urea bond for the design of reversible and self-healing polymers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438999/
https://www.ncbi.nlm.nih.gov/pubmed/24492620
http://dx.doi.org/10.1038/ncomms4218
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