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Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking
Covalent organic frameworks (COFs) are network polymers with long-range positional order whose properties can be tuned using the isoreticular chemistry approach. Making COFs from strong bonds is challenging because irreversible rapid formation of the network produces amorphous materials with locked-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654755/ https://www.ncbi.nlm.nih.gov/pubmed/29066848 http://dx.doi.org/10.1038/s41467-017-01423-5 |
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author | Stewart, David Antypov, Dmytro Dyer, Matthew S. Pitcher, Michael J. Katsoulidis, Alexandros P. Chater, Philip A. Blanc, Frédéric Rosseinsky, Matthew J. |
author_facet | Stewart, David Antypov, Dmytro Dyer, Matthew S. Pitcher, Michael J. Katsoulidis, Alexandros P. Chater, Philip A. Blanc, Frédéric Rosseinsky, Matthew J. |
author_sort | Stewart, David |
collection | PubMed |
description | Covalent organic frameworks (COFs) are network polymers with long-range positional order whose properties can be tuned using the isoreticular chemistry approach. Making COFs from strong bonds is challenging because irreversible rapid formation of the network produces amorphous materials with locked-in disorder. Reversibility in bond formation is essential to generate ordered networks, as it allows the error-checking that permits the network to crystallise, and so candidate network-forming chemistries such as amide that are irreversible under conventional low temperature bond-forming conditions have been underexplored. Here we show that we can prepare two- and three-dimensional covalent amide frameworks (CAFs) by devitrification of amorphous polyamide network polymers using high-temperature and high-pressure reaction conditions. In this way we have accessed reversible amide bond formation that allows crystalline order to develop. This strategy permits the direct synthesis of practically irreversible ordered amide networks that are stable thermally and under both strong acidic and basic hydrolytic conditions. |
format | Online Article Text |
id | pubmed-5654755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56547552017-10-26 Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking Stewart, David Antypov, Dmytro Dyer, Matthew S. Pitcher, Michael J. Katsoulidis, Alexandros P. Chater, Philip A. Blanc, Frédéric Rosseinsky, Matthew J. Nat Commun Article Covalent organic frameworks (COFs) are network polymers with long-range positional order whose properties can be tuned using the isoreticular chemistry approach. Making COFs from strong bonds is challenging because irreversible rapid formation of the network produces amorphous materials with locked-in disorder. Reversibility in bond formation is essential to generate ordered networks, as it allows the error-checking that permits the network to crystallise, and so candidate network-forming chemistries such as amide that are irreversible under conventional low temperature bond-forming conditions have been underexplored. Here we show that we can prepare two- and three-dimensional covalent amide frameworks (CAFs) by devitrification of amorphous polyamide network polymers using high-temperature and high-pressure reaction conditions. In this way we have accessed reversible amide bond formation that allows crystalline order to develop. This strategy permits the direct synthesis of practically irreversible ordered amide networks that are stable thermally and under both strong acidic and basic hydrolytic conditions. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5654755/ /pubmed/29066848 http://dx.doi.org/10.1038/s41467-017-01423-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Stewart, David Antypov, Dmytro Dyer, Matthew S. Pitcher, Michael J. Katsoulidis, Alexandros P. Chater, Philip A. Blanc, Frédéric Rosseinsky, Matthew J. Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title | Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title_full | Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title_fullStr | Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title_full_unstemmed | Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title_short | Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
title_sort | stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654755/ https://www.ncbi.nlm.nih.gov/pubmed/29066848 http://dx.doi.org/10.1038/s41467-017-01423-5 |
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