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Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering
The ordered porous frameworks like MOFs and COFs are generally constructed using the monomers through distinctive metal-coordinated and covalent linkages. Meanwhile, the inter-structural transition between each class of these porous materials is an under-explored research area. However, such altered...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636044/ https://www.ncbi.nlm.nih.gov/pubmed/37945788 http://dx.doi.org/10.1038/s41598-023-46573-3 |
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author | Mohammed, Abdul Khayum Gaber, Safa Raya, Jésus Skorjanc, Tina Elmerhi, Nada Stephen, Sasi Sánchez, Pilar Pena Gándara, Felipe Hinder, Steven J. Baker, Mark A. Polychronopoulou, Kyriaki Shetty, Dinesh |
author_facet | Mohammed, Abdul Khayum Gaber, Safa Raya, Jésus Skorjanc, Tina Elmerhi, Nada Stephen, Sasi Sánchez, Pilar Pena Gándara, Felipe Hinder, Steven J. Baker, Mark A. Polychronopoulou, Kyriaki Shetty, Dinesh |
author_sort | Mohammed, Abdul Khayum |
collection | PubMed |
description | The ordered porous frameworks like MOFs and COFs are generally constructed using the monomers through distinctive metal-coordinated and covalent linkages. Meanwhile, the inter-structural transition between each class of these porous materials is an under-explored research area. However, such altered frameworks are expected to have exciting features compared to their pristine versions. Herein, we have demonstrated a chemical-induction phase-engineering strategy to transform a two-dimensional conjugated Cu-based SA-MOF (Cu-Tp) into 2D-COFs (Cu-TpCOFs). The structural phase transition offered in-situ pore size engineering from 1.1 nm to 1.5–2.0 nm. Moreover, the Cu-TpCOFs showed uniform and low percentage-doped (~ 1–1.5%) metal distribution and improved crystallinity, porosity, and stability compared to the parent Cu-Tp MOF. The construction of a framework from another framework with new linkages opens interesting opportunities for phase-engineering. |
format | Online Article Text |
id | pubmed-10636044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106360442023-11-11 Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering Mohammed, Abdul Khayum Gaber, Safa Raya, Jésus Skorjanc, Tina Elmerhi, Nada Stephen, Sasi Sánchez, Pilar Pena Gándara, Felipe Hinder, Steven J. Baker, Mark A. Polychronopoulou, Kyriaki Shetty, Dinesh Sci Rep Article The ordered porous frameworks like MOFs and COFs are generally constructed using the monomers through distinctive metal-coordinated and covalent linkages. Meanwhile, the inter-structural transition between each class of these porous materials is an under-explored research area. However, such altered frameworks are expected to have exciting features compared to their pristine versions. Herein, we have demonstrated a chemical-induction phase-engineering strategy to transform a two-dimensional conjugated Cu-based SA-MOF (Cu-Tp) into 2D-COFs (Cu-TpCOFs). The structural phase transition offered in-situ pore size engineering from 1.1 nm to 1.5–2.0 nm. Moreover, the Cu-TpCOFs showed uniform and low percentage-doped (~ 1–1.5%) metal distribution and improved crystallinity, porosity, and stability compared to the parent Cu-Tp MOF. The construction of a framework from another framework with new linkages opens interesting opportunities for phase-engineering. Nature Publishing Group UK 2023-11-09 /pmc/articles/PMC10636044/ /pubmed/37945788 http://dx.doi.org/10.1038/s41598-023-46573-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mohammed, Abdul Khayum Gaber, Safa Raya, Jésus Skorjanc, Tina Elmerhi, Nada Stephen, Sasi Sánchez, Pilar Pena Gándara, Felipe Hinder, Steven J. Baker, Mark A. Polychronopoulou, Kyriaki Shetty, Dinesh Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title | Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title_full | Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title_fullStr | Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title_full_unstemmed | Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title_short | Crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
title_sort | crystallizing covalent organic frameworks from metal organic framework through chemical induced-phase engineering |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636044/ https://www.ncbi.nlm.nih.gov/pubmed/37945788 http://dx.doi.org/10.1038/s41598-023-46573-3 |
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