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Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies
The size of single crystals of the metal‐organic framework CPO‐27‐Ni was incrementally increased through a series of modulated syntheses. A novel linker modulated synthesis using 2,5‐dihydroxyterephthalic acid and the isomeric ligand 4,6‐dihydroxyisophthalic acid yielded large single crystals of CPO...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251849/ https://www.ncbi.nlm.nih.gov/pubmed/33783895 http://dx.doi.org/10.1002/chem.202100528 |
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author | Vornholt, Simon M. Elliott, Caroline G. Rice, Cameron M. Russell, Samantha E. Kerr, Peter J. Rainer, Daniel N. Mazur, Michal Warren, Mark R. Wheatley, Paul S. Morris, Russell E. |
author_facet | Vornholt, Simon M. Elliott, Caroline G. Rice, Cameron M. Russell, Samantha E. Kerr, Peter J. Rainer, Daniel N. Mazur, Michal Warren, Mark R. Wheatley, Paul S. Morris, Russell E. |
author_sort | Vornholt, Simon M. |
collection | PubMed |
description | The size of single crystals of the metal‐organic framework CPO‐27‐Ni was incrementally increased through a series of modulated syntheses. A novel linker modulated synthesis using 2,5‐dihydroxyterephthalic acid and the isomeric ligand 4,6‐dihydroxyisophthalic acid yielded large single crystals of CPO‐27‐Ni (∼70 μm). All materials were shown to have high crystallinity and phase purity through powder X‐ray diffraction, electron microscopy methods, thermogravimetry, and compositional analysis. For the first time single‐crystal structure analyses were carried out on CPO‐27‐Ni. High BET surface areas and nitric oxide (NO) release efficiencies were recorded for all materials. Large single crystals of CPO‐27‐Ni showed a prolonged NO release and proved suitable for in situ single‐crystal diffraction experiments to follow the NO adsorption. An efficient activation protocol was developed, leading to a dehydrated structure after just 4 h, which subsequently was NO‐loaded, leading to a first NO loaded single‐crystal structural model of CPO‐27‐Ni. |
format | Online Article Text |
id | pubmed-8251849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82518492021-07-07 Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies Vornholt, Simon M. Elliott, Caroline G. Rice, Cameron M. Russell, Samantha E. Kerr, Peter J. Rainer, Daniel N. Mazur, Michal Warren, Mark R. Wheatley, Paul S. Morris, Russell E. Chemistry Full Papers The size of single crystals of the metal‐organic framework CPO‐27‐Ni was incrementally increased through a series of modulated syntheses. A novel linker modulated synthesis using 2,5‐dihydroxyterephthalic acid and the isomeric ligand 4,6‐dihydroxyisophthalic acid yielded large single crystals of CPO‐27‐Ni (∼70 μm). All materials were shown to have high crystallinity and phase purity through powder X‐ray diffraction, electron microscopy methods, thermogravimetry, and compositional analysis. For the first time single‐crystal structure analyses were carried out on CPO‐27‐Ni. High BET surface areas and nitric oxide (NO) release efficiencies were recorded for all materials. Large single crystals of CPO‐27‐Ni showed a prolonged NO release and proved suitable for in situ single‐crystal diffraction experiments to follow the NO adsorption. An efficient activation protocol was developed, leading to a dehydrated structure after just 4 h, which subsequently was NO‐loaded, leading to a first NO loaded single‐crystal structural model of CPO‐27‐Ni. John Wiley and Sons Inc. 2021-05-07 2021-06-10 /pmc/articles/PMC8251849/ /pubmed/33783895 http://dx.doi.org/10.1002/chem.202100528 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Vornholt, Simon M. Elliott, Caroline G. Rice, Cameron M. Russell, Samantha E. Kerr, Peter J. Rainer, Daniel N. Mazur, Michal Warren, Mark R. Wheatley, Paul S. Morris, Russell E. Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title | Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title_full | Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title_fullStr | Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title_full_unstemmed | Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title_short | Controlled Synthesis of Large Single Crystals of Metal‐Organic Framework CPO‐27‐Ni Prepared by a Modulation Approach: In situ Single‐Crystal X‐ray Diffraction Studies |
title_sort | controlled synthesis of large single crystals of metal‐organic framework cpo‐27‐ni prepared by a modulation approach: in situ single‐crystal x‐ray diffraction studies |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251849/ https://www.ncbi.nlm.nih.gov/pubmed/33783895 http://dx.doi.org/10.1002/chem.202100528 |
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