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Uracil Derivatives for Halogen-Bonded Cocrystals
Among non-covalent interactions, halogen bonding is emerging as a new powerful tool for supramolecular self-assembly. Here, along with a green and effective method, we report three new halogen-bonded cocrystals containing uracil derivatives and 1,2,4,5-tetrafluoro-3,6-diiodobenzene as X-bond donor c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508742/ https://www.ncbi.nlm.nih.gov/pubmed/34639004 http://dx.doi.org/10.3390/ijms221910663 |
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author | Benito, Mónica Roselló, Yannick Barceló-Oliver, Miquel Frontera, Antonio Molins, Elies |
author_facet | Benito, Mónica Roselló, Yannick Barceló-Oliver, Miquel Frontera, Antonio Molins, Elies |
author_sort | Benito, Mónica |
collection | PubMed |
description | Among non-covalent interactions, halogen bonding is emerging as a new powerful tool for supramolecular self-assembly. Here, along with a green and effective method, we report three new halogen-bonded cocrystals containing uracil derivatives and 1,2,4,5-tetrafluoro-3,6-diiodobenzene as X-bond donor coformer. These multicomponent solids were prepared both by solvent-drop grinding and solution methods and further characterized by powder and single-crystal X-ray diffraction, Fourier-transformed infrared spectroscopy, and thermal methods (TGA-DSC). In order to study the relative importance of hydrogen versus halogen bonds in the crystal packing, computational methods were applied. |
format | Online Article Text |
id | pubmed-8508742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85087422021-10-13 Uracil Derivatives for Halogen-Bonded Cocrystals Benito, Mónica Roselló, Yannick Barceló-Oliver, Miquel Frontera, Antonio Molins, Elies Int J Mol Sci Article Among non-covalent interactions, halogen bonding is emerging as a new powerful tool for supramolecular self-assembly. Here, along with a green and effective method, we report three new halogen-bonded cocrystals containing uracil derivatives and 1,2,4,5-tetrafluoro-3,6-diiodobenzene as X-bond donor coformer. These multicomponent solids were prepared both by solvent-drop grinding and solution methods and further characterized by powder and single-crystal X-ray diffraction, Fourier-transformed infrared spectroscopy, and thermal methods (TGA-DSC). In order to study the relative importance of hydrogen versus halogen bonds in the crystal packing, computational methods were applied. MDPI 2021-10-01 /pmc/articles/PMC8508742/ /pubmed/34639004 http://dx.doi.org/10.3390/ijms221910663 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Benito, Mónica Roselló, Yannick Barceló-Oliver, Miquel Frontera, Antonio Molins, Elies Uracil Derivatives for Halogen-Bonded Cocrystals |
title | Uracil Derivatives for Halogen-Bonded Cocrystals |
title_full | Uracil Derivatives for Halogen-Bonded Cocrystals |
title_fullStr | Uracil Derivatives for Halogen-Bonded Cocrystals |
title_full_unstemmed | Uracil Derivatives for Halogen-Bonded Cocrystals |
title_short | Uracil Derivatives for Halogen-Bonded Cocrystals |
title_sort | uracil derivatives for halogen-bonded cocrystals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508742/ https://www.ncbi.nlm.nih.gov/pubmed/34639004 http://dx.doi.org/10.3390/ijms221910663 |
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