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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...

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Detalles Bibliográficos
Autores principales: Benito, Mónica, Roselló, Yannick, Barceló-Oliver, Miquel, Frontera, Antonio, Molins, Elies
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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