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Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde
The title compound (systematic name: 3-chloro-5-fluoro-2-hydroxybenzaldehyde), C(7)H(4)ClFO(2), is a dihalogenated salicylaldehyde derivative that has been studied for its antibacterial characteristics. The salicylaldehyde engages in intramolecular hydrogen bonding with an O—H⋯O distance of 2....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784655/ https://www.ncbi.nlm.nih.gov/pubmed/33520258 http://dx.doi.org/10.1107/S2056989020014425 |
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author | Triggs, Christopher T. Tanski, Joseph M. |
author_facet | Triggs, Christopher T. Tanski, Joseph M. |
author_sort | Triggs, Christopher T. |
collection | PubMed |
description | The title compound (systematic name: 3-chloro-5-fluoro-2-hydroxybenzaldehyde), C(7)H(4)ClFO(2), is a dihalogenated salicylaldehyde derivative that has been studied for its antibacterial characteristics. The salicylaldehyde engages in intramolecular hydrogen bonding with an O—H⋯O distance of 2.6231 (19) Å while the molecules pack together via weak intermolecular C—H⋯O, C—H⋯F and F⋯O interactions and offset face-to-face π-stacking. |
format | Online Article Text |
id | pubmed-7784655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-77846552021-01-29 Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde Triggs, Christopher T. Tanski, Joseph M. Acta Crystallogr E Crystallogr Commun Research Communications The title compound (systematic name: 3-chloro-5-fluoro-2-hydroxybenzaldehyde), C(7)H(4)ClFO(2), is a dihalogenated salicylaldehyde derivative that has been studied for its antibacterial characteristics. The salicylaldehyde engages in intramolecular hydrogen bonding with an O—H⋯O distance of 2.6231 (19) Å while the molecules pack together via weak intermolecular C—H⋯O, C—H⋯F and F⋯O interactions and offset face-to-face π-stacking. International Union of Crystallography 2020-11-03 /pmc/articles/PMC7784655/ /pubmed/33520258 http://dx.doi.org/10.1107/S2056989020014425 Text en © Triggs and Tanski 2020 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Research Communications Triggs, Christopher T. Tanski, Joseph M. Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title | Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title_full | Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title_fullStr | Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title_full_unstemmed | Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title_short | Crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
title_sort | crystallographic and spectroscopic characterization of 3-chloro-5-fluorosalicylaldehyde |
topic | Research Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784655/ https://www.ncbi.nlm.nih.gov/pubmed/33520258 http://dx.doi.org/10.1107/S2056989020014425 |
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