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The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes

In order to improve pharmaceutical properties of drugs, complexes are synthesized as combinations with other chemical substances. The complexes of fenamic acid and its derivatives, such as mefenamic-, tolfenamic- and flufenamic acid, with acridine were obtained and the X-ray structures were discusse...

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Autores principales: Krawczyk, Marta S., Sroka, Adam, Majerz, Irena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156396/
https://www.ncbi.nlm.nih.gov/pubmed/34065674
http://dx.doi.org/10.3390/molecules26102956
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author Krawczyk, Marta S.
Sroka, Adam
Majerz, Irena
author_facet Krawczyk, Marta S.
Sroka, Adam
Majerz, Irena
author_sort Krawczyk, Marta S.
collection PubMed
description In order to improve pharmaceutical properties of drugs, complexes are synthesized as combinations with other chemical substances. The complexes of fenamic acid and its derivatives, such as mefenamic-, tolfenamic- and flufenamic acid, with acridine were obtained and the X-ray structures were discussed. Formation of the crystals is determined by the presence of the intermolecular O–H(…)N hydrogen bond that occur between fenamic acids and acridine. Intermolecular interactions stabilizing the crystals such as π(…)π stacking, C–H(…)X (X = O, Cl) intermolecular hydrogen bonds as well as C–H(…)π and other dispersive interactions were analyzed by theoretical methods: the quantum theory of atoms in molecules (QTAIM) and noncovalent interaction (NCI) approaches.
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spelling pubmed-81563962021-05-28 The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes Krawczyk, Marta S. Sroka, Adam Majerz, Irena Molecules Article In order to improve pharmaceutical properties of drugs, complexes are synthesized as combinations with other chemical substances. The complexes of fenamic acid and its derivatives, such as mefenamic-, tolfenamic- and flufenamic acid, with acridine were obtained and the X-ray structures were discussed. Formation of the crystals is determined by the presence of the intermolecular O–H(…)N hydrogen bond that occur between fenamic acids and acridine. Intermolecular interactions stabilizing the crystals such as π(…)π stacking, C–H(…)X (X = O, Cl) intermolecular hydrogen bonds as well as C–H(…)π and other dispersive interactions were analyzed by theoretical methods: the quantum theory of atoms in molecules (QTAIM) and noncovalent interaction (NCI) approaches. MDPI 2021-05-16 /pmc/articles/PMC8156396/ /pubmed/34065674 http://dx.doi.org/10.3390/molecules26102956 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
Krawczyk, Marta S.
Sroka, Adam
Majerz, Irena
The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title_full The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title_fullStr The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title_full_unstemmed The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title_short The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
title_sort crystal structure and intermolecular interactions in fenamic acids–acridine complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156396/
https://www.ncbi.nlm.nih.gov/pubmed/34065674
http://dx.doi.org/10.3390/molecules26102956
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