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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Main Authors: Marta S. Krawczyk, Adam Sroka, Irena Majerz
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/10/2956
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spelling doaj-eaaae85f4446424ebd074cfbf1345e042021-06-01T00:10:49ZengMDPI AGMolecules1420-30492021-05-01262956295610.3390/molecules26102956The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine ComplexesMarta S. Krawczyk0Adam Sroka1Irena Majerz2Faculty of Pharmacy, Wrocław Medical University, Borowska 211a, 50-556 Wrocław, PolandFaculty of Pharmacy, Wrocław Medical University, Borowska 211a, 50-556 Wrocław, PolandFaculty of Pharmacy, Wrocław Medical University, Borowska 211a, 50-556 Wrocław, PolandIn 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<sup>…</sup>N hydrogen bond that occur between fenamic acids and acridine. Intermolecular interactions stabilizing the crystals such as π<sup>…</sup>π stacking, C–H<sup>…</sup>X (X = O, Cl) intermolecular hydrogen bonds as well as C–H<sup>…</sup>π and other dispersive interactions were analyzed by theoretical methods: the quantum theory of atoms in molecules (QTAIM) and noncovalent interaction (NCI) approaches.https://www.mdpi.com/1420-3049/26/10/2956fenamic acidsacridinecomplexQTAIMNCI approach
collection DOAJ
language English
format Article
sources DOAJ
author Marta S. Krawczyk
Adam Sroka
Irena Majerz
spellingShingle Marta S. Krawczyk
Adam Sroka
Irena Majerz
The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes
Molecules
fenamic acids
acridine
complex
QTAIM
NCI approach
author_facet Marta S. Krawczyk
Adam Sroka
Irena Majerz
author_sort Marta S. Krawczyk
title 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_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_sort crystal structure and intermolecular interactions in fenamic acids–acridine complexes
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-05-01
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<sup>…</sup>N hydrogen bond that occur between fenamic acids and acridine. Intermolecular interactions stabilizing the crystals such as π<sup>…</sup>π stacking, C–H<sup>…</sup>X (X = O, Cl) intermolecular hydrogen bonds as well as C–H<sup>…</sup>π and other dispersive interactions were analyzed by theoretical methods: the quantum theory of atoms in molecules (QTAIM) and noncovalent interaction (NCI) approaches.
topic fenamic acids
acridine
complex
QTAIM
NCI approach
url https://www.mdpi.com/1420-3049/26/10/2956
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