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One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations

In one pot, the self-assembly of AgNO(3) and 2-chloroquinoxaline (2Cl-quinox) in water–ethanol mixture afforded two novel crystalline Ag(I) complexes. The major product is the polymeric complex [Ag(2Cl-quinox)(NO(3))](n); (1), while the minor product (2) comprises two molecules which are the monomer...

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Autores principales: El-Naggar, Mostafa A., Sharaf, Mona Mohammed, Albering, Jörg H., Abu-Youssef, Morsy A. M., Kassem, Taher S., Soliman, Saied M., Badr, Ahmed M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719528/
https://www.ncbi.nlm.nih.gov/pubmed/36463246
http://dx.doi.org/10.1038/s41598-022-24030-x
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author El-Naggar, Mostafa A.
Sharaf, Mona Mohammed
Albering, Jörg H.
Abu-Youssef, Morsy A. M.
Kassem, Taher S.
Soliman, Saied M.
Badr, Ahmed M. A.
author_facet El-Naggar, Mostafa A.
Sharaf, Mona Mohammed
Albering, Jörg H.
Abu-Youssef, Morsy A. M.
Kassem, Taher S.
Soliman, Saied M.
Badr, Ahmed M. A.
author_sort El-Naggar, Mostafa A.
collection PubMed
description In one pot, the self-assembly of AgNO(3) and 2-chloroquinoxaline (2Cl-quinox) in water–ethanol mixture afforded two novel crystalline Ag(I) complexes. The major product is the polymeric complex [Ag(2Cl-quinox)(NO(3))](n); (1), while the minor product (2) comprises two molecules which are the monomeric [Ag(2Cl-quinox)(2)(NO(3))]; (2a) and polymeric [Ag(2Cl-quinox)(NO(3))](n); (2b) complexes. The single crystal X-ray structure revealed that 1 and 2b are made up of two-dimensional infinite sheets. In contrast, 2a is a monomeric complex which has a highly distorted tetrahedral geometry around Ag(I) center. In all cases, the 2Cl-quinox molecule acts as a terminal monodentate ligand. Complexes 1 and 2b have similar molecular structures and also have almost similar crystal packing. Using Hirshfeld surface analysis, the O…H hydrogen bonds and π–π stacking interactions contributed significantly to the molecular packing. Both complexes have broad-spectrum action towards multi drug-resistance bacteria. The most effective function of 2 is against Proteus morganii, with a MIC value of 8 μg/mL. Complex 2 (IC(50) = 5.93 ± 0.52 μg/mL) has remarkably greater cytotoxic effect against lung carcinoma (A-549) than cis-platin (IC(50) = 7.5 ± 0.69 μg/mL) and AgNO(3) (IC(50) = 14.7 ± 0.53 μg/mL). The higher Ag-content in 2 could be the main reason for its higher cytotoxicity than 1.
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spelling pubmed-97195282022-12-05 One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations El-Naggar, Mostafa A. Sharaf, Mona Mohammed Albering, Jörg H. Abu-Youssef, Morsy A. M. Kassem, Taher S. Soliman, Saied M. Badr, Ahmed M. A. Sci Rep Article In one pot, the self-assembly of AgNO(3) and 2-chloroquinoxaline (2Cl-quinox) in water–ethanol mixture afforded two novel crystalline Ag(I) complexes. The major product is the polymeric complex [Ag(2Cl-quinox)(NO(3))](n); (1), while the minor product (2) comprises two molecules which are the monomeric [Ag(2Cl-quinox)(2)(NO(3))]; (2a) and polymeric [Ag(2Cl-quinox)(NO(3))](n); (2b) complexes. The single crystal X-ray structure revealed that 1 and 2b are made up of two-dimensional infinite sheets. In contrast, 2a is a monomeric complex which has a highly distorted tetrahedral geometry around Ag(I) center. In all cases, the 2Cl-quinox molecule acts as a terminal monodentate ligand. Complexes 1 and 2b have similar molecular structures and also have almost similar crystal packing. Using Hirshfeld surface analysis, the O…H hydrogen bonds and π–π stacking interactions contributed significantly to the molecular packing. Both complexes have broad-spectrum action towards multi drug-resistance bacteria. The most effective function of 2 is against Proteus morganii, with a MIC value of 8 μg/mL. Complex 2 (IC(50) = 5.93 ± 0.52 μg/mL) has remarkably greater cytotoxic effect against lung carcinoma (A-549) than cis-platin (IC(50) = 7.5 ± 0.69 μg/mL) and AgNO(3) (IC(50) = 14.7 ± 0.53 μg/mL). The higher Ag-content in 2 could be the main reason for its higher cytotoxicity than 1. Nature Publishing Group UK 2022-12-03 /pmc/articles/PMC9719528/ /pubmed/36463246 http://dx.doi.org/10.1038/s41598-022-24030-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
El-Naggar, Mostafa A.
Sharaf, Mona Mohammed
Albering, Jörg H.
Abu-Youssef, Morsy A. M.
Kassem, Taher S.
Soliman, Saied M.
Badr, Ahmed M. A.
One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title_full One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title_fullStr One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title_full_unstemmed One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title_short One pot synthesis of two potent Ag(I) complexes with quinoxaline ligand, X-ray structure, Hirshfeld analysis, antimicrobial, and antitumor investigations
title_sort one pot synthesis of two potent ag(i) complexes with quinoxaline ligand, x-ray structure, hirshfeld analysis, antimicrobial, and antitumor investigations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719528/
https://www.ncbi.nlm.nih.gov/pubmed/36463246
http://dx.doi.org/10.1038/s41598-022-24030-x
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