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Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes
ONO-Pincer Schiff base salicylidene (HSaln ligand) complexes with VO(2+), UO(2)(2+), MoO(2)(2+) and Mn(2+) ions (MSaln complexes = VOSaln, UO(2)Saln, MoO(2)Saln and MnSaln, respectively) were synthesized and fully characterized by different physico-chemical tools. The VOSaln complex was further trea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074042/ https://www.ncbi.nlm.nih.gov/pubmed/35529964 http://dx.doi.org/10.1039/c9ra06816c |
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author | Adam, Mohamed Shaker S. El-Hady, Omar M. Ullah, Farman |
author_facet | Adam, Mohamed Shaker S. El-Hady, Omar M. Ullah, Farman |
author_sort | Adam, Mohamed Shaker S. |
collection | PubMed |
description | ONO-Pincer Schiff base salicylidene (HSaln ligand) complexes with VO(2+), UO(2)(2+), MoO(2)(2+) and Mn(2+) ions (MSaln complexes = VOSaln, UO(2)Saln, MoO(2)Saln and MnSaln, respectively) were synthesized and fully characterized by different physico-chemical tools. The VOSaln complex was further treated with 1,10-phenanthroline which afforded a new VO-complex (VOSaln-Ph). All complexes and their ligands, as eco-friendly reagents, were explored for their biological potential as antibacterial and antifungal agents. Reactivity of MSaln complexes against the tested pathogen strains exhibited a remarkable inhibitory effect compared to the coordinated ligand (HSaln) and applicable standard drugs. Moreover, the MSaln complex-DNA interaction was investigated by ultraviolet-visible spectroscopy, viscosity and gel electrophoresis techniques affording binding strengths in the order: UO(2)Saln > MnSaln > MoO(2)Saln > VOSaln-Ph > VOSaln. Additionally, the biological potential of the investigated compounds was further explored by molecular docking to illustrate the nature of the drug–DNA interactions. All MSaln complexes show respectable anti-proliferative potential as anticancer agents against selected human carcinoma cell lines. Aside from the biological activities these complexes (MSaln complexes) were also investigated for catalytic efficiency in the Suzuki–Miyaura cross-coupling system of phenylboronic acid with 2-bromopyridine in water, sustainably. The results indicated that the MnSaln catalyst performed well with high yield. The catalytic potential of MnSaln was compared in water, water–ionic liquid mixtures and ionic liquids. |
format | Online Article Text |
id | pubmed-9074042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90740422022-05-06 Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes Adam, Mohamed Shaker S. El-Hady, Omar M. Ullah, Farman RSC Adv Chemistry ONO-Pincer Schiff base salicylidene (HSaln ligand) complexes with VO(2+), UO(2)(2+), MoO(2)(2+) and Mn(2+) ions (MSaln complexes = VOSaln, UO(2)Saln, MoO(2)Saln and MnSaln, respectively) were synthesized and fully characterized by different physico-chemical tools. The VOSaln complex was further treated with 1,10-phenanthroline which afforded a new VO-complex (VOSaln-Ph). All complexes and their ligands, as eco-friendly reagents, were explored for their biological potential as antibacterial and antifungal agents. Reactivity of MSaln complexes against the tested pathogen strains exhibited a remarkable inhibitory effect compared to the coordinated ligand (HSaln) and applicable standard drugs. Moreover, the MSaln complex-DNA interaction was investigated by ultraviolet-visible spectroscopy, viscosity and gel electrophoresis techniques affording binding strengths in the order: UO(2)Saln > MnSaln > MoO(2)Saln > VOSaln-Ph > VOSaln. Additionally, the biological potential of the investigated compounds was further explored by molecular docking to illustrate the nature of the drug–DNA interactions. All MSaln complexes show respectable anti-proliferative potential as anticancer agents against selected human carcinoma cell lines. Aside from the biological activities these complexes (MSaln complexes) were also investigated for catalytic efficiency in the Suzuki–Miyaura cross-coupling system of phenylboronic acid with 2-bromopyridine in water, sustainably. The results indicated that the MnSaln catalyst performed well with high yield. The catalytic potential of MnSaln was compared in water, water–ionic liquid mixtures and ionic liquids. The Royal Society of Chemistry 2019-10-25 /pmc/articles/PMC9074042/ /pubmed/35529964 http://dx.doi.org/10.1039/c9ra06816c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Adam, Mohamed Shaker S. El-Hady, Omar M. Ullah, Farman Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title | Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title_full | Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title_fullStr | Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title_full_unstemmed | Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title_short | Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes |
title_sort | biological and catalytic potential of sustainable low and high valent metal-schiff base sulfonate salicylidene pincer complexes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074042/ https://www.ncbi.nlm.nih.gov/pubmed/35529964 http://dx.doi.org/10.1039/c9ra06816c |
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