Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base

The bivalent Co(II), Ni(II), Cu(II), and Zn(II) complexes (A, B, C, D) of novel Schiff base ligand such as 2-((E)-(5-(trifluoromethyl)-2-methoxyphenylimino)methyl)-4-chlorophenol (HL1) have been synthesized. The structural analysis have been carried by elemental analysis, NMR, FTIR, ESI-mass, UV–Vis...

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Main Authors: M. Swathi, Dasari Ayodhya, Shivaraj
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Results in Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211715623004708
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author M. Swathi
Dasari Ayodhya
Shivaraj
author_facet M. Swathi
Dasari Ayodhya
Shivaraj
author_sort M. Swathi
collection DOAJ
description The bivalent Co(II), Ni(II), Cu(II), and Zn(II) complexes (A, B, C, D) of novel Schiff base ligand such as 2-((E)-(5-(trifluoromethyl)-2-methoxyphenylimino)methyl)-4-chlorophenol (HL1) have been synthesized. The structural analysis have been carried by elemental analysis, NMR, FTIR, ESI-mass, UV–Visible, ESR, TGA and these results confirmed that Ni(II) and Cu(II) complexes were exhibit square planar geometry, whereas Co(II) and Zn(II) complexes exhibits octahedral geometry. DNA binding interaction studies such as UV absorption, viscosity, fluorescence techniques revealed that the mode of binding of complexes with DNA is intercalative mode. DNA cleavage studies revealed that all the complexes were cleaved into Form I & II. The pathological studies of all the complexes were screened against microbial strains in-vitro, which revealed that Cu(II) complexes are more potent compared to other complexes and free ligands. The antidiabetic and antioxidant activity studies revealed that Cu(II) complex exhibit slight higher activity. Cytotoxicity studies on cell lines (KB3 & MCF7 cell lines) revealed that the all synthesized complexes were showed superior activity compared to the ligand.
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spelling doaj.art-83ca51759acd4c30bc07ea90d64fa70b2023-12-03T05:41:07ZengElsevierResults in Chemistry2211-71562024-01-017101231Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff baseM. Swathi0Dasari Ayodhya1 Shivaraj2Department of Chemistry, Osmania University, Hyderabad, Telangana 500007, IndiaDepartment of Chemistry, Osmania University, Hyderabad, Telangana 500007, India; Chemical Group, Intellectual Property India, Patent Office, Guindy, Chennai, Tamil Nadu 600032, IndiaDepartment of Chemistry, Osmania University, Hyderabad, Telangana 500007, India; Corresponding author.The bivalent Co(II), Ni(II), Cu(II), and Zn(II) complexes (A, B, C, D) of novel Schiff base ligand such as 2-((E)-(5-(trifluoromethyl)-2-methoxyphenylimino)methyl)-4-chlorophenol (HL1) have been synthesized. The structural analysis have been carried by elemental analysis, NMR, FTIR, ESI-mass, UV–Visible, ESR, TGA and these results confirmed that Ni(II) and Cu(II) complexes were exhibit square planar geometry, whereas Co(II) and Zn(II) complexes exhibits octahedral geometry. DNA binding interaction studies such as UV absorption, viscosity, fluorescence techniques revealed that the mode of binding of complexes with DNA is intercalative mode. DNA cleavage studies revealed that all the complexes were cleaved into Form I & II. The pathological studies of all the complexes were screened against microbial strains in-vitro, which revealed that Cu(II) complexes are more potent compared to other complexes and free ligands. The antidiabetic and antioxidant activity studies revealed that Cu(II) complex exhibit slight higher activity. Cytotoxicity studies on cell lines (KB3 & MCF7 cell lines) revealed that the all synthesized complexes were showed superior activity compared to the ligand.http://www.sciencedirect.com/science/article/pii/S2211715623004708Coats redfern methodGeometrical optimizationThermodynamic parametersAnti-diabetic activityDNA interactionCytotoxicity study
spellingShingle M. Swathi
Dasari Ayodhya
Shivaraj
Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
Results in Chemistry
Coats redfern method
Geometrical optimization
Thermodynamic parameters
Anti-diabetic activity
DNA interaction
Cytotoxicity study
title Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
title_full Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
title_fullStr Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
title_full_unstemmed Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
title_short Design, structural characterization, DNA interaction studies, antibacterial, antioxidant, and cytotoxicity studies of Co(II), Ni(II), Cu((II), Zn((II) complexes containing 2-methoxy 5-trifluoromethyl benzenamine Schiff base
title_sort design structural characterization dna interaction studies antibacterial antioxidant and cytotoxicity studies of co ii ni ii cu ii zn ii complexes containing 2 methoxy 5 trifluoromethyl benzenamine schiff base
topic Coats redfern method
Geometrical optimization
Thermodynamic parameters
Anti-diabetic activity
DNA interaction
Cytotoxicity study
url http://www.sciencedirect.com/science/article/pii/S2211715623004708
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