oa South African Journal of Chemistry - Synthesis, characterization and antimicrobial activity of copper(II) complexes of some ortho-substituted aniline Schiff bases; crystal structure of bis(2-methoxy-6-imino)methylphenol copper(II) complex : research article
|Article Title||Synthesis, characterization and antimicrobial activity of copper(II) complexes of some ortho-substituted aniline Schiff bases; crystal structure of bis(2-methoxy-6-imino)methylphenol copper(II) complex : research article|
|© Publisher:||South African Chemical Institute (SACI)|
|Journal||South African Journal of Chemistry|
|Affiliations||1 Lagos State University, Nigeria, 2 Rhodes University, 3 Rhodes University and 4 Nelson Mandela Metropolitan University|
|Publication Date||Jan 2014|
|Pages||45 - 51|
|Keyword(s)||Antimicrobial activity, Cu(II) complexes, o-Vanillin, Schiff bases and Substituted-aniline|
This study presents the synthesis, characterization and antimicrobial activity of copper(II) complexes of some ortho-substituted aniline Schiff bases (L1-L8). The Schiff bases and their respective copper(II) complexes were characterized by a combination of elemental analysis, infrared and UV/Visible studies. The structures of the ligands were also confirmed from 1H- and 13C-NMR spectral data. The infrared and electronic transition studies showed that the ligands are bidentate coordinating via the imine nitrogen and the phenolic oxygen atoms in a planar configuration. Introduction of aqueous ammonia to the ethanolic solution of L3/L4 and Cu(OAc)2. H2O aliquot yielded an ammonia-based complex due to the hydrolysis of the imine bond. The crystal structure of the resulting complex indicated a square planar geometry. The copper(II) ion crystallizes in the monoclinic system with a space group of P21/c having a = 10.9309, b = 4.85600, c = 17.7030, α = γ = 90 ° and β = 119.658 °. The geometry is slightly distorted from planarity with O1-Cu1-N1 bond angles of 92.19 ° and 87.8 °. The Schiff base ligands and their respective copper(II) complexes were screened for their in vitro antibacterial and antifungal activity against Escherichia coli ATCC® 8739*, Staphylococcus aureus subsp. aureus ATCC® 6538*, Bacillus subtilis subsp. spizizenii ATCC® 6633* and Candida albicans ATCC® 2091*. The o-vanillin-based ligands exhibited higher activity than the salicylaldehyde derivatives which were virtually non-active against the tested organisms.
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