One-pot synthesis, characterization, photocatalytic activity and biological studies of Co(II), Ni(II) and Cu(II) complexes of a tetraazamacrocyclic Schiff base

Template condensation between pentane-1,5-dial and triethylenetetramine in the presence of divalent metal salts in methanolic solution resulted in mononuclear 15-membered tetraazamacrocyclic Schiff base metal complexes, [M(C 11 H 22 N 4 )X 2 ], where M = Co(II), Ni(II) and Cu(II), X = Cl − and C 11...

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Bibliographic Details
Published inJournal of coordination chemistry Vol. 76; no. 5-6; pp. 729 - 748
Main Authors Remiya, J. P., Shyni, B., Sikha, T. S., Parvathy, U. R.
Format Journal Article
LanguageEnglish
Published Abingdon Taylor & Francis 19.03.2023
Taylor & Francis Ltd
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Summary:Template condensation between pentane-1,5-dial and triethylenetetramine in the presence of divalent metal salts in methanolic solution resulted in mononuclear 15-membered tetraazamacrocyclic Schiff base metal complexes, [M(C 11 H 22 N 4 )X 2 ], where M = Co(II), Ni(II) and Cu(II), X = Cl − and C 11 H 22 N 4 is the tetradentate macrocyclic ligand. The bonding and overall geometry of the complexes are inferred through elemental analysis, FT-IR, UV-vis, 1 H/ 13 C NMR, ESI-mass, molar conductance, magnetic susceptibility and TG measurements. On the basis of the absorption bands in UV-vis spectra and magnetic moment analyses, a six-coordinate octahedral geometry is proposed for all the metal complexes. The formulation of the metal chelates is compatible with the thermal decomposition profiles. Photocatalytic efficiency of the macrocyclic Ni(II) complex was studied using solar water-splitting. The in vitro antimicrobial activity of metal complexes has been tested against certain bacterial and fungal species. The scavenging ability of DPPH free radicals was used to test the antioxidant activity of the complexes. In addition, MTT assay was used to assess the cytotoxicity of Cu(II) chloro complex against L929 mouse fibroblast cell lines.
ISSN:0095-8972
1029-0389
DOI:10.1080/00958972.2023.2199440