Search

Two mononuclear complexes of Co(II) and Zn(II) with a [MO6] coordination sphere, [Co(L)2(H2O)2] (1) and [Zn(L)2(H2O)2] (2), are prepared and characterized through spectral, single crystal X-ray and DFT/TD-DFT studies. The X-ray structure reveals an octahedral geometry with all the oxygen donor sets around the metal ion. DFT studies confirm the cobalt complex is high spin with a +2 oxidation state. Time dependent density functional theory (TD-DFT) shows the electronic transitions to be metal to ligand (MLCT) and intra-ligand charge transfer (ILCT) type. The complexes consolidate the crystal lattice via extensive non-covalent interactions, which are verified by Hirshfeld surface analysis. These non-covalent interactions are also responsible for the enhanced DNA binding affinity of the complexes as confirmed theoretically by molecular docking studies. The Zn(II) complex binds to DNA with more affinity due to the lesser HOMO–LUMO energy gap calculated by DFT analysis. The complexes are assessed for catecholase like activity for oxidation of 3,5-DTBC to 3,5-DTBQ in ethanol. 1 shows catecholase activity with the parameters Kcat = 168.5 h−1, KM = 0.00043 M and Vmax = 4.68 × 10−2 M min−1. ESI-MS identifies possible intermediates formed during the catalytic cycle while EPR and cyclic voltammetry confirm the mechanism of the catalytic oxidation to be metal centered rather than radical formation. The catecholase activity of 1 and inactivity of 2 are also corroborated by density functional theory (DFT) analysis. The theoretical analysis results are in good agreement with the experimental findings concerning the structure, electronic spectra, DNA binding affinity and catecholase like activity. Most interestingly, the present Co(II) complex is discovered to be a better catecholase mimic and the activity could be tuned by modifications in the metal or structural features of the ligand(s) and complexes. [ABSTRACT FROM AUTHOR]

Abstract A homodinuclear Cu(II) complex, [Cu 2 (H 2 tea) 2 (4-methoxybenzoate) 2 ]·2H 2 O (1) [H 3 tea = triethanolamine] containing a methoxy benzoate auxiliary was crystallized out and characterized by spectral and single crystal X-ray crystallography. Both the Cu(II) ions adopt a distorted octahedral geometry. Non-covalent C H··· π interactions generate a 1D chain thus consolidating the crystal lattice of 1. The complex was studied for the binding properties with Ct-DNA employing UV–visible, fluorescence, viscosity measurements, circular dichroism (CD) and cyclic voltammetric (CV) techniques. The theoretical analyses (molecular docking and DFT) corroborate well the experimental results. Graphical abstract A homodinuclear Cu(II) complex binds with CT DNA in a non-intercalating mode as studied by experimental and theoretical (docking and DFT) studies. Image 1 Highlights • A homodinuclear Cu(II) complex of triethanolamine has been prepared and characterized. • Crystal structure analysis reveals a distorted octahedral geometry around the Cu(II) ion. • DNA binding studies are performed using spectral, viscosity, CD and CV techniques. • Experimental DNA binding results are corroborated well with DFT and docking studies. [ABSTRACT FROM AUTHOR]