The effect of structural configuration on the DNA binding and in vitro antioxidant properties of new copper(ii) N2O2 Schiff base complexes. (20th June 2022)

• Record Type: Journal Article
• Authors: Yusuf, Tunde Lewis; Akintayo, Damilola Caleb; Oladipo, Segun Daniel; Adeleke, Adesola Abimbola; Olofinsan, Kolawole; Vatsha, Banele; Mabuba, Nonhlagabezo
• Is Part Of: New journal of chemistry. Volume 46:Number 27(2022)
• Page Start: 12968
• Page End: 12980
• Publication Date: 2022-06-20
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d2nj01477g
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : DNA interaction with cis and trans -copper NO complexes favours the cis configuration due to low energies observed in the cis configuration. Abstract : The interaction of transition metal complexes with DNA and plasma protein gives insight into the development of new materials for medical and biotechnology applications. Thus, we synthesized new series of copper(ii ) N, O-Schiff base complexes, [Cu(L 1 )2 ] (1 ), [Cu(L 2 )2 ] (2 ) and [Cu(L 3 )2 ] (3 ) (HL 1 = 2-(((2-chlorophenyl)imino)methyl)phenol, HL 2 = 2-(((2-isopropylphenyl)imino)methyl)phenol, and HL 3 = 2-(((2-methoxyphenyl)imino)methyl)phenol). The complexes were elucidated by X-ray crystallography, mass spectrometry, cyclic voltammetry, elemental analysis, FT-IR, and UV-visible spectroscopies. The crystal structures of complexes 1 & 2 reveal that the copper(ii ) centre adopts a slightly distorted square planar geometry bearing two bidentate Schiff base ligands L 1, L 2, respectively. The ligands adopted a κ 2 N:O coordination mode via the imine nitrogen and phenolate oxygen atoms. The geometry around the copper(ii ) centre in complex 3 deviates significantly from an ideal square planar geometry with bond angles O(1) 1 –Cu(1)–O(1) and N(1) 1 –Cu(1)–N(1) at 88.69(12)° and 99.27(11)°, respectively. The N, N, O, O coordinating atoms from the two ligands adopt a trans -configuration in 1 & 2 and cis -configuration in 3 . The interaction of these complexes with calf thymus–DNA by UV/Vis spectroscopies indicated high intrinsic binding constants ( K b ) in the range of 10 4 to 10 6 M −1 . From the binding constant values ( K b ), we noted that complex 3 with cis -configuration had the highest K b value. The in vitro antioxidant properties of the complexes were evaluated using four different assays at different concentrations to evaluate their antioxidant potential. Complex 1, with the lowest IC50 value of 93.28 μM has the highest NO˙ scavenging ability than other complexes and ascorbic acid (reference drug) with IC50 values of 133.41 μM. This study revealed that complex 3 containing the methoxy substituent and cis -configuration had the highest CT-DNA binding affinity and radical scavenging ability. Ab initio simulations of the electronic and structural properties of the complexes were carried out to estimate some quantum chemical properties of these complexes.