Tuned structure and DNA binding properties of metal complexes based on a new 4-acylpyrazolone derivative. (23rd January 2020)

• Record Type: Journal Article
• Authors: Xi, Wei; Song, Fu-Qiang; Xia, Xue-Li; Song, Xue-Qin
• Is Part Of: New journal of chemistry. Volume 44:Number 6(2020)
• Page Start: 2281
• Page End: 2290
• Publication Date: 2020-01-23
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c9nj05948b
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : The structure and DNA binding performance of three transition metal compounds based on a new pyrazolone ligand were tuned effectively by changing both metal cations and anions. Abstract : It is common knowledge that the spatial structure of substrates is the major influencing factor in DNA binding. To tune the binding affinity of DNA, a new 4-acylpyrazolone derivative ligand, (2-hydroxy- N ′-((5-hydroxy-3-methyl-1-(4-nitrophenyl)-4, 5-dihydro-1 H -pyrazol-4-yl)(phenyl)methylene)benzohydrazide) (H2 L ) and its three complexes have been prepared and well characterized. Reaction of H2 L with CuCl2 resulted in a mononuclear compound with tetra-coordinated quadrilateral plane, [Cu(HL)Cl] (1 ). When H2 L was coordinated to Cu(OAc)2, a dinuclear Cu(ii ) compound with chemical formula of [Cu2 L2 (CH3 OH)2 ]·CH3 OH (2 ) was obtained, and the coordination geometry of Cu(ii ) is a square pyramid. Upon assembly of H2 L with Mn(OAc)2, a quite different dinuclear compound with chemical composition of [Mn2 L2 (O CH3 )2 (H2 O)2 ]·CH3 OH (3 ) was afforded, where Mn(iii ) displayed distorted octahedral configurations. DNA binding studies were performed on H2 L and its three complexes by means of electron absorption titration and EB–DNA competition experiments, and the results indicate they all bind DNA in an intercalation mode, and their binding affinity follows the order of 1 > 2 > 3 > H2 L . In addition, time-dependent density functional theory (TD-DFT) calculations were performed for H2 L and its three complexes to better clarify the electronic transitions in the UV-vis spectra.