Co(III) and Ni(II) complexes of an anthracene appended aroyl hydrazone: Synthesis, crystal structures, DNA binding and catecholase activity

被引:48
|
作者
Mondal, Satyajit [1 ]
Pakhira, Bholanath [1 ]
Blake, Alexander J. [2 ]
Drew, Mike G. B. [3 ]
Chattopadhyay, Shyamal Kumar [1 ]
机构
[1] Indian Inst Engn Sci & Technol, Dept Chem, Sibpur 711103, Howrah, India
[2] Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, Notts, England
[3] Univ Reading, Dept Chem, Reading RG6 6AD, Berks, England
基金
英国工程与自然科学研究理事会;
关键词
Co(III) complex; Crystal structure; Voltammetry; DNA binding; Catecholase activity; COBALOXIME(II)-CATALYZED OXIDATIVE DEHYDROGENATION; 2,6-DIACETYLPYRIDINE DAP HYDRAZONES; TRINUCLEAR COPPER(II) COMPLEX; EFFECTIVE CORE POTENTIALS; MIXED-LIGAND COMPLEXES; MOLECULAR CALCULATIONS; COBALT(III) COMPLEXES; PROTONIC MODULATION; ENERGIES; OXIDASE;
D O I
10.1016/j.poly.2016.05.052
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The Co(III) and Ni(II) complexes [Co(L-2)(2)(bpy)]Cl (1) and [Ni(L-2)(2)(phen)] (2) (where L-2 is a monoanionic bidentate hydrazone ligand and bpy = 2,2'-bipyridine, phen = 1,10-phenanthroline) have been synthesized and characterized by infra-red, UV-Vis, ESI-MS spectroscopies and elemental analyses. Complexes 1 and 2 were structurally characterized by single crystal X-ray diffraction. Structural analysis reveals a distorted octahedral coordination environment around the metal center with an MN4O2 chromophore [M = Co(III) and NOD], with the hydrazone ligand acting as a monoanionic bidentate N, O-donor. Binding of complexes 1 and 2 with calf thymus DNA (CT-DNA) was investigated by UV-Vis absorption, fluorescence spectroscopy and viscosity measurements. Complex 1 shows excellent catecholase mimicking activity with 3,5-di-tert-butylcatechol (3,5-DTBCH2) as the substrate. Kinetic measurements suggest the rate of catechol oxidation follows saturation kinetics with respect to the substrate and the k(cat) value was found to be quite high, with a value of 1.00 x 10(5) h(-1). (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:327 / 337
页数:11
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