Citation: ZHANG Yong-Po, YANG Jia-Jia, LÜ Jia-Yuan, GAO Chun-Yan, ZHAO Jin-Zhong. Syntheses, Structures, DNA/BSA Binding and DNA Cleavage of Mononuclear Manganese(Ⅱ) and Cobalt(Ⅱ) Complexes with N,O-Chelating Quinoline Derivative Ligand[J]. Chinese Journal of Inorganic Chemistry, ;2016, 32(12): 2172-2182. doi: 10.11862/CJIC.2016.265 shu

Syntheses, Structures, DNA/BSA Binding and DNA Cleavage of Mononuclear Manganese(Ⅱ) and Cobalt(Ⅱ) Complexes with N,O-Chelating Quinoline Derivative Ligand

1.
College of Arts and Sciences, Shanxi Agricultural University, Taigu, Shanxi 030801, China

Corresponding author: GAO Chun-Yan, ZHAO Jin-Zhong,
Received Date: 15 June 2016
Available Online: 29 September 2016
Fund Project:

Two new mononuclear complexes[ML(H₂O)₃]·H₂O (M=Mn(1) and Co(2)) of quinoline derivative ligand (Na₂L=sodium 8-(carboxylatomethoxy)quinoline-2-carboxylate) have been synthesized and characterized. The complexes are isostructural and both metal centers are heptacoordinated with O₆N donor sets and the geometry around metal centers can be best described as distorted pentagonal bipyramidal. Interactions of the complexes with CT-DNA and BSA have been explored by absorption and emission spectral methods. Binding abilities of the complexes to CT-DNA display a relative order:2>1, while the quenching mechanisms of BSA by both complexes are static procedures and the binding constant values follow the order:1>2. In the presence of H₂O₂ as a revulsant or an activator, compared with complex 1, the DNA cleavage efficiency of 2 exhibited more remarkable increases at the same conditions. Oxidative mechanism has been demonstrated by adding standard radical scavengers and the reactive oxygen species (ROS) responsible for the DNA cleavage is likely hydroxyl radicals (OH·).
- complexes;quinoline ligand;DNA/BSA binding;DNA cleavage
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沈阳化工大学材料科学与工程学院沈阳 110142