Citation: Xiao-Hong LI, Xian-Wei WU, Yuan WANG, Wei-Na WU. Synthesis, Crystal Structures, and DNA-Binding Properties of Cd(Ⅱ)/Fe(Ⅲ) Complexes with 4-Fluorophenyl-N-(quinolin-2-ylmethylene)thiosemicarbazide[J]. Chinese Journal of Inorganic Chemistry, ;2022, 38(9): 1790-1798. doi: 10.11862/CJIC.2022.176 shu

Synthesis, Crystal Structures, and DNA-Binding Properties of Cd(Ⅱ)/Fe(Ⅲ) Complexes with 4-Fluorophenyl-N-(quinolin-2-ylmethylene)thiosemicarbazide

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  • Two complexes [Cd2(L)2(NO3)2] (1) and [Fe(L)2]NO3·3CH3OH (2), as well as (H2L)NO3 (HL=4-fluorophenyl-N-(quinolin-2-ylmethylene)thiosemicarbazide) have been synthesized and structurally determined by single-crystal X-ray diffraction, elemental analysis, and IR. The results show that 1 is a centrosymmetry binuclear complex, in which each central Cd(Ⅱ) ion is coordinated by one independent anionic ligand L- with a [N2S] donor set, one bidentate nitrate anion, and another μ2-bridged S atom from the adjacent thiosemicarbazone, thus providing a distorted octahedron geometry. The Fe(Ⅲ) ion in complex 2 displays the same coordination geometry as the Cd(Ⅱ) ion in 1, while is surrounded by two tridentate L- ligands. The fluorescence spectra, the absorption spectra, and the viscosity measurements indicate that complex 2 could effectively bind with ct-DNA through intercalation mode, while HL and complex 1 might interact with ct-DNA by outside groove binding mode, and the binding affinity of complex 2 with ct-DNA was stronger than those of HL and complex 1. In addition, the results of cytotoxicity experiments showed that complex 2 had the strongest ability to inhibit the proliferation of HeLa tumor cells among the three compounds.
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