Synthesis, structural characterization, DNA/Protein binding and in vitro cytotoxicity of isomeric ruthenium carbonyl complexes

被引:16
|
作者
Kalaivani, P. [1 ]
Prabhakaran, R. [1 ]
Dallemer, F. [2 ]
Vaishnavi, E. [3 ]
Poornima, P. [4 ]
Padma, V. Vijaya [4 ]
Renganathan, R. [3 ]
Natarajan, K. [1 ]
机构
[1] Bharathiar Univ, Dept Chem, Coimbatore 641046, Tamil Nadu, India
[2] Aix Marseille Univ, Ctr St Jerome, Lab Madirel, CNRS,UMR7246, F-13397 Marseille 20, France
[3] Bharathidasan Univ, Dept Chem, Tiruchirappalli 620015, India
[4] Bharathiar Univ, Dept Biotechnol, Coimbatore 641046, Tamil Nadu, India
关键词
Ruthenium(II) complexes; Salicylaldehyde-4(N)-ethylthiosemicarbazone; CT-DNA binding; Lysozyme protein binding; Three-dimensional fluorescence spectroscopy; Cytotoxicity; NITRIC-OXIDE SYNTHASE; HUMAN SERUM-ALBUMIN; THIOSEMICARBAZONE COMPLEXES; PALLADIUM(II) COMPLEXES; COORDINATION MODE; SCHIFF-BASE; 2-ACETYLPYRIDINE THIOSEMICARBAZONES; HYPOXIC SELECTIVITY; REDOX PROPERTIES; DONOR LIGANDS;
D O I
10.1016/j.jorganchem.2014.04.003
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of salicylaldehyde-4(N)-ethylthiosemicarbazone, [H-2-(Sal-etsc)] with [RuHCl(CO)(PPh3)(3)] afforded two isomeric ruthenium(II) carbonyl complexes namely [Ru(H-Sal-etsc)(CO)Cl(PPh3)(2)] (1) and [Ru(Sal-etsc)(CO)(PPh3)(2)]center dot Cl (2). The new complexes were characterized by various spectroscopic techniques (IR, Electronic, H-1 NMR and P-31 NMR) and X-ray crystallography. In this reaction, bidentate monobasic coordination with the formation of more strain NS four member chelate in (1) and tridentate monobasic coordination with the formation of ONS five and six member rings in (2) were observed. The binding interaction of complexes (1 and 2) to calf thymus(CT) DNA/Lysozyme has been explored. The cytotoxic nature of the complexes was evaluated on human lung/liver cancer cells, A549 and HepG2. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:67 / 80
页数:14
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