Department of Chemistry, Bharathiar University, Coimbatore 641 046, India.
Eur J Med Chem. 2012 Sep;55:420-31. doi: 10.1016/j.ejmech.2012.08.001. Epub 2012 Aug 10.
Bivalent, ruthenium organometallics containing hydrazone ligands with the composition [RuH(CO)(PPh(3))(2)(L(1-3))] (4-6) have been synthesised from the reactions of [RuH(2)(CO)(PPh(3))(3)] and benzoic acid pyridine-2-ylmethylene-hydrazide (HL(1)) (1) /benzoic acid (1-pyridin-2-yl-ethylidene)-hydrazide (HL(2)) (2)/benzoic acid (phenyl-pyridin-2-yl-methylene)-hydrazide (HL(3)) (3) and characterised by various physico-chemical techniques. The X-ray crystal structure of one of the above complexes, [RuH(CO)(PPh(3))(2)(L(3))] (6) demonstrated a distorted octahedral coordination geometry around the metal centre. Results of our investigation on the effect of substitution (H or CH(3) or C(6)H(5)) at the azomethine carbon of coordinated hydrazone in these ruthenium chelates on the potential binding with DNA/BSA, free radical scavenging and cytotoxicity is presented.
二价钌有机金属配合物,含有腙配体,其组成为[RuH(CO)(PPh(3))(2)(L(1-3))](4-6),是由[RuH(2)(CO)(PPh(3))(3)]和苯甲酸吡啶-2-基亚甲基腙(HL(1))(1)/苯甲酸(1-吡啶-2-基亚乙基)腙(HL(2))(2)/苯甲酸(苯并吡啶-2-基亚甲基)腙(HL(3))(3)反应合成的,并通过各种物理化学技术进行了表征。上述配合物之一[RuH(CO)(PPh(3))(2)(L(3))](6)的 X 射线晶体结构表明,金属中心周围的配位几何形状为扭曲的八面体。我们研究了配位腙中与氮相连的亚胺碳原子上的取代基(H 或 CH(3)或 C(6)H(5))对这些钌配合物与 DNA/BSA 的潜在结合、自由基清除和细胞毒性的影响。