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Original Articles

DNA-binding and anti-oxidation properties of binuclear lanthanide(III) complexes of 8-hydroxyquinoline-7-carbaldehyde-(isonicotinyl)hydrazone

, , , , &
Pages 2041-2054 | Received 27 Dec 2011, Accepted 07 Mar 2012, Published online: 22 May 2012
 

Abstract

Binuclear complexes [LnL(NO3)(H2O)2]2 were prepared from the Schiff base 8-hydroxyquinoline-7-carbaldehyde-(isonicotinyl)hydrazone (H2L) and equivalent molar amounts of Ln(NO3)3 · 6H2O (Ln = La3+, Nd3+, Sm3+, Eu3+, Gd3+, Dy3+, Ho3+, Er3+, Yb3+), respectively. The ligand is dibasic tetradentate and the dimerization occurs through the phenolate oxygen atoms leading to a central four-membered (LnO)2-ring. The ligand and all the Ln(III) complexes can bind to calf thymus DNA through intercalation with binding constants of 105–106 (mol L−1)−1, and they show strong scavenging abilities on hydroxyl radicals and superoxide radicals. The values of SC 50 of Ln(III) complexes for HO and are 2.344−13.33 and 4.459−28.48 µmol L−1, respectively. Ln(III) complexes present stronger binding abilities to DNA and stronger anti-oxidation properties than ligand. Complex containing hydroxyl unit shows stronger scavenging abilities on hydroxyl radical, while complex containing N-heteroaromatic substituent shows stronger scavenging abilities on superoxide radicals. Furthermore, earlier rare metal complexes show stronger scavenging abilities on both hydroxyl radicals and superoxide radicals.

Acknowledgments

This study was supported by China NNSF (20975046) and Gansu Educational Fund SRP (1010B-04).

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