ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Syntheses, Crystal Structure, and Nuclease Activity of Oxalato-Bridged Dicopper(II) Complexes with Planar N-Donor Heterocyclic Bases

Thomas, Anitha M and Neelakanta, Girish and Mahadevan, Subramony and Nethaji, Munirathinam and Chakravarty, Akhil R (2002) Syntheses, Crystal Structure, and Nuclease Activity of Oxalato-Bridged Dicopper(II) Complexes with Planar N-Donor Heterocyclic Bases. In: European Journal of Inorganic Chemistry, 2002 (10). pp. 2720-2726.

[img] PDF
Restricted to Registered users only

Download (154kB) | Request a copy


Oxalato-bridged dicopper(II) complexes $[{CuL(H_2O)}_2(\mu - ox)]-(ClO_4)_2 (1-4)$, where L is a bidentate chelating heterocyclic base such as 2,2'-bipyridine (bpy, 1), 1,10-phenanthroline (phen, 2), dipyridoquinoxaline (dpq, 3) and dipyridophenazine (dppz, 4), were prepared by treatment of copper(II) perchlorate hexahydrate with sodium oxalate and L in aqueous ethanol. Complex 3 has been structurally characterised. The coordination geometry of the copper centres is essentially square-pyramidal. The ${CuL(H_2O)}$ units are bridged by an oxalate moiety to form the discrete dimeric core. Magnetic studies in the 20-300 K temperature range show the presence of an antiferromagnetically coupled dicopper(II) unit, giving -2J values in the $346-384 cm^{-1}$ range. The redox-active complexes retain the dimeric core in solution, and two quasireversible $Cu^{II}/Cu^I$ couples are observed in the potential range from 0.2 to -0.4 V vs. SCE in a DMF/tris-HCl/0.1 M KCl buffer system (1:1, v/v, pH = 7.2) with a glassy carbon working electrode. The binding and cleavage of DNA by the complexes have been studied. The intercalating ability of the planar bases, determined from the decrease of the fluorescence intensity of ethidium bromide bound calf thymus DNA on addition of the complex, gave the order: 3 > 4 > 2 >> 1. The nuclease activity of the complexes with supercoiled pUC19 DNA in DMF/tris-HCl/NaCl buffer (pH = 7.2) in the presence of ascorbic acid follows the order: 3 > 2 >> 4 > 1. The dpq complex exhibits the most efficient DNA binding and cleavage activity. The dppz complex shows good binding ability but poor nuclease activity.

Item Type: Journal Article
Publication: European Journal of Inorganic Chemistry
Publisher: Wiley-VCH Verlag GmbH
Additional Information: The copyright belongs to Wiley-VCH Verlag GmbH.
Keywords: catalysis;copper;crystal structure;magnetic properties;nuclease activity
Department/Centre: Division of Biological Sciences > Molecular Reproduction, Development & Genetics
Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 06 Mar 2006
Last Modified: 19 Sep 2010 04:23
URI: http://eprints.iisc.ac.in/id/eprint/5602

Actions (login required)

View Item View Item