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Hydrolytic Cleavage of DNA by Ternary Amino Acid Schiff Base Copper( II ) Complexes Having Planar Heterocyclic Ligands
Author(s) -
Reddy Pattubala A. N.,
Nethaji Munirathinam,
Chakravarty Akhil R.
Publication year - 2004
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200300514
Subject(s) - chemistry , schiff base , square pyramidal molecular geometry , coordination geometry , stereochemistry , copper , salicylaldehyde , ligand (biochemistry) , phenanthroline , crystallography , medicinal chemistry , crystal structure , hydrogen bond , molecule , organic chemistry , receptor , biochemistry
The ternary copper( II ) complexes [Cu(salgly)L] (L = phen, 1 ; dpq, 2 ), [Cu(salala)L] (L = phen, 3 ; dpq, 4 ) and [Cu(salphe)L] (L = phen, 5 ; dpq, 6 ), where salgly, salala and salphe are tridentate Schiff‐base ligands derived from the condensation of salicylaldehyde with glycine, L ‐alanine and L ‐phenylalanine, respectively, are prepared and their nuclease activity studied (phen, 1,10‐phenanthroline; dpq, dipyridoquinoxaline). The crystal structure of 3 displays a distorted square‐pyramidal (4+1) coordination geometry in which the ONO‐donor Schiff base is bonded to the metal atom in the basal plane. The chelating phen ligand displays an axial−equatorial mode of bonding. The complexes exhibit a d−d band near 670 nm and a charge transfer band near 370 nm in methanol. The one‐electron paramagnetic complexes display axial EPR spectra in DMF glass at 77 K, indicating a {d x 2− y 2} 1 ground state. The complexes are redox‐active and exhibit a quasi‐reversible Cu II /Cu I couple in DMF at approximately −0.6 V vs. SCE. They show catalytic activity in the oxidation of ascorbic acid by molecular oxygen. The ability of the complexes to bind calf thymus (CT) DNA follows the order: 2 ≈ 4 ≈ 6 > 1 ≈ 3 ≈ 5 . Complexes 1 − 6 show oxidative DNA cleavage activity in the presence of mercaptopropionic acid as a reducing agent. All the complexes show hydrolytic cleavage activity in the absence of light or any reducing agent. The oxidative and hydrolytic DNA cleavage efficiencies follow the order: 2 ≈ 4 ≈ 6 > 1 ≈ 3 ≈ 5 . The dpq complexes, which have a greater DNA binding ability, display enhanced nuclease activity than their phen analogues. The hydrolytic DNA cleavage rate of 1.8 h −1 , observed for 2 , is significantly high relative to most of the known copper‐based synthetic hydrolases. Mechanistic pathways involved in the nuclease activity of the complexes are discussed. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)