Article

New homodi-and heterotrinuclear metal complexes of Schiff base compartmental ligand: interaction studies of copper complexes with calf thymus DNA

Central European Journal of Chemistry (impact factor: 1.07). 04/2012; 4(3):502-522. DOI:10.2478/s11532-006-0020-6 pp.502-522

ABSTRACT The new homodinuclear complexes 1–4 of the type [LMII
2Cl2], heterotrinuclear complexes 5 and 6 of the type [LMII
2SnIVCl6] where M = CuII, MnII, CoII, NiII and CuII and NiII, respectively have been synthesized and characterized by elemental analysis and various spectroscopic techniques. The homodinuclear
complexes possess two different environments (N2 and N2O2donor sets) for holding the metal ions. The metal ion in N2 set exhibits square planar geometry with two chloride ions in the inner sphere but rhombic structure is found in tetradentate
N2O2 Schiff base cavity while in heterotrinuclear complexes SnIV atom is in the octahedral environment. The interaction of complexes 1 and 5 with calf thymus DNA was carried out by absorption spectroscopy and cyclic voltammetry. The intrinsic binding constants (K

b
) of complex 1 and 5 were determined as 3.2 × 103 M−1 and 9.6 × 103 M−1, respectively suggesting that complex 5 binds more strongly to CT-DNA than complex 1. Fluorescence studies along with viscosity measurements have also been checked to authenticate the binding of metal complexes
with DNA.

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Keywords

chloride ions
 
complex 1
 
complex 1. Fluorescence studies
 
complex 5 binds
 
complexes 1
 
elemental analysis
 
exhibits square planar geometry
 
heterotrinuclear complexes 5
 
heterotrinuclear complexes SnIV atom
 
inner sphere
 
intrinsic binding constants
 
metal complexes
 
metal ion
 
metal ions
 
MnII
 
new homodinuclear complexes 1–4
 
rhombic structure
 
various spectroscopic techniques
 
viscosity measurements
 

Suvigya Mathur