Applied Organometallic Chemistry · 2014 · 19 citations · 38 references
Natural SciencesChemistryMolecular BiologyInorganic ChemistryNucleic Acid ChemistryStructural BiologyCoordination ChemistryDna ChemistryLigand BindingMetal-ligand BondingReceptor-ligand InteractionsTransition Metal ComplexesComplexation ChemistryIntermolecular Metal-ligand InteractionsOctahedral ComplexesOctahedral CoordinationQuinoxaline ChemistryQuinoxaline SynthesisSpectroscopic Characterization Of Metal-ligand BondsSupramolecular Coordination Complexes
Three new mononuclear cobalt(II) complexes containing ligands with extended planar quinoxaline moieties, {dipyrido[3,2‐a:2′,3′‐c]phenazine (dppz) or dipyrido[3,2‐d:2′,3′‐f]quinoxaline (dpq)}, viz. [Co(dppz)(acac) 2 ] · CH 3 OH ( 1 ), [Co(dpq)(tfnb) 2 ] ( 2 ) and [Co(dpq)(dbm) 2 ] ( 3 ), where acac = acetylacetonate, tfnb = benzoyltrifluoroacetone and dbm = dibenzoylmethane, have been synthesized and structurally characterized as octahedral complexes. The binding ability of the complexes with calf thymus (CT)‐DNA has been investigated by spectroscopic and viscosity measurements. Results indicate that all complexes bind to CT‐DNA via intercalative mode, and the DNA binding affinity of dppz complex 1 is apparently stronger than that of dpq complexes 2 and 3 . Furthermore, DNA photocleavage experiments indicate that these complexes are efficient DNA cleaving agents in UV‐A (365 nm) and hydroxyl radical (HO · ), singlet oxygen ( 1 O 2 ) and superoxide anion ( 1 O 2 − ) serve as the major cleavage active species. In addition, interaction of the complexes with bovine serum albumin (BSA) was investigated using UV − visible and fluorescence methods, which indicated that all complexes could quench the intrinsic fluorescence of BSA in a static quenching process. Copyright © 2014 John Wiley & Sons, Ltd.
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