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Synthesis, characterization and DNA-binding and DNA-photocleavage studies of two Ru(II) complexes containing two main ligands and one ancillary ligand
Authors:Jing Sun  Shuo WuHuo-Yan Chen  Feng GaoJie Liu  Liang-Nian JiZong-Wan Mao
Affiliation:a School of Pharmacy, Guangdong Medical College, Dongguan 523808, China
b MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
c Department of Chemistry, Jinan University, Guangzhou 510632, China
Abstract:
DNA-binding and DNA-photocleavage properties of two Ru(II) complexes, [Ru(L1)(dppz)2](PF6)4 (1) and [Ru(L2)(dppz)2](PF6)4 (2) (L1 = 5,5′-di(1-(triethylammonio)methyl)-2,2′-dipyridyl cation; L2 = 5,5′-di(1-(tributylammonio)methyl)-2,2′-dipyridyl cation; dppz = dipyrido[3,2-a:2′,3′-c]phenazine, have been investigated. Experimental results show that the DNA-binding affinity of complex 1 is greater than that of 2, both complexes emit luminescence in aqueous solution, either alone or in the presence of DNA, complex 1 can bind to DNA in an intercalative mode while 2 most likely interacts with DNA in a partial intercalation fashion, and complex 2 serves as a better candidate for enantioselective binding to CT-DNA compared with 1. Moreover, complex 1 reveals higher efficient DNA cleavage activity than 2, during which supercoiled DNA is converted to nicked DNA with both complexes. Theoretical calculations for the two complexes have been carried out applying the density functional theory (DFT) method at the level of the B3LYP/LanL2DZ basis set. The calculated results can reasonably explain the obtained experimental trends in the DNA-binding affinities and binding constants (Kb) of these complexes.
Keywords:Synthesis   Ru(II) complexes   DNA-binding   Photocleavage   Density functional theory (DFT)
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