Synthesis, characterization and DNA-binding and DNA-photocleavage studies of two Ru(II) complexes containing two main ligands and one ancillary ligand

被引:21
|
作者
Sun, Jing [2 ,3 ]
Wu, Shuo [1 ]
Chen, Huo-Yan [3 ]
Gao, Feng [3 ]
Liu, Jie [1 ]
Ji, Liang-Nian [3 ]
Mao, Zong-Wan [3 ]
机构
[1] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
[2] Guangdong Med Coll, Sch Pharm, Dongguan 523808, Peoples R China
[3] Sun Yat Sen Univ, MOE Key Lab Bioinorgan & Synthet Chem, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Synthesis; Ru(II) complexes; DNA-binding; Photocleavage; Density functional theory (DFT); DENSITY-FUNCTIONAL THEORY; EFFECTIVE CORE POTENTIALS; RUTHENIUM(II) COMPLEXES; MOLECULAR CALCULATIONS; DEOXYRIBONUCLEIC-ACID; BASE-PAIRS; LUMINESCENCE; TRIS(PHENANTHROLINE)RUTHENIUM(II); 1,10-PHENANTHROLINE; INTERCALATORS;
D O I
10.1016/j.poly.2011.04.047
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
DNA-binding and DNA-photocleavage properties of two Ru(II) complexes, [Ru(L-1)(dppz)(2)](PF6)(4) (1) and [Ru(L-2)(dPPz)(2)](PF6)(4) (2) (L-1 = 5,5'-di(1-(triethylammonio)methyl)-2,2'-dipyridyl cation; L-2 = 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 (K-b) of these complexes. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1953 / 1959
页数:7
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