Synthesis, characterization, DNA-binding and spectral properties of complexes [Ru(L)4(dppz)]2+ (L = Im and MeIm)

被引:123
作者
Chen, Lan-Mei [1 ]
Liu, Jie [1 ]
Chen, Jin-Can [1 ]
Tan, Cai-Ping [1 ]
Shi, Shuo [1 ]
Zheng, Kang-Cheng [1 ]
Ji, Liang-Nian [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Bioinorgan & Synth Chem, Guangzhou 510275, Peoples R China
[2] Tongji Univ, Dept Chem, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Ru(II) complex; imidazole; DNA-binding; spectral property; DFT/TDDFT;
D O I
10.1016/j.jinorgbio.2007.09.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two new Ru(II) complexes [Ru(L)(4)(dppz)](2+) (L = imidazole (Im), 1-methylimidazole (MeIm); dppz = dipyrido[3,2-a:2',3'-c]phenazine), have been synthesized and characterized in detail by elemental analysis, H-1 NMR, Electrospray ionization mass spectrometry (ESI-MS) and UV-visible (UV-Vis) spectroscopic techniques. The interaction of these complexes with calf thymus DNA (CT-DNA) has been explored by using electronic absorption titration, competitive binding experiment, circular dichroism (CD), thermal denaturation and viscosity measurements. The experimental results show that: both the two complexes can bind to DNA in an intercalation mode; the DNA-binding affinity of complex [Ru(Im)(4)(dppz)](2+) 1 (K-b=2.5 x 10(6) M-1) is greater than that of complex [Ru(MeIM)(4)(dppz)](2+) 2 (K-b = 1.1 x 10(6) M-1). Moreover, it is very interesting to find that the circular dichroic spectrum of DNA-complex 1 adduct, in which both bands centered at 277 nm and 236 nm are all negative, is very different from those of DNA-complex 2 adduct and other Ru(II) complexes binding to DNA in general intercalation mode. It may be due to the hydrogen-bonding effect or the contribution of induced CD signals of complex 1. Another interesting finding is that the hypochromism of the complexes is not linear relation to their DNA-binding affinities. In order to deeply study these experimental phenomena and trends, the density functional theory (DFT) and time-dependent DFT (TDDFT) computations were carried out, and on the basis of the DFT/TDDFT results and the frontier molecular orbital theory, the trend in DNA-binding affinities, the spectral properties as well as the interesting phenomena of larger extent of hypochromism but relatively smaller K-b values for the title complexes have been reasonably explained. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:330 / 341
页数:12
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