Chemical modulation of the luminescence of a DNA-bound diruthenium(II) complex by copper(II) ion and EDTA

被引:9
作者
Li, Qian [1 ]
Chao, Hui [2 ]
Chen, Miao-Jing [1 ]
Li, Hong [1 ]
Xu, Zheng-He [1 ]
机构
[1] S China Normal Univ, Sch Chem & Environm, Key Lab Technol Electrochem Energy Storage & Powe, Guangzhou 510006, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Chem, Guangzhou 510275, Guangdong, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
LIGHT-SWITCH; BINDING; LIGAND; INTERCALATION; SOLVENTS; BEHAVIOR; DUPLEX; DAMAGE;
D O I
10.1007/s11243-010-9383-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A method for the chemical modulation of the photoluminescence of a DNA-bound diruthenium(II) complex, [(bipy)(2)Ru(bpib)Ru(bipy)(2)](4+) (bipy = 2,2'-bipyridine, bpib = 1,4-bis([1, 10]phenanthroline [5,6-d]imidazol-2-yl) benzene) by the introduction of Cu2+ ion and EDTA has been developed. The diruthenium(II) complex showed strong photoluminescence both in buffer solutions and on an indium-tin oxide (ITO) surface, which was not modulated by Cu2+ or EDTA. The DNA-bound [(bipy)(2)Ru(bpib)Ru(bipy)(2)](4+) with a binding constant of 3.8 x 10(4) M-1 showed an enhancement in the luminescence based on the electrostatic interaction between the complex and DNA. The presence of Cu2+ was found to quench the luminescence of DNA-bound [(bipy)(2)Ru(bpib)Ru(bipy)(2)](4+), but the quenched luminescence was recovered by addition of an equimolar concentration of EDTA. Hence, the photoluminescence of DNA-bound [(bipy)(2)Ru(bpib)Ru(bipy)(2)](4+) depends strongly on the introduction of Cu2+ and EDTA.
引用
收藏
页码:707 / 711
页数:5
相关论文
共 28 条
[1]   Charge separation in a ruthenium-quencher conjugate bound to DNA [J].
Augustyn, Katherine E. ;
Stemp, E. D. A. ;
Barton, Jacqueline K. .
INORGANIC CHEMISTRY, 2007, 46 (22) :9337-9350
[2]   [Ru(bpy)2dppz]2+ light-switch mechanism in protic solvents as studied through temperature-dependent lifetime measurements [J].
Brennaman, MK ;
Meyer, TJ ;
Papanikolas, JM .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (45) :9938-9944
[3]   A luminescent pH sensor based on a diruthenium(II) complex: 'off-on-off' switching via the protonation/deprotonation of an imidazole-containing ligand [J].
Chao, H ;
Ye, BH ;
Zhang, QL ;
Ji, LN .
INORGANIC CHEMISTRY COMMUNICATIONS, 1999, 2 (08) :338-340
[4]   Luminescence properties of a di-ruthenium(II) complex with an intramolecular hydrogen bond modulated by DNA and copper(II) ion [J].
Chen, Pei-Liang ;
Chao, Hui ;
Xu, Juan ;
Wang, Li ;
Li, Hong .
TRANSITION METAL CHEMISTRY, 2009, 34 (07) :773-778
[5]   Oxidative damage by ruthenium complexes containing the dipyridophenazine ligand or its derivatives: A focus on intercalation [J].
Delaney, S ;
Pascaly, M ;
Bhattacharya, PK ;
Han, K ;
Barton, JK .
INORGANIC CHEMISTRY, 2002, 41 (07) :1966-1974
[6]   MOLECULAR LIGHT SWITCH FOR DNA - RU(BPY)2(DPPZ)2+ [J].
FRIEDMAN, AE ;
CHAMBRON, JC ;
SAUVAGE, JP ;
TURRO, NJ ;
BARTON, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (12) :4960-4962
[7]   A light-controlled reversible DNA photoligation via carbazole-tethered 5-carboxyvinyluracil [J].
Fujimoto, Kenzo ;
Yoshino, Hideaki ;
Ami, Takehiro ;
Yoshimura, Yoshinaga ;
Saito, Isao .
ORGANIC LETTERS, 2008, 10 (03) :397-400
[8]   Oxidative DNA damage through long-range electron transfer [J].
Hall, DB ;
Holmlin, RE ;
Barton, JK .
NATURE, 1996, 382 (6593) :731-735
[9]   Enhanced DNA photocleavage properties of Ru(II) terpyridine complexes upon incorporation of methylphenyl substituted terpyridine and/or the polyazine bridging ligand dpp (2,3-bis(2-pyridyl)pyrazine) [J].
Jain, Avijita ;
Slebodnick, Carla ;
Winkel, Brenda S. J. ;
Brewer, Karen J. .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2008, 102 (10) :1854-1861
[10]   ssDNA templated self-assembly of chromophores [J].
Janssen, Pim G. A. ;
Vandenbergh, Joke ;
van Dongen, Joost L. J. ;
Meijer, E. W. ;
Schenning, Albertus P. H. J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (19) :6078-+