Journal
TRANSITION METAL CHEMISTRY
Volume 34, Issue 7, Pages 773-778Publisher
SPRINGER
DOI: 10.1007/s11243-009-9261-5
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Funding
- Natural Science Foundation of Guangzhou
- Guangdong Province of the People's Republic of China
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Modulation of the luminescence properties of a di-ruthenium(II) complex [(bpy)(2)Ru(BL)Ru(bpy)(2)](4+) (bpy = 2,2'-bipyridine, BL = 2-hydroxyl-5-methyl-1,3-bis([1,10]phenanthroline-[5,6-d]imidazol-2-yl)benzene) by DNA and/or Cu2+ ion has been investigated. It is found that the ruthenium(II) complex can coordinate to the Cu2+ ion in both the absence and presence of DNA. Binding to DNA is through electrostatic interactions and the intramolecular hydrogen bond in the complex is located outside of the DNA. The binding constant is 1.6 x 10(4) M-1. Moreover, it is demonstrated that DNA has the ability to enhance the luminescence intensities of both the di-ruthenium(II) complex and the tri-metallic system generated by chelating with Cu2+. Conversely, Cu2+ ion can quench the luminescence of both the free ruthenium(II) complex and the DNA-bound ruthenium(II) complex.
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