Chem. J. Chinese Universities

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Formation and Luminescent Properties of New Heterobimetallic Complexes

ZHANG Qian-Ling1, LIU Jian-Hong1, REN Xiang-Zhong1, ZHANG Pei-Xin1, WANG Fang1, LI Cui-Hua1, LIU Jian-Zhong2, JI Liang-Nian2   

    1. Department of Chemistry and Biology, Normal College, Shenzhen University, Shenzhen 518060, China;
    2. The Key Laboratory of Gene Engineering of Ministry of Education, Colledge of Life Science, Zhongshan University, Guangzhou 510275, China
  • Received:2006-02-20 Revised:1900-01-01 Online:2006-10-10 Published:2006-10-10
  • Contact: LIU Jian-Hong

Abstract: The formation of new heterobimetallic complexes obtained via the coordination reactions of [Ru(bpy)2TPPHZ]2+(TPPHZ=tetrapyrido[3,2-a: 2',3'-c: 3",2"-h: 2'",3'"-j]phenazine) and [Ru(bpy)2ODHIP]2+(ODHIP=3,4-dihydroxyl-imidazo[4,5-f][1,10]phenanthroline) with Ni2+ were investigated by spectroscopic methods. The DNA-binding and luminescent properties of the complexes after coordinating with Ni2+ were also studied. The experimental results indicate that both [Ru(bpy)2TPPHZ]2+ and [Ru(bpy)2ODHIP]2+ could coordinate with Ni2+ to form the heterobimetallic
complexes [Ru(bpy)2(TPPHZ)Ni]4+ and [Ru(bpy)2(ODHIP)Ni]4+. The emission intensity of the complexes decreased with increasing the amounts of Ni2+. After binding to DNA, both complexes could coordinate with Ni2+ to form the heterobimetallic complexes. [Ru(bpy)2(TPPHZ)Ni]4+ kept binding to DNA by intercalation, and the luminescence of complex almost disappeared at n(Ni)/n(Ru)=1. While the binding mode of [Ru(bpy)2(ODHIP)Ni]4+ changed from groove binding to intercalation, and the emission intensity of the complex decreased.

Key words: Polypyridyl ruthenium(Ⅱ) complex, DNA, Ni2+, Luminescence, Intercalation

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