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作 者:张黔玲[1] 刘剑洪[1] 任祥忠[1] 李翠华[1] 张培新[1] 刘建忠[2] 计亮年[2]
机构地区:[1]深圳大学师范学院化生系,深圳518060 [2]中山大学教育部基因工程重点实验室,广州510275
出 处:《无机化学学报》2006年第5期885-889,共5页Chinese Journal of Inorganic Chemistry
基 金:广东省自然科学基金博士启动基金(No.04300882);深圳市科技计划资助项目(No.200328)
摘 要:The formation of heterobimetallic complex [Co(bpy)2(ODHIP)Zn]5+ by [Co(bpy)2ODHIP]3+ and Zn2+ was investigated. The luminescent property of complex was also studied. The results indicated that the nonluminescent monometallic complex [Co(bpy)2ODHIP]3+ could coordinated with Zn2+ to form the luminescent heterobimetallic complex [Co(bpy)2(ODHIP)Zn]5+, the emission intensity increased as increasing the amounts of Zn2+. The luminescence became the strongest at the ratio of CZn / CCo of 1. After binding to DNA, [Co(bpy)2ODHIP]3+ must change its binding mode from partial intercalation to intercalation to make the peripheral coordination site on the ODHIP ligand accessible for Zn2+, the coordination occurred from the opposite side of helix with respect to the intercalated [Co(bpy)2ODHIP]3+, and the luminescent heterobimetallic complex [Co(bpy)2(ODHIP)Zn]5+ was formed. On the other hand, [Co(bpy)2(ODHIP)Zn]5+ bound to DNA by intercalation and situated the region of the intercalated [Co(bpy)2ODHIP]3+ between the base pairs of DNA, while the remained monometallic complex [Co(bpy)2ODHIP]3+ bound to DNA by partial intercalation.The formation of heterobimetallic complex [Co(bpy)2(ODHIP)Zn]^5+by [Co(bpy)2ODHIP]^3+ and Zn^2+ was investigated. The luminescent property of complex was also studied. The results indicated that the nonluminescent monometallic complex [Co(bpy)2ODHIP]^3+ could coordinated with Zn^2+ to form the luminescent heterobimetallic complex [Co(bpy)2(ODHIP)Zn]^5+, the emission intensity increased as increasing the amounts of Zn^2+. The luminescence became the strongest at the ratio of Czn/Cco of 1. After binding to DNA, [Co(bpy)2ODHIP]^3+ must change its binding mode from partial intercalation to intercalation to make the peripheral coordination site on the ODHIP ligand accessible for Zn^2+, the coordination occurred from the opposite side of helix with respect to the intercalated [Co(bpy)2ODHIP]^3+, and the luminescent heterobimetallic complex [Co(bpy)2(ODHIP)Zn]^5+ was formed. On the other hand, [Co(bpy)2(ODHIP)Zn]^5+ bound to DNA by intercalation and situated the region of the intercalated [Co(bpy)2ODHIP]^3+ between the base pairs of DNA, while the remained monometallic complex [Co(bpy)2ODHIP]^3+ bound to DNA by partial intercalation.
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