| 钌(Ⅱ)配合物与DNA相互作用的瞬态发光特性 |
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| 引用本文： | 朱伟玲,刘学文,王惠,于会娟,黎爱珍,巢辉,郑康成,计亮年.钌(Ⅱ)配合物与DNA相互作用的瞬态发光特性[J].发光学报,2007,28(4):510-514. |
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| 作者姓名： | 朱伟玲 刘学文 王惠 于会娟 黎爱珍 巢辉 郑康成 计亮年 |
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| 作者单位： | 1. 中山大学, 光电材料与技术国家重点实验室, 广东, 广州, 510275;2. 中山大学, 化学与化学工程学院, 广东, 广州, 510275;3. 茂名学院, 技术物理系, 广东, 茂名, 525000 |
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| 基金项目： | 国家自然科学基金(60478013)，广东省自然科学重点基金(05101819)，茂名学院科研基金(203346)资助项目 |
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| 摘 要： | 以三种新合成的钌配合物Ru(bpy)2(7-CH3-dppz)]2+、Ru(bpy)2(7-F-dppz)]2+、Ru(phen)2(7-F-dppz)]2+为研究对象,采用时间分辨的荧光光谱技术分别测量了这三种钌配合物与小牛胸腺DNA相互作用时的瞬态荧光动力学过程。结果表明:Ru(bpy)2(7-CH3-dppz)]2+的发光寿命最长(约382 ns),而Ru(bpy)2(7-F-dppz)]2+的发光寿命最短(约65 ns)。分析表明:钌配合物的发光来源于配合物分子中的电荷转移态到基态的辐射跃迁。通过钌配合物与DNA的相互作用,使得配合物激发态分子的无辐射弛豫几率减小,从而导致发光寿命的增加。配合物的分子与DNA相互作用越强,激发态分子的无辐射弛豫几率越小,发光寿命也越长,最终导致高的发光效率。配合物的分子结构对配合物的分子与DNA的相互作用具有重要的影响。
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| 关 键 词： | 钌配合物 DNA 瞬态发光 超快光谱技术 |
| 文章编号： | 1000-7032（2007）04-0510-05 |
| 收稿时间： | 2006-11-02 |
| 修稿时间： | 2006-11-022006-12-11 |
Property of Transient Luminescence in Ru(Ⅱ) Complexes Bond to DNA |
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| ZHU Wei-ling,LIU Xue-wen,WANG Hui,YU Hui-juan,LI Ai-zhen,CHAO Hui,ZHENG Kang-cheng,JI Liang-nian.Property of Transient Luminescence in Ru(Ⅱ) Complexes Bond to DNA[J].Chinese Journal of Luminescence,2007,28(4):510-514. |
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| Authors: | ZHU Wei-ling LIU Xue-wen WANG Hui YU Hui-juan LI Ai-zhen CHAO Hui ZHENG Kang-cheng JI Liang-nian |
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| Institution: | 1. Sate Key Laboratory of Optoelectronics Materials and Technologies of Zhongshan University, Guangzhou 510275, China;2. Institute of Chemical and Chemical Enginner of Zhongshan University, Guangzhou 510275, China;3. Department of Technical Physics, Maoming College, Maoming 525000, China |
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| Abstract: | To study the emission dynamics for the Ru(Ⅱ) complexes bond to DNA,and show the effects of the molecular structure of complexes on bonding to DNA,three kinds of Ru(Ⅱ) complexes Ru(bpy)2(7-CH3-dppz)]2+,Ru(bpy)2(7-F-dppz)]2+ and Ru(phen)2(7-F-dppz)]2+,bpy=2,2′-bipyridine,dppz=dipyrido3,2-a:2′,3′-c]phenazine,phen=1,10-phenanthroline],have been synthesized.Their electronic absorption spectras and steady-state fluorescence spectra have been investigated.The electronic absorption spectra show that the wavelength of metal-to-ligand charge transfer(MLCT) peaks of the three kinds of Ru complexes are all at about 400 nm.Under the same power of photoexcitation at the wavelength of the MLCT peaks,the binding of Ru(bpy)2(7-CH3-dppz)]2+ to calf thymus DNA has the strongest fluorescence,and Ru(bpy)2(7-F-dppz)]2+ to calf thymus DNA has the feeblest one.On the base of the study for the absorption spectra and steady-state fluorescence spectra,the transient luminescence in three kinds of Ru(Ⅱ) complexes bond to DNA have been studied by using picosecond time resolved spectroscopy.The results show that the fluorescence decay for the Ru(Ⅱ) complexes bond to DNA exhibits as a biexponential form.Among the three kinds of Ru(Ⅱ) complexes,Ru(bpy)2(7-CH3-dppz)]2+ bonds to DNA has the longest luminescence lifetime(about 382 ns and 108 ns),Ru(bpy)2(7-F-dppz)]2+ bonds to DNA has the shortest lifetime(about 65 ns and 16 ns),and Ru(phen)2(7-F-dppz)]2+ bonds to DNA has the lifetime(about 326 ns and 37 ns) shorter then Ru(bpy)2(7-CH3-dppz)]2+ and longer then Ru(bpy)2(7-F-dppz)]2+.The possible origin of the luminescence dynamics has been discussed.The luminescence is attribute to radiative decay from the MLCT excited state to the ground state.Through the interaction with the DNA,the radiativeless rate of the photoexcited Ru(Ⅱ) complex molecules is decreased,which results in the increase of luminescence lifetime and efficiency.The more stronger for the interaction,the more longer for the luminescence lifetime and higher for luminescence efficiency.The molecular structure of the Ru(Ⅱ) complex has an important impact on the interaction with DNA. |
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| Keywords: | Ru complex DNA transient luminescence ultrafast spectroscopic technology |
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