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一种钌配合物与DNA相互作用发光增强的超快过程研究
引用本文:沈涵,于会娟,朱伟玲,巢晖,王惠,计亮年.一种钌配合物与DNA相互作用发光增强的超快过程研究[J].光学学报,2007,27(7):333-1337.
作者姓名:沈涵  于会娟  朱伟玲  巢晖  王惠  计亮年
作者单位:中山大学光电材料与技术国家重点实验室,广州 510275;中山大学光电材料与技术国家重点实验室,广州 510275;中山大学化学与化工学院,广州 510275;中山大学光电材料与技术国家重点实验室,广州 510275;茂名学院技术物理系,茂名 525000
基金项目:国家自然基金(60478013,20571089),广东省自然基金重点项目(05101819),博士点基金(20040558031),茂名学院科研基金(203346)资助课题
摘    要:采用时间分辩激光光谱技术,研究了一种钌配合物Ru(dmb)2(mitatp)]2 发光增强的超快过程。采用比较方法测量了Ru(dmb)2(mitatp)]2 和Ru(dmb)2(mitatp)]2 /DNA复合物的瞬态发光弛豫过程。Ru(dmb)2(mitatp)]2 和Ru(dmb)2(mitatp)]2 /DNA复合物的发光均来源于Ru(dmb)2(mitatp)]2 中的电荷转移单态和三重态到基态的辐射跃迁。通过钌配合物与DNA的相互作用,Ru(dmb)2(mitatp)]2 的荧光寿命由339 ns延长至589 ns;磷光寿命由16μs延长至21μs,总的发光强度增强了约1个数量级。分析表明,Ru(dmb)2(mitatp)]2 发光寿命和发光强度的增加可能来源于Ru(dmb)2(mitatp)]2 与DNA之间的电荷转移态的形成,它导致Ru(dmb)2(mitatp)]2 的最低激发单态和三重态到基态的无辐射概率的减小,增强了Ru(dmb)2(mitatp)]2 发光效率。

关 键 词:激光与光电子学  瞬态发光动力学  超快激光光谱技术  钌配合物和DNA
文章编号:0253-2239(2007)07-1333-5
收稿时间:2006/8/8
修稿时间:2006-08-08

Study on Ultrafast Dynamics of Luminescence Enhancement in a [DNA and Ru] Complex
Shen Han,Yu Huijuan,Zhu Weiling,Chao Hui,Wang Hui,Ji Liangnian.Study on Ultrafast Dynamics of Luminescence Enhancement in a [DNA and Ru] Complex[J].Acta Optica Sinica,2007,27(7):333-1337.
Authors:Shen Han  Yu Huijuan  Zhu Weiling  Chao Hui  Wang Hui  Ji Liangnian
Institution:1.State Key Laboratory of Optoelectronic Materials and Technologies, Sun Yat-Sen University, Guangzhou 510275; 2. Institite of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275; 3. Department of Technologic Physics, Maoming Institute, Maoming 525000
Abstract:The ultrafast dynamics of the luminescence enhancement in Ru(dmb)2(mitatp)]2+ and Ru(dmb)2(mitatp)]2+/DNA complex has been studied by use of time-resolved luminescence spectroscopy. The transient luminescence relaxation processes of Ru(dmb)2(mitatp)]2+ and Ru(dmb)2(mitatp)]2+/DNA complex have been measured with comparison method. The luminescence is due to the transition between charge transfer singlet and triplet states. The results show that after interaction with DNA, the lifetimes of fluorescence and phosphorescence of Ru(dmb)2(mitatp)]2+ complex are prolonged from 339 ns to 589 ns and from 16 μs respectively, and the total luminescence intensity is enhanced by one order of magnitude. The possible origin may be the formation of the new energy levels of the photoexcited charge-transfer singlet and triplet states by the interaction between Ru(dmb)2(mitatp)]2+ and DNA resulting in the decrease of the nonradiative decay rate from the lowest excited state to the ground state and the increase of the luminescence efficiency.
Keywords:laser and optoelectronics  transient luminescence dynamics  ultrafast laser and spectroscopic technology  Ru complex and DNA
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