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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and DNA photocleavage study of Ru(bpy)(3)(2+)-(CH2)(n)-MV2+ complexes
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Synthesis and DNA photocleavage study of Ru(bpy)(3)(2+)-(CH2)(n)-MV2+ complexes

机译:Ru(bpy)(3)(2 +)-(CH2)(n)-MV2 +复合物的合成及DNA光解研究

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A series of Ru(bpy)(3)(2+)-(CH2)(n)-MV2+ complexes (1, n = 3, 4, 7) used for DNA photocleavage have been designed and synthesized. Under the irradiation of visible light, complexes 1 can cleave supercoiled plasmid DNA (pBR322) both in air and under Ar atmosphere. Radical species such as O2(-center dot), (OH)-O-center dot and the light-induced charge-separated (CS) oxidation state Ru(bpy)(3)(3+)-(CH2)(n)-MV+center dot are responsible for the cleavage. The longer the carbon chain linkage, the higher the DNA photocleavage efficiency. It is noted that backwards intramolecular electron transfer (ET) that exist in complexes 1 can lead to some decreasing effect on the cleavage result, while inclusion of complexes 1 with cucurbit[8]uril (CB[8]) inhibits the backwards ET to some extent, thereby increasing photocleavage efficiency.
机译:设计并合成了一系列用于DNA光裂解的Ru(bpy)(3)(2 +)-(CH2)(n)-MV2 +配合物(1,n = 3,4,7)。在可见光的照射下,复合物1可以在空气中和Ar气氛下裂解超螺旋质粒DNA(pBR322)。自由基物种,例如O2(中心点),(OH)-O-中心点和光诱导的电荷分离(CS)氧化态Ru(bpy)(3)(3 +)-(CH2)(n) -MV +中心点负责切割。碳链键越长,DNA的光裂解效率越高。值得注意的是,配合物1中存在的向后分子内电子转移(ET)可能对裂解结果产生某些降低的影响,而配合物1与葫芦科[8] uril(CB [8])则将向后分子ET抑制到一定程度。程度,从而提高光解效率。

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