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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Synthesis, DNA-binding and photocleavage studies of [Ru(phen)_2(pbtp)]~2+ and [Ru(bpy)_2(pbtp)]~2+ (phen= 1,10-phenanthroline; bpy=2,2'-bipyridine; pbtp = 4,5,9,11,14-pentaaza-benzo[b]triphenylene)
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Synthesis, DNA-binding and photocleavage studies of [Ru(phen)_2(pbtp)]~2+ and [Ru(bpy)_2(pbtp)]~2+ (phen= 1,10-phenanthroline; bpy=2,2'-bipyridine; pbtp = 4,5,9,11,14-pentaaza-benzo[b]triphenylene)

机译:[Ru(phen)_2(pbtp)]〜2 +和[Ru(bpy)_2(pbtp)]〜2 +(phen = 1,10-菲咯啉; bpy = 2.2)的合成,DNA结合和光裂解研究'-联吡啶; pbtp = 4,5,9,11,14-五氮杂-苯并[b]三亚苯基)

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摘要

Based on the ligand dppz (dppz = dipyrido-[3,2-a:2',3'-c]phenazine), a new ligand pbtp (pbtp = 4,5,9,11,14_pentaaza-benzo[b]triphenylene) and its polypyridyl ruthenium(II) complexes [Ru(phen)_2(pbtp)]~2+ (1) (phen =1,10-phenanthroline and [Ru(bpy)_2(pbtp)]~2+ (2) (bpy = 2,2'-bipyridine) have been synthesized and characterized by elemental analysis, ES-MS and 1H NMR spectroscopy. The DNA-binding of these complexes were investigated by spectroscopic methods and viscosity measurements. The experimental results indicate that both complexes 1 and 2 bind to CT-DNA in classical intercalation mode, and can enantioselectively interact with CT-DNA. It is interesting to note that the pbtp ruthenium(II) complexes, in contrast to the analogous dppz complexes, do not show fluorescent behavior when intercalated into DNA. When irradiated at 365 nm, both complexes promote the photocleavage of pBR 322 DNA.
机译:基于配体dppz(dppz =双吡啶-[3,2-a:2',3'-c]吩嗪),一个新的配体pbtp(pbtp = 4,5,9,11,14_pentaaza-苯并[b]三苯撑)及其聚吡啶基钌(II)络合物[Ru(phen)_2(pbtp)]〜2 +(1)(phen = 1,10-菲咯啉和[Ru(bpy)_2(pbtp)]〜2 +(2) (bpy = 2,2'-bipyridine)的合成,通过元素分析,ES-MS和1H NMR光谱进行表征,并通过光谱法和粘度测量研究了这些配合物的DNA结合力,实验结果表明这两种配合物1和2以经典的嵌入模式与CT-DNA结合,并且可以与CT-DNA对映选择性地相互作用,有趣的是,与类似的dppz配合物相比,pbtp钌(II)配合物在以下情况下不显示荧光行为当在365 nm处照射时,两种复合物均会促进pBR 322 DNA的光裂解。

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