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单核钴(III)和镍(II)配合物与多吡啶配体,[Co(phen)2(taptp)]3+ 和 [Ni(phen) 2(taptp)]2+:合成、光解和 DNA 结合。

Mononuclear Co(III) and Ni(II) complexes with polypyridyl ligands, [Co(phen)2(taptp)]3+ and [Ni(phen) 2(taptp)]2+: synthesis, photocleavage and DNA-binding.

机构信息

Institute for Advanced Studies in Basic Sciences, 45195, Zanjan, Iran.

出版信息

J Fluoresc. 2013 Mar;23(2):259-64. doi: 10.1007/s10895-012-1143-0. Epub 2012 Nov 2.

Abstract

Two novel, mixed ligand complexes of cobalt(III) and nickel(II), Co(phen)2(taptp) (1) and Ni(phen)2(taptp) (2) (phen = 1,10-phenanthroline and taptp = 4,5,9,18-tetraazaphenanthreno [9,10-b]triphenylene), were synthesized and characterized by elemental analyses, UV-visible and NMR spectroscopies. The binding interactions of the two complexes with DNA have been investigated using absorption and emission spectroscopy methods and electrophoresis measurement mode. The intrinsic binding constants for these complexes to DNA are in the order of 10(5). In Tris buffer, the Co(III) complex shows a moderate luminescence which was enhanced after binding to DNA. However for complex Ni(II), no emission was observed in Tris buffer. The Co(phen)2(taptp) and Ni(phen)2(taptp) can cause the photocleavage of DNA supercoiled pBR322 upon irradiation by 360 nm light. Based on the data, an intercalative mode of DNA binding is suggested for the two complexes.

摘要

两种新型的钴(III)和镍(II)混合配体配合物,[Co(phen)2(taptp)]3+ (1) 和 [Ni(phen)2(taptp)]2+ (2) (phen = 1,10-菲咯啉,taptp = 4,5,9,18-四氮杂菲并[9,10-b]三苯并),通过元素分析、紫外-可见和 NMR 光谱法进行了合成和表征。使用吸收和发射光谱法以及电泳测量模式研究了两个配合物与 DNA 的结合相互作用。这些配合物与 DNA 的固有结合常数为 10(5)。在 Tris 缓冲液中,Co(III)配合物显示出中等强度的发光,与 DNA 结合后增强。然而,对于 Ni(II)配合物,在 Tris 缓冲液中没有观察到发射。[Co(phen)2(taptp)]3+ 和 [Ni(phen)2(taptp)]2+可以在 360nm 光照射下引起超螺旋 pBR322 DNA 的光解。基于这些数据,提出了两种配合物与 DNA 结合的插入模式。

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