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Synthesis,Crystal structure and DNA Binding of of a chiral new Cu(II) complex with (1R, 2R)-1,2-hexanediamine

机译:对(1R,2R)-1,2-己二胺的手性新Cu(II)复合物的合成,晶体结构和DNA结合

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The compound 1, (R,R)-N,N’-bis(benzaldehyde)-1,2-cyclohexanediamine schiff base was synthesized and characterized by ~1H-NMR spectra, MS spectra and IR spectra. And the coordination reaction of 1 with nitrate of Cu (II) was studied. The reaction of 1 with Cu~(II) salt [Cu(NO_3)_2.2H_2O] generates a new compound 2. The compound 2 was determined by IR spectra, elemental analysis and single-crystal X-ray diffraction. Crystal data for 2: space group P2(1)2(1)2(1), with a= 9.632(12)?, b = 9.706(12)?, c = 22.04(3)?, α=90.00 o,β=90.00 o, γ=90.00 o, Flack=0.02(3), Z=4, V= 2061(4) ? 3, Dc=1.457 mg.m~(-3), μ=1.109mm~(-1), F(000)=956. There are 6 coordination sites around Cu~(2+) of 2, which are respectively occupied by two oxygen atoms (all from two H2O) and four nitrogen atoms all from two cyclohexanediamine molecule. The Cu atom and four chelating nitrogen atoms are coplanar. There exist intra-molecular H-bond and intermolecular H-bond. The DNA binding behaviors of 2 has been examined by viscosity measurements, fluorescent spectroscopy, absorption spectra and cyclic voltammetric techniques. Results suggest that the compound 2 binds to DNA with a non-classical intercalative mode and static interaction mode. The observed efficient nuclease activity of the compound 2 is interesting and may have further influences in the chemistry of DNA binders.
机译:合成化合物1,(R,R)-N,N'-BIS(苯甲醛)-1,2-环己烷二胺席基席基,其特征在于〜1H-NMR光谱,MS光谱和IR光谱。研究了用硝酸盐(II)的1的配位反应。用Cu〜(II)盐[Cu(NO_3)_2.2H_2O]的反应产生新的化合物2.化合物2通过IR光谱,元素分析和单晶X射线衍射测定。 2:空间组P2(1)2(1)2(1)的晶体数据,具有A = 9.632(12)?,B = 9.706(12)?,C = 22.04(3)?,α= 90.00 o, β= 90.00 o,γ= 90.00 o,脆= 0.02(3),z = 4,v = 2061(4)? 3,DC = 1.457 mg.m〜(-3),μ= 1.109mm〜(-1),f(000)= 956。 Cu〜(2+)的6个配位位点2,其分别由两个氧原子(来自两个H 2 O)和来自两个环己二胺分子的四个氮原子占据。 Cu原子和四个螯合氮原子是共面的。存在分子内H键和分子间H键。已经通过粘度测量,荧光光谱,吸收光谱和循环伏安技术检查了2的DNA结合行为。结果表明,化合物2具有非典型的插入模式和静态相互作用模式与DNA结合。所观察到的化合物2的有效核酸酶活性是有趣的,并且可能在DNA粘合剂的化学中具有进一步的影响。

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