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首页> 外文期刊>Journal of Coordination Chemistry >Syntheses of phenoxo-bridged Zn(II) and metallamacrocyclic Hg(II) complexes of organochalcogen (Se, Te) substituted Schiff-bases: structure and DNA-binding studies of Zn(II) complexes
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Syntheses of phenoxo-bridged Zn(II) and metallamacrocyclic Hg(II) complexes of organochalcogen (Se, Te) substituted Schiff-bases: structure and DNA-binding studies of Zn(II) complexes

机译:有机硫属元素(Se,Te)取代席夫碱的酚氧桥联的Zn(II)和金属环Hg(II)配合物的合成:Zn(II)配合物的结构和DNA结合研究

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The coordination of organochalcogen (especially Se and Te) substituted Schiff-bases L1H, L2H, L3H, and L4H toward Zn(II) and Hg(II) has been studied. Reactions of these ligands with ZnCl2 in 1 : 1 molar ratio gave binuclear complexes [{2-[PhX(CH2) n N = C(Ph)]-6-[PhCO]-4-MeC6H2O}2Zn2Cl2] (where X = Se, n = 2 (1); X = Se, n = 3 (2); X = Te, n = 2 (3); and X = Te, n = 3 (4)) with partial hydrolytic cleavage of proligands. In these complexes, two partially hydrolyzed ligand fragments coordinate tridentate (NOO) with two Zn's. Reaction of HgBr2 with L1H and L2H in 1 : 1 molar ratio gave monometallic complexes [C6H2(4-Me)(OH)[2,6-{C(Ph) = N(CH2) n Se(Ph)}2HgBr2]] (n = 2 (5) or 3 (6)) and under similar conditions with L3H and L4H gave bimetallic complexes [C6H2(4-Me)(OH)[2,6-{C(Ph) = N(CH2) n Te(Ph)}2Hg2Br4]] (n = 2 (7) or 3 (8)) in which the ligands coordinate with metal through selenium or tellurium, leaving the imino nitrogen and phenolic oxygen uncoordinated. The proligands L1H, L2H give 14- or 16-membered metallamacrocycles through Se-Hg-Se linkages and L3H, L4H give 16- or 18-membered metallamacrocycles through Te-Hg-Br-Hg-Te linkages. All the complexes were characterized by elemental analyses, ESIMS, FTIR, multinuclear NMR, UV-Vis, and conductance measurements. The redox properties of the complexes were investigated by cyclic voltammetry (CV). Complexes 1-4 exhibited ligand-centered irreversible oxidation processes. Complexes 5 and 6 showed metal-centered quasi-reversible single electron transfer, whereas dinuclear complexes 7 and 8 displayed two quasi-reversible, one-electron transfer steps. A single-crystal X-ray structure determination of 1 showed that the coordination unit is centrosymmetric with Zn(II) in square-pyramidal coordination geometry and the two square pyramids sharing an edge. The Zn ··· Zn separation is 3.232 à . The DNA-binding properties of 1 and 3 with calf thymus DNA were explored by a spectrophotometric method and CV.View full textDownload full textKeywordsOrganoselenium/tellurium, Schiff-base, Zn(II) and Hg(II) complexes, X-ray structure, Cyclic voltammetry, DNA-bindingRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/00958972.2011.639874
机译:有机硫属元素(尤其是Se和Te)取代的席夫碱L 1 H,L 2 H,L 3 H和L <研究了对Zn(II)和Hg(II)的sup> 4 H。这些配体与ZnCl 2 的摩尔比为1 :: 1的反应给出了双核配合物[{2- [PhX(CH 2 n < / sub> N == C(Ph)]-6- [PhCO] -4-MeC 6 H 2 O} 2 Zn 2 Cl 2 ](其中X == Se,n == 2(1); X == ≥Se,n = 3(2); X = = Te,n = 2(3);和X = Te,n,n = ≥3(4))与配体的部分水解裂解。在这些络合物中,两个部分水解的配体片段将三齿(NOO)与两个Zn配位。 HgBr 2 与L 1 H和L 2 H在1 :: 1摩尔比下的反应生成单金属配合物[C < sub> 6 H 2 (4-Me)(OH)[2,6- {C(Ph)≥= N(CH 2 n Se(Ph)} 2 HgBr 2 ]]](n == 2(5)或3( 6))并在相似的条件下用L 3 H和L 4 H生成双金属配合物[C 6 H 2 (4-Me)(OH)[2,6- {C(Ph)≥= N(CH 2 n Te(Ph) } 2 Hg 2 Br 4 ]](n == 2(7)或3(8))配体通过硒或碲与金属配位,使亚氨基氮和酚氧不配位。配体L 1 H,L 2 H通过Se-Hg-Se键和L 3 H给出14或16元金属环L 4 H通过Te-Hg-Br-Hg-Te键生成16或18元金属环。所有的配合物都通过元素分析,ESIMS,FTIR,多核NMR,UV-Vis和电导测量来表征。通过循环伏安法(CV)研究了配合物的氧化还原性质。配合物1-4表现出以配体为中心的不可逆氧化过程。配合物5和6显示出以金属为中心的准可逆单电子转移,而双核配合物7和8显示出两个准可逆的单电子转移步骤。 X射线单晶结构的确定为1,表明在金字塔形的金字塔结构中,配位单元与Zn(II)是中心对称的,并且两个正方形的金字塔共享一个边。 Zn····Zn分离为3.232。通过分光光度法和CV探索了1和3与小牛胸腺DNA的DNA结合特性。查看全文下载全文关键词循环伏安法,DNA绑定4dff56cd6bb1830b“};添加到候选列表链接永久链接http://dx.doi.org/10.1080/00958972.2011.639874

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