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Synthesis and Crystal Structure of the Azo Copper(Ⅱ)-complex
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作者 任跃红 董金龙 +1 位作者 王自卫 任建国 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第3期376-379,共4页
The single crystals of the azo copper(Ⅱ)-complex have been obtained from the solution of the compound dissolved in the ethanol by slow evaporation at room temperature. The structure was successfully determined by s... The single crystals of the azo copper(Ⅱ)-complex have been obtained from the solution of the compound dissolved in the ethanol by slow evaporation at room temperature. The structure was successfully determined by single-crystal X-ray diffraction. The crystal is of triclinic system, space group P1 with a = 7.8843(12), b = 11.5998(17), c = 13.955(2) A, α = 112.214(2), β = 95.105(2), γ = 97.616(2)o, V = 1157.6(3) A^3, Mr = 586.97, Z = 2, F(000) = 600, Dc = 1.684 g/cm^3, μ(MoKα) = 1.120 mm-1, the final R = 0.0419 and wR = 0.1259 for 3475 observed reflections with I 〉 2σ(I). The coordination around copper(II) atom is a slightly distorted square-pyramidal geometry involving [Cu(C16H11N4O8S)(OH)H2O]-cation, one Na+ anion and one C2H5OH solvate molecule. The hydrogen bonds and π···π stacking interactions extend the complex into a three-dimensional framework. 展开更多
关键词 copper(ⅱ)-complex crystal structure hydrogen bonds π…π stacking interactions
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Synthesis and Crystal Structure of a Dinuclear Compound Cu_2[(O=PPh_2)_2N]_2(μ-O_2PPh_2)_2
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作者 王欣 项生昌 +3 位作者 盛天录 傅瑞标 李亚敏 吴新涛 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第4期459-464,共6页
A neutral dinuclear compound Cu2[(O=PPh2)2N]2(μ-O2PPh2)2 has been unexpectedly prepared from the reaction of [Cu2(dppa)2(MeCN)4](ClO4)2 (dppa = bis(diphenylphosphino)- amine) and Sn(edt)2(edt = ethan... A neutral dinuclear compound Cu2[(O=PPh2)2N]2(μ-O2PPh2)2 has been unexpectedly prepared from the reaction of [Cu2(dppa)2(MeCN)4](ClO4)2 (dppa = bis(diphenylphosphino)- amine) and Sn(edt)2(edt = ethane-1,2-dithiolate) in dichloromethane in air. ESR spectrum shows that the original Cu^+ ion has been oxidized. The crystal structure determined by an X-ray single diffractometer displays that the concurrence of the redox and hydrolysis of the origin ligand dppa is taken with the formation of two new ligands. The complex crystallizes in triclinic, space group P1^- with a = 9.4269(13), b = 10.7522(13), c = 16.787(2)A^°, α= 92.042(5), β= 104.591(7), γ = 96.167(6)°, V= 1633.6(4) A^°3, C72H60 Cu2N2O8P6, Mr = 1394.12, Z = 1, D,. = 1.419 g/cm^3, F(000) = 718,μ = 0.856 mm^-1, the final R = 0.0530 and wR = 0.1096 for 4210 observed reflections with I 〉 2σ(I). 展开更多
关键词 copper(ⅱ)-complex crystal structure oxidation hydrolysis
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双核铜(Ⅱ)配合物在H_2O_2存在下对DNA的氧化切割活性(英文) 被引量:5
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作者 张寿春 邵颖 《无机化学学报》 SCIE CAS CSCD 北大核心 2006年第9期1733-1739,共7页
A novel dinuclear copper(Ⅱ) complex, [Cu2(phen)(dipic)2(H2O)2]·2H2O (phen=1,10-phenanthroline, dipicH2=2,6-pyridinedicarboxylic acid), has been prepared and structurally characterized. The complex crystallizes i... A novel dinuclear copper(Ⅱ) complex, [Cu2(phen)(dipic)2(H2O)2]·2H2O (phen=1,10-phenanthroline, dipicH2=2,6-pyridinedicarboxylic acid), has been prepared and structurally characterized. The complex crystallizes in the triclinic system, space group P1 with cell parameters a=0.846 0(17) nm, b=1.289 5(3) nm, c=1.452 7(3) nm, α=77.42(3)°, β=79.11(3)°, γ=87.08(3)°, and V=1.518 8(6) nm3. The dinuclear complex shows potential DNA cleavage activity at micromolar concentration in the presence of H2O2 and exhibits higher nuclease efficiency than mononuclear complex [Cu(dipic)(H2dipic)]·H2O. Without external reductants, the added H2O2 may contribute to the generation of hydroxyl radicals that result in DNA strand scission.CCDC:291786. 展开更多
关键词 双核铜()配合物 DNA 氧化切割 晶体结构
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二氯二(2-吡啶-N-氧化物)二硒醚合铜配合物的合成及晶体结构 被引量:1
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作者 马德良 张红剑 +3 位作者 李婷婷 沈震 葛赟 牛德仲 《徐州师范大学学报(自然科学版)》 CAS 2009年第2期73-77,共5页
由(PySe)2和CuCl2.2H2O在溶剂CH2Cl2和乙醇中合成了化合物[Cu(PySe)2Cl2]((PySe)2=二(2-吡啶-N-氧化物)二硒醚,HPySe=2-硒吡啶-N-氧化物),并用单晶X射线衍射法测定了该化合物的晶体结构(C20H16Cl2CuN4O4Se4).该配合物空间群为P2(1)/n,... 由(PySe)2和CuCl2.2H2O在溶剂CH2Cl2和乙醇中合成了化合物[Cu(PySe)2Cl2]((PySe)2=二(2-吡啶-N-氧化物)二硒醚,HPySe=2-硒吡啶-N-氧化物),并用单晶X射线衍射法测定了该化合物的晶体结构(C20H16Cl2CuN4O4Se4).该配合物空间群为P2(1)/n,晶体学参数:a=1.6496(2),b=0.9872(6),c=1.6870(2)nm,β=111.405(2)°,V=2.558(5)nm3,Z=4,Dc=2.147g·cm-3,Mr=394.5,μ=6.790mm-1,F(000)=1580.最终结构偏离因子R=0.1226,Rw=0.2551;S=1.019.最终差值电子密度的最大值和最小值分别为1804nm-3和-1852nm-3.中心离子Cu(Ⅱ)的配位环境呈四方锥构型. 展开更多
关键词 2-硒吡啶-N-氧化物 铜配合物 合成 晶体结构
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六氮杂三十元大环双核铜配合物的合成及其水解动力学性质
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作者 刘捷 郑玉娟 《河南工程学院学报(自然科学版)》 2016年第1期27-32,共6页
利用对苯二甲醛和二丙烯三胺制备了一个三十元六氮杂大环配体L(L=3,7,11,18,22,26-hexaazatricyclo[26.2.2.213,16]tetratriaconta-1(30),13,15,28,31,33-hexaene),合成了一个新颖的双核铜配合物[Cu_2L](CO_3)_2,用X-单晶衍射分析技术... 利用对苯二甲醛和二丙烯三胺制备了一个三十元六氮杂大环配体L(L=3,7,11,18,22,26-hexaazatricyclo[26.2.2.213,16]tetratriaconta-1(30),13,15,28,31,33-hexaene),合成了一个新颖的双核铜配合物[Cu_2L](CO_3)_2,用X-单晶衍射分析技术表征了其结构:Cu(Ⅱ)与环上的3个氮原子及来自CO32-上的2个氧原子配位,分别形成配位构型不同的变形四方锥构型和三角双锥构型,采用紫外-可见分光光度法研究了配合物催化p-硝基苯酚醋酸酯(NA)的水解动力学性质.结果表明,催化水解速率对底物NA及配合物的浓度均呈一级反应且催化水解速率受酸碱平衡控制,当pH值=9.00时,水解速率常数为0.034 mol/s,推测其催化机制可能为Lewis acid机制. 展开更多
关键词 三十元大环双核铜配合物 晶体结构 p-硝基苯酚醋酸酯 催化水解动力学
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