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CRYSTAL STRUCTURE OF A 2D SHEET-LIKE μ-CYANIDO-OXAMIDATO BRIDGED Fe(III)-Cu(II) HETERNUCLEAR COMPLEX
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作者 Nei Fang Wu Zhong Ning CHEN Jun QIU and Wen Xia TANG (State Key Laboratory of Coordination Chemistry,Nanjing University, Manjing 210093)Jing Ling WANG and Fang Ming NIAO(Department of Chemistry, Tianjin Normal University, Tianjin 300074) 《Chinese Chemical Letters》 SCIE CAS CSCD 1994年第8期713-714,共2页
The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal s... The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal space group Puma. with a=11 .413(4), b=22.242(5), c=7.736(2) A, and Z=4.The structure was refined to conventionat discrepancy factors R=0.047 and Pw=0.054. The Cu(II ) and Fe(III)centers are bridged by oxpn and cyanide, the formal behaves as a his-terdentate tigand bound to cooper(II)ion to form (II) dimers. whereas the latter bridges Cu(II) and Fe(III) centers in both symmetric and asymetric end- to-end bis-monodentate fashions, spreading out along be plane to form a 20 network. The Structure is made up of CuFe unit with Cu(II) and Fe(III) ions locating in a distorted square-based pyramid and a compressed octahedron, respectively. 展开更多
关键词 iii OXAMIDATO COMPLEX CRYSTAL CYANIDO HETERNUCLEAR ii LIKE OF BRIDGED Fe cu
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FERROMAGNETICALLY COUPLED Gd(III)Cu(II)Gd(III)TRINUCLEAR COMPLEXES
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作者 Ming Ming MIAO Dai Zheng LIAO +1 位作者 Zone Hui JIANG and Geng Lin WANG (Department of Chemistry.Nankai University,Tianjin.300071) 《Chinese Chemical Letters》 SCIE CAS CSCD 1995年第6期533-536,共4页
Three new heterotrinuclear complexes have been synthesized and characterized, namely {[Gd(L)(2)](2)[Cu(pbaOH)]}(ClO4)(4), where pbaOH denotes 2-hydroxy-1,3-propylenebis(oxamato), L stands for 1,10-phenanthroline (phen... Three new heterotrinuclear complexes have been synthesized and characterized, namely {[Gd(L)(2)](2)[Cu(pbaOH)]}(ClO4)(4), where pbaOH denotes 2-hydroxy-1,3-propylenebis(oxamato), L stands for 1,10-phenanthroline (phen), 5-nitro-1,10-phenanthroline (NO2-phen) or 2,2'-bipyridyl (bpy). The temperature dependence of the magnetic susceptibility of ([Gd(phen)(2)(ClO4)](2)[Cu(pbaOH)])(ClO4)(2) has been studied in the 4-300K range, giving the exchange integral J = 6.69 cm(-1). This indicates a weak ferromagnetic interaction between the copper(II) and gadolinium(III) ions. 展开更多
关键词 ii)Gd iii)TRINUCLEAR COMPLEXES cu
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Cu(Ⅱ)-稀土异双核配合物的研究
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作者 朱学栋 朱子彬 +1 位作者 焉翠蔚 李延团 《华东理工大学学报(自然科学版)》 CAS CSCD 北大核心 1997年第4期397-402,共6页
利用液相化学合成技术,成功制备了六种含草酰胺桥的新型异双核配合物Cu(oxap)Ln(phen)2(ClO4)3(Ln:Y,Ce,Pr,Eu,Gd,Yb)。基于元素分析、红外光谱、电子光谱、ESR谱及变温磁化率等测试... 利用液相化学合成技术,成功制备了六种含草酰胺桥的新型异双核配合物Cu(oxap)Ln(phen)2(ClO4)3(Ln:Y,Ce,Pr,Eu,Gd,Yb)。基于元素分析、红外光谱、电子光谱、ESR谱及变温磁化率等测试手段对这些异双核配合物进行了表征。测定了Cu(oxap)Gd(phen)2(ClO4)3的变温磁化率(4.2~300K),对由自旋Hamiltonian算符H=-2JS1·S2导出的磁方程用最小二乘法拟合,求得交换积分J=2.18cm-1,表明配合物中Cu(I)和Gd(II)离子间存在弱的铁磁性超交换作用。 展开更多
关键词 草酰胺桥 合成 稀土元素 双核配合物
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使用支撑液膜从Fe^(3+)/Cu^(2+)溶液中选择分离Fe^(3+)的研究(I)液液萃取实验(英文)
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作者 张保成 G.Gozzelino 《膜科学与技术》 CAS CSCD 北大核心 2001年第5期57-57,共1页
支撑液膜在水溶液金属离子的分离中有着独特的优势 .报道了从Fe3+/Cu2 +溶液中选择分离Fe3+液 /液萃取研究结果 .水相为Fe3+/Cu2 +硫酸溶液 ,萃取相为正癸醇 (n -de canol) ,载体为二 (2 -乙基己基 )磷酸 (D2EHPA) .实验研究了溶液相中... 支撑液膜在水溶液金属离子的分离中有着独特的优势 .报道了从Fe3+/Cu2 +溶液中选择分离Fe3+液 /液萃取研究结果 .水相为Fe3+/Cu2 +硫酸溶液 ,萃取相为正癸醇 (n -de canol) ,载体为二 (2 -乙基己基 )磷酸 (D2EHPA) .实验研究了溶液相中硫酸浓度以及有机相中载体D2EHPA浓度对金属离子萃取速率的影响 .研究发现水溶液的酸浓度对Fe3+的萃取影响较明显 ,而对Cu2 +的萃取影响很小 .在两相界面处Fe3+与D2EHPA的反应速度比Cu2 +快很多 .Fe3+、Cu2 +与D2EHPA的络合物在有机相中的扩散速度都较慢 ,但是Fe3+与D2EHPA的络合物的界面反应速度比络合物的扩散速度快 .有机相中载体浓度对金属离子萃取速率的影响也很明显 .液液萃取研究结果显示 ,在使用支撑液膜进行铁离子选择分离时 ,可以通过改变溶液相酸的浓度 ,有机相中载体浓度 ,或者通过缩短分离时间来提高选择率 . 展开更多
关键词 支撑液膜 分离 液液萃取 实验 铁/铜溶液 铁离子
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Mechanistic Study and Kinetic Determination of Cu(Ⅱ) by the Catalytic Kinetic Spectrophotometric Method 被引量:1
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作者 ZHANG Haoshuang LIU Li JI Hongwei 《Journal of Ocean University of China》 SCIE CAS CSCD 2019年第1期144-150,共7页
A highly sensitive and selective catalytic kinetic spectrophotometric method for the determination of Cu(Ⅱ) is proposed. It is based on the catalytic effect of Cu(Ⅱ) on the oxidation of glutathione(GSH) by potassium... A highly sensitive and selective catalytic kinetic spectrophotometric method for the determination of Cu(Ⅱ) is proposed. It is based on the catalytic effect of Cu(Ⅱ) on the oxidation of glutathione(GSH) by potassium hexacyanoferrate(Ⅲ) in acidic medium at 25.0℃. The reaction is monitored spectrophotometrically by measuring the decrease in absorbance of oxidant at 420 nm using the fix-time method. Under the optimum conditions, the proposed method allows the determination of Cu(Ⅱ) in a range of 0-35.0 ng m L^(-1) with good precision and accuracy and the limit of detection is down to 0.04 ng m L^(-1). The relative standard deviation(RSD) is 1.02%. The reaction orders with respect to each reagent are found to be 1, 1/2, and 1/2 for potassium hexacyanoferrate(Ⅲ), glutathione and Cu(Ⅱ) respectively. On the basis of these values, the rate equation is obtained and the possible mechanism is established. Moreover, few anions and cations can interfere with the determination of Cu(Ⅱ). The new proposed method can be successfully used to the determination of Cu(Ⅱ) in fresh water samples and seawater samples. It is found that the proposed method has fairly good selectivity, high sensitivity, good repeatability, simplicity and rapidity. 展开更多
关键词 cu(Ⅱ) catalytic kinetic method SPECTROPHOTOMETRY GLUTATHIONE potassium hexacyanoferrate(Ⅲ)
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酚氧桥联希夫碱Gd~ⅢCu~Ⅱ双核配合物磁学性质理论研究 被引量:1
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作者 黄仁义 罗树常 +2 位作者 刘秋秋 王双凤 梅红 《山东化工》 CAS 2018年第6期13-16,共4页
采用DFT-BS方法,选择GGA、混合泛函、meta-GGA方法和不同基组对酚氧桥联席夫碱Gd~ⅢCu~Ⅱ双核配合物[Cu(valaepy)_2Gd(O_2NO)_3]磁学性质进行研究。结果表明,在B3P86/TZVP(Gd为SARC2-DKH-QZVP)水平下计算的数值与实验值最吻合。分子磁... 采用DFT-BS方法,选择GGA、混合泛函、meta-GGA方法和不同基组对酚氧桥联席夫碱Gd~ⅢCu~Ⅱ双核配合物[Cu(valaepy)_2Gd(O_2NO)_3]磁学性质进行研究。结果表明,在B3P86/TZVP(Gd为SARC2-DKH-QZVP)水平下计算的数值与实验值最吻合。分子磁轨道分析表明,分子磁轨道主要由Gd~Ⅲ离子的4f轨道、Cu~Ⅱ离子3d_(x^2-y^2)的轨道、席夫碱中酚氧桥联配位O原子的p轨道组成。自旋布居分析表明,Gd~Ⅲ以自旋极化为主,Cu~Ⅱ以自旋离域为主。 展开更多
关键词 DFT-BS 酚氧桥 席夫碱 Gdiiicuii双核配合物 磁学性质
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席夫碱铜和镍配合物的合成与表征
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作者 佟龙 尹霈仪 +6 位作者 葛迎迎 陈越南 苏静琼 金红广 陈丹骅 吴杨阳 蔡跃鹏 《华南师范大学学报(自然科学版)》 CAS 北大核心 2011年第B06期15-18,共4页
合成了新型含氮-氧螯合型席夫碱(HL)配体的铜(II)配合物和镍(III)配合物,并通过X射线单晶衍射、红外光谱、核磁共振氢谱、紫外-可见光谱、质谱和电子光谱等手段对其进行了表征.通过分析配合物1表明它属于单晶系,空间群为P21/... 合成了新型含氮-氧螯合型席夫碱(HL)配体的铜(II)配合物和镍(III)配合物,并通过X射线单晶衍射、红外光谱、核磁共振氢谱、紫外-可见光谱、质谱和电子光谱等手段对其进行了表征.通过分析配合物1表明它属于单晶系,空间群为P21/n.中心Cu原子的几何配位结构为扭曲四方锥(考虑到Cu···N之间的弱作用).而配合物2属于单斜晶系,空间群为P21/c.中心Ni离子的几何配位结构为扭曲八面体,与此同时,中性分子单元[Ni^IIIL2(N3)]是通过氢键C—H…N的连接形成一维的无限链. 展开更多
关键词 cu(ii)配合物 Ni(iii)配合物 席夫碱 N N-二甲基乙二胺 水杨醛
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Synthesis and ferromagnetic interaction in oxamido- bridged heterodinuclear copper (Ⅱ)- chromium (Ⅲ) complexes
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作者 李延团 焉翠蔚 廖代正 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1999年第1期24-31,1,共9页
Four μ-oxamido heterodinuclear complexes, [Cu(oxae)Cr(L)2] (NO3)3,where oxae denotes the N, N’-bis (2-aminoethyl) oxamido dianion and L represents 1, 10-phenanthroline ( phen); 5-nitro-1, 10-phenanthroline (NO2-phen... Four μ-oxamido heterodinuclear complexes, [Cu(oxae)Cr(L)2] (NO3)3,where oxae denotes the N, N’-bis (2-aminoethyl) oxamido dianion and L represents 1, 10-phenanthroline ( phen); 5-nitro-1, 10-phenanthroline (NO2-phen); 5-methyl-1, 10-phenanthroline (Me-phen) and 2,2’-bipyridine (bpy), have been synthesized and characterized by elemental analyses, magnetic moments (at room temperature) and molar conductivity measurements and spectroscopy. It is proposed that these complexes have extended oxamido-bridged structures consisting of a copper (Ⅱ) ion and a chromium (Ⅲ) ion, which have a square planar environment and octahedral environment, respectively. The cryomagnetic properties of the [Cu(oxae)Cr(bpy)2] (NO3)3(1) and [Cu(oxae)Cr(phen)2] (NO3)3(2) complexes have been measured over the range of 4.2-300 K. The least-squares fit of the experimental data based on the spin Hamiltonian, H = - 2JS1·S2, the exchange integrals (J) were evaluated as + 36.9 cm-1 for 1 and +35.8 cm-1 for 2. The results have confirmed 展开更多
关键词 Qxamido-bridge ferromagnetic interaction cu(ii)-cr(iii) binuclear complex
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