对甲苯磺酸铜的电化学表征

合成了对甲苯磺酸铜,用X光单晶衍射确定了其结构.实验结果表明,该盐容易脱除全部结晶水,在空气中不潮解.分别测定了对甲苯磺酸铜(Cu(p-OTs)2)在H2O、CH3OH和DMF中的电化学参数.实验结果表明Cu(p-OTs)2在不同溶剂中的反应机理各异. Cu(II)的电化学还原在H2O中是分两步进行,而在CH3OH和DMF中的电化学还原是一步两电子过程.对实验结果进行了分析讨论.     

乙二胺铜－铁氰复合修饰电极薄膜的电沉积和结构表征及电化学性质

乙二胺铜－铁氰复合修饰电极薄膜的电沉积和结构表征及电化学性质陈昌国，李海梅，黄宗卿（重庆大学化工学院重庆６３００４４）关键词：铜、乙二胺，铁氰，修饰电极，光谱普鲁士兰（ＰＢ）修饰电极因其独特的电致变色现象而倍受关注。在１９７８年以来的十余年间里已相继...     

Complexing properties of methyl and phenyl glycine derivatives in their compounds with H+, Ni(II), Cu(II), and Zn(II)

The influence of the solvent and the substituents on the complexing properties of methyl and phenyl glycine derivatives is discussed. On the basis of a computer analysis of potentiometric titration results, the composition and the stability constants of the complexes ofN-methylglycine,N,N-dimethylglycine,N-phenylglycine and phenylglycine with H⁺ and with Ni(II), Cu(II), Zn(II) were determined. The ligand-metal coordination mode as well as the zwitterion level in percent in ligand/proton systems were determined by spectral analyses and equilibria studies.

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Komplexbildung der Methyl- und Phenylglycin-Derivate in ihren Verbindungen mit dem Proton und Ni(II), Cu(II) und Zn(II)

Zusammenfassung Der Einfluß des Lösungsmittels und der Substituenten auf die komplexbildenden Eigenschaften der Methyl- und Phenylglycin-Derivate wird diskutiert. Anhand einer Computer-Analyse von potentiometrischen Daten wurden die Zusammensetzung und die Beständigkeitskonstanten der Komplexe vonN-Methylglycin,N,N-Dimethylglycin,N-Phenylglycin und Phenylglycin mit H⁺, Ni(II), Cu(II) und Zn(II) festgestellt. Mittels spektroskopischer Methoden und Gleichgewichtstudien wurde der Koordinationstyp des Liganden mit dem Metall festgestellt sowie der Prozentanteil des Zwitterions im Ligand/Proton-System.

     

流动注射分光光度法测定微量铜的研究

研究了在ＴｒｉｔｏｎＮ－１０１存在下，２－羟基－３－羧基－５－磺酸基苯重氮氨基偶氮苯（ＨＣＳ－ＤＡＡ）显色流动注射光度测定微量铜的新方法，用ｐＨ０．４～１１．５Ｎａ２Ｂ４Ｏ７－ＮａＯＨ缓冲溶液作载流，ＨＣＳＤＡＡ和ＴｒｉｔｏｎＮ－１０１的混合试剂作试剂流，采双道流路，５３０ｎｍ检测反应生成红色配合物，方法线性范围是０．０２４～０．２０μｇ／ｍＬ，检出限为８ｎｇ／ｍＬ，进样频率为１００样次／ｈ，直接     

A Novel Hybrid Solid Constructed from Tetramolybdate and Copper Complexes with Mixed Ligands: [{(Cu·phen)2(tp)}{(Cu·phen·H2O)2(tp)}{Mo4O14}]

A novel copper molybdate with mixed ligands, [{(Cu·phen)2(tp)}{(Cu·phen·H2O)2(tp)}{Mo4O14}] (phen=1,10-phenanthroline, tp=terephthalate) 1, has been hydrothermally synthesized and structurally characterized. The crystal belongs to monoclinic system, space group P21/c with a=13.1711(7), b=19.6132(10), c=13.6910(7) (A), β=117.6870(10)°, V=3131.8(3)(A)3, Z=2, C64H44Cu4Mo4N8O24, Mr=1946.99, Dc=2.065 g/cm3, F(000)=1920, μ(MoKα) (A) 2.198 mm-1, R=0.0810 and wR=0.2012 for 4233 observed reflections (Ⅰ ＞ 2σ(Ⅰ)). The structural analysis indicates that the title compound contains a discrete tetramolybdate cluster decorated with copper complex fragments and tp ligands bridging the clusters into a wave-like layer. The hydrogen bonding between adjacent layers further extends the compound into a 3-D framework.     

酞菁铜与Q-CdS超微粒子界面的光致电荷转移研究

半导体超微粒子与有机分子界面的光致电行转移过程是当前光化学和材料科学研究的一个活跃领域［‘，2］；研究的目的主要有两个方面，一是研究半导体超微粒子表面光致电行转移的特性；二是研究有机分子对超微粒子的光敏化作用．目前，超微粒子的功能化研究日益深入，其独特的光     

Synthesis, crystal structure and magnetic properties of a novel complex [Cu(NIT2Py)(PDA)(H2O)]·(CH3OH)(H2O)

A novel complex [Cu(NIT2Py)(PDA)(H₂O)]·(CH₃OH)(H₂O) has been synthesized and structurally characterized by X-ray diffraction methods. It crystallizes in the monoclinic space group P2(1)/c. The structure consists of [Cu(NIT2Py)(PDA)(H₂O)] moiety, one solvent methanol molecule and one water molecule. The copper(II) ion is in a distorted octahedral environment: one nitrogen atom and one oxygen atom from the NIT2Py, one nitrogen atom from the PDA (2,6-pyridine dicarboxylic acid) and one oxygen atom from the aqueous in the basal plane; two oxygen atoms from the PDA in the axial position. The units of [Cu(NIT2Py)(PDA)(H₂O)] were connected as one dimension chain by the intermolecular hydrogen bonds. The complex exhibits intramolecular antiferromagnetic interactions between the Cu(II) ion and the NIT2Py.     

痕量铜的合并带法流动注射分析——Fe~(3+)-S_2 O_3~(2-)-Cu~(2+)催化体系

本文基于 Cu~(2+)对三价铁离子与硫代硫酸盐反应生成深紫蓝色物质的褪色反应的催化作用采用流动注射合并带技术,建立了痕量铜(Ⅱ)的快速分析方法。方法的线性范围在0～350μg/L 检出限为10μg/L,相对标准偏差为1.68％,进样频率可达100样次/小时,具有很高的选择性。     

Syntheses of TiO2(B) nanowires and TiO2 anatase nanowires by hydrothermal and post-heat treatments

TiO₂(B) nanowires and TiO₂ anatase nanowires were synthesized by the hydrothermal processing in 10 M NaOH aq. at 150 °C followed by the post-heat treatment at 300-800 °C. As-synthesized Na-free titanate nanowires (prepared by the hydrothermal treatment and repeated ion exchanging by HCl (aq.) were transformed into TiO₂(B) structure with maintaining 1-D morphology at 300-500 °C, and further transformed into anatase structure at 600-800 °C with keeping 1-D shape. At 900 °C, they transformed into rod-shaped rutile grains. Microstructure of these 1-D TiO₂ nanomaterials is reported.     

铜、钴、镍同时分离工艺的研究

稀土体系三种元素同时分离的工艺最近已有发表,但非稀土方面的工作尚未见报导.对Cu、Co、Ni三种元素,通常是将Cu、Co作为一个组份与Ni分离.本工作对组成为Cu:Co:Ni=1:1:1的水相合成料液设计了两种工艺,进行了串级实验,实现了该三种元素的同时分离, 串级实验以HEH(EHP)作萃取剂,煤油为稀释剂,其它试剂均用分析纯.