Hydrothermal Synthesis and X‐Ray Structural Characterization of Manganese,Nickel, and Cadmium Coordination Polymers Containing 2,3‐Pyridinedicarboxylate as Multidentate Ligands

Three divalent transiton‐metal complexes of 2,3‐pyridinedicarboxylate (2,3‐pda²), [Mn(2,3‐pda)‐(H₂O)3]_∞ ( 7 ), [Ni(2,3‐pda)(H₂O)3]_∞ ( 8 ), and [Cd2(2,3‐pda)₂(H₂O)]_∞ ( 9 ) have been hydrothermally synthesized and structurally characterized. X‐ray diffraction analyses reveal that compounds 7 and 8 are zigzag‐ and linear‐type one‐dimension (1D) coordination polymers, respectively, whereas compound 9 is a three‐dimension (3D) coordination polymer. A simple comparison of the coordination geometries with the available neutral analogues {M_x(2,3‐pda)_x(H₂O)_y}_∞ containing one or two divalent transition‐metal atoms and equal ligands in the presence or absence of coordinated water molecules is also presented.     

Synthesis and structure of Mn(II) and Zn(II) complexes containing 1,10-phenanthroline unit

The Mn(II) and Zn(II) complexes of N,N′-diisopropyl-1,10-phenanthroline-2,9-dimethanamine have been synthesised, and the structure of the two complexes have been studied by X-ray crystallography.     

聚硅氧烷涂敷的反相高效液相色谱固定相

用甲基乙烯基聚硅氧烷涂敷于硅烷化的微粒硅胶上，制备出一种新型的涂敷型反相高效液相色谱固定相。该固定相对极性、非极性和碱性化合物均有良好的分离能力，峰对称性好。对其恶性循环 了考察，连续使用三个月后，固定相的碳量和色谱性能仍保持不变。     

2,6—二氯—4—溴偶氮胂光度法测定微量铀（Ⅵ）

本报道用了２，６－二氯－４－溴偶氮胂作显色剂测定微量铀（Ⅵ）的光度法。在Ｈ２ＳＯ４介质中，铀（Ⅵ与）２，６－二氯－４－溴偶氮胂形成１：２络合物，其λｍａｘ＝６４０ｎｍ；表观摩尔吸光系数为１．１×１０＾５Ｌ．ｍｏｌ＾－＾１．ｃｍ＾－＾１；铀的浓度在０．０－２２．０μｇ／ｍｌ内符合比耳定律。方法具有灵敏度高，选择性好，操作方便等特点并已用于废水及矿样中微量铀（Ⅵ）的测定。     

Determination of medecamycin by adsorptive stripping voltammetry with an activated electrode

The adsorptive and electrochemical behaviors of medecamycin were investigated on a glassy carbon electrode (GCE) pretreated by anodic oxidation at +1.8 V for 5 min in 0.025 mol l^–1 NH₃-NH₄Cl (pH 8.6) solution. An adsorptive stripping voltammetric method for the determination of medecamycin at the pretreated glassy carbon electrode has been developed. Medecamycin was accumulated in NH₃-NH₄Cl buffer (pH 9.0) at a potential of –0.7 V (vs. saturated calomel electrode (SCE)) for a certain time, and then determined by second-order differential anodic stripping voltammetry. The second-order differential anodic stripping peak current at +0.72 V was proportional to the concentration of medecamycin in the range 2.0 g ml^–1 to 50.0 g ml^–1. The detection limit (three times the signal-to-noise) was 1.0 g ml^–1 and the relative standard deviation of the results was 3.28% for eight successive determinations of 10.0 g ml^–1 medecamycin. This method has been applied to the direct determination of medecamycin in commercial tablets and spiked urine samples with satisfactory results.     

Transient response of a Brownian particle with general damping

We study the transient response of a Brownian particle with general damping in a system of metastable potential well. The escape rate is evaluated as a function of time after an infinite wall is removed from the potential barrier. It takes a relaxation time for the rate to reach its limit value and this rate relaxation time differs from the relaxation time of the majority of the probability around the bottom of the potential well. The rate relaxation time is found to depend on the temperature as well as the damping constant. It involves the diffusion time and the instanton time, in general agreement with recent studies of the overdamped case by Bier et al. [Phys. Rev. E 59, 6422 (1999)].     

Large-scale synthesis of globotriose derivatives through recombinant E. coli

The carbohydrate chains decorating cell membranes and secreted proteins participate in a range of important biological processes. However, their ultimate significance and possible therapeutic potential have not been fully explored due to the lack of economical methods for their production. This study is an example of the use of a genetically engineered bacterial strain in the preparation of diverse oligosaccharides. Based on an ex vivo biosynthetic pathway, an artificial gene cluster was constructed by linking the genes of five associated enzymes on a plasmid vector. This plasmid was inserted into the E. coli NM522 strain to form globotriose-producing cells ('superbug' pLDR20-CKTUF). The specific strain was conveniently applied to the synthesis of globotriose trisaccharide and its derivatives, as potential neutralizers for Shiga toxin. This work demonstrates a novel and economical method for generating ligand diversity for carbohydrate drug development.     

电吸附技术的应用与研究

本文综述了活性炭、活性炭纤维、炭气凝胶及活性氧化铝等材料的电吸附/脱附技术的研究进展。主要介绍了其在去除水中无机和有机污染物方面的应用，并对今后的研究方向提出了建议。     

Distance dependence of electron transfer in rigid,cofacially compressed,pi-stacked porphyrin-bridge-quinone systems

The electron-transfer (ET) dynamics of a series of unusually rigid pi-stacked porphyrin-quinone (P-Q) systems, in which sub-van der Waals interplanar distances separate juxtaposed porphyryl, aromatic bridge, and quinonyl components of these assemblies, are reported. The photoinduced charge separation (CS) and thermal charge recombination (CR) ET reactions of [5-[8'-(2',5'-benzoquinonyl)-1'-naphthyl]-10,20-diphenylporphinato]zinc(II) (1a-Zn), [5-[8'-(4'-[8'"-(2'"',5'"'-benzoquinonyl)-1'"-naphthyl]-1'-phenyl)-1'-naphthyl]-10,20-diphenylporphinato]zinc(II) (2a-Zn), and [5-(8'-[4'-(8'"-[4'"'-(8'"-[2'"',5'"'-benzoquinonyl]-1'"-naphthyl)-1'"'-phenyl]-1'"-naphthyl)-1'-phenyl]-1'-naphthyl)-10,20-diphenylporphinato]zinc(II) (3a-Zn) in CH(2)Cl(2) were investigated by pump-probe transient absorption spectroscopy. Analyses of these data show that the phenomenological ET distance dependence (beta) for both the CS and CR reactions in these systems is soft (beta(CS) = 0.43 A(-1); beta(CR) = 0.35 +/- 0.16 A(-1)). This work demonstrates that simple aromatic building blocks such as benzene, which are characterized by highly stabilized filled molecular orbitals and large HOMO-LUMO gaps, can provide substantial D-A electronic coupling when organized within a pi-stacked structural motif that features a modest degree of arene-arene interplanar compression.     

Y3+,W6+掺杂的矿物锂快离子导体Li1.2+x-yYxTi1.9-xAl0.1Si0.1WyP2.9-yO12系统的合成与表征

以LiTi2(PO4)3为母体,以天然高岭石为起始原料,经高温固相反应制得了一系列新的锂快离子导体Li1.2+x-yYxTi1.9-xAl0.1Si0.1WyP2.9-yO12(以下简称Y-W-Lisicon).X射线粉末衍射分析结果表明,在x＝0.10,y≤0.20及x＝0.20,y≤0.20的组成范围内能得到空间群为R3c,类似于Nasicon的三方结构,但在上述组成范围内均有杂相存在.应用交流阻抗技术测定电导率的结果表明,起始组成为x=0.10,y=0.10的样品在室温下具有较高的离子电导率,为1.65×10-5 S·cm-1;组成为x=0.20,y=0.10的样品在573 K时具有较高的离子电导率,为6.53×10-3 S·cm-1,该样品的分解电压为3.0 V.