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991.
992.
Jing-An Zhang Mei Pan Rui Yang Zhi-Gang She Wolfgang Kaim Zhi-Jin Fan Cheng-Yong Su 《Polyhedron》2010
The semirigid tridentate 8-(2-pyridinylmethylthio)quinoline ligand (Q1) is shown to form the structurally characterized transition metal complexes [Cu(Q1)Cl2] (1), [Co(Q1)(NO3)2] (2), [Cd(Q1)(NO3)2] (3), [Cd(Q1)I2] (4). [Cu(Q1)2](BF4)2·(H2O)2 (5), [Cu(Q1)2](ClO4)2·(CH3COCH3)2 (6), [Zn(Q1)2](ClO4)2(H2O)2 (7), [Cd2(Q1)2Br4] (8), [Ag2(Q1)2(ClO4)2] (9), and [Ag2(Q1)2(NO3)2] (10). Four types of structures have been observed: ML-type in complexes 1–4, in which the anions Cl−, NO3− or I− also participate in the coordination; ML2− type in complexes 5–7 without direct coordination of the anions BF4− or ClO4− and with more (Cu2+) or less (Zn2+) distorted bis-fac coordinated Q1; M2L2-type in complex 8, in which two Br− ions act as bridges between two metal ions; and M2(μ-L)2-type in complexes 9 and 10, in which the ligand bridges two anion binding and Ag–Ag bonded ions. Depending on electron configuration and size, different coordination patterns are observed with the bonds from the metal ions to Npyridyl longer or shorter than those to Nquinoline. Typically Q1 acts as a facially coordinating tridentate chelate ligand except for the compounds 9 and 10 with low-coordinate silver(I). Except for 6 and 8, the complexes exhibit distinct constraining effects against both G(+) and G(-) bacteria. Complexes 1, 3, 4, 5, 7 have considerable antifungal activities and complexes 1, 5, 7, and 10 show selective effects to restrain certain botanic bacteria. Electrochemical studies show quasi-reversible reduction behavior for the copper(II) complexes 1, 5 and 6. 相似文献
993.
Mei Wang Nathalie Simon Gaelle Charrier Muriel Bouttemy Arnaud Etcheberry Musen Li Rabah Boukherroub Sabine Szunerits 《Electrochemistry communications》2010,12(3):351-354
While it is clearly established that oxidation of as-grown boron-doped diamond (BDD) interfaces results in the introduction of different surface oxygen functions such as ether, carbonyl and hydroxyl groups, there is no reported approach which can clearly distinguish between the different surface functions. For further surface functionalization, it is important to quantify the presence of each group on the diamond surface. In this paper, the presence and amount of surface hydroxyl groups is identified using esterification of the COH groups with trifluoroacetic acid. The presence of CF3 group in the acid allowed the identification and estimation of the amount of surface hydroxyl groups using X-ray photoelectron spectroscopy (XPS). 相似文献
994.
Shao Rong Luan Yi Hua Zhu Yu Qing Jia Qing Cao 《Journal of Thermal Analysis and Calorimetry》2010,99(2):523-530
A complex of thiourea and bismuth trichloride has been synthesized. Its composition is Bi3Cl9[SC(NH2)2]7. Crystallographic data are a = 7.141(2) Å, b = 8.820(3) Å, c = 16.365(5) Å, α = 99.389(4)°, β = 95.422(4)°, γ = 106.177(4)°, triclinic system. There are the mononuclear anion [BiCl5SC(NH2)2]2? and the dinuclear cation {Bi2Cl4[SC(NH2)2]6}2+ with the Bi–Cl–Bi bridge bonds in the complex. The electric conductance of the absolute methanol solution contained the complex indicates that the complex is an ionic compound. Raman spectra indicate that the bismuth ion is coordinated by the sulfur atoms of the thiourea. The thermal analysis verifies the structure of complex. The TG–MASS curves show the structure rearrangement in the complex at about 118 °C. The DSC curves and calculation means that the structure rearrangement is irreversible. 相似文献
995.
Mingfei Shao Jingbin Han Wenying Shi Min Wei Xue Duan 《Electrochemistry communications》2010,12(8):1077-1080
The ordered ultrathin film based on iron(III) porphyrin and Co–Al layered double hydroxide (Co–Al LDH) nanosheets has been fabricated via the layer-by-layer (LBL) method. The film modified electrode demonstrates a couple of well-defined reversible redox peaks attributed to Co(III)/Co(II), with iron(III) porphyrin serving as an efficient mediator for facilitating the electron transfer. Furthermore, it exhibits excellent electrocatalytic behavior for H2O2 with a wide linear range of response, high sensitivity and low detection limit. 相似文献
996.
Jiang F Wang Y Hu X Shao N Na N Delanghe JR Ouyang J 《Journal of separation science》2010,33(21):3393-3399
The application of pore-gradient polyacrylamide gel electrophoresis (PG-PAGE) incorporated with carbon nanotube modified by Triton X-100 and carboxylation so as to improve the separation of human serum proteins is reported. The novel PG-PAGE was made by adding water-soluble single-walled carbon nanotubes (CNTs) when preparing the polyacrylamide gel. Significant improvements in separation of complement C3 protein and haptoglobin (Hp) in human serum were achieved. It was estimated that the interactions between the hydrophilic groups on the proteins and the surface of the CNTs result in different adsorption kinetics of complement C3 and Hp subtype on the nanoparticles incorporated in the gel, thus enhancing the separation of the two proteins in serum. This new CNT matrix-assisted PG-PAGE method for enhanced separation of complement C3 and Hp in human serum was successfully applied to distinguish the samples from liverish patients and healthy people. 相似文献
997.
Cationic hyperbranched BPEI was immobilized on the surface of MWNTs via electrostatic interactions between the positively charged protonated amines within the polymer and the carboxyl groups on the chemically oxidized MWNT surface. The functionalized BPEI‐MWNTs were characterized by FT‐IR, TGA, TEM and surface charge analysis, and it was used as a bio‐sorbent for the adsorption of proteins. CD spectra showed no conformational change of BSA during the adsorption/desorption process. A dynamic adsorption capacity of 167 mg · g?1 for BSA was achieved. With a sample volume of 2.0 mL, an enrichment factor of 10 was obtained along with an adsorption efficiency of 100%, a recovery of 100%, a sampling frequency of 10 h?1 and a RSD of 2.6% at 25 µg · mL?1 BSA.
998.
Yingliang Wei Qing Zhang Chen Shao Chao Li Luping Zhang Xianli Li 《Journal of Analytical Chemistry》2010,65(4):398-403
A rapid and convenient electrochemical method is described for the determination of salbutamol based on multi-carbon nanotubes
(MWNT) film coated glassy carbon electrode (GCE). The electrochemical behavior of salbutamol at this modified electrode was studied by square wave voltammetry, which indicated
that the oxidation peak potential of salbutamol shifted on 40 mV to less positive potential and the peak current increased
4.5 fold, in contrast to that at a bare electrode. Various experimental parameters such as pH value of supporting electrolyte,
the amount of modifier, and accumulation time were optimized. Under optimal measurement conditions, there is a good linear
relationship between the peak current (I
pa) and salbutamol concentration in the range from 8.0 × 10−7 to 1.0 × 10−5 M, and the detection limit is 2.0 × 10−7 M (S/N = 3) at 2 min accumulation. The method has been successfully employed to detect salbutamol in pharmaceutical formulations. 相似文献
999.
负载钯催化的Suzuki偶联反应研究进展 总被引:4,自引:0,他引:4
负载钯催化的Suzuki偶联反应,由于产物易分离、催化剂可重复使用,已引起人们的广泛关注.综述了近年来负载钯催化的Suzuki偶联反应研究进展,载体包括活性碳、金属氧化物、硅铝酸盐微孔分子筛、二氧化硅材料、活性粘土和聚合物等. 相似文献
1000.
高效液相色谱的4种商品手性柱对38种手性化合物的拆分研究 总被引:5,自引:1,他引:4
采用纤维素-三(3,5-二甲基苯基氨基甲酸酯)涂敷型手性固定相(Chiralcel OD柱)、直链淀粉-三(3,5-二甲基苯基氨基甲酸酯)涂敷型手性固定相(Chiralpak AD柱)、直链淀粉-三(3,5-二甲基苯基氨基甲酸酯)键合型手性固定相(Chiralpak IA柱)和Pirkle型的(S,S)-Whelk-01手性固定相对38种外消旋体化合物进行手性拆分。实验结果表明,4种固定相的手性识别能力为:OD>AD>IA>(S,S)-Whelk-01,OD固定相的手性识别率达到60%,并且它们之间的手性识别性能还具有一定的互补性。本研究对4种常用手性固定相的拆分能力进行了对比,为拆分手性化合物时有的放矢地选择手性固定相提供了参考。 相似文献