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941.
Dr. László Beda 《Journal of Thermal Analysis and Calorimetry》1995,44(2):513-516
The curing of composition containing epoxy bond is complicated chemical and technological process where under temperature and pressure conditions a change of its structure occurs. The structure changes are possible to know by thermal methods as DSC, DTA, etc. and also by measurement of dielectrical response under the low frequency electrical field. 相似文献
942.
CrystalStructureandMolecularAbsoluteConfigurationof(+)-Isocedranol(C_(15)H_(26)O)¥LiuJie;ChenMin-Qin(CenterofAnalysis&Measurem... 相似文献
943.
Xiao-pingYan Bao-linHe JieZhang Han-fanLiua 《高分子科学》2005,(4):393-399
Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%) obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn^2 but with a certain decrease in activity. The reaction parameters in the presence of Zn^2 were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations. 相似文献
944.
Li Jiang Fushen Lu Qing Chang Yang Liu Huibiao Liu Yuliang Li Wei Xu Guanglei Cui Junpeng Zhuang Xiaofang Li Shu Wang Yinglin Song Daoben Zhu 《Chemphyschem》2005,6(3):481-486
An ultrathin composite film containing anionic Ag-His complexes (His: L-Histidine) and oppositely charged BH-PPV was fabricated by means of the electrostatic layer-by-layer self-assembly technique. UV/Vis spectra showed a continuous deposition process of Ag-His complexes and BH-PPV. The film structure was characterized by using small-angle X-ray diffraction, AFM, and SEM. The nonlinear optical properties of the ultrathin film were studied by using the Z-scan technique with a laser duration of 8 ns at a wavelength of 532 nm. The film sample exhibited a strong nonlinear saturated absorption, with an alpha2 value of -3.9 x 10(-5) mW(-1) and a self-defocusing effect with an n2 value of -4.78 x 10 (-12) m2W(-1). 相似文献
945.
The 1,3-dipolar cycloaddition reaction of meso-tetraaryl porphyrin with 2,6-dichlorobenzonitrile oxide yielded novel isoxazoline-fused chlorins and two stereoisometric bacteriochlorins. The crystal structure of bacteriochlorin was characterized by X-ray diffraction. 相似文献
946.
Analysis of acyclovir by high performance capillary electrophoresis with on-column amperometric detection 总被引:1,自引:0,他引:1
The separation of acyclovir (ACV) by high performance capillary electrophoresis (HPCE) with on-column amperometric detection using alpha-amino-5-mercapto-3,4-dithiazole (AMD) as internal standard is described. The calibration line was linear in the range of 0.5-20 mg/L of ACV. The detection limit was 0.15 mg/L of ACV. Its recovery ranged from 98 to 101% with relative standard deviations (RSDs) from 1.9 to 3.2% (n = 5). This method was successfully used for determining ACV in some pharmaceuticals and human urine. Comparable results with HPCE with ultraviolet (UV) detection and amperometric detection were obtained. 相似文献
947.
Reaction of the semi-rigid ligand 2,4-bis(1-imidazolylmethyl)-mesitylene (m-bimms) with CdCl2 afforded a boat-like molecular rectangle [Cd(m-bimms)Cl2]2 · 1/2H2O (1), with the orientation of the two imidazolyl arms of the ligand in syn-conformation and bridging chloride ions bisecting the macrocycle. Weak Cl· · ·H—C interations further extended the dimers into 1D infinite chains with nanoscopic channels. An analogous reaction with Cd(NO3)2 gave a 1D coordination polymer [Cd(m-bimms)2(NO3)2]n · 2nH2O (2) composed of nanoscopic metallamacrocycles, where the two imidazolyl arms adopt an anti-conformation. Different anions result in different ligand conformations and thus determine the varied molecular architectures. 相似文献
948.
949.
Nonaqueous capillary electrophoretic (NACE) method for the separation of nine structurally similar chiral anticholinergic drugs was developed. The eight drug enantiomers were separated on baseline within 18 min using 20mM phosphoric acid and 10 mM NaOH, containing 10 mM heptakis(2,3-dimethyl-6-sulfato)-4beta-cyclodextrin (HDMS-beta-CD) in methanol. The results were compared with those obtained in the high performance liquid chromatography system. 相似文献
950.
Xiong JY Narayanan J Liu XY Chong TK Chen SB Chung TS 《The journal of physical chemistry. B》2005,109(12):5638-5643
Kinetics as well as the evolution of the agarose gel topology is discussed, and the agarose gelation mechanism is identified. Aqueous high melting (HM) agarose solution (0.5% w/v) is used as the model system. It is found that the gelation process can be clearly divided into three stages: induction stage, gelation stage, and pseudoequilibrium stage. The induction stage of the gelation mechanism is identified using an advanced rheological expansion system (ARES, Rheometric Scientific). When a quench rate as large as 30 deg C/min is applied, gelation seems to occur through a nucleation and growth mechanism with a well-defined induction time (time required for the formation of the critical nuclei which enable further growth). The relationship between the induction time and the driving force which is determined by the final setting temperature follows the 3D nucleation model. A schematic representation of the three stages of the gelation mechanism is given based on turbidity and rheological measurements. Aggregation of agarose chains is promoted in the polymer-rich phase and this effect is evident from the increasing mass/length ratio of the fiber bundles upon gelation. Continuously increasing pore size during gelation may be attributed to the coagulation of the local polymer-rich phase in order to achieve the global minimum of the free energy of the gelling system. The gel pore size determined using turbidity measurements has been verified by electrophoretic mobility measurements. 相似文献