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81.
The reduction of triphenyltin piperidyl dithiocarbamate in acetone has been investigated using d.c. polarography and cyclic
voltammetry. Polarographic reduction yielded four well-defined waves, two of which were diffusion-controlled and two of which
appear to represent adsorption processes. The cyclic voltammetric study yielded results in close agreement with the polarographic
data. Results appear to indicate the release of the dithiocarbamate moiety, followed by reduction to form the triphenyltin
radical, which undergoes dimerization, as well as reduction to the triphenyltin anion. For comparison, the polarographic reduction
of triphenyltinchloride was investigated. A mechanism similar to that proposed by earlier authors for the polarographic behaviour
of tributyltin oxide was found.
For convenience, the more commonly used terminology of piperidyl dithiocarbamate is used throughout the paper, in place of
(piperidine-1-carbodithioato) triphenyltin (IV). 相似文献
82.
83.
Photovoltaic and spectral properties of tetraphenyloporphyrin and metallotetraphenyloporphyrin dyes 总被引:1,自引:0,他引:1
Spectroscopical properties and photocurrent (or photovoltage) of tetraphenyloporphyrins and metallotetraphenyloporphyrins in nematic liquid crystal have been studied. Photoelectric response has been measured in an electrochemical cell made of the semitransparent semiconducting and golden electrodes with porphyrin dyes embedded in liquid crystal. Fluorescence, time-resolved luminescence in microsecond time scale and photoacoustic spectra have also been measured. The competition between radiative, non-radiative processes and charge transfer is discussed. It has been shown that effectivity of porphyrins for photocurrent generation depends on the presence/absence of central metal in the macrocycle of porphyrin skeleton and the kind of metal. The schematic model of the contributions of the dye molecule and semiconducting electrode in the electron transfer process is shown. 相似文献
84.
Wen-Jia Zhou Shu-Juan Bao Yan-Yu Liang Ben-Lin He Hu-Lin Li 《Journal of Solid State Electrochemistry》2006,10(5):277-282
Pure-phase and well-crystallized spinel LiMn2O4 powders were successfully synthesized by a simple rheological phase method. The thermal behavior and structure properties
of the powders prepared by the rheological phase method compared with the solid-state reaction were investigated by thermogravimetry,
powder X-ray diffraction , scanning electron microscopy and transmission electron microscopy. According to the results of
the electrochemical tests, it is obvious that the sample resulting from the rheological phase method shows higher discharge
capacity and better cycling stability than one formed in the solid-state reaction. The cyclic voltammogram and columbic efficiency
curves also confirm that the product by the rheological phase method has a good cycling performance due to its fine cubic
spinel structure and morphology. 相似文献
85.
Merlin C. E. Bandeira Franci D. Prochnow Lúcia K. Noda Norberto S. Gonçalves Isolda Costa Hercílio G. de Melo Joe A. Crayston César V. Franco 《Journal of Solid State Electrochemistry》2004,8(4):244-251
The electropolymerization of trans-[RuCl2(vpy)4] (vpy=4-vinylpyridine) monomer on Nd-Fe-B magnets was studied by electrochemical impedance spectroscopy (EIS). Impedance diagrams obtained during the polymerization process were used to monitor film formation. The EIS results gave insight into the electrochemical phenomena occurring at the magnet surface as the polymerization process progressed. The film structure and morphology were also studied by X-ray photoelectron spectroscopy, scanning electron microscopy and Raman spectroscopy. The Raman spectroscopy results showed that the polymerization takes place at the vinyl groups of the monomer and also that the redox polymer structure is very similar to that of the monomer. The ratio of the intensity of the XPS peaks for fluorine (from the electrolyte PF6
–) and ruthenium present in the film showed that the polymer on Nd-Fe-B contained an equal proportion of Ru2+ and Ru3+, indicating that part of the film is positively charged, i.e. {[RuCl2(vpy)4]+}
n
. 相似文献
86.
L. G. Lin Y. Wang J. W. Yan Y. Z. Yuan J. Xiang B. W. Mao 《Electrochemistry communications》2003,5(12):995-999
We report an in situ STM study of a potential-dependent long-range surface restructuring of Au(1 1 1) electrode in neat 1-butyl-3-methylimidazolium tetrafluoroborates (BMIBF4) ionic liquid. Au(1 1 1) undergoes a significant long-range surface restructuring upon cathodic excursion to −1.0 V vs. Pt quasi-reference. The restructuring involves the formation of tiny pits, which then develops into a stable worm-like network with an average width of the network grids 2 nm. Electrochemical annealing occurs at the cathodic limit with the presence of a reduction product of cation BMI+. A smooth surface is recovered with the appearance of the typical (√3 × 22) reconstruction of Au(1 1 1). The surface restructuring is reestablished upon anodic excursion to −1.3 V after the adsorbed reduction product is oxidized. The long-range surface restructuring phenomenon is tentatively explained as a result of partial charge transfer to the weakly adsorbed BMI+, which reduces the metal–metal cohesive energy. In addition, the synergetic effect of the counter anion BF4− may also be involved. The results provide a knowledge of Au(1 1 1) electrode behavior in the neat ionic liquid and are beneficial to understanding in situ STM results involving surface morphological changes in such a media. 相似文献
87.
Mechanical properties of BPDA-ODA polyimide fibers 总被引:1,自引:0,他引:1
An aromatic polyimide was synthesized via a one-step polycondensation reaction between biphenyltetracarboxylic dianhydride (BPDA) and 4,4′-oxydianiline (ODA) in p-chlorophenol. The polyimide (BPDA-ODA) solution dopes were spun into fibers by means of dry-jet wet spinning. The as-spun fibers were drawn and treated in heating tubes for improving the mechanical properties. The thermal treatment on the fibers resulted in a relatively high tensile strength and modulus. Thermal mechanical analysis (TMA) was employed to study the linear coefficient of thermal expansion (CTE). Thermal gravimetry analysis (TGA) spectra showed that the BPDA-ODA fibers possessed an excellent property of thermo-oxidative degradation resistance. The sonic modulus Es of the polyimide fibers was measured. 相似文献
88.
Nada F. Atta 《European Polymer Journal》2005,41(12):3018-3025
Polymeric films derived from thioflavin S were electrosynthesized on mild steel and silver electrodes in sulfuric acid and lithium perchlorate-containing aqueous solutions. The introduction of thioflavin S in an acidic solution protected the surface of steel from corrosion. The electrochemical behavior of the steel coated with a layer of poly(thioflavin) was examined by electrochemical impedance spectroscopy. The films exhibited a capacitive behavior and were semi-conductive in nature. Infra red reflectance measurements of the polymer films at the steel surface showed that the polymer structure retained the aromatic structure of the benzene and thiazole rings with the distinction of a nitrogen quinone vibrational band. Surface morphology of the polymer film was examined with scanning electron microscopy. The films are yellow, compact and dense when electrochemically formed onto steel surfaces when compared to a blue rather porous when formed onto silver electrode. The mechanism of electropolymerization of thioflavin is given and found similar to that of aniline with the possibility of metal chelation with the sulfur and/or nitrogen in the thiazole ring. 相似文献
89.
Molecularly imprinted polymers (MIPs) selective for fluorescein, rhodamine or 2,4-dichlorophenoxyacetic acid (2,4-D) were electropolymerized onto graphite electrodes using an aqueous solution equimolar in resorsinol/ortho-phenylenediamine and in the presence of the template molecule. For the dyes, the MIP-coated electrodes showed higher affinity for their template molecule than for a non-template dye. The 2,4-D-MIP-coated electrode showed a concentration dependent response for 2,4-D as compared to the polymer-coated electrode prepared in the absence of template molecule. 相似文献
90.
Cheng Chu Zeng Li Ming Hu Jia Zeng Ru Gang Zhong College of Life Science & Bioengineering Beijing University of Technology Beijing China 《中国化学快报》2007,18(2):130-132
The anodic oxidation of caffeic acid in the presence of acetylacetone or methyl acetoacetate in aqueous solution has been studied by cyclic voltammetry and controlled-potential electrolysis techniques. The result showed that caffeic acid was oxidized to the corresponding o-benzoquinone, which underwent further Michael-addition with acetylacetone or methyl acetoacetate to produce caffeic acid derivative 3,4-dihydroxy-6-(1-acetylacetone)-yl cinnamic acid 4a or 3,4-dihydroxy-6-(1-acetyl-methylacetate)-yl cinnamic acid 4b. 相似文献