Search results for "Roche"
showing 10 items of 2666 documents
Over-Oxidation as the Key Step in the Mechanism of the MoCl5-Mediated Dehydrogenative Coupling of Arenes.
2015
Molybdenum pentachloride is an unusually powerful reagent for the dehydrogenative coupling of arenes. Owing to the high reaction rate using MoCl5, several labile moieties are tolerated in this transformation. The mechanistic course of the reaction was controversially discussed although indications for a single electron transfer as the initial step were found recently. Herein, based on a combined study including synthetic investigations, electrochemical measurements, EPR spectroscopy, DFT calculations, and mass spectrometry, we deduct a highly consistent mechanistic scenario: MoCl5 acts as a one-electron oxidant in the absence of TiCl4 and as two-electron oxidant in the presence of TiCl4, bu…
Vis/NIR spectroelectrochemical analysis of poly-(Azure A) on ITO electrode
2006
Electrochromic behavior of poly-(Azure A) on indium–tin oxide electrode is analyzed in an aqueous potassium nitrate solution. The dependence of the absorbance on the applied potential during cyclic voltammograms proves very interesting at two selected characteristic wavelengths: at 925 nm, attributed to an intermediate species and another at 735 nm, attributed to the oxidized form of the polymer. Molar absorptivity coefficients for both species have been calculated from the relationship between current and the derivative of absorbance with respect to time. Voltammograms of formation of the intermediate are simulated from spectroelectrochemical results. Keywords: Poly-(Azure A), Spectroelect…
Conversion electron Mössbauer study of low carbon steel polarized in aqueous sulfate and sulfite containing sulfate solutions
1993
Abstract The passivation of low carbon steel was studied in aqueous solutions of 0.5 M Na 2 SO 4 (pH = 3.5 and 6.5) and of 0.5 M Na 2 SO 4 + 0.001 M NaHSO 3 (pH 3.5 and 6.5). The used conversion electron Mossbauer spectroscopy (CEMS) with the complementary electrochemical, microscopic and spectrophotometric investigations proved that the presence of sulfite ion induces pitting corrosion. The compositions and thichnesses of the passive films formed during the electrochemical treatments are determined from the conversion electron Mossbauer spectra. γ-FeOOH was found in each case as a major component. At pH = 3.5, the sextet belonging to Fe 3 C appears in the spectra in most cases, and also Fe…
In situ AFM study of proton-assisted electrochemical oxidation/reduction of microparticles of organic dyes
2008
In situ atomic force microscopy (AFM) images of crystals of organic dyes alizarin, indigo and morin have been monitored during the course of their solid-state electrochemical oxidation/reduction in contact with aqueous acetate buffer. Such images indicate that proton-assisted reduction and oxidation processes are localized in a shallow layer in the vicinity of the particle/electrolyte interface, in agreement with expectances from the Lovric and Scholz model with significantly restricted proton diffusion across the solids. Keywords: Voltammetry of nanoparticles, Atomic force microscopy, Organic dyes, Diffusion
Facile synthesis and characterization of functionalized, monocrystalline rutile TiO2 nanorods.
2006
Functionalized, monocrystalline rutile TiO2 nanorods were prepared from TiCl4 in aqueous solution under acidic conditions in the presence of dopamine, followed by aging and hydrothermal treatment at 150 degrees C. The surface-bound organic ligand controls the morphology as well as the crystallinity and the phase selection of TiO2. The presence of monocrystalline rutile TiO2 was confirmed by X-ray powder diffraction and HRTEM investigations. The as-prepared nanorods are soluble in water at pH3. The surface functionalization was analyzed by IR and 1H NMR, confirming the presence of dopamine on the surface. The surface amine groups can be tailored further with functional molecules such as dyes…
Calculation of the surface concentration of Zn(I) from the anodic voltammetric peak of zinc combined with the QCM results
2004
Deconvolution of voltammograms of anodic dissolution of zinc has proved to be possible through the electrochemical quartz crystal microbalance data and the F(dm/dQ) function. This deconvolution allows to calculate the surface concentration of Zn(I) and to obtain an estimation for the kinetic constant of the second single-electron transfer. Keywords: Zinc anodic dissolution, EQCM, Surface concentration, Deconvolution and kinetic constant
Partitioning of macrocyclic compounds in a cationic and an anionic micellar solution: a small-angle neutron scattering study.
2004
Following a previous investigation on partitioning of some macrocycle compounds in sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) aqueous solutions and their effect on the micellar structure, a small-angle neutron scattering (SANS) study has been performed at fixed surfactant content (0.20 mol/L) and varying macrocycle concentrations from 0.20 up to 1.0 mol/L. Conductivity measurements have been also performed in order to evaluate the effect of the presence of macrocycles on the critical micellar concentration (cmc) of the two surfactants. SANS experimental data were fitted successfully by means of a core-plus-shell monodisperse prolate ellipsoid model. It has been…
Analysis of an impedance function of zinc anodic dissolution
2004
Zinc anodic dissolution has been studied by means of electrochemical impedance spectroscopy (EIS). The kinetic study of the oxidation mechanism has allowed us to propose a theoretical impedance function for this system in deaerated sulphate medium. Relevant information on the faradaic process is provided by analysis of the theoretical impedance function. Kinetic parameters of this system can be calculated from the fitting of experimental data to the faradaic impedance function deduced theoretically. The physical measurements of this function are analysed by means of the dependence of simulated EIS spectra on kinetic parameters.
Distribution potential in electrified microemulsions with potential determining salts
2018
Abstract The electrical polarization of lamellar and water-in-oil microemulsions composed of the aqueous solution of a potential determining salt (PDS), an organic solvent and a nonionic surfactant has been studied. The distribution of the PDS ions across the interface between two immiscible electrolyte solutions (ITIES) generates an electrical potential difference which can be used to control charge transfer processes. In macroscopic ITIES, this distribution potential is independent of the PDS concentration and can be determined from the electroneutrality condition far from the interface. In microemulsions, on the contrary, the distribution potential is smaller in magnitude and depends on …
The role of lithium, perchlorate and water during electrochemical processes in poly(3,4-ethylenedioxythiophene) films in LiClO4 aqueous solutions
2021
Abstract Thin films of poly(3,4-ethylendioxythiophene) (PEDOT) were electrochemically deposited on gold electrodes in aqueous media. The role of perchlorate, lithium, and water during the charge/discharge of PEDOT films was investigated by cyclic voltammetry together with EQCM, vis − NIR spectroscopy, and acoustic impedance, also by means of ac-electrogravimetry in a 0.1 M LiCl O 4 aqueous solutions. In this way, it has been possible to correlate the electrical, mass, color and electromechanical properties changes during the electrochemical reactions of this polymer. Both, hydrated lithium cations and perchlorate anions can act as counterions during the electrochemical reactions, however, a…