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21.
Haines TJ Bionta RM Blewitt G Bratton CB Casper D Claus R Cortez BG Errede S Foster GW Gajewski W Ganezer KS Goldhaber M Jones TW Kielczewska D Kropp WR Learned JG Lehmann E LoSecco JM Matthews J Park HS Price LR Reines F Schultz J Seidel S Shumard E Sinclair D Sobel HW Stone JL Sulak L Svoboda R van der Velde JC Wuest C 《Physical review letters》1986,57(16):1986-1989
22.
Observation of a neutrino burst in coincidence with supernova 1987A in the Large Magellanic Cloud 总被引:1,自引:0,他引:1
Bionta RM Blewitt G Bratton CB Casper D Ciocio A Claus R Cortez B Crouch M Dye ST Errede S Foster GW Gajewski W Ganezer KS Goldhaber M Haines TJ Jones TW Kielczewska D Kropp WR Learned JG LoSecco JM Matthews J Miller R Mudan MS Park HS Price LR Reines F Schultz J Seidel S Shumard E Sinclair D Sobel HW Stone JL Sulak LR Svoboda R Thornton G van der Velde JC Wuest C 《Physical review letters》1987,58(14):1494-1496
23.
Virginie Lair Amandine Calmet Valrie Albin Sophie Griveau Michel Cassir 《Electroanalysis》2019,31(1):22-30
Small fiber peripheral neuropathy is an early complication of diabetes. Electric skin response to some stimulus, as electrochemical skin conductance ECS, is a promising route in the early follow‐up of such diseases. It is related to sweat gland innervations and their permeability to chlorides and protons; it is non‐invasive, quantitative and reproducible. In routine clinical use, it could allow to better adapt the treatments and improve the adhesion for preventing pathological progress, thus reducing colossal healthcare costs. To optimize the measurements and understand the electrochemical behavior of electrodes, an original electrolytic cell was designed in lab scale. Thereby, an electrolyte is chosen to mimic sweat composition. For achieving currents range of ESC in vivo measurements, the original idea was to play on electrolyte viscosity by adding sucrose. In this paper, the novel electrolytic lab cell is presented with its limiting kinetics processes. A model of chloride migration to the anode and global electric model dedicated to the cell are proposed. Cell parameters are thoroughly studied, e. g. the resistance, which is equivalent to the inverse of ESC, by exploiting the models and through in vitro experiments, with protocols focusing on reproducibility. This original approach establishes, inter alia, an important result: the resistance is accurately retrieved using linear voltammetry, whereas single voltage measurement fails notably and is, therefore, unsatisfactory. 相似文献
24.
An alternating direction scheme on a nonuniform mesh for reaction-diffusion parabolic problems 总被引:1,自引:0,他引:1
Clavero C; Jorge JC; Lisbona F; Shishkin={paragraph} GI 《IMA Journal of Numerical Analysis》2000,20(2):263-280
In this paper we develop a numerical method for two-dimensionaltime-dependent reaction-diffusion problems. This method, whichcan immediately be generalized to higher dimensions, is shownto be uniformly convergent with respect to the diffusion problems.This method, which can immediately be generalized to higherdimensions, is shown to be uniformly convergent with respectto the diffusion parameter. 相似文献
25.
Fortage J Peltier C Nastasi F Puntoriero F Tuyèras F Griveau S Bedioui F Adamo C Ciofini I Campagna S Lainé PP 《Journal of the American Chemical Society》2010,132(46):16700-16713
The multifaceted potentialities of expanded pyridiniums (EPs), based on one pyridinium core bearing a 4-pyridyl or 4-pyridylium as the N-pyridinio group, are established at both experimental and theoretical levels. Two classes of head-to-tail (htt) EPs were designed, and their first representative elements were synthesized and fully characterized. The branched (B) family is made up of 2,6-diphenyl-4-aryl-1,4'-bipyridin-1-ium (or 1,1'-diium) species, denoted 1B and 2B for monocationic EPs (with aryl = phenyl and biphenyl, respectively) and 1B(Me) and 2B(Me) for related quaternarized dicationic species. The series of fused (F) analogues comprises 9-aryl-benzo[c]benzo[1,2]quinolizino[3,4,5,6-ija][1,6]naphthyridin-15-ium species, denoted 1F and 2F, and their 2,15-diium derivatives referred to as 1F(Me) and 2F(Me). Electrochemistry (in MeCN vs SCE) reveals that branched EPs undergo a single reversible bielectronic reduction at ca. -0.92 V for 1B/2B and -0.59 V for 1B(Me)/2B(Me), whereas pericondensed species show two reversible monoelectronic reductions at ca. -0.83 and -1.59 V for 1F/2F and ca. -0.42 and -1.07 V for 1F(Me)/2F(Me). Regarding electronic absorption features, all htt-EP chromophores show absorptivity in the range of ca. 1-4 × 10(4) M(-1) cm(-1), with red-edge absorptions extending toward 450 and 500 nm (in MeCN) for 2B(Me) and 2F(Me), respectively. These lowest-energy pi-pi* transitions are ascribed to intramolecular charge transfer between the electron-releasing biphenyl group and the htt-bipyridinium electron-withdrawing subsystems. EPs display room-temperature photoemission quantum yields ranging from 10% to 50%, with the exception of 1B, and branched luminophores are characterized by larger Stokes shifts (8000-10?000 cm(-1)) than fused ones. Lastly, a method to predict the efficiency of photobiscyclization of branched EPs into fused ones, based on the analysis of computed difference maps in total electron density for singlet excited states, is proposed. 相似文献
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28.
Argüello JE Costentin C Griveau S Savéant JM 《Journal of the American Chemical Society》2005,127(14):5049-5055
Cobalt(I) cobalamin and cobinamide are efficient catalysts of the hydrogenolysis of aliphatic chloro compounds. Taking chloroacetonitrile as example, the first requirement for high catalytic efficiency is fulfilled by the high reactivity of the Co(I) complex toward the substrate, leading to the alkylcobalt(III) complex. This is further reduced into the alkylcobalt(II) complex. However, the fact that these two reactions are fast is not enough to ensure an efficient catalysis: in DMF catalysis is very poor, while it is high in water. The experiments carried out in DMF with addition of an acid show that a crucial step in the catalytic process is the proton transfer decomposition of the alkylcobalt(II) complex, leading to the product, and closing the catalytic loop by regeneration of the cobalt(I) complex. Another important feature of these catalytic reactions is the role played by axial ligands present in the solution, particularly those that are produced by the catalytic reaction itself, namely, chloride ions and the counteranion of the added acid. The stronger these ligands, the more negative the potential required for the reduction of the alkylcobalt(III) complex. This amounts to a self-moderation effect: the more efficient catalysis, the slower its second step, i.e., the conversion of the alkylcobalt(III) complex into the alkylcobalt(II). 相似文献
29.
Andreea Cernat Sophie Griveau Cyrille Richard Fethi Bedioui Robert Săndulescu 《Electroanalysis》2013,25(6):1369-1372
We propose the fabrication of nanostructured glassy carbon (GC) electrodes modified with horseradish peroxidase (HRP) for the detection of paracetamol. This was accomplished by inducing the nanostructuration of GC via the adsorption of polystyrene nanospheres (900 nm diameter) followed by electropolymerization of N‐(10‐azidodecyl)pyrrole. The nanospheres were then removed and nanostructured polypyrrole‐GC was submitted to click reaction in presence of ethynyl‐biotin that was further coupled to HRP‐avidin. The electrode was then used to sense the electrochemical reduction of the enzymatically generated electroactive oxidized species of acetaminophen (NAPQI) in the presence of hydrogen peroxide. The nanostructured electrode with HRP exhibits a fast response towards NAPQI reduction and improved performances in terms of sensitivity and limit of detection compared to non structured electrode. 相似文献
30.
Preparation and Characterization of Electrodes Modified with Pyrrole Surfactant,Multiwalled Carbon Nanotubes and Metallophthalocyanines for the Electrochemical Detection of Thiols 下载免费PDF全文
Magdalena Rangel Argote Elizabeth Sánchez Guillén Ana Gabriela Gutiérrez Porras Oracio Serrano Torres Cyrille Richard José H. Zagal Fethi Bedioui Silvia Gutierrez Granados Sophie Griveau 《Electroanalysis》2014,26(3):507-512
Our aim was to prepare hybrid electrodes active towards the electrooxidation of thiols by the co‐immobilization of native carbon nanotubes (CNTs) and cobalt phthalocyanine (CoPc) from aqueous solutions. This strategy was adopted to avoid the oxidation of CNTs that can induce a modification of their exceptional properties. To do so, a hydrosoluble pyrrole surfactant was used to get homogeneous aqueous dispersions of CNTs and CoPc and to trap both materials on the electrode via the electropolymerization of the pyrrole surfactant. The hybrid electrodes exhibit a good electrocatalytic activity towards the oxidation of L ‐cysteine and glutathione. Their performances in terms of limit of detection (0.01 mM) are compatible with the detection of these thiols in biological samples. 相似文献