Electrochemical generation

Azamar-Barrios J A, Munoz E P and Penicaud A 1997 Electrochemical generation of the higher fullerene radicals Tmoisture-free conditions and their observation by EPR J. Chem. Soc.,... 

Mediator Electrochemically Generated Reagent Generator-Electrode Reaction Representative Application ... 

Type of Reaction Mediator Electrochemically Generated Reagent G en erato r-E1 ectrod e Reaction Representative Reaction ... 

Electrochemical Generation of Chlorine Dioxide from Chlorite. The electrochemical oxidation of sodium chlorite is an old, but not weU-known method of generating chlorine dioxide. Concentrated aqueous sodium chlorite, with or without added conductive salts, is oxidized at the anode of an electrolytic cell having a porous diaphragm-type separator between the anode and cathode compartments (122—127). The anodic reaction is... 

G. Cowley, M. Lips2tajn, and Z. Twaidowski, "Electrochemical Generation of Chloric Acid at High Current Efficiencies," iu Ref. 64. 

Fuel cells, which rely on electrochemical generation of electric power, could be used for nonpolluting sources of power for motor vehicles. Since fuel cells are not heat engines, they offer the potential for extremely low emissions with a higher thermal effidency than internal combustion engines. Their lack of adoption by mobile systems has been due to their cost, large size, weight, lack of operational flexibility, and poor transient response. It has been stated that these problems could keep fuel cells from the mass-produced automobile market until after the year 2010 (5). 

Electrochemically generated trifluoromethyl radicals add to 1-hexyne to give a 1 4 mixture of ( )- and (Z)-l,l,l-trifluoro-2-heptene [22] Kinetic data on the addition of photochemically generated trifluoromethyl radicals to acetylene and substituted acetylenes were reported [2J]. Alcohols and aldehydes add to hexa-fluoro-2-butyne in the presence of peroxide and y-ray initiation [24] (equations 16 and 17). 

Electrochemically generated nickel is very selective for the reduction of ai compounds into anilines, in which alkenyl, alkyhyl, halo, cytino, formyl, ind benzyloxy groups are not affected. Sodium snlfide has been used for the selective reduction of at group in the presence of aliphatic nitro groups (Tq. 6.44. ... 

Allylation of aldehydes and ketones by reagents, electrochemically generated at the cadmium anode from allyl bromides, are also known30. 

D. Tsiplakides, S. Neophytides, and C.G. Vayenas, Investigation ofthe state ofthe electrochemically generated adsorbed O species on Au films interfaced with Y203-doped-ZrOj, Ionics, submitted (2001). 

Tris(4-bromophenyl)ammoniumyl hexachloroantimonate (TBPA) differs from the other promoters in that its cation is a radical, and as such produces radical cationic sulfonium ions as glycosylating species from thioglycosides.85 The use of this promoter arose from earlier work on the electrochemical generation of 5-glycosyl radical cations as glycosylating species. 

The reactivity of electrochemically generated phosphonyl radicals has been recently reviewed by Kargin and Budnikova [8] and will not be considered here. The reactivity of phosphonyl radicals is mainly accounted for by the three processes [9] shown in Scheme 2 radical addition (1), atom transfer (2 and 3), and electron transfer (4). 

The electrochemical generation and reactivity of phosphoniumyl and related charged radicals have been recently reviewed by Kargin and Bunikova [8]. In 1995, Yasui reviewed the reactivity of trivalent phosphorus compounds in single electron transfer (SET) processes [41] and, in 1990, the EPR features and reactivity of phosphoniumyl radicals were reviewed by Tordo [42]. 

The photoelectrochemical behavior of ZnSe-coated CdSe thin Aims (both deposited by vacuum evaporation on Ti) in polysulflde solution has been described by Russak and Reichman [112] and was reported to be similar to MIS-type devices. Specifically, Auger depth profiling showed the ZnSe component of the (ZnSe)CdSe heterostructures to convert to ZnO after heat treatment in air, thus forming a (ZnO)CdSe structure, while the ZnO surface layer was further converted to a ZnS layer by cycling the electrode in polysulfide electrolyte. This electrochemically generated ZnS layer provided an enhanced open-circuit potential compared to CdSe alone. Efficiencies as high as 5.4% under simulated AM2 conditions were recorded for these electrodes. 

In addition, this review has been prepared to promote the term voltaic cell in honor of Alessandro Volta, the inventor of the pile, i.e., an electrochemical generator of electricity. Up to now this name has been used in only a few papers. This term is a logical analogue to the term galvanic cell, particularly in discussions of Volta potential and Gal-vani potential concepts. 

Electrochemical reactors (cells, tanks) are used for the practical realization of electrolysis or the electrochemical generation of electrical energy. In developing such reactors one must take into account the purpose of the reactor as well as the special features of the reactions employed in it. Most common is the classical reactor type with plane-parallel electrodes in which positive and negative electrodes alternate and all electrodes having the same polarity are connected in parallel. Reactors in which the electrodes are concentric cylinders and convection of the liquid electrolyte can be realized by rotation of one of the electrodes are less common. In batteries, occasionally the electrodes are in the form of two long ribbons with a separator in between which are wound up as a double spiral. 

Fuel-cell-based power plants (or electrochemical generators, the rather appropriate Russian term) have several constituent parts (1) the fuel cell battery or stack itself (2) vessels for the reactants (hydrogen or methanol oxygen when needed) (3) special devices controlling the supply of reactants and withdrawal of the reaction products according to their consumption and formation in the electrochemical reactions ... 

Le Mest Y, L Her M. 1995. Electrochemical generation of a new type of dioxygen carrier complex. Reversible fixation of dioxygen by the highly electron-deficient two-electron oxidized derivative of a dicobalt face-to-face diporphyrin. J Chem Soc Chem Commun 1441. 

In pioneering studies [47], the SECM feedback mode was used to study the ET reaction between ferrocene (Fc), in nitrobenzene (NB), and the aqueous mediator, FcCOO, electrochemically generated at the UME by oxidation of the ferrocenemonocar-boxylate ion, FcCOO. Tetraethylammonium perchlorate (TEAP) was applied in both phases as the partitioning electrolyte. The results of this study indicated that the reaction at the ITIES was limited by the ET process, provided that there was a sufficiently high concentration of TEAP in both phases. 

Electrochemically generated products can be readily characterized by in situ measurement of their absorption spectra in the ultraviolet and visible regions. Optically transparent electrodes (OTEs) prepared from thin layers... 

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