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Redox Reactions reversibility

Redox reactions. Reversal of oxidation states in hydroxyaldehydes results when Oppenaur oxidation and Meerwein-Ponndorf-Verley reduction operate at the responsive functional groups. ... [Pg.176]

Influence of the Kinetics of Electron Transfer on the Faradaic Current The rate of mass transport is one factor influencing the current in a voltammetric experiment. The ease with which electrons are transferred between the electrode and the reactants and products in solution also affects the current. When electron transfer kinetics are fast, the redox reaction is at equilibrium, and the concentrations of reactants and products at the electrode are those specified by the Nernst equation. Such systems are considered electrochemically reversible. In other systems, when electron transfer kinetics are sufficiently slow, the concentration of reactants and products at the electrode surface, and thus the current, differ from that predicted by the Nernst equation. In this case the system is electrochemically irreversible. [Pg.512]

In the previous section we saw how voltammetry can be used to determine the concentration of an analyte. Voltammetry also can be used to obtain additional information, including verifying electrochemical reversibility, determining the number of electrons transferred in a redox reaction, and determining equilibrium constants for coupled chemical reactions. Our discussion of these applications is limited to the use of voltammetric techniques that give limiting currents, although other voltammetric techniques also can be used to obtain the same information. [Pg.527]

Electrochemical Reversibility and Determination of m In deriving a relationship between 1/2 and the standard-state potential for a redox couple (11.41), we noted that the redox reaction must be reversible. How can we tell if a redox reaction is reversible from its voltammogram For a reversible reaction, equation 11.40 describes the voltammogram. [Pg.527]

Photochromism Based on Redox Reactions. Although the exact mechanism of the reversible electron transfer is often not defined, several viologen salts (pyridinium ions) exhibit a photochromic response to uv radiation in the crystalline state or in a polar polymeric matrix, for example,... [Pg.163]

Redox Reaction a reversible reduction-oxidation reaction. [Pg.1372]

The complex reacts with CO reversibly via a series of redox reactions. Rh(TMPP)2+ forms adducts with bulky isocyanides RNC (R = Bu , Pr ), retaining the +2 state but changing to a trans-geometry (Figure 2.34) with monodentate phosphines (and uncoordinated ethers) (R = Bu , Mefr = 2.04 B gj. = 2.45, g = 1.96). [Pg.107]

So-called reverse ATRP has been described where a conventional radical initiator (e.g. AIBN) and a transition metal complex in its Higher oxidation state are used. 85"288 One of the first systems explored was ( uBr- 133 AIBN VI VIA. It is important that the initiator is completely consumed early in the polymerization. The use of peroxide initiators in reverse ATRP can be problematical depending on the catalyst used and the reaction temperature.286 289 The system CuBr2/133/BPO/MMA at 60°C was found to provide no control,286 In ATRP at lower temperatures (40 °C), the system CuCl/133/BPO/MMA was successful though dispersities obtained were relatively broadf89 Radicals are produced from the redox reaction between the catalyst in its reduced form and BPO. [Pg.491]

The oxidation states and reversible redox reactions of metalloporphyrins. J. H. Furhrhop, Struct. Bonding (Berlin), 1974,18,1-67 (221). [Pg.43]

The stoichiometry of the redox reactions of conducting polymers (n and m in reactions 1 and 2) is quite variable. Under the most widely used conditions, polypyrroles and polythiophenes can be reversibly oxidized to a level of one hole per ca. 3 monomer units (i.e., a degree of oxidation, n, of ca. 0.3).7 However, this limit is dictated by the stability of the oxidized film under the conditions employed (Section V). With particularly dry and unreactive solvents, degrees of oxidation of 0.5 can be reversibly attained,37 and for poly-(4,4 -dimethoxybithiophene), a value of n = 1 has been reported.38 Although much fewer data are available for n-doping, it appears to involve similar stoichiometries [i.e., m in Eq. (2) is typically ca. 0.3].34,39"41 Polyanilines can in principle be reversibly p-doped to one... [Pg.553]

Due to its electronic conductivity, polypyrrole can be grown to considerable thickness. It also constitutes, by itself, as a film on platinum or gold, a new type of electrode surface that exhibits catalytic activity in the electrochemical oxidation of ascorbic acid and dopamine in the reversible redox reactions of hydroquinones and the reduction of molecular oxygen iV-substituted pyrroles are excellent... [Pg.57]

Polynuclear transition metal cyanides such as the well-known Prussian blue and its analogues with osmium and ruthenium have been intensely studied Prussian blue films on electrodes are formed as microcrystalline materials by the electrochemical reduction of FeFe(CN)g in aqueous solutionThey show two reversible redox reactions, and due to the intense color of the single oxidation states, they appear to be candidates for electrochromic displays Ion exchange properties in the reduced state are limited to certain ions having similar ionic radii. Thus, the reversible... [Pg.58]

The Nemst equation is applicable only if the redox reaction is reversible. Not all reactions are... [Pg.188]

Polysulfides are the key reactants in the high-density sodium-sulfur and Hthium-sulfur batteries [4] which are based on the following reversible redox reaction taking place in the polysulfide melt ... [Pg.128]

Fuhrhop J-H (1974) The Oxidation States and Reversible Redox Reactions of Metallopor-phyrins. 18 1-67... [Pg.246]

The relatively simple chemistry of this redox reaction is one reason why nickel-cadmium batteries are rechargeable. As we show later in this chapter, applying an external voltage can reverse this reaction. [Pg.1389]

Bruce PG, Irvine ITS (2001) Insertion Compounds. In Encyclopedia of Materials Science and Technology, Elsevier Science Ltd Oxford ISBN 0-08-0431526, pp. 4115-4121 SchoUhom R (1980) Reversible topotactic redox reactions of solids by electron/ion transfer. Angew Chem Int Ed Engl 19 983-1003... [Pg.54]

The surface waves were simulated assuming the presence of two different functionalities, each undergoing a reversible two electron redox reaction. It was assumed that these surface functionalities were qulnones In Nernstlan equilibrium with the electrode potential before each DPV pulse. It was also assumed that the current during... [Pg.587]

The present technique enables light-induced redox reaction UV light-induced oxidative dissolution and visible light-induced reductive deposition of silver nanoparticles. Reversible control of the particle size is therefore possible in principle. The reversible redox process can be applied to surface patterning and a photoelectrochemical actuator, besides the multicolor photochromism. [Pg.263]

Applying the common equations for the thermodynamics of reversible cells, it is possible to extract energetic parameters for the adatom redox reaction. This approach requires the measurement of voltammograms at different temperatures. If we consider that the adatom oxidation reaction involves the formation of the hydroxide, we can write the following equation for the overall cell reaction ... [Pg.219]

B Uses a redox reaction that cannot easily be reversed... [Pg.41]

For a redox reaction in an electrochemical cell the decrease in free enthalpy (- AG) is in accordance with the energy delivered by the transfer of electrons through an external circuit if this takes place in a reversible way, i.e., at a rate slow enough to allow complete attainment of equilibrium, the conversion of 1 gram mole will deliver an electrical energy of - AG = z FE. In total cell reaction mred, + n ox2 m ox, + nred2, where m81 = nS2 electrons are transfered (<5, and S2 represent the respective valence differences of the two redox systems), we have... [Pg.46]

Quinhydrone electrode. If the equimolar compound formed by (benzo)quin-one (Q) and (benzo)hydroquinone (QH2), the so-called quinhydrone (Q2H2), is dissolved in water, it dissociates to the extent of about 90% into the two components. In conjunction with H+ ions and electrons an equilibrium is established on the basis of a completely reversible redox reaction ... [Pg.60]

The quinone-hydroquinone system represents a classic example of a fast, reversible redox system. This type of reversible redox reaction is characteristic of many inorganic systems, such as the interchange between oxidation states in transition metal ions, but it is relatively uncommon in organic chemistry. The reduction of benzoquinone to hydroquinone... [Pg.82]


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See also in sourсe #XX -- [ Pg.297 ]




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