Redox reactions applications

A general kinetics model for all photochemical reaction orders, and a photosystem designed to harvest visible light as a source of electrons for use in redox reactions applicable to organic synthesis have also been described. ... 

Lui, S.M., W. Liang, A. Soriano, and JJ. Cowan (1994). Enzymatic reduction of inorganic anions-variable-temperature steady-state and pre-steady-state kinetics experiments to map the energy profile of an enzymatic multielectron redox reaction — application to the dissimilatory sulfite reductase from desulfovibrio-vulgaris (Hildenborough). J. Am. Chem. Soc. 116, 4531-4536. 

Highly protective layers can also fonn in gaseous environments at ambient temperatures by a redox reaction similar to that in an aqueous electrolyte, i.e. by oxygen reduction combined with metal oxidation. The thickness of spontaneously fonned oxide films is typically in the range of 1-3 nm, i.e., of similar thickness to electrochemical passive films. Substantially thicker anodic films can be fonned on so-called valve metals (Ti, Ta, Zr,. ..), which allow the application of anodizing potentials (high electric fields) without dielectric breakdown. 

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. 

Determining Equilibrium Constants for Coupled Chemical Reactions Another important application of voltammetry is the determination of equilibrium constants for solution reactions that are coupled to a redox reaction occurring at the electrode. The presence of the solution reaction affects the ease of electron transfer, shifting the potential to more negative or more positive potentials. Consider, for example, the reduction of O to R... 

A number of reductive procedures have found general applicability. a-Azidoketones may be reduced catalytically to the dihydropyrazines (80OPP265) and a direct conversion of a-azidoketones to pyrazines by treatment with triphenylphosphine in benzene (Scheme 55) has been reported to proceed in moderate to good yields (69LA(727)23l). Similarly, a-nitroketones may be reduced to the a-aminoketones which dimerize spontaneously (69USP3453279). The products from this reaction are pyrazines and piperazines and an intermolecular redox reaction between the initially formed dihydropyrazines may explain their formation. Normally, if the reaction is carried out in aqueous acetic acid the pyrazine predominates, but in less polar solvents over-reduction results in extensive piperazine formation. 

A phenomenological model for redox reactions in solution application to aquocobalt(III) systems. 

One of the most useful applications of standard potentials is in the calculation of equilibrium constants from electrochemical data. The techniques that we develop here can be applied to any kind of reaction, including neutralization and precipitation reactions as well as redox reactions, provided that they can be expressed as the difference of two reduction half-reactions. 

The field of modified electrodes spans a wide area of novel and promising research. The work dted in this article covers fundamental experimental aspects of electrochemistry such as the rate of electron transfer reactions and charge propagation within threedimensional arrays of redox centers and the distances over which electrons can be transferred in outer sphere redox reactions. Questions of polymer chemistry such as the study of permeability of membranes and the diffusion of ions and neutrals in solvent swollen polymers are accessible by new experimental techniques. There is hope of new solutions of macroscopic as well as microscopic electrochemical phenomena the selective and kinetically facile production of substances at square meters of modified electrodes and the detection of trace levels of substances in wastes or in biological material. Technical applications of electronic devices based on molecular chemistry, even those that mimic biological systems of impulse transmission appear feasible and the construction of organic polymer batteries and color displays is close to industrial use. 

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

First, the simple thermodynamic description of pe (or Eh) and pH are both most directly applicable to the liquid aqueous phase. Redox reactions can and do occur in the gas phase, but the rates of such processes are described by chemical kinetics and not by equilibrium concepts of thermodynamics. For example, the acid-base reaction... 

Electrochemical reactions have many practical applications. Some are spontaneous, and others are driven uphill by applying an external potential. In this section, we present practical examples of spontaneous redox processes. We describe externally driven redox reactions in Section 19-1. 

Besides improving stability, a practical goal of surface modification has been to utilize redox reactions, otherwise not applicable, to yield better electrical characteristics such as higher open-circuit photovoltage, and to promote high conversion efficiencies. 

MEMED has also been used to investigate the nature of coupled ion-transfer processes involved in spontaneous electron transfer at ITIES [80]. In this application, a key strength of MEMED is that all of the reactants and products involved in the reaction can be measured, as shown in Figs. 19 and 20. The redox reaction studied involved the oxidation of either ferrocene (Fc) or decamethylferrocene (DMFc) in a DCE phase (denoted by Fcdce) by either IrCle or Fe(CN)g in the aqueous phase (denoted by Ox ) ... 

Metal/metal oxides are the materials of choice for construction of all-solid-state pH microelectrodes. A further understanding of pH sensing mechanisms for metal/metal oxide electrodes will have a significant impact on sensor development. This will help in understanding which factors control Nemstian responses and how to reduce interference of the potentiometric detection of pH by redox reactions at the metal-metal oxide interface. While glass pH electrodes will remain as a gold standard for many applications, all-solid-state pH sensors, especially those that are metal/metal oxide-based microelectrodes, will continue to make potentiometric in-vivo pH determination an attractive analytical method in the future. 

The participation of cations in redox reactions of metal hexacyanoferrates provides a unique opportunity for the development of chemical sensors for non-electroactive ions. The development of sensors for thallium (Tl+) [15], cesium (Cs+) [34], and potassium (K+) [35, 36] pioneered analytical applications of metal hexacyanoferrates (Table 13.1). Later, a number of cationic analytes were enlarged, including ammonium (NH4+) [37], rubidium (Rb+) [38], and even other mono- and divalent cations [39], In most cases the electrochemical techniques used were potentiometry and amperometry either under constant potential or in cyclic voltammetric regime. More recently, sensors for silver [29] and arsenite [40] on the basis of transition metal hexacyanoferrates were proposed. An apparent list of sensors for non-electroactive ions is presented in Table 13.1. 

In conclusion, the unique properties of Prussian blue and other transition metal hexa-cyanoferrates, which are advantageous over existing materials concerning their analytical applications, should be mentioned. First, metal hexacyanoferrates provide the possibility to develop amperometric sensors for non-electroactive cations. In contrast to common smart materials , the sensitivity and selectivity of metal hexacyanoferrates to such ions is provided by thermodynamic background non-electroactive cations are entrapped in the films for charge compensation upon redox reactions. 

Definitions. Titrimetric Reactions. Acid-base Titrations. Applications of Acid-base Titrations. Redox Titrations. Applications of Redox Titrations. Complexometric Titrations. Ethylenediaminetetraacetic Acid (EDTA). Applications of EDTA Titrations. Titrations with Complexing Agents Other Than EDTA. Precipitation Titrations. ... 

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