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Oxidation potentials organic compounds

In such a synthesis the lengths of the pulses are variable as well as the potentials of the square wave. Recently a potential-time profile has been used to maintain the activity of an electrode during the oxidation of organic compounds (Clark et al., 1972) at a steady potential the current for the oxidation process was observed to fall, but a periodic short pulse to cathodic potentials was sufficient to prevent this decrease in electrode activity. [Pg.165]

One-electron reduction or oxidation of organic compounds provides a useful method for the generation of anion radicals or cation radicals, respectively. These methods are used as key processes in radical reactions. Redox properties of transition metals can be utilized for the efficient one-electron reduction or oxidation (Scheme 1). In particular, the redox function of early transition metals including titanium, vanadium, and manganese has been of synthetic potential from this point of view [1-8]. The synthetic limitation exists in the use of a stoichiometric or excess amount of metallic reductants or oxidants to complete the reaction. Generally, the construction of a catalytic redox cycle for one-electron reduction is difficult to achieve. A catalytic system should be constructed to avoid the use of such amounts of expensive and/or toxic metallic reagents. [Pg.64]

An acidic bromate solution can oxidize various organic compounds and the reaction is catalyzed by species like cerous and manganous ions that can generate 1-equivalent oxidants with quite positive reduction potential. Belousov (1959) first observed oscillations in Celv]/[Cem] during Ce (III) catalysed oxidation of citric acid by bromate ion. Zhabotinskii made extensive studies of both temporal and spatial oscillations and also demonstrated that instead of Ce (III), weak 1- equivalent reductants like Mn(II) and Fe (II) can also be used. The reaction is called Belousov-Zhabotinskii reaction. This reaction, most studied and best understood, can be represented as... [Pg.122]

Polyoxometalates undoubtedly have enormous catalytic potential in liquid phase selective oxidation of organic compounds. Various strategies for immobilization of POMs on solid matrices have been developed during the past two decades and opened new opportunities for practical applications. The most developed and widely used technique is electrostatic... [Pg.290]

The oxidation potentials of compounds having Si-Si bonds, the disilanes and polysilanes, are interesting (Table 9). The oxidation potentials decrease with increasing chain length [145]. Decrease of the HOMO level with chain length seems to be responsible for this phenomena. The oxidation potentials of polysilanes also depend on the nature of the organic group on silicon [146]. [Pg.782]

Derivation Bromination of dimethylhydantoin. Use Controlled bromination and oxidation of organic compounds, water treatment, polymerization catalyst, potential germicide and sanitizer. [Pg.393]

Transition metals are potentially important participants in the abiotic oxidation of organic compounds. Higher-valent transition metals may participate directly, by oxidizing a stoichiometric amount of organic substrate, or indirectly, by catalyzing reactions of O2. Iron is the most abundant and... [Pg.240]


See other pages where Oxidation potentials organic compounds is mentioned: [Pg.459]    [Pg.64]    [Pg.913]    [Pg.463]    [Pg.319]    [Pg.107]    [Pg.571]    [Pg.574]    [Pg.641]    [Pg.869]    [Pg.46]    [Pg.6]    [Pg.1]    [Pg.17]    [Pg.61]    [Pg.59]    [Pg.258]    [Pg.99]    [Pg.340]    [Pg.344]    [Pg.514]    [Pg.4184]    [Pg.226]    [Pg.869]    [Pg.913]    [Pg.53]    [Pg.309]    [Pg.1997]    [Pg.360]    [Pg.246]    [Pg.27]    [Pg.50]    [Pg.7014]    [Pg.138]    [Pg.299]    [Pg.81]    [Pg.31]    [Pg.301]    [Pg.257]    [Pg.227]    [Pg.47]    [Pg.49]   
See also in sourсe #XX -- [ Pg.852 ]

See also in sourсe #XX -- [ Pg.852 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.852 ]




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Organic compounds, oxidation

Organic oxidant

Organic oxidation

Oxidation potential

Oxidizing potential

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