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Aromatic compounds redox potentials

The low specificity of electron-donating substrates is remarkable for laccases. These enzymes have high redox potential, making them able to oxidize a broad range of aromatic compounds (e.g. phenols, polyphenols, methoxy-substituted phenols, aromatic amines, benzenethiols) through the use of oxygen as electron acceptor. Other enzymatic reactions they catalyze include decarboxylations and demethylations [66]. [Pg.142]

Besides the applications of the electrophilicity index mentioned in the review article [40], following recent applications and developments have been observed, including relationship between basicity and nucleophilicity [64], 3D-quantitative structure activity analysis [65], Quantitative Structure-Toxicity Relationship (QSTR) [66], redox potential [67,68], Woodward-Hoffmann rules [69], Michael-type reactions [70], Sn2 reactions [71], multiphilic descriptions [72], etc. Molecular systems include silylenes [73], heterocyclohexanones [74], pyrido-di-indoles [65], bipyridine [75], aromatic and heterocyclic sulfonamides [76], substituted nitrenes and phosphi-nidenes [77], first-row transition metal ions [67], triruthenium ring core structures [78], benzhydryl derivatives [79], multivalent superatoms [80], nitrobenzodifuroxan [70], dialkylpyridinium ions [81], dioxins [82], arsenosugars and thioarsenicals [83], dynamic properties of clusters and nanostructures [84], porphyrin compounds [85-87], and so on. [Pg.189]

Redox shuttles based on aromatic species were also tested. Halpert et al. reported the use of tetracyano-ethylene and tetramethylphenylenediamine as shuttle additives to prevent overcharge in TiS2-based lithium cells and stated that the concept of these built-in overcharge prevention mechanisms was feasible. Richardson and Ross investigated a series of substituted aromatic or heterocyclic compounds as redox shuttle additives (Table 11) for polymer electrolytes that operated on a Li2Mn40g cathode at elevated temperatures (85 The redox potentials of these... [Pg.136]

Substituent effects on redox potentials can be rationalized by free energy relationships in many cases Although 1 can be related to aromatic compounds, a linear correlation with Hammett s a-constants fails. As can be seen from the substituents -N(CH3)2 Ik) and -OCH3 11) the electron attracting effect is the dominating one and not the resonance effect. Therefore Taft s a "-constants describe the substituent effects more correctly. According to (1)... [Pg.4]

A variety of four-membered ring compounds can be obtained with photochemical reactions of aromatic compounds, mainly with the [2 + 2] (ortho) photocycloaddition of alkenes. In the case of aromatic compounds of the benzene type, this reaction is often in competition with the [3 + 2] (meta) cycloaddition, and less frequently with the [4 + 2] (para) cycloaddition (Scheme 5.7) [38-40]. When the aromatic reaction partner is electronically excited, both reactions can occur at the 7t7t singlet state, but only the [2 + 2] addition can also proceed at the %% triplet state. Such competition was also discussed in the context of redox potentials of the reaction partners [17]. Most frequently, it is the electron-active substituents on the aromatic partner and the alkene which direct the reactivity. The [2 + 2] photocycloaddition is strongly favored when electron-withdrawing substituents are present in the substrates. In such a reaction, crotononitrile 34 was added to anisole 33 (Scheme 5.8, reaction 15) [41 ], and only one regioisomer (35) was obtained in good yield. In this transformation, the... [Pg.144]

The amino acid residues at the environment of the catalytic tryptophan described above (Fig. 3.6) could be responsible for the differences observed in the oxidation of high redox-potential aromatic substrates by VP and LiP. In this regard, LiP needs redox mediators for oxidation of some compounds that are directly oxidized by VP, such as Reactive Black 5 (RB5) and even polymeric lignin (although model dimers are directly oxidized) [10]. In contrast, VP exhibits a lower efficiency oxidizing VA than LiP. [Pg.50]

Perez-Boada M, Ruiz-Duenas FJ, Pogni R et al (2005) Versatile peroxidase oxidation of high redox potential aromatic compounds Site-directed mutagenesis, spectroscopic and... [Pg.57]

As the two one-electron redox potentials involved are close to 1V, many aromatic compounds can be oxidized to a radical cation. This is a common source of free radical production during intoxication with xenobiotics [31]. The large difference in redox potential between the two couples O2/H2O2 and H2O2/H2O provides a thermodynamic driving force for H2O2 dismutation catalyzed by catalase ... [Pg.29]


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See also in sourсe #XX -- [ Pg.496 ]

See also in sourсe #XX -- [ Pg.496 ]




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Aromatic redox potentials

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Redox potentials

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