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Oxidants molecular oxygen

In the cases of the selective oxidation reactions over metal oxide catalysts the so-called Mars-van Krevelen or redox mechanism [4], involving nucleophilic oxide ions 0 is widely accepted. A possible role of adsorbed electrophilic oxygen (molecularly adsorbed O2 and / or partially reduced oxygen species like C , or 0 ) in complete oxidation has been proposed by Haber (2]. However, Satterfield [1] queried whether surface chemisorbed oxygen plays any role in catalytic oxidation. [Pg.484]

For catalytic oxidations opt for hydrogen peroxide or molecular oxygen as oxidant for catalytic reductions opt for molecular hydrogen as reductant. [Pg.119]

Secondary alcohol oxidases catalyze the oxidation of secondary alcohols to ketones using molecular oxygen as oxidant. A secondary alcohol oxidase from polyvinyl alcohol-degrading bacterium Pseudomonas vesicularis var. povalolyticus PH exhibited activity toward several... [Pg.159]

The vast majority of the studies in this field relate to the oxidation of iron ions by molecular oxygen. The oxidation of Fe2+ is first-order with respect to dioxygen and,... [Pg.402]

Copper is part of several essential enzymes including tyrosinase (melanin production), dopamine beta-hydroxylase (catecholamine production), copper-zinc superoxide dismutase (free radical detoxification), and cytochrome oxidase and ceruloplasmin (iron conversion) (Aaseth and Norseth 1986). All terrestrial animals contain copper as a constituent of cytochrome c oxidase, monophenol oxidase, plasma monoamine oxidase, and copper protein complexes (Schroeder et al. 1966). Excess copper causes a variety of toxic effects, including altered permeability of cellular membranes. The primary target for free cupric ions in the cellular membranes are thiol groups that reduce cupric (Cu+2) to cuprous (Cu+1) upon simultaneous oxidation to disulfides in the membrane. Cuprous ions are reoxidized to Cu+2 in the presence of molecular oxygen molecular oxygen is thereby converted to the toxic superoxide radical O2, which induces lipoperoxidation (Aaseth and Norseth 1986). [Pg.133]

Platinum supported on carbon (Pt/C) was tested as solid catalysts in the oxidation of sucrose using molecular oxygen as oxidant (Scheme 10). The reaction was carried out in water and under atmospheric pressure. The support strongly influences the reaction and Pt/C was found more efficient than Pt/Alumina at 353 K. Over Pt/C, at a pH of 9, mono-, di-, and tricarboxylate derivatives were mainly obtained with a tricarboxylate yield of 35% [103]. [Pg.81]

Lipid hydroperoxides are also generated in singlet molecular oxygen mediated oxidations and by the action of enzymes such as lipoxygenases and cyclooxygenases. Chemiluminescence (CL) arising from lipid peroxidation has been used as a sensitive detector of oxidative stress both in vitro and in vivo . Several authors have attributed ultra-weak CL associated with lipid peroxidation to the radiative deactivation of O2 and to triplet-excited carbonyls (63, 72) (equations 35 and 36) " . It has been proposed that the latter emitters arise from the thermolysis of dioxetane intermediates (61, 62) (equation 35), endoperoxide (73) (equation 37) and annihilation of aUtoxyl, as well as peroxyl radicals ... [Pg.949]

The mechanism proposed for SSAO-catalyzed oxidations is shown in Scheme 1 [16], A molecular oxygen-dependent oxidation converts the reduced cofactor back to the quinone with the formation of hydrogen peroxide and ammonia. [Pg.664]

Figure 1. Initial rate of isotopic exchange of the oxygen of oxides with molecular oxygen at 370°C, Curve 1 and their relative activity in hydrogen oxidation at 340°C, Curve 2. The activity of lanthanum oxide is taken to be unity (1). Figure 1. Initial rate of isotopic exchange of the oxygen of oxides with molecular oxygen at 370°C, Curve 1 and their relative activity in hydrogen oxidation at 340°C, Curve 2. The activity of lanthanum oxide is taken to be unity (1).
Table 9.1 Oxidation of sulfides ArSR to sulfones catalyzed by LDH-OSO4 using molecular oxygen as oxidant. Table 9.1 Oxidation of sulfides ArSR to sulfones catalyzed by LDH-OSO4 using molecular oxygen as oxidant.

See other pages where Oxidants molecular oxygen is mentioned: [Pg.122]    [Pg.704]    [Pg.1481]    [Pg.587]    [Pg.20]    [Pg.248]    [Pg.119]    [Pg.700]    [Pg.180]    [Pg.67]    [Pg.213]    [Pg.965]    [Pg.306]    [Pg.359]    [Pg.34]    [Pg.220]    [Pg.260]    [Pg.162]    [Pg.487]    [Pg.247]    [Pg.269]    [Pg.352]    [Pg.83]    [Pg.164]    [Pg.1474]    [Pg.11]    [Pg.105]    [Pg.352]    [Pg.357]    [Pg.283]    [Pg.6]    [Pg.14]    [Pg.46]    [Pg.50]    [Pg.211]    [Pg.144]    [Pg.151]   
See also in sourсe #XX -- [ Pg.209 ]




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Alkenes oxidation with molecular oxygen

Aromatic rings oxidation with molecular oxygen

Cyclic disilanes, oxidation with molecular oxygen

Disilenes, oxidation with molecular oxygen

Ethylene oxide molecular oxygen

Liquid-Phase Oxidations with Hydrogen Peroxide and Molecular Oxygen Catalyzed by Polyoxometalate-Based Compounds

Molecular Oxygen Binding and Activation Oxidation Catalysis

Molecular Oxygen as Terminal Oxidant

Molecular Oxygen as the Oxidant

Molecular oxygen as oxidant

Molecular oxygen cyclic disilane oxidation

Molecular oxygen disilene oxidation

Molecular oxygen, oxidation anionic

Molecular oxygen, oxidation aromatic

Molecular oxygen, oxidation cationic

Molecular oxygen, oxidation ionic

Molecular oxygen, oxidation organometallic compound

Molecular oxygen, oxidation rearrangements

Molecular oxygen, oxidation ring opening

Oxidation by molecular oxygen

Oxidation molecular oxygen

Oxidation molecular oxygen

Oxidation of hydrocarbons by molecular oxygen

Oxidation with Molecular Oxygen

Oxygen, molecular hydrocarbon oxidation processes

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