Active oxygen, formation

Figure 5. Active oxygen formation in ozonolyses at 0°C. Average composite of four runs. Conditions are same as in Figure 3...

Oxidative mineralization using active oxygen Formation of adsorbed hydroxide H20— H+ + OH ads + e-... 

The standard potential for the anodic reaction is 1.19 V, close to that of 1.228 V for water oxidation. In order to minimize the oxygen production from water oxidation, the cell is operated at a high potential that requires either platinum-coated or lead dioxide anodes. Various mechanisms have been proposed for the formation of perchlorates at the anode, including the discharge of chlorate ion to chlorate radical (87—89), the formation of active oxygen and subsequent formation of perchlorate (90), and the mass-transfer-controUed reaction of chlorate with adsorbed oxygen at the anode (91—93). Sodium dichromate is added to the electrolyte ia platinum anode cells to inhibit the reduction of perchlorates at the cathode. Sodium fluoride is used in the lead dioxide anode cells to improve current efficiency. 

Similarly the active oxygen of oxaziranes can be transferred to triphenylphosphine with the formation of ]ihosphine oxide and to tertiary amines yielding amine oxides. ... 

There are several available terminal oxidants for the transition metal-catalyzed epoxidation of olefins (Table 6.1). Typical oxidants compatible with most metal-based epoxidation systems are various alkyl hydroperoxides, hypochlorite, or iodo-sylbenzene. A problem associated with these oxidants is their low active oxygen content (Table 6.1), while there are further drawbacks with these oxidants from the point of view of the nature of the waste produced. Thus, from an environmental and economical perspective, molecular oxygen should be the preferred oxidant, because of its high active oxygen content and since no waste (or only water) is formed as a byproduct. One of the major limitations of the use of molecular oxygen as terminal oxidant for the formation of epoxides, however, is the poor product selectivity obtained in these processes [6]. Aerobic oxidations are often difficult to control and can sometimes result in combustion or in substrate overoxidation. In... 

What happens to the methoxy formed by this process is strongly temperature dependent. At low temperature (up to - 340K) it is stable on the surface and forms the beautiful structures shown in fig.2. Since the active oxygen is used in such reactions then the methoxy must (i) not block the active site at its formation or (ii) diffuses away from the active site. Our evidence indicates the latter to be the case since methoxy is present at sites away from the oxygen islands. Above approximately 340 K the methoxy is unstable and decomposes to yield formaldehyde and hydrogen in the gas phase. Above approximately 400 K, the stoichiometry of the reaction changes to... 

Relatively detailed study has been done for the reaction pathways over Au/Ti02 catalysts mainly because of simplicity in catalytic material components. The rate of PO formation at temperatures around 323 K does not depend on the partial pressure of C3H6 up to 20vol% and then decreases with an increase, while it increases monotonously with the partial pressure of O2 and H2 [57]. A kinetic isotope effect of H2 and D2 was also observed [63]. These rate dependencies indicate that active oxygen species are formed by the reaction of O2 and H2 and that this reaction is rate-determining [57,63,64]. 

Figure 8. Formation of active oxygen as a function of irradiation time during photolysis (k = 313 nm) of +00+ (2 mol/L) in 2,4-dimethylpentane in the presence of 0>. Additives amine 11 and nitroxide 1...

The same pathway of activation has been postulated in the formation of quinones, although the putative 6-hydroxyBP precursor has never been isolated (19,20). In this mechanism, formation of quinones would proceed by autoxidation of 6-hydroxyBP (20). However, substantial evidence indicates that the first step in formation of quinones does not involve the typical attack of the electrophilic active oxygen to yield 6-hydroxyBP, but instead consists of the loss of one electron from BP to produce the radical cation. 

Cervera and Levine [81] studied the mechanism of oxidative modification of glutamine synthetase from Escherichia coli. It was found that active oxygen species initially caused inactivation of the enzyme and generated a more hydrophilic protein, which still was not a substrate for the protease. Continuous action of oxygen species resulted in the formation of oxidized protein subjected to the proteolytic attack of protease. 

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