Hydrogen reduction mechanism

It is worthwhile noticing that, while v and n are arbitrary quantities that depend on the way we write the stoichiometric equation, the electron number njv is characteristic of the electrode reaction kinetics. In the Tafel hydrogen reduction mechanism, njv = and indicates the... 

When the cathodic reaction is the evolution of hydrogen, reduction mechanism may be... 

Although considered an active participant in the process cycle, the tetrahydroaLkylanthraquinone (10) may not be a significant part of the catalytic hydrogenation because, dependent on the concentration in the working solution, these could all be converted to the hydroquinone by the labile shift per equation 17 and not be available to participate. None of the other first- or second-generation anthraquinone derivatives produce hydrogen peroxide, but most are susceptible to further reaction by oxidative or reductive mechanisms. 

The mechanism for reduction by LiAlH4 is very similar. However, since LiAlH4 reacts very rapidly with protic solvents to form molecular hydrogen, reductions with this reagent must be carried out in aprotic solvents, usually ether or tetrahydrofuran. 

Aromatic diazo compounds can be reduced in water via a radical process (Scheme 11.5).108 The reduction mechanism of arenediazo-nium salts by hydroquinone was studied in detail.109 Arenediazonium tetrafluoroborate salts undergo facile electron-transfer reactions with hydroquinone in aqueous phosphate-buffered solution containing the hydrogen donor solvent acetonitrile. Reaction rates are first order in a... 

Further mechanistic insights into hydrogenations catalyzed by HRuCl(PPh3)3 (7, p. 83) have been obtained indirectly, from studies on hydrogenation of some ruthenium(III) phosphine complexes (83). A frequently considered mechanism for hydrogen reduction of metal salts involves slow formation of an intermediate monohydride, followed by a faster reaction between the hydride and starting complex (/, p. 72), Eqs. (2) and (3) ... 

As seen from the above scheme, XO reduces dioxygen into hydrogen peroxide by two-electron reduction mechanism and into superoxide by one-electron reduction mechanism. The efficiency of superoxide production depends on the nature of the substrate (in addition to... 

The reaction mechanism for the solid state reduction is the same as that described above for the hydrogen reduction of haematite, namely the formation of a porous iron product which results from the penetration of pores in the reacting pellets by reducing gases, and the migration of the reaction products, C02 and H20 through these pores back into the gaseous phase. 

Although detailed mechanistic studies are not reported, the postulated mechanism for the reductive cyclization of allenic carbonyl compounds involves entry into the catalytic cycle via silane oxidative addition. Allene silylrhodation then provides the cr-allylrhodium hydride A-18, which upon carbometallation of the appendant aldehyde gives rise to rhodium alkoxide B-14. Oxygen-hydrogen reductive elimination furnishes the hydrosilylation-cyclization product... 

TPR of supported bimetallic catalysts often reveals whether the two metals are in contact or not. The TPR pattern of the 1 1 FeRh/SiOi catalyst in Fig. 2.4 shows that the bimetallic combination reduces largely in the same temperature range as the rhodium catalyst does, indicating that rhodium catalyzes the reduction of the less noble iron. This forms evidence that rhodium and iron are well mixed in the fresh catalyst. The reduction mechanism is as follows. As soon as rhodium becomes metallic it causes hydrogen to dissociate atomic hydrogen migrates to iron oxide in contact with metallic rhodium and reduces the oxide instantaneously. 

The lower the slope, the lower the activation loss for the O2 reduction reaction in acid media, the observed slope is 0.060 V/ decade and it can be obtained theoretically by assuming the oxygen discharge step as the slowest one (the rate determining step, the r.d.s. ( 7)). For hydrogen the mechanism is different and the r.d.s. is the atomic dissociation and in this case a Tafel slope of 0.030... 

Pilling-Bedworth ratio of 1 96, anatase phase films can show cracks and fissures with, consequendy, a loss of mechanical stability, however a hydrogen reduction treatment above 600°C leads to phase transition from anatase (101) to rutile (110) [43] with XRD detecting TiH2 upon prolonged hydrogen treatment of titania. As shown in Fig. 4.4, introduction of vanadium increases the intensity of the anatase Ti02 peak above 700°C disappearance of the vanadium (001) peak and the simultaneous appearance of the rutile (110) peak are observed, but anatase continues to dominate even after heat treatment at 800° C. A sharp vanadium (001) peak is observed for heat treatments carried out in air, while no vanadium peak has been seen in the case of heat treatment at 600°C in presence of Ar/H2. 

Mechanism and stereochemistry of reductions of ketones, 66 Mechanism of dehydrohalogenation, 292 Mechanism of hydrogenation, 111 Mechanism of reduction of aromatic compounds, 12... 

Recent mechanistic studies on transition metal-catalysed hydrogen transfer reactions have been reviewed. Experimental and theoretical studies showed that hydrogen transfer reactions proceed through different pathways. For transition metals, hydridic routes are the most common. Within the hydridic family there are two main groups the monohydride and dihydride routes. Experimentally, it was found that whereas rhodium and iridium catalysts favour the monohydride route, the mechanism for ruthenium catalysts proceeds by either pathway, depending on the ligands. A direct hydrogen transfer mechanism has been proposed for Meerwein-Ponndorf-Verley (MPV) reductions.352... 

Whereas iV-tosylimines do not coordinate diethylzinc well in polar solvents (and thus tend to give ethylated product), solvents such as toluene favour coordination, leading to reduction of the imine to secondary amines under mild conditions, via a /3-hydrogen transfer mechanism 48... 

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