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Kinetic hydride

Other approaches to classify the L M-H bond in terms of hydridicity are based on kinetic or thermodynamic studies of hydride transfer reactions. Selected examples can be found in the work of Cheng, Brunschwig and Bullock [17], who determined kinetic hydridicities by the reaction of TMHs with the trityl cation, and in the work of Sarker and Bruno [18], who used the equilibration of both types of species to establish a thermodynamic scale of hydridicities. [Pg.99]

There are many compounds in existence which have a considerable positive enthalpy of formation. They are not made by direct union of the constituent elements in their standard states, but by some process in which the necessary energy is provided indirectly. Many known covalent hydrides (Chapter 5) are made by indirect methods (for example from other hydrides) or by supplying energy (in the form of heat or an electric discharge) to the direct reaction to dissociate the hydrogen molecules and also possibly vaporise the other element. Other known endothermic compounds include nitrogen oxide and ethyne (acetylene) all these compounds have considerable kinetic stability. [Pg.77]

Extensive studies on the Wacker process have been carried out in industrial laboratories. Also, many papers on mechanistic and kinetic studies have been published[17-22]. Several interesting observations have been made in the oxidation of ethylene. Most important, it has been established that no incorporation of deuterium takes place by the reaction carried out in D2O, indicating that the hydride shift takes place and vinyl alcohol is not an intermediate[l,17]. The reaction is explained by oxypailadation of ethylene, / -elimination to give the vinyl alcohol 6, which complexes to H-PdCl, reinsertion of the coordinated vinyl alcohol with opposite regiochemistry to give 7, and aldehyde formation by the elimination of Pd—H. [Pg.22]

Propose a mechanism that could account for the overall four-thirds-order kinetics and the appearance of the dialkylaluminum hydride concentration to the one-third power. [Pg.255]

Interestingly, true hydrides, such as NaH and KH, do not reduce carbonyl groups. Using energies of hydride and methoxide (at left), calculate AH xn for the reduction of formaldehyde by H. Is this reaction more or less favorable than those based on ZH4 Can the low reactivity of NaH and KH be attributed to thermodynamic factors, or must kinetic factors be responsible ... [Pg.140]

Kinetic inertness, evidently caused by the electronic configuration, leads to a remarkable unreactivity of the Rh-H bond to hydrolysis. In the absence of air, it is unaffected by ammonia solution in dilute solution, the ammonia tram to hydride is reversibly replaced by water, showing that the hydride has a trans-effect parallel to its trans-influence. [Pg.118]

Kinetic study [141] of complexes of the type trans-Pt(PEt3)2XCl was of great value in establishing the strong trans-effect of hydride (Table 3.13) examination of the data for a wide range of reactions gives rise to a series... [Pg.237]

Moreover, in the case of hydride intervention, still a further factor, namely the kinetics of hydrogen diffusion into the metal, influences also the overall kinetics by removing a reactant from a reaction zone. In order to compare the velocity of reaction of hydrogen, catalyzed by palladium, with the velocity of the same reaction proceeding on the palladium hydride catalyst, it might be necessary to conduct the kinetic investigations under conditions when no hydride formation is possible and also when a specially prepared hydride is present in the system from the very beginning. [Pg.256]

Scholten and Konvalinka (9) in 1966 published the results of their studies on the kinetics and the mechanism of (a) the conversion of para-hydrogen and ortho-deuterium and (b) hydrogen-deuterium equilibration. At first the a-phase of the Pd-H system was used as catalyst, and then the results were compared with those obtained when the palladium had previously been transformed into its /3-hydride phase. [Pg.256]

A ten to hundredfold decrease in the velocity of the reaction, seen as a break down of the Arrhenius plot, is observed at a temperature which, for any given pressure, is always higher than that thermodynamically foreseen for the beginning of the a-/3 transition (this discrepancy is smallest at 265 mm Hg pressure). The marked decrease of the rate of reaction is characteristic of the appearance of the /3-hydride phase. The kinetics of reaction on the hydride follows the Arrhenius law but with different values of its parameters than in the case of the a-phase. [Pg.257]

Table III lists the kinetic equations for the reactions studied by Scholten and Konvalinka when the hydride was the catalyst involved. Uncracked samples of the hydride exhibit far greater activation energy than does the a-phase, i.e. 12.5 kcal/mole, in good accord with 11 kcal/mole obtained by Couper and Eley for a wire preexposed to the atomic hydrogen. The exponent of the power at p amounts to 0.64 no matter which one of the reactions was studied and under what conditions of p and T the kinetic experiments were carried out. According to Scholten and Konvalinka this is a unique quantitative factor common to the reactions studied on palladium hydride as catalyst. It constitutes a point of departure for the authors proposal for the mechanism of the para-hydrogen conversion reaction catalyzed by the hydride phase. Table III lists the kinetic equations for the reactions studied by Scholten and Konvalinka when the hydride was the catalyst involved. Uncracked samples of the hydride exhibit far greater activation energy than does the a-phase, i.e. 12.5 kcal/mole, in good accord with 11 kcal/mole obtained by Couper and Eley for a wire preexposed to the atomic hydrogen. The exponent of the power at p amounts to 0.64 no matter which one of the reactions was studied and under what conditions of p and T the kinetic experiments were carried out. According to Scholten and Konvalinka this is a unique quantitative factor common to the reactions studied on palladium hydride as catalyst. It constitutes a point of departure for the authors proposal for the mechanism of the para-hydrogen conversion reaction catalyzed by the hydride phase.
The catalytic system studied by Rennard and Kokes was in fact very complex. It can be expected that the satisfactory prolongation of the reaction should, however, result in a deviation from the formulated kinetics. Unfortunately no investigation comparable to that of Scholten and Kon-valinka has been done in the case of olefin hydrogenation. Such a study of the catalytic activity of the pure /3-phase of palladium hydride in comparison with the a- or (a + /3)-phases would supplement our knowledge concerning catalytic hydrogenation on palladium. [Pg.265]

Fig. 13. Arrhenius plots of the kinetics of H atom recombination on a Ni77Cu23 alloy film catalyst. Above room temperature—active NiCu film with low activation energy. Below room temperature—film deactivated owing to a 0-hydride phase formation activation energy markedly increased. After Karpinski el al. (65). Fig. 13. Arrhenius plots of the kinetics of H atom recombination on a Ni77Cu23 alloy film catalyst. Above room temperature—active NiCu film with low activation energy. Below room temperature—film deactivated owing to a 0-hydride phase formation activation energy markedly increased. After Karpinski el al. (65).
Fig. 15. Kinetics of the ethylene hydrogenation on Ni and 0-Ni-hydride film catalysts m denotes mass of films, which as known is connected with the thickness and crystallite sizes of the films involved. Blank points—rate of reaction proceeding on Ni film catalysts black points—rate of reaction proceeding on nickel previously exposed to the atomic hydrogen action, i.e. transformed to some extent into /3-Ni-hydride. Fig. 15. Kinetics of the ethylene hydrogenation on Ni and 0-Ni-hydride film catalysts m denotes mass of films, which as known is connected with the thickness and crystallite sizes of the films involved. Blank points—rate of reaction proceeding on Ni film catalysts black points—rate of reaction proceeding on nickel previously exposed to the atomic hydrogen action, i.e. transformed to some extent into /3-Ni-hydride.

See other pages where Kinetic hydride is mentioned: [Pg.164]    [Pg.338]    [Pg.164]    [Pg.338]    [Pg.322]    [Pg.203]    [Pg.49]    [Pg.184]    [Pg.480]    [Pg.71]    [Pg.66]    [Pg.71]    [Pg.21]    [Pg.38]    [Pg.257]    [Pg.235]    [Pg.214]    [Pg.618]    [Pg.783]    [Pg.46]    [Pg.229]    [Pg.216]    [Pg.74]    [Pg.246]    [Pg.253]    [Pg.256]    [Pg.263]    [Pg.266]    [Pg.267]    [Pg.268]    [Pg.268]    [Pg.281]    [Pg.281]    [Pg.282]    [Pg.284]    [Pg.284]    [Pg.285]    [Pg.538]   
See also in sourсe #XX -- [ Pg.382 ]




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