Acceptors activation energy

Perhaps the best approach at present is to compare the measured exciton binding energy Ex with the hydrogenic donor activation energy EDH = 33 meV [8] to obtain an estimate for a hole mass which can be used in the hydrogen model to estimate the acceptor activation energy EA = (mh/me)ED. The appropriate relation is ... 

We roughly attempted to compare the acceptor ionization energies between the experimental and calculated values, for the monovalent substitutional impurities of group-VA elements at the host O site. The comparison was made for group-VA elements because of the existence of the most reliable data for them. The experimental values [20,22,29-31] of the acceptor activation energies for group-VA elements were already described in Section 4.1 to be 0.170-0.200 eV for N,... 

The majority of SiC-based devices employ lightly doped regions of n-type material whereas the heavily doped ones are p-type. Aluminium is strongly preferred as a p-type dopant due to its lower acceptor activation energy and its high solubility. The main advantage of... 

The contribution of this polar structure to the bonding lowers the energy of the transition state. This may be viewed as a lower activation energy for the addition step and thus a factor which promotes this particular reaction. The effect is clearly larger the greater the difference in the donor-acceptor properties of X and Y. The transition state for the successive addition of the same monomer (whether X or Y substituted) is structure [V] ... 

Nitrobenzenediazoate can be considered as an azo compound comparable to an azobenzene having one electron acceptor and one donor on each side of the azo group the acceptor-donor relationship is more dominant in the (Z) -> (E) diazoate pair than in the diazohydroxide pair. The N=N rotation mechanism of the diazoate pair is therefore the favored process (E = 84 kJ mol-1 Lewis and Hanson, 1967). On the other hand, 4-C1 is not a substituent with a —M effect therefore it does not reduce the double-bond character of the N = N bond and the mechanism involving inversion at the N((3)-atom becomes dominant. The activation energy of the latter process (E = 104 kJ mol-1 Schwarz and Zollinger, 1981) is higher than that of the N = N rotation mechanism for the 4-nitro derivative, but it is reasonable to assume that it is lower than that for N = N rotation in the 4-chloro derivative. Furthermore, one can conclude that N-inversion is more favorable in the diazohydroxide than in the diazoate. ... 

On K modified Ni(100) and Ni(lll)62,63 and Pt(lll)64 the dissociative adsorption of hydrogen is almost completely inhibited for potassium coverages above 0.1. This would imply that H behaves as an electron donor. On the other hand the peaks of the hydrogen TPD spectra shift to higher temperatures with increasing alkali coverage, as shown in Fig. 2.22a for K/Ni(lll), which would imply an electron acceptor behaviour for the chemisorbed H. Furthermore, as deduced from analysis of the TPD spectra, both the pre-exponential factor and the activation energy for desorption... 

Ferrocen-l,l -diylbismetallacycles are conceptually attractive for the development of bimetal-catalyzed processes for one particular reason the distance between the reactive centers in a coordinated electrophile and a coordinated nucleophile is self-adjustable for specific tasks, because the activation energy for Cp ligand rotation is very low. In 2008, Peters and Jautze reported the application of the bis-palladacycle complex 56a to the enantioselective conjugate addition of a-cyanoacetates to enones (Fig. 31) [74—76] based on the idea that a soft bimetallic complex capable of simultaneously activating both Michael donor and acceptor would not only lead to superior catalytic activity, but also to an enhanced level of stereocontrol due to a highly organized transition state [77]. An a-cyanoacetate should be activated by enolization promoted by coordination of the nitrile moiety to one Pd(II)-center, while the enone should be activated as an electrophile by coordination of the olefinic double bond to the carbophilic Lewis acid [78],... 

Therefore, the activation energy of quasi-equilibrium conductivity changes as a logarithm of concentration of adsorption particles which, when the linear dependence between Nt and P is available, corresponds to situation observed in experiment [155]. We should note that due to small value m function (1.91) satisfactorily approximates the kinetics oit) A - B n(i + t/t>) observed in experiments [51, 167, 168]. Moreover, substantially high partial pressures of acceptor gas, i.e. at high concentrations of Nt expression (1.81) acquires the shape ait) Oait/toc) it,Nty " when t>toc>. This suggests that for... 

It has been proposed that when a triplet sensitizer has insufficient exdta-tation energy to promote an acceptor to its triplet state, this deficiency can be supplied as an activation energy ... 

During the last two decades, more studies have been conducted to explore the catalytic effects of different redox mediators on the bio-transformation processes. Redox mediators, also referred to as electron shuttles, have been shown to play an important role not only as final electron acceptor for many recalcitrant organic compounds, but also facilitating electron transfer from an electron donor to an electron acceptor, for example, azo dyes [8, 11, 12], Redox mediators accelerate reactions by lowering the activation energy of the total reaction, and are organic molecules that can reversibly be oxidized and reduced, thereby conferring the capacity to serve as an electron carrier in multiple redox reactions. 

Fig. 11. Capacitive transient spectra of defect states associated with dislocations in ultra-pure germanium (crystal 281 grown along [100] under 1 atmosphere of H2) The micrographs show the etch pits produced by dislocations on a (100) surface. DLTS peak b has an activation energy of Ev + 20 meV. The net-shallow acceptor concentration is 1010 cm-3.

This reaction was proposed by Farmer [44]. Miller and Mayo observed this reaction experimentally in oxidized styrene [45]. The rate constant of this reaction was measured by the free radical acceptor method by Denisova and Denisov [46]. This reaction is endothermic. The activation energies of these reactions are sufficiently higher than their enthalpy values. 

The concurrent slow homolytic reaction gives rise to free radicals [14]. The occurrence of the homolytic reaction can be revealed by the consumption of free radical acceptors [8,15], CL [16], or NMR spectroscopy [17,18]. The introduction of phosphite into the hydroperoxide-containing cumene causes an initiation, pro-oxidative effect related to the formation of free radicals [6]. The yield of radicals from aliphatic phosphites is much lower (0.01-0.02%) than that from aromatic phosphites (up to 5%) [17]. The homolytic reaction of phosphites with hydroperoxide has a higher activation energy than the heterolytic reaction, which results in the predominance of the former reaction at elevated temperatures. 

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