Binary encounter mechanism

The quantum-mechanical ionization cross section is derived using one of several approximations—for example, the Born, Ochkur, two-state, or semi-classical approximations—and numerical computations (Mott and Massey, 1965). In some cases, a binary encounter approximation proves useful, which means that scattering between the incident particle and individual electrons is considered classically, followed by averaging over the quantum-mechanical velocity distribution of the electrons in the atom (Gryzinski, 1965a-c). However, Born s approximation is the most widely used one. This is discussed in the following paragraphs. 

If the von Smoluchowski rate law (Eq. 6.10) is to be consistent with the formation of cluster fractals, then it must in some way also exhibit scaling properties. These properties, in turn, have to be exhibited by its second-order rate coefficient kmn since this parameter represents the flocculation mechanism, aside from the binary-encounter feature implicit in the sequential reaction in Eq. 6.8. The model expression for kmn in Eq. 6.16b, for example, should have a scaling property. Indeed, if the assumption is made that DJRm (m = 1, 2,. . . ) is constant, Eq. 6.16c applies, and if cluster fractals are formed, Eq. 6.1 can be used (with R replacing L) to put Eq. 6.16c into the form... 

Addition of the L-732,531 FKBP binary complex to a calcineurin activity assay resulted in increasingly nonlinear progress curves with increasing binary complex concentration. The htting of the data to Equation (6.3) revealed an inhibitor concentration effect on v-, as well as on vs and obs, consistent with a two-step mechanism of inhibition as in scheme C of Figure 6.3. Salowe and Hermes analyzed the concentration-response effects of the binary complex on v, and determined an IC50 of 0.90 pM that, after correction for I.S I/A (assuming competitive inhibition), yielded a A) value for the inhibitor encounter complex of 625 nM. 

However, at still larger concentrations only DET/UT is capable of reaching the kinetic limit of the Stem-Volmer constant and the static limit of the reaction product distribution. On the other hand, this theory is intended for only irreversible reactions and does not have the matrix form adapted for consideration of multistage reactions. The latter is also valid for competing theories based on the superposition approximation or nonequilibrium statistical mechanics. Moreover, most of them address only the contact reactions (either reversible or irreversible). These limitations strongly restrict their application to real transfer reactions, carried out by distant rates, depending on the reactant and solvent parameters. On the other hand, these theories can be applied to reactions in one- and two-dimensional spaces where binary approximation is impossible and encounter theories inapplicable. 

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