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Rate constants macroscopic

Predicting the solvent or density dependence of rate constants by equation (A3.6.29) or equation (A3.6.31) requires the same ingredients as the calculation of TST rate constants plus an estimate of and a suitable model for the friction coefficient y and its density dependence. While in the framework of molecular dynamics simulations it may be worthwhile to numerically calculate friction coefficients from the average of the relevant time correlation fiinctions, for practical purposes in the analysis of kinetic data it is much more convenient and instructive to use experimentally detemiined macroscopic solvent parameters. [Pg.849]

Using the coordinates of special geometries, minima, and saddle points, together with the nearby values of potential energy, you can calculate spectroscopic properties and macroscopic therm ody-riatriic and kinetic parameters, sncfi as enthalpies, entropies, and thermal rate constants. HyperChem can provide the geometries and energy values for many of these ealeulatiori s. [Pg.32]

The low-temperature chemistry evolved from the macroscopic description of a variety of chemical conversions in the condensed phase to microscopic models, merging with the general trend of present-day rate theory to include quantum effects and to work out a consistent quantal description of chemical reactions. Even though for unbound reactant and product states, i.e., for a gas-phase situation, the use of scattering theory allows one to introduce a formally exact concept of the rate constant as expressed via the flux-flux or related correlation functions, the applicability of this formulation to bound potential energy surfaces still remains an open question. [Pg.132]

The first theoretical attempts in the field of time-resolved X-ray diffraction were entirely empirical. More precise theoretical work appeared only in the late 1990s and is due to Wilson et al. [13-16]. However, this theoretical work still remained preliminary. A really satisfactory approach must be statistical. In fact, macroscopic transport coefficients like diffusion constant or chemical rate constant break down at ultrashort time scales. Even the notion of a molecule becomes ambiguous at which interatomic distance can the atoms A and B of a molecule A-B be considered to be free Another element of consideration is that the electric field of the laser pump is strong, and that its interaction with matter is nonlinear. What is needed is thus a statistical theory reminiscent of those from time-resolved optical spectroscopy. A theory of this sort was elaborated by Bratos and co-workers and was published over the last few years [17-19]. [Pg.265]

Assuming that the spin conversion is a nonadiabatic process, the macroscopic rate constant may be expressed, following Levich [125], in terms of the thermally averaged transition probability, the averaging being extended over the initial vibronic levels, as ... [Pg.95]

In subsequent works, Marcus developed his theory further in a series of papers providing expressions for the work terms, the reorganization energy and the macroscopic ET rate constants [3 6]. Assuming a sharp liquid-liquid boundary, the solution of the mean molar volume of reactants yields an expression for of the form... [Pg.197]

From a study of overall rate constant k(T) for a reaction in the bulk and its dependence on concentrations of reactants, catalyst/inhibitor, temperature etc., the kinetics come up with a mechanism by putting together a lot of direct and indirect evidences. The determination of the overall rate constant k(T) using transition state theory was a more sophisticated approach. But the macroscopic theories such as transition state theory in different versions are split to some extent in some cases, e.g. for very fast reactions. The experimental and theoretical studies in reaction dynamics have given the indications under which it becomes less satisfactory and further work in this direction may contribute much more to solve this problem. [Pg.204]

A connection between microscopic quantities such as state-to-state cross sections, state-to-state rate constant and macroscopic quantities such as overall rate constant k(T) is summarized in Flow Chart 1. [Pg.205]

The link between the microscopic description of the reaction dynamics and the macroscopic kinetics that can be measured in a catalytic reactor is a micro-kinetic model. Such a model will start from binding energies and reaction rate constants deduced from surface science experiments on well defined single crystal surfaces and relate this to the macroscopic kinetics of the reaction. [Pg.81]

Using eqns. (42)-(44) and assuming T > co /2n, i.e. that the temperature is not too low, we have that tunneling does not practicably influence the macroscopic reaction rate constant at high pressures when the molecules have an equilibrium energy distribution. In this case... [Pg.58]

The macroscopically observed reaction rate, W, is proportional to the product of the rate constant and the magnitude of the active surface ... [Pg.73]

Macroscopic and microscopic rate constants Except in the simplest mechanisms, the observed rate constant for the reaction as a whole will not correspond to any one of the microscopic rate constants k characterizing the individual steps. The term observed rate constant, kobs, is used for the overall rate constant for the complete reaction. [Pg.91]


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See also in sourсe #XX -- [ Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 , Pg.114 , Pg.115 , Pg.116 , Pg.117 , Pg.118 ]




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Equation and Macroscopic Rate Constants

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