Molecular activation-limited rate constant

Diffusion of particles in the polymer matrix occurs much more slowly than in liquids. Since the rate constant of a diffusionally controlled bimolecular reaction depends on the viscosity, the rate constants of such reactions depend on the molecular mobility of a polymer matrix (see monographs [1-4]). These rapid reactions occur in the polymer matrix much more slowly than in the liquid. For example, recombination and disproportionation reactions of free radicals occur rapidly, and their rate is limited by the rate of the reactant encounter. The reaction with sufficient activation energy is not limited by diffusion. Hence, one can expect that the rate constant of such a reaction will be the same in the liquid and solid polymer matrix. Indeed, the process of a bimolecular reaction in the liquid or solid phase occurs in accordance with the following general scheme [4,5] ... 

As mentioned earlier, ascorbate and ubihydroquinone regenerate a-tocopherol contained in a LDL particle and by this may enhance its antioxidant activity. Stocker and his coworkers [123] suggest that this role of ubihydroquinone is especially important. However, it is questionable because ubihydroquinone content in LDL is very small and only 50% to 60% of LDL particles contain a molecule of ubihydroquinone. Moreover, there is another apparently much more effective co-antioxidant of a-tocopherol in LDL particles, namely, nitric oxide [125], It has been already mentioned that nitric oxide exhibits both antioxidant and prooxidant effects depending on the 02 /NO ratio [42]. It is important that NO concentrates up to 25-fold in lipid membranes and LDL compartments due to the high lipid partition coefficient, charge neutrality, and small molecular radius [126,127]. Because of this, the value of 02 /N0 ratio should be very small, and the antioxidant effect of NO must exceed the prooxidant effect of peroxynitrite. As the rate constants for the recombination reaction of NO with peroxyl radicals are close to diffusion limit (about 109 1 mol 1 s 1 [125]), NO will inhibit both Reactions (7) and (8) and by that spare a-tocopherol in LDL oxidation. 

The biological chemistry of NO is ultimately defined by its activity at the molecular level. For example, NO readily reacts with other free radicals such as HO to give nitrite or with O2 to give peroxynitrite (Eq. (44)) at near diffusion-limited second-order rate constants (e.g. k2 1010 1VT1 s 1 for 02 ) (97). 

One point of interest deriving from the equations of TST (and Arrhenius theory) is that the upper limit for the 298 K rate constant of a unimolecular reaction that takes place with zero activation energy (of whatever sort) is roughly 10 sec . This is, in some sense, a conceptually obvious result since that is on the order of a molecular vibrational frequency, which is thought of as the mechanism by which a transition state goes to its products. 

Another way of evaluating enzymatic activity is by comparing k2 values. This first-order rate constant reflects the capacity of the enzyme-substrate complex ES to form the product P. Confusingly, k2 is also known as the catalytic constant and is sometimes written as kcal. It is in fact the equivalent of the enzyme s TOF, since it defines the number of catalytic cycles the enzyme can undergo in one time unit. The k2 (or kcat) value is obtained from the initial reaction rate, and thus pertains to the rate at high substrate concentrations. Some enzymes are so fast and so selective that their k2/Km ratio approaches molecular diffusion rates (108—109 m s-1). This means that every substrate/enzyme collision is fruitful, and the reaction rate is limited only by how fast the substrate molecules diffuse to the enzyme. Such enzymes are called kinetically perfect enzymes [26],... 

A very recent study240 reveals that an activation energy of at least 19 6 kJmol-1 can be estimated from the upper limit for the rate constant of the insertion of germylene into molecular hydrogen (equation 47). 

For the overall rate of a catalytic reaction, this is an important conclusion because the rate of a catalytic reaction is proportional to the site occupancy and the rate constant of molecular activation, when the latter step is rate limiting. For a monomolecular reaction this follows from an elementary expression for the overall rate r ... 

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