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Induced kinetic stability

Myers (1960) recognized two kinds of stability, viz., inherent stability as a function of time, and induced stability as a function of stimuli. Induced kinetic stability necessitates the expenditure of work exceeding .12 Acceptance of a stabilization role for water has not been universal Jirgensons (1946) argued against it, enunciating instead the influence of particle shape and the mutual chemical affinity between atomic groups at the solid-liquid interface. [Pg.64]

The nature of the nucleation site as well as the kinetics of formation and dissociation of the H-induced and stabilized platelets have yet to be experimentally studied in detail. However, their generation in float-zone (Johnson and Herring, 1988b) as well as Czochralski-grown (Fig. 8) silicon argues against the involvement of oxygen or carbon in platelet nucleation. [Pg.145]

For such supramolecular systems, diffusion NMR may be extremely important for the determination of the structure and dynamics of the system. Diffusion is also extremely important in determining the association constant in systems, which on their formation induce a small change in the NMR spectra, and in systems in which chemical shift changes occur for reasons other than complexation, for example when protonation takes place. Diffusion NMR can also easily be used to probe the kinetic stability of multicomponent systems just by monitoring the effect of a small excess of one of the components on the diffusion coefficient of the supramolecular system. [Pg.215]

To study the UAG3T UAG3T quadruplexes kinetics, the authors performed different types of experiments. Addition of an excess of the complementary strand induces a time-dependent formation of the duplex, whose kinetics are related to quadruplex unfolding. A single exponential function perfectly fits the data for each form. At temperature below 40°C, the parallel quadruplex unfolds faster than the antiparallel one. As the antiparallel quadruplex has slightly higher activation energy of dissociation (Eob = +43 kcal moN v.s. +34 kcal mol for the parallel form), kinetic stability is reversed above 40°C. At 37°C, the lifetimes of the two quadruplexes are very close, around 2 h. To study their kinetics of... [Pg.51]

Their work showed that mutations which influence the amyloid-forming ability of a protein are possible without concomitant changes in the rate of partial denaturation. The most severe forms of transthyretin-induced disease appear to be those where there is a reduction in both thermodynamic and kinetic stability. [Pg.31]

Finally, let us make a remark that may enlighten the significance of relative asymptotic stability. As is known (from Exercise 1 of 4.1.3) the solutions of the induced kinetic differential equation of the reaction... [Pg.44]

Figure 4. The relationship between temperature, water content, and stability (after Franks, F.f In a dilute aqueous suspension, a biochemically active molecule is structural stabile but is vulnerable to a wide range of environmental degradative forces such as hydrolysis, oxidation and racemization. In a surface immobilized or dehydrated state, a biochemically active molecule achieves peater kinetic stability at a cost of thermodynamic instability. From a dilute state (A) through supersaturation (S) with progressive water loss on the way to a solid glassy state (B), a biochemcially active molecule passes through a thermodynamically defined (entropic loss of water and enthalpy of adsorption) transition zone (stippled) where irreversible conformational changes may occur. We have observed that the disaccharides used to fabricate Aquasomes appear to stabilize biochemically active molecules in this zone during surface-induced dehydration. The dashed line represent the freeze-drying pathway between the eutectic point and Tg. Figure 4. The relationship between temperature, water content, and stability (after Franks, F.f In a dilute aqueous suspension, a biochemically active molecule is structural stabile but is vulnerable to a wide range of environmental degradative forces such as hydrolysis, oxidation and racemization. In a surface immobilized or dehydrated state, a biochemically active molecule achieves peater kinetic stability at a cost of thermodynamic instability. From a dilute state (A) through supersaturation (S) with progressive water loss on the way to a solid glassy state (B), a biochemcially active molecule passes through a thermodynamically defined (entropic loss of water and enthalpy of adsorption) transition zone (stippled) where irreversible conformational changes may occur. We have observed that the disaccharides used to fabricate Aquasomes appear to stabilize biochemically active molecules in this zone during surface-induced dehydration. The dashed line represent the freeze-drying pathway between the eutectic point and Tg.
This repulsion facilitates diffusion separation of the products, i.e. kinetically stabilizes the final state. It is not excluded that in enzymatic reactions involving charge transfer this factor induces the conformational rearrangement of the protein, thus preparing the enzyme for the next step of a multistage process[306]. [Pg.171]

In summary, genotoxicity studies of endosulfan have provided evidence that this compound is mutagenic and clastogenic, and that it induces effects on cell cycle kinetics in two different mammalian species. However, some of these data may be suspect because some formulations of endosulfan have contained epichlorohydrin, a known genotoxic chemical, as a stabilizer (Hoechst 1990). It should be noted that humans may also be exposed to epichlorohydrin along with endosulfan. [Pg.166]

Neutrons readily induce nuclear reactions, but they always produce nuclides on the high neutron-proton side of the belt of stability. Protons must be added to the nucleus to produce an unstable nuclide with a low neutron-proton ratio. Because protons have positive charges, this means that the bombarding particle must have a positive charge. Nuclear reactions with positively charged particles require projectile particles that possess enough kinetic energy to overcome the electrical repulsion between two positive particles. [Pg.1574]


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See also in sourсe #XX -- [ Pg.64 ]




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