The peroxides from methylrhenium trioxide (MTO) and hydrogen peroxide, CH 3ReO 2(η 2-O 2), A, and CH 3Re(O)(η 2-O 2) 2(H 2O), B, have been fully characterized in both organic and aqueous media by spectroscopic means (NMR and UV−vis). In aqueous solution, the equilibrium constants for their formation are K 1 = 16.1 ± 0.2 L mol - 1 and K 2 = 132 ± 2 L mol - 1 at pH 0, μ = 2.0 M, and 25 °C.

This Perspective presents a personal overview of the current status of the theory of chemical kinetics and mechanisms for complex processes. We attempt to assess the status of the field for reactions in the gas phase, at gas–solid interfaces, in liquid solutions, in enzymes, and for protein folding. Some unifying concepts such as potential energy surfaces, free energy, master equations,. Chemical kinetics, also known as reaction kinetics, is the study of rates of chemical processes. Chemical kinetics includes investigations of how different experimental conditions can influence the speed of a chemical reaction and yield information about the reaction's mechanism and transition states, as well as the construction of mathematical models that can describe the characteristics of a chemical reaction.

In the presence of hydrogen peroxide the catalyst decomposes to methanol and perrhenate ions with a rate that is dependent on [H 2O 2] and [H 3O +]. The complex peroxide and pH dependences could be explained by one of two possible pathways: attack of either hydroxide on A or HO 2 - on MTO. The respective second-order rate constants for these reactions which were deduced from comprehensive kinetic treatments are k A = (6.2 ± 0.3) × 10 9 and k MTO = (4.1 ± 0.2) × 10 8 L mol - 1 s - 1 at μ = 0.01 M and 25 °C. The plot of log k ψ versus pH for the decomposition reaction is linear with a unit slope in the pH range 1.77−6.50. The diperoxide B decomposes much more slowly to yield O 2 and CH 3ReO 3. This is a minor pathway, however, amounting to.

Alternatively, in adult patients an induction dose of 1 mg to 2 mg/kg intravenous ketamine at a rate of 0.5 mg/kg/min may be used for induction of anesthesia. Chertezh angara iz metallokonstrukcij.

The serious study of the reaction mechanisms of transition metal com­ plexes began some five decades ago. Work was initiated in the United States and Great Britain; the pioneers ofthat era were, inalphabetical order, F. Higgision, E.1.

Wilkins.A larger community of research scientists then entered the field, many of them stu­ dents ofthose just mentioned. Interest spread elsewhere as well, principally to Asia, Canada, and Europe. Before long, the results ofindividual studies were being consolidated into models, many of which traced their origins to the better-established field of mechanistic organic chemistry.

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