Quasiclassical trajectory study of O(1D) + N2O --> NO + NO: classification of reaction paths and vibrational distribution.

Quasiclassical trajectory calculations for the planar reaction of O(1D) + N2O --> NO + NO are performed on a newly constructed ab initio potential energy surface. In spite of the reduced dimension approximation, the agreement between the computational and experimental results is largely satisfactory, especially on the similar amount of excitation of the two kinds of NO products found by Akagi et al. [J.

Experimental verification of the Smoluchowski theory for a bimolecular diffusion-controlled reaction in liquid phase.

We report experimental verification of the Smoluchowski theory for diffusion-controlled reactions in solution at the steady-state limit. We have determined both the diffusion coefficients and the self-termination reaction rates of the diphenylmethyl radical simultaneously. Smoluchowski theory is insufficient to discuss the reaction rate for the self-termination reaction of the diphenylmethyl radical, so the reaction rate of an encounter complex based on the Collins-Kimball treatment is estimated.

Exit interaction effect on nascent product state distribution of O(1D)+N2O-->NO+NO.

We have determined the rotational state distributions of NO(v'=0,1,2) products produced from the reaction O(1D)+N2O. This is the first full characterization of the product rotational distribution of this reaction. The main part of each rotational distribution (up to j' approximately 80) has rotational temperature approximately 20,000 K and all these distributions are quite near to those predicted by the phase space theory (PST).

Efficient and rapid C-Si bond cleavage in supercritical water.

Arylsilanes, alkenylsilanes, allylic silanes, and alkylsilanes were found to undergo extremely facile and rapid C-Si bond cleavage in supercritical water. The rapid C-Si bond cleavage occurred even with robust unactivated tetraalkylsilanes. The control experiments revealed the dramatic difference between supercritical and subcritical conditions and that between supercritical water and supercritical methanol, attesting to a unique reactivity of supercritical water in C-Si bond cleavage.