Eley–Rideal reaction dynamics between O atoms on β-cristobalite (100) surface: A new interpolated potential energy surface and classical trajectory study

Reaction Dynamics of NH2+OH on an Interpolated Potential Energy Surface

QCT calculations were performed to study the behavior of energized NH2OH formed by association collision of NH2 radical with OH radical. A potential energy surface that describes the behavior of the title reaction has been constructed by interpolation of ab initio data. H2O, HON, HNO, NH3, O, H2NO, cis or trans-HONH, and H products and two vibrationally energized NH2OH and NH3O adducts were obs...

Quasiclassical trajectory study of the dynamics of the H + N 2 O reaction on a new potential energy surface

reaction dynamics of nh2+oh on an interpolated potential energy surface

qct calculations were performed to study the behavior of energized nh2oh formed by association collision of nh2 radical with oh radical. a potential energy surface that describes the behavior of the title reaction has been constructed by interpolation of ab initio data. h2o, hon, hno, nh3, o, h2no, cis or trans-honh, and h products and two vibrationally energized nh2oh and nh3o adducts were obs...

Dynamics of the O( ) + HCl reaction on the electronic state: A new ab initio potential energy surface, quasi-classical trajectory study, and comparison to experiment

A new potential energy surface for the lowest electronic state of the O( ) + HCl system is presented. This surface is based on electronic energies calculated at the multireference configuration interaction level of theory with the Davidson correction (MR-CI+Q) using the Dunning cc-pVTZ one-electron basis sets. The ab initio energies thus obtained are scaled using the Scaled External Correlation...

The dynamics of the H2 + CO+ reaction on an interpolated potential energy surface.

A potential energy surface that describes the title reaction has been constructed by interpolation of ab initio data. Classical trajectory studies on this surface show that the total reaction rate is close to that predicted by a Langevin model, although the mechanism is more complicated than simple ion-molecule capture. Only the HCO(+) + H product is observed classically. An estimate of the mag...