The classical collision dynamics of a model atom-molecule non-integrable collision system is studied, and the energy transfer (ET) moment is examined as a function of the initial semiclassical level of the molecule. A recently derived classical scaling theory is shown to be valid in the case when the molecular motion remains regular throughout the collision, and the ET variation is then characterized by a polynomial dependence on the initial (semiclassical) quantum numbers. When chaotic motions participate, the ET no longer follows the scaling law. The utility of the scaling theory in providing the proper interpolation form for extending classical trajectory data in non-integrable collision systems is discussed
The dynamics of rotational energy transfer in atom-molecule collisions is studied formally, and comp...
A model for energy transfer in the collision between an atom and a highly excited target molecule ha...
We introduce a model to study the collisions of two ultracold diatomic molecules in one dimension in...
The classical mechanical treatment of non-reactive scattering processes is cast into a convenient fo...
Classical energy transfer in a simple collinear collisionsystem is studied within the framework of a...
We recently developed the so-called classical-discrete (CD) fluctua¬tion model for inelastic molecul...
366-372Energy transfer in nonreactive collisions of atom-diatomic molecules has been studied in thre...
The scaling principle in classical molecular collisions given earlier by DePristo [J. Chem. Phys. 75...
Two new theoretical developments are presented in this article. First an energy corrected sudden (EC...
Using an analogy with Statistical Thermodynamics and the Einstein equation for fluctuation probabili...
In molecular dynamics applications there is a growing interest in mixed quantum-classical models. Th...
A recently developed classical model for electronically nonadiabatic collision processes is applied ...
A method of analysing classical trajectory data, based on recently derived scaling principles, is ap...
The existence of multiple time scales in molecular dynamics poses interesting and challenging questi...
Thtecdimensional classical trajectory calculations have been carried out for the quenching of Br*(‘P...
The dynamics of rotational energy transfer in atom-molecule collisions is studied formally, and comp...
A model for energy transfer in the collision between an atom and a highly excited target molecule ha...
We introduce a model to study the collisions of two ultracold diatomic molecules in one dimension in...
The classical mechanical treatment of non-reactive scattering processes is cast into a convenient fo...
Classical energy transfer in a simple collinear collisionsystem is studied within the framework of a...
We recently developed the so-called classical-discrete (CD) fluctua¬tion model for inelastic molecul...
366-372Energy transfer in nonreactive collisions of atom-diatomic molecules has been studied in thre...
The scaling principle in classical molecular collisions given earlier by DePristo [J. Chem. Phys. 75...
Two new theoretical developments are presented in this article. First an energy corrected sudden (EC...
Using an analogy with Statistical Thermodynamics and the Einstein equation for fluctuation probabili...
In molecular dynamics applications there is a growing interest in mixed quantum-classical models. Th...
A recently developed classical model for electronically nonadiabatic collision processes is applied ...
A method of analysing classical trajectory data, based on recently derived scaling principles, is ap...
The existence of multiple time scales in molecular dynamics poses interesting and challenging questi...
Thtecdimensional classical trajectory calculations have been carried out for the quenching of Br*(‘P...
The dynamics of rotational energy transfer in atom-molecule collisions is studied formally, and comp...
A model for energy transfer in the collision between an atom and a highly excited target molecule ha...
We introduce a model to study the collisions of two ultracold diatomic molecules in one dimension in...