Reference : Analysis of kinetic energy release distributions by the maximum entropy method. |

Scientific journals : Article | |||

Physical, chemical, mathematical & earth Sciences : Chemistry | |||

http://hdl.handle.net/2268/979 | |||

Analysis of kinetic energy release distributions by the maximum entropy method. | |

English | |

[fr] L'analyse des distributions d'énergie cinétique par la méthode du maximum d'entropie. | |

Leyh, Bernard [Université de Liège - ULg > Département de chimie (sciences) > Laboratoire de dynamique moléculaire >] | |

Gridelet, E. [> > > >] | |

Locht, Robert [Université de Liège - ULg > Département de Chimie (Faculté des Sciences) > Laboratoire de dynamique Moléculaire (Sciences) >] | |

Lorquet, Jean-Claude [Université de Liège - ULg > Département de Chimie (Faculté des sciences) > Laboratoire de Dynamique Moléculaire (Sciences) > >] | |

2006 | |

International Journal of Mass Spectrometry | |

Elsevier Science Bv | |

249-250 | |

Chava Lifshitz Memorial Issue | |

330-339 | |

Yes (verified by ORBi) | |

International | |

1387-3806 | |

Amsterdam | |

Netherlands | |

[en] angular momentum ; ergodicity ; maximum entropy ; translational energy release ; nonadiabatic reactions | |

[en] Energy is not always fully randomized in an activated molecule because of the existence of dynamical constraints. An analysis of kinetic energy release distributions (KERDs) of dissociation fragments by the maximum entropy method (MEM) provides information on the efficiency of the energy flow between the reaction coordinate and the remaining degrees of freedom during the fragmentation. For example, for barrierless cleavages, large translational energy releases are disfavoured while energy channeling into the rotational and vibrational degrees of freedom of the pair of fragments is increased with respect to a purely statistical partitioning. Hydrogen atom loss reactions provide an exception to this propensity rule. An ergodicity index, F, can be derived. It represents an upper bound to the ratio between two volumes of phase space: that effectively explored during the reaction and that in principle available at the internal energy E. The function F(E) has been found to initially decrease and to level off at high internal energies. For an atom loss reaction, the orbiting transition state version of phase space theory (OTST) is especially valid for low internal energies, low total angular momentum, large reduced mass of the pair of fragments, large rotational constant of the fragment ion, and large polarizability of the released atom. For barrierless dissociations, the major constraint that results from conservation of angular momentum is a propensity to confine the translational motion to a two-dimensional space. For high rotational quantum numbers, the influence of conservation of angular momentum cannot be separated from effects resulting from the curvature of the reaction path. The nonlinear relationship between the average translational energy <epsilon > and the internal energy E is determined by the density of vibrational-rotational states of the pair of fragments and also by non-statistical effects related to the incompleteness of phase space exploration. The MEM analysis of experimental KERDs suggests that many simple reactions can be described by the reaction path Hamiltonian (RPH) model and provides a criterion for the validity of this method. Chemically oriented problems can also be solved by this approach. A few examples are discussed: determination of branching ratios between competitive channels, reactions involving a reverse activation barrier, nonadiabatic mechanisms, and isolated state decay. (c) 2005 Elsevier B.V. All rights reserved. | |

Laboratoire de Dynamique Moléculaire | |

Fonds de la Recherche Scientifique (Communauté française de Belgique) - FNRS, ARC Contract n° 99-04/245 | |

Researchers | |

http://hdl.handle.net/2268/979 | |

10.1016/j.ijms.2005.12.005 | |

http://www.sciencedirect.com/science/journal/13873806 | |

- PDF-version of Editor's Postprint available on request - Version-pdf du tiré-à-part disponible sur demande |

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