Reference : Ground and Excited State Dissociation Dynamics of Ionized 1,1-Difluoroethene
Scientific journals : Article
Physical, chemical, mathematical & earth Sciences : Chemistry
Ground and Excited State Dissociation Dynamics of Ionized 1,1-Difluoroethene
[fr] Dynamique de la dissociation des états fondamental et excité du 1,1-difluoroéthylène ionisé.
Gridelet, Evelyne [> > > >]
Dehareng, Dominique mailto [Université de Liège - ULg > > Centre d'ingénierie des protéines >]
Locht, Robert mailto [Université de Liège - ULg > Département de Chimie (Faculté des Sciences) > Laboratoire de Dynamique Moléculaire (Sciences) >]
Lorquet, Andrée mailto [Université de Liège - ULg > Département de chimie (sciences) > Laboratoire de dynamique moléculaire >]
Lorquet, Jean-Claude mailto [Université de Liège - ULg > Département de Chimie (Faculté des sciences) > Laboratoire de Dynamique Moléculaire (Sciences) > >]
Leyh, Bernard mailto [Université de Liège - ULg > Département de chimie (sciences) > Laboratoire de dynamique moléculaire >]
Journal of Physical Chemistry A
Amer Chemical Soc
Yes (verified by ORBi)
[en] Kinetic energy release distributions ; Dissociative photoionization ; Two sector mass spectrometer ; Maximum entropy method ; Orbiting transition state theory ; Ab initio calculations
[fr] Conical intersection ; 1,1-C2H2F2
[en] The kinetic energy release distributions (KERDs) for the fluorine atom loss from the 1,1-difluoroethene cation have been recorded with two spectrometers in two different energy ranges. A first experiment uses dissociative photoionization with the He(I) and Ne(I) resonance lines, providing the ions with a broad internal energy range, up to 7 eV above the dissociation threshold. The second experiment samples the metastable range, and the average ion internal energy is limited to about 0.2 eV above the threshold. In both energy domains, KERDs are found to be bimodal. Each component has been analyzed by the maximum entropy method. The narrow, low kinetic energy components display for both experiments the characteristics of a statistical, simple bond cleavage reaction: constraint equal to the square root of the fragment kinetic energy and ergodicity index higher than 90%. Furthermore, this component is satisfactorily accounted for in the metastable time scale by the orbiting transition state theory. Potential energy surfaces corresponding to the five lowest electronic states of the dissociating 1,1-C2H2F2+ ion have been investigated by ab initio calculations at various levels. The equilibrium geometry of these states, their dissociation energies, and their vibrational wavenumbers have been calculated, and a few conical intersections between these surfaces have been identified. It comes out that the ionic ground state (X) over tilde B-2(1) is adiabatically correlated with the lowest dissociation asymptote. Its potential energy curve increases in a monotonic way along the reaction coordinate, giving rise to the narrow KERD component. Two states embedded in the third photoelectron band ( (B) over tilde (2)A(1), at 15.95 eV and (C) over tilde B-2(2) at 16.17 eV) also correlate with the lowest asymptote at 14.24 eV. We suggest that their repulsive behavior along the reaction coordinate be responsible for the KERD high kinetic energy contribution.
Laboratoire de Dynamique Moléculaire
ARC Contract n°99/04-245, PAI Contract n°P4/03, FNRS ; Politique Scientifique Fédérale (Belgique) = Belgian Federal Science Policy

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