The Water Exchange Mechanism in the First ...
Type de document :
Compte-rendu et recension critique d'ouvrage
DOI :
Titre :
The Water Exchange Mechanism in the First Excited State of Hydrated Uranyl(VI)
Auteur(s) :
Wåhlin, Pernilla [Auteur]
Vallet, Valérie [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Wahlgren, Ulf [Auteur]
Nordic Institute for Theoretical Physics [NORDITA]
Grenthe, Ingmar [Auteur]
Vallet, Valérie [Auteur]
Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523 [PhLAM]
Wahlgren, Ulf [Auteur]
Nordic Institute for Theoretical Physics [NORDITA]
Grenthe, Ingmar [Auteur]
Titre de la revue :
Inorganic Chemistry
Pagination :
11310
Éditeur :
American Chemical Society
Date de publication :
2009-10-30
ISSN :
0020-1669
Mot(s)-clé(s) en anglais :
actinide
ab initio
uranyl
water exchange
ab initio
uranyl
water exchange
Discipline(s) HAL :
Physique [physics]/Physique [physics]/Chimie-Physique [physics.chem-ph]
Résumé en anglais : [en]
The water exchange mechanism of the uranyl(VI) aquo ion in the luminescent state, <sup>3</sup>Δ<sub>g</sub> in the spin-orbit free nomenclature, has been investigated using quantum chemical methods and compared to the ...
Lire la suite >The water exchange mechanism of the uranyl(VI) aquo ion in the luminescent state, <sup>3</sup>Δ<sub>g</sub> in the spin-orbit free nomenclature, has been investigated using quantum chemical methods and compared to the corresponding reaction in the electronic ground state. The reaction mechanism was studied by calculation of the enthalpy of reaction of the A and D intermediates relative to the reactant, using a penta-aquo ion model with one additional water molecule in the second hydration sphere. The reaction barriers around the intermediates are low and they are therefore a good approximation for the activation enthalpy. The energy of the D-intermediate is significantly larger than that of the A-intermediate both in the luminescent and ground states, suggesting that the water exchange is the same in both states. This suggestion is supported by the experimental rate constants for luminescence decay and water exchange in the electronic ground state that are 0.5x10<sup>6</sup> s<sup>-1</sup> and 1.3x10<sup>6</sup> s<sup>-1</sup>, respectively.Lire moins >
Lire la suite >The water exchange mechanism of the uranyl(VI) aquo ion in the luminescent state, <sup>3</sup>Δ<sub>g</sub> in the spin-orbit free nomenclature, has been investigated using quantum chemical methods and compared to the corresponding reaction in the electronic ground state. The reaction mechanism was studied by calculation of the enthalpy of reaction of the A and D intermediates relative to the reactant, using a penta-aquo ion model with one additional water molecule in the second hydration sphere. The reaction barriers around the intermediates are low and they are therefore a good approximation for the activation enthalpy. The energy of the D-intermediate is significantly larger than that of the A-intermediate both in the luminescent and ground states, suggesting that the water exchange is the same in both states. This suggestion is supported by the experimental rate constants for luminescence decay and water exchange in the electronic ground state that are 0.5x10<sup>6</sup> s<sup>-1</sup> and 1.3x10<sup>6</sup> s<sup>-1</sup>, respectively.Lire moins >
Langue :
Anglais
Vulgarisation :
Non
Commentaire :
4 pages
Source :