Ground state of the (H2O)(2)(+) radical cation: DFT versus post-Hartree-Fock methods

Mariona Sodupe, Juan Bertran, Luis Rodríguez-Santiago, E. J. Baerends

Producció científica: Contribució a una revistaArticleRecercaAvaluat per experts

227 Cites (Scopus)


Correlated calculations show the proton-transferred OH-H3O+ isomer to be the ground-state structure of the (H2O)2+ dimer ion, with the C2h hemibond structure being ca. 8 kcal/mol less stable. Modern density functionals however favor the hemibond structure, overestimating the strength of the three-electron bond by ca. 17 kcal/ mol. The wrong prediction of the relative stability of the two isomers is attributed to overestimation by the exchange functionals of the self-interaction part of the exchange energy in the hemibond ion due to its delocalized electron hole. It is cautioned that this erroneous behavior of the density functionals for exchange, if unrecognized, may lead to wrong predictions for ground-state structures of systems with a three-electron bond. © 1999 American Chemical Society.
Idioma originalEnglish
Pàgines (de-a)166-170
RevistaJournal of Physical Chemistry A
Estat de la publicacióPublicada - 7 de gen. 1999


Navegar pels temes de recerca de 'Ground state of the (H2O)(2)(+) radical cation: DFT versus post-Hartree-Fock methods'. Junts formen un fingerprint únic.

Com citar-ho