Electronic structure and molecular properties of the heptacyanorhenate [Re(CN)(7)](3-) and [Re(CN)(7)](4-) complexes

David J.; Mendizabal, F; Arratia-Perez, R

Abstract

We report scalar relativistic and Dirac scattered wave (DSW) calculations on the heptacyanorhenate [Re(CN)7]3- and Re(CN) 7 4- complexes. Both the ground and lowest excited states of each complex split by spin-orbit interaction by about 0.3 eV. The calculated molecular electronegativities χ indicate that the open-shell complex is less reactive than the closed-shell complex, in agreement with experimental observations. The calculations indicate that the ground state spin density is highly anisotropic and that spin-orbit effects are responsible for the magnetic anisotropy of the molecular g tensor of the Re(CN)7 3- complex. The calculated optical electronic transitions for both complexes with a polarizable continuum model using a time-dependent density functional (TDDFT)/B3LYP formalism are in reasonable agreement with those observed in the absorption spectrum. © 2006 American Chemical Society.

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Título según WOS: Electronic structure and molecular properties of the heptacyanorhenate [Re(CN)(7)](3-) and [Re(CN)(7)](4-) complexes
Título según SCOPUS: Electronic structure and molecular properties of the heptacyanorhenate [Re(CN)7]3- and [Re(CN)7]4- complexes
Título de la Revista: JOURNAL OF PHYSICAL CHEMISTRY A
Volumen: 110
Número: 3
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2006
Página de inicio: 1072
Página final: 1077
Idioma: English
URL: http://pubs.acs.org/doi/abs/10.1021/jp055884t
DOI:

10.1021/jp055884t

Notas: ISI, SCOPUS