Resonant Circular Dichroism of Chiral Metal-Organic Complex (Articolo in rivista)

Type
Label
  • Resonant Circular Dichroism of Chiral Metal-Organic Complex (Articolo in rivista) (literal)
Anno
  • 2012-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1103/PhysRevLett.108.083001 (literal)
Alternative label
  • D. Catone, M. Stener, P. Decleva, G. Contini, N. Zema, T. Prosperi, V. Feyer, K. C. Prince, S. Turchini (2012)
    Resonant Circular Dichroism of Chiral Metal-Organic Complex
    in Physical review letters (Print); APS, American physical society, College Park, MD (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • D. Catone, M. Stener, P. Decleva, G. Contini, N. Zema, T. Prosperi, V. Feyer, K. C. Prince, S. Turchini (literal)
Pagina inizio
  • 083001 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 108 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 8 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto Struttura della Materia, C.N.R. Via Del Fosso del Cavaliere 100, 00133 Roma, Italy Dipartimento di Scienze Chimiche e Farmaceutiche, Università di Trieste, Via Licio Giorgieri 1, I-34127 Trieste, Italy Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali, INSTM, Unitá di Trieste, Trieste, Italy DEMOCRITOS CNR-IOM National Simulation Center, Trieste, Italy Sincrotrone Trieste, I-34149 Basovizza, Trieste, Italy IOM-CNR, I-34149, Basovizza, Trieste, Italy (literal)
Titolo
  • Resonant Circular Dichroism of Chiral Metal-Organic Complex (literal)
Abstract
  • A sizable enhancement of the circular dichroism in photoelectron spectroscopy has been measured and computed for the metal complex ?-cobalt(III) tris-acetylacetonate highest occupied molecular orbital state in the region of the Co 3p->3d Fano resonance. In the resonance the dichroism reaches the maximum value of 5% and even changes its sign as compared to the direct photoionization channel. We ascribe this enhancement to electron correlation processes, namely, with the coupling between discrete excitations and the continuum, which is correctly described in the time dependent density functional theory (TDDFT) framework. These findings open new physical aspects of photoelectron circular dichroism that now can be interpreted not only via the simple direct ionization, but also through more complex electron correlation processes. (literal)
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