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Metal-Metal Bonding in Actinide Dimers: U2 and U2.
Ciborowski, Sandra M; Mitra, Abhishek; Harris, Rachel M; Liu, Gaoxiang; Sharma, Prachi; Khetrapal, Navneet; Blankenhorn, Moritz; Gagliardi, Laura; Bowen, Kit H.
Afiliação
  • Ciborowski SM; Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
  • Mitra A; Department of Chemistry, Pritzker School of Molecular Engineering, James Franck Institute, Chicago Center for Theoretical Chemistry, The University of Chicago, Chicago, Illinois 60637, United States.
  • Harris RM; Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
  • Liu G; Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
  • Sharma P; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Khetrapal N; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Blankenhorn M; Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
  • Gagliardi L; Department of Chemistry, Pritzker School of Molecular Engineering, James Franck Institute, Chicago Center for Theoretical Chemistry, The University of Chicago, Chicago, Illinois 60637, United States.
  • Bowen KH; Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.
J Am Chem Soc ; 143(41): 17023-17028, 2021 Oct 20.
Article em En | MEDLINE | ID: mdl-34609860
ABSTRACT
Understanding direct metal-metal bonding between actinide atoms has been an elusive goal in chemistry for years. We report for the first time the anion photoelectron spectrum of U2-. The threshold of the lowest electron binding energy (EBE) spectral band occurs at 1.0 eV, which corresponds to the electron affinity (EA) of U2, whereas the vertical detachment energy of U2- is found at EBE ∼ 1.2 eV. Electronic structure calculations on U2 and U2- were carried out with state-of-the-art theoretical methods. The computed values of EA(U2) and EA(U) and the difference between the computed dissociation energies of U2 and U2- are found to be internally consistent and consistent with experiment. Analysis of the bonds in U2 and U2- shows that while U2 has a formal quintuple bond, U2- has a quadruple bond, even if the effective bond orders differ only by 0.5 unit instead of one unit. The resulting experimental-computational synergy elucidates the nature of metal-metal bonding in U2 and U2-.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2021 Tipo de documento: Article