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Excess electrons bound to H2S trimer and tetramer clusters.
Liu, Gaoxiang; Díaz-Tinoco, Manuel; Ciborowski, Sandra M; Martinez-Martinez, Chalynette; Lyapustina, Svetlana; Hendricks, Jay H; Ortiz, Joseph Vincent; Bowen, Kit H.
Afiliação
  • Liu G; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
  • Díaz-Tinoco M; Department of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. jvo0001@auburn.edu.
  • Ciborowski SM; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
  • Martinez-Martinez C; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
  • Lyapustina S; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
  • Hendricks JH; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
  • Ortiz JV; Department of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. jvo0001@auburn.edu.
  • Bowen KH; Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA. kbowen@jhu.edu.
Phys Chem Chem Phys ; 22(6): 3273-3280, 2020 Feb 14.
Article em En | MEDLINE | ID: mdl-32003384
ABSTRACT
We have prepared the hydrogen sulfide trimer and tetramer anions, (H2S)3- and (H2S)4-, measured their anion photoelectron spectra, and applied high-level quantum chemical calculations to interpret the results. The sharp peaks at low electron binding energies in their photoelectron spectra and their diffuse Dyson orbitals are evidence for them both being dipole-bound anions. While the dipole moments of the neutral (H2S)3 and (H2S)4 clusters are small, the excess electron induces structural distortions that enhance the charge-dipolar attraction and facilitate the binding of diffuse electrons.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article