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Photoinduced Dissociative Electron Capture Processes in Binary Ion-Molecule Complexes

  • Donna M. Cyr
  • Mark A. Johnson
Part of the NATO ASI Series book series (NSSB, volume 326)

Abstract

Molecular negative ions are distinct from their neutral counter parts in that while their ground electronic states can be quite stable, their first excited electronic states often correspond to the electron detachment continuum, with the lowest valence excited states embedded in the continuum.1,2 Thus, the absence of the long range coulomb attraction between the excess electron and the neutral core often completely eliminates the infinite number of bound Rydberg states present in all neutral molecules near their ionization potentials. There are, however, a few recently discovered cases in which the dipole moment of a neutral molecule is sufficiently large that the electrostatic (i.e. charge-dipole) interaction with the excess electron is sufficient to create an additional bound electronic state just below the continuum.3 Water dimer anion, (H2O)2’ -4 presents a spectacular case in which a dipole bound state actually forms the ground state since all the valence states are unstable with respect to autodetachment.

Keywords

Photoelectron Spectrum Charge Transfer Band Binary Complex Iodine Atom Neutral Surface 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 1994

Authors and Affiliations

  • Donna M. Cyr
    • 1
  • Mark A. Johnson
    • 1
  1. 1.Department of Chemistry, Sterling Chemistry LaboratoryYale UniversityNew HavenUSA

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