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The Role of A and A’ States in the Geminate Recombination of Molecular Iodine

  • D. F. Kelley
  • N. A. Abul-Haj
Part of the Springer Series in Chemical Physics book series (CHEMICAL, volume 38)

Abstract

The photodissociation and recombination dynamics of solution phase molecular iodine have been extensively studied both theoretically and experimentally. The simplicity of the reaction, I2→I+I→I2, along with iodine’s well understood spectroscopy [1],have resulted in numerous picosecond laser experiments [2–6] as well as molecular dynamics[5], generalized Langevi n[7] and other theoretical studies.[8–10] Despite these efforts, several fundamental questions have remained unanswered. For example, the rate of vibrational relaxation in the ground electronic state has not been directly determined. However, recent experimental [5] and theoretical [5,7,8] studies have suggested that vibrational relaxation may take ~100ps. Furthermore, recent rare gas matrix isolation studies by FLYNN[11] and theoretical studies by MILLER[9] have suggested that recombination into excited electronic states may be an important relaxation mechanism. The results presented here will further address these questions of electronic and vibrational relaxation.

Keywords

Ground Electronic State Excited Electronic State Vibrational Relaxation Molecular Iodine Ground State Atom 
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-Verlag Berlin Heidelberg 1984

Authors and Affiliations

  • D. F. Kelley
    • 1
  • N. A. Abul-Haj
    • 1
  1. 1.Department of Chemistry and BiochemistryUniversity of California Los AngelesLos AngelesUSA

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