Determining the branching ratios of site-specific water and hydronium formation from ethanol

POSTER

Abstract

In ethanol, water and hydronium cations may be formed by single or double hydrogen migration, respectively. Due to the geometric structure of ethanol, the migrating hydrogens can originate from either the CH$_3$ or CH$_2$ sites to form bonds with the OH moiety. To determine the site-specific branching ratios of water and hydronium formation induced by an ultrafast intense laser field, we employ coincidence momentum imaging to measure the fragmentation of a variety of isotopologues of ethanol. We also briefly highlight how this method can be used to determine the site-specific branching ratios of H$_2^+$ and H$_3^+$ formation.

*Supported by the Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office for Science, U.S. Department of Energy under Award \# DE-FG02-86ER13491.

Authors

  • Travis Severt

    • J. R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, KS 66506 USA
    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
    • J.R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan KS, USA
    • Department of Physics, Kansas State University, Manhattan KS, USA
    • J.R. Macdonald Laboratory, Kansas State University, Manhattan, KS 66506
  • K. Borne

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • F. Ziaee

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • B. Jochim

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • P. Feizollah

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506
  • B. Kaderiya

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • P. Kanaka Raju

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • K. D. Carnes

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • D. Rolles

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • A. Rudenko

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • I. Ben-Itzhak

    • J.R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, KS 66506, USA
  • N. Ekanayake

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • M. Nairat

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • N. P. Weingartz

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • B. M. Farris

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • B. G. Levine

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • J. E. Jackson

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA
  • M. Dantus

    • Department of Chemistry, Michigan State University, East Lansing, MI 48824, USA