Photo-fragmentation of the closo-carboranes

ORAL

Abstract

Single and multi-cation ionic fragmentation of three isomeric carborane cage compounds [closo-1,2-orthocarborane, closo-1,7-metacarborane, closo-1,12-paracarborane (C$_{2}$B$_{10}$H$_{12})$] following B 1s and C 1s excitation were studied by time of flight mass analysis. The energetic cycles were constructed to gain some insights into some of decomposition processes. CH$^{+}$ or BH$_{2}^{+}$ fragment dominates the single ion fragmentation of the closo-carboranes. Double ion fragmentation yields and charge separation mass spectra of all three isomers are generally quite similar in that H$^{+}$ and BH$_{2}^{+}$/CH$^{+}$ ion pairs, BH$_{2}^{+}$/CH$^{+}$ and Y$_{11}^{+ }$ion pairs (where Y = (BH) or (CH)), Y$_{3}^{+}$ and Y$_{9}^{+ }$ion pairs (where Y = (BH) or (CH)) yields dominate. The H$^{+}$ and BH$_{2}^{+}$/CH$^{+}$ ion pairs dominate at the B 1s threshold for ortho- and metacarborane, while Y$_{1}^{+}$ and Y$_{11}^{+ }$ion pairs (where Y = (BH) or (CH)) dominates the multi-photofragment ion yield of paracarborane at the B1s threshold.

Authors

  • Jing Liu

    Physics and Astronomy, Univ. of Nebraska-Lincoln, Dept. of Physics and Astronomy, University of Nebraska-Lincoln

  • Danqin Feng

    Dept. of Physics and Astronomy, University of Nebraska-Lincoln

  • P.A. Dowben

    Dept. of Physics and Astronomy, University of Nebraska-Lincoln

  • A.P. Hitchcock

    Dept. of Chemistry, McMaster University, Canada

  • A.L.D. Kilcoyne

    Advanced Light Source, Lawrence-Berkeley Laboratory

  • T. Tyliszczak

    Advanced Light Source, Lawrence-Berkeley Laboratory

  • J.D. Bozek

    Stanford Synchrotron Radiation Laboratory

  • E. R\"uhl

    Institut f\"ur Physikalische Chemie, Freie Universit\"at Berlin, Germany