Table of Contents
Laser Chemistry
Volume 10, Issue 3, Pages 177-184

Uv Multiphoton Induced Chemistry of Nitrobenzene in Solution

1Department of Chemistry, Dartmouth College, Hanover NH 03755, USA
2Department of Chemistry, University of New Hampshire, Durham NH03824, USA

Received 27 July 1989; Accepted 5 September 1989

Copyright © 1990 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The technique of Multiphoton Induced Chemistry (MPIC) has been employed to initiate ion-molecule chemistry of organic molecules in solution. We report one of the first examples of the use of liquid phase multiphoton ionization (MPI) to prepare organic cations, which then react with the solvent in ionmolecule processes. The products obtained in this chemical sequence are significantly different from those observed in conventional or multiphoton-induced neutral chemistry in the same solvent. The particular example explored in this work is the reactivity of the nitrobenzene cation in methanol solvent. Products of the ion-molecule chemistry, detected by gas chromatography/mass spectrometry, are phenol and benzyl alcohol. These products depend upon the square of the laser intensity. It is shown by ionization current measurements in a conductance cell, that ionic species are produced as precursors to the observed products. The implications of this application of MPI are briefly discussed. A preliminary report on the unimolecular chemistry of the highly excited neutral molecule is also included. The product of this channel is nitrosobenzene. It is shown, in this case, that the reactive state is most likely a highly vibrationally excited ground state molecule, not the lowest triplet level invoked in conventional photochemistry.