Affiliation:
1. Department of Chemistry, Dartmouth College, Hanover NH 03755, USA
2. Department of Chemistry, University of New Hampshire, Durham NH03824, USA
Abstract
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.
Subject
Spectroscopy,Biochemistry,Atomic and Molecular Physics, and Optics
Cited by
4 articles.
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