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Updated: Jan 6, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Infrared Spectroscopy of Radical-Cation Clusters (NH3)n=4-6
Amandeep Singh1, Arisa Iguchi2,3, Zane Golpariani1
1Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States.
Abstract:
Radical-cation clusters of ammonia ((NH3)n=4-6+) were produced inside helium droplets and studied via infrared laser spectroscopy in the NH stretching region. The clusters have multiple isomers, whose structures were studied with quantum chemical calculations. The comparison of the measured and calculated spectra of the free NH stretches shows that each cluster has an NH4+ core, solvated by NH3 molecules and an NH2 radical through hydrogen bonds, as their respective global minima states. The spectra of (NH3)n=4-6+ contain the arrays of strong bands in the frequency range of 2300-3200 cm-1, which stem from the interaction between the hydrogen bond bridge vibrations of the ammonium core NH4+ and the overtones of its bending modes. The spectra of (NH3)5+ and (NH3)6+ indicate the presence of some additional higher-energy isomers, which have a free NH stretch of the NH4+ core.
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