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Updated: May 27, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Resonance electron attachment and long-lived negative ions of phthalimide and pyromellitic diimide
Stanislav A Pshenichnyuk1, Alexander S Vorob'ev, Alberto Modelli
1Institute of Physics of Molecules and Crystals, Ufa Research Center, Russian Academy of Sciences, October Avenue, 151, 450075 Ufa, Russia. sapsh@anrb.ru
Abstract:
Resonance attachment of low energy (0-15 eV) electrons to imide-containing molecules, phthalimide (PTI) and pyromellitic diimide (PMDI), was investigated in the gas-phase by means of Electron Transmission Spectroscopy (ETS) and Dissociative Electron Attachment Spectroscopy (DEAS). Among a variety of low intensity negatively charged fragments formed by DEA, in both compounds the dominant species was found to be a long-lived (μs) parent molecular anion formed at zero energy. In addition, in PMDI long-lived molecular anions were also observed at 0.85 and 2.0 eV. The experimentally evaluated detachment times from the molecular anions as a function of incident electron energy are modeled with a simple computational approach based on the RRKM theory. The occurrence of radiationless transitions to the ground anion state, followed by internal vibrational relaxation, is believed to be a plausible mechanism to explain the exceptionally long lifetime of the PMDI molecular anions formed above zero energy.
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