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Updated: May 25, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Studies of impulsive vibrational influence on ultrafast electronic excitation transfer
Jason D Biggs1, Jeffrey A Cina
1Department of Chemistry and Oregon Center for Optics, University of Oregon, Eugene, Oregon 97403, USA.
Abstract:
We investigated electronic energy-transfer dynamics in three model dimers within which coherent intramonomer nuclear motion had been induced by impulsive Raman excitation using an optimized, electronically preresonant control pulse. Calculations of the donor-survival probability, the ultrafast pump-probe signal, and the pump-probe difference signal are presented for dithia-anthracenophane and homodimers of 2-difluoromethylanthracene and 2-trifluoromethylanthracene. Survival probabilities and signals, along with phase-space analyses, elucidated the mechanisms, extent, and spectroscopic manifestations of external vibrational or torsional control over electronic excitation transfer.
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