Thio- and selenofenchone were synthesized and characterized by microwave and infrared spectroscopy, and calculated spectra for telluro- and polonofenchone predict a strong nuclear-charge scaling of chirality-sensitive effects.
Excited state assignment and state-resolved photoelectron circular dichroism in chalcogen-substituted fenchones
1 Pith paper cite this work. Polarity classification is still indexing.
abstract
Excited electronic states of fenchone, thiofenchone, and selenofenchone are characterized and assigned with different gas-phase spectroscopic methods and \textit{ab initio} quantum chemical calculations. With an increasing atomic number of the chalcogen, we observe increasing bathochromic (red) shifts, which vary in strength for Rydberg states, valence-excited states, and ionization energies. The spectroscopic insight is used to state-resolve the contributions in multi-photon photoelectron circular dichroism with femtosecond laser pulses. This is shown to be a sensitive observable of molecular chirality in all studied chalcogenofenchones. Our work contributes new spectroscopic information, particularly on thiofenchone and selenofenchone. It may open a perspective for future coherent control experiments exploiting resonances in the visible and or near-ultraviolet spectral regions.
fields
physics.chem-ph 1years
2025 1verdicts
CONDITIONAL 1representative citing papers
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Heavier chalcogenofenchones for fundamental gas-phase studies of molecular chirality
Thio- and selenofenchone were synthesized and characterized by microwave and infrared spectroscopy, and calculated spectra for telluro- and polonofenchone predict a strong nuclear-charge scaling of chirality-sensitive effects.