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Vibrationally Resolved Inner-Shell Photoexcitation of the Molecular Anion C 2 .

Stefan SchippersP-M HillenbrandAlexander Perry-SassmannshausenT BuhrS FuchsS ReinwardtFlorian TrinterAlfred MüllerMichael Martins
Published in: Chemphyschem : a European journal of chemical physics and physical chemistry (2023)
Carbon 1s core-hole excitation of the molecular anion C 2 - has been experimentally studied at high resolution by employing the photon-ion merged-beams technique at a synchrotron light source. The experimental cross section for photo-double-detachment shows a pronounced vibrational structure associated with 1 σ u → 3 σ g ${1\sigma _u \to 3\sigma _g }$ and 1 σ g → 1 π u ${1\sigma _g \to 1\pi _u }$ core excitations of the C 2 - ground level and first excited level, respectively. A detailed Franck-Condon analysis reveals a strong contraction of the C 2 - molecular anion by 0.2 Å upon this core photoexcitation. The associated change of the molecule's moment of inertia leads to a noticeable rotational broadening of the observed vibrational spectral features. This broadening is accounted for in the present analysis which provides the spectroscopic parameters of the C 2 - 1 σ u - 1 3 σ g 2 2 Σ u + ${1\sigma _u^{ - 1} \,3\sigma _g^2 \;^2 \Sigma _u^ + }$ and 1 σ g - 1 3 σ g 2 2 Σ g + ${1\sigma _g^{ - 1} \,3\sigma _g^2 \;^2 \Sigma _g^ + }$ core-excited levels.
Keyphrases
  • high resolution
  • ionic liquid
  • molecular dynamics simulations
  • density functional theory
  • molecular docking
  • quantum dots
  • smooth muscle
  • contrast enhanced
  • electron transfer