Far-IR absorption of neutral polycyclic aromatic hydrocarbons (PAHs): light on the mechanism of IR–UV ion dip spectroscopy

Autor: Sébastien Gruet, Sanjana Panchagnula, Wybren Jan Buma, Alexander K. Lemmens, Johannes M. M. Thunnissen, Melanie Schnell, Daniël B. Rap, Anouk M. Rijs, Alexander G. G. M. Tielens, Amanda L. Steber
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: The journal of physical chemistry letters 11(21), 8997-9002 (2020). doi:10.1021/acs.jpclett.0c02714
The Journal of Physical Chemistry Letters
Journal of Physical Chemistry Letters, 11(21), 8997–9002
Journal of Physical Chemistry Letters, 11, 8997-9002
Journal of Physical Chemistry Letters, 11, 21, pp. 8997-9002
J. Phys. Chem. Lett.
ISSN: 1948-7185
DOI: 10.1021/acs.jpclett.0c02714
Popis: The journal of physical chemistry letters 11(21), 8997 - 9002 (2020). doi:10.1021/acs.jpclett.0c02714
Gas-phase IR–UV double-resonance laser spectroscopy is an IR absorption technique that bridges the gap between experimental IR spectroscopy and theory. The IR experiments are used to directly evaluate predicted frequencies and potential energy surfaces as well as to probe the structure of isolated molecules. However, a detailed understanding of the underlying mechanisms is, especially in the far-IR regime, still far from complete, even though this is crucial for properly interpreting the recorded IR absorption spectra. Here, events occurring upon excitation to vibrational levels of polycyclic aromatic hydrocarbons by far-IR radiation from the FELIX free electron laser are followed using resonance-enhanced multiphoton ionization spectroscopy. These studies provide detailed insight into how ladder climbing and anharmonicity influence IR–UV spectroscopy and therefore the resulting IR signatures in the far-IR region. Moreover, the potential energy surfaces of these low-frequency delocalized modes are investigated and shown to have a strong harmonic character.
Published by ACS, Washington, DC
Databáze: OpenAIRE