https://doi.org/10.1140/epjd/s10053-023-00727-0
Regular Article – Molecular Physics and Chemical Physics
Revisiting photoisomerization in fluorinated analogues of acetylacetone trapped in cryogenic matrices
1
Institut des Sciences Moléculaires d’Orsay, CNRS, Université Paris-Sacla, 91405, Orsay, France
2
Instituto Superior de Tecnologías y Ciencias Aplicadas (InSTEC), Universidad de La Habana, Ave. Salvador Allende No. 1110, 10400, Plaza de la Revolución, La Habana, Cuba
3
Université de Pau et des Pays de l’Adour, E2S UPPA, CNRS, IPREM, Pau, France
4
Institute of Chemical Physics, Vilnius University, Vilnius, Lithuania
a
a.gutierrez-quintanilla@univ-pau.fr
e
claudine.crepin-gilbert@universite-paris-saclay.fr
Received:
18
April
2023
Accepted:
5
July
2023
Published online:
16
August
2023
UV-induced processes are commonly studied in acetylacetone analogues. In this contribution, we revisit the existing work on the photoisomerization process in some of the fluorinated analogues of acetylacetone, i.e., trifluoroacetylacetone (F3-acac) and hexafluoroacetylacetone (F6-acac). We performed selective UV laser excitation of these molecules trapped in soft cryogenic matrices, namely neon and para-hydrogen, and probed by vibrational spectroscopy. Clear spectroscopy of 3 isomers of F6-acac and 6 isomers of F3-acac is obtained, including the first characterization of a second open enol isomer of hexafluoroacetylacetone. In addition, we present the electronic absorption spectra of both molecules in cryogenic matrices before and after specific UV irradiations, giving new data on the electronic transitions of photoproducts. Vibrational and electronic experimental results are analyzed and discussed within comparisons with DFT and TD-DFT calculations. Our findings contribute to a deeper understanding of the photoisomerization process in these molecules after electronic excitation in gas and condensed phase.
Supplementary Information The online version contains supplementary material available at https://doi.org/10.1140/epjd/s10053-023-00727-0.
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© The Author(s), under exclusive licence to EDP Sciences, SIF and Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.