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Title: Photochemistry of glycolaldehyde in cryogenic matrices

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4881605· OSTI ID:22420086
; ;  [1];  [2];  [3]
  1. Institut des Sciences Moléculaires d’Orsay, CNRS UMR 8214, Université Paris-Sud, 91405 Orsay (France)
  2. DSM/IRAMIS/SIS2M (CEA-CNRS UMR3299), Commissariat à l’Énergie Atomique, 91191 Gif-sur-Yvette (France)
  3. Department of General Physics and Spectroscopy, Vilnius University, 01315 Vilnius (Lithuania)

The photochemistry of glycolaldehyde (GA) upon irradiation at 266 nm is investigated in argon, nitrogen, neon, and para-hydrogen matrices by IR spectroscopy. Isomerization and fragmentation processes are found to compete. The hydrogen-bonded Cis-Cis form of GA is transformed mainly to the open Trans-Trans conformer and to CO and CH{sub 3}OH fragments and their mixed complexes. Different photo-induced behaviours appear depending on the matrix. In nitrogen, small amounts of Trans-Gauche and Trans-Trans conformers are detected after deposition and grow together upon irradiation. The Trans-Gauche conformer is characterized for the first time. In para-hydrogen due to a weaker cage effect additional H{sub 2}CO and HCO fragments are seen. Calculations of the potential energy surfaces of S{sub 0}, S{sub 1}, and T{sub 1} states – to analyse the torsional deformations which are involved in the isomerization process – and a kinetic analysis are presented to investigate the different relaxation pathways of GA. Fragmentation of GA under UV irradiation through the CO+CH{sub 3}OH molecular channel is a minor process, as in the gas phase.

OSTI ID:
22420086
Journal Information:
Journal of Chemical Physics, Vol. 140, Issue 22; Other Information: (c) 2014 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English

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