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Hydrocarboxyl Radical as a Product of α-Alanine Ultraviolet Photolysis.

Brendan MooreShin Yi TohY T Angel WongTermeh BashiriAlexandra McKinnonYonnie WaiKa Wing Alethea LeePolina OvchinnikovChih-Yu ChiangPavle DjuricaninTakamasa Momose
Published in: The journal of physical chemistry letters (2021)
UV photodissociation of α-alanine was studied by parahydrogen matrix isolation infrared spectroscopy. The temporal behavior of Fourier transform infrared spectra revealed that UV irradiation at 213 nm yielded the HOCO radical as a direct photoproduct from the S2 excited state. The concentration of HOCO quickly approached a steady state due to secondary photodissociation of HOCO to produce CO2 + H or CO + OH. On the other hand, no photoproducts were detected by S1 excitation at 266 nm. Irradiation of fully deuterated α-alanine at 213 nm yielded ∼2 times more cis-DOCO radicals than the lower energy isomer trans-DOCO, indicating that the conformation of the hydroxyl group is fairly well-preserved upon photodissociation of α-alanine. The present study suggests that HOCO may be a good tracer species in the search for amino acids in interstellar space.
Keyphrases
  • photodynamic therapy
  • amino acid
  • light emitting
  • radiation induced
  • aqueous solution
  • pet ct
  • genetic diversity