Open AccessSpin-Forbidden Carbon–Carbon Bond Formation in Vibrationally Excited α-CO
Author(s) -
Jessalyn A. DeVine,
Arnab Choudhury,
Jascha A. Lau,
Dirk Schwarzer,
Alec M. Wodtke
Publication year - 2022
Publication title -
the journal of physical chemistry. a/the journal of physical chemistry. a.
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/acs.jpca.2c01168
Subject(s) - chemistry , excited state , intersystem crossing , singlet state , excitation , spin (aerodynamics) , molecule , atomic physics , photochemistry , chemical physics , molecular physics , physics , organic chemistry , quantum mechanics , thermodynamics
Fourier transform infrared spectroscopy of laser-irradiated cryogenic crystals shows that vibrational excitation of CO leads to the production of equal amounts of CO 2 and C 3 O 2 . The reaction mechanism is explored using electronic structure calculations, demonstrating that the lowest-energy pathway involves a spin-forbidden reaction of (CO) 2 yielding C( 3 P) + CO 2 . C( 3 P) then undergoes barrierless recombination with two other CO molecules forming C 3 O 2 . Calculated intersystem crossing rates support the spin-forbidden mechanism, showing subpicosecond spin-flipping time scales for a (CO) 2 geometry that is energetically consistent with states accessed through vibrational energy pooling. This spin-flip occurs with an estimated ∼4% efficiency; on the singlet surface, (CO) 2 reconverts back to CO monomers, releasing heat which induces CO desorption. The discovery that vibrational excitation of condensed-phase CO leads to spin-forbidden C-C bond formation may be important to the development of accurate models of interstellar chemistry.