Modeling the Ground- and Excited-State Unimolecular Decay of the Simplest Fluorinated Criegee Intermediate, HFCOO, Formed from the Ozonolysis of Hydrofluoroolefin Refrigerants.

Hydrofluoroolefins (HFO) are fourth-generation refrigerants designed to function as efficient refrigerants with no ozone depletion potential and zero global warming potential. Despite extensive studies on their chemical and physical properties, the ground- and excited-state chemistry of their atmospheric oxidation products is less well understood. This study focuses on the ground- and excited-state chemistry of the simplest fluorinated Criegee intermediate (CI), fluoroformaldehyde oxide (HFCOO), which is the simplest fluorinated CI formed from the ozonolysis of HFOs. HFCOO contains syn- and anti-conformers, which have Boltzmann populations of, respectively, 87 and 13% at 298 K. For both conformers, the calculated ground-state reaction energy profiles associated with cyclization to form fluorodioxirane is lower than the equivalent unimolecular decay path in the simplest CI, H 2 COO, with anti-HFCOO returning a barrier height more than half of that of H 2 COO. The excited-state dynamics reveal that photoexcitation to the bright S 2 state of syn-HFCOO and anti-HFCOO is expected to undergo a prompt O-O fission─with the former conformer expected to dissociate with an almost unity quantum yield and to form both O ( 1 D) + HFCO (S 0 ) and O ( 3 P) + HFCO (T 1 ) products. In contrast, photoexcitation of anti-HFCOO is expected to undergo an O-O bond fission with a non-unity quantum yield. The fraction of photoexcited anti-HFCOO that dissociates is predicted to exclusively form O ( 1 D) + HFCO (S 0 ) products, which is in sharp contrast to H 2 COO. The wider implications of our results are discussed from both physical and atmospheric chemistry perspectives.