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Collision-free photochemistry of methylazide: observation of unimolecular decomposition of singlet methylnitrene
Authors:Larson Christopher  Ji Yuanyuan  Samartzis Petros  Wodtke Alec M  Lee Shih-Huang  Lin Jim Jr-Min  Chaudhuri Chanchal  Ching Tao-Tsung
Institution:Department of Chemistry and Biochemistry, University of California, Santa Barbara, Santa Barbara, California 93106, USA. clarson@chem.ucsb.edu
Abstract:Methylazide photolysis at 248 nm has been investigated by ionizing photofragments with synchrotron radiation in a photofragmentation translational spectroscopy study. CH3N and N2 were the only observed primary products. The translational energy release suggests a simple bond rupture mechanism forming singlet methylnitrene, 1CH3N, and N2. Thus, these experiments reveal the unimolecular decomposition of this highly unstable species. We explain our observations through a mechanism which is initiated by the isomerization of 1CH3N to a highly internally excited methanimine H2C=NH isomer, which decomposes by 1,1-H2 elimination forming HNC+H2 as well as sequential H-atom loss (N-H followed by C-H bond cleavage), to form HCN. No evidence for dynamics on the triplet manifold of surfaces is found.
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