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Title: Effect of charged and excited states on the decomposition of 1,1-diamino-2,2-dinitroethylene molecules

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.2741530· OSTI ID:20991285
; ; ;  [1]
  1. Department of Physics, University of Nevada, Las Vegas, Nevada 89154 and Department of Physics and Astronomy, University College London, London WC1E 6BT (United Kingdom)

The authors have calculated the electronic structure of individual 1,1-diamino-2,2-dinitroethylene molecules (FOX-7) in the gas phase by means of density functional theory with the hybrid B3LYP functional and 6-31+G(d,p) basis set and considered their dissociation pathways. Positively and negatively charged states as well as the lowest excited states of the molecule were simulated. They found that charging and excitation can not only reduce the activation barriers for decomposition reactions but also change the dominating chemistry from endo- to exothermic type. In particular, they found that there are two competing primary initiation mechanisms of FOX-7 decomposition: C-NO{sub 2} bond fission and C-NO{sub 2} to CONO isomerization. Electronic excitation or charging of FOX-7 disfavors CONO formation and, thus, terminates this channel of decomposition. However, if CONO is formed from the neutral FOX-7 molecule, charge trapping and/or excitation results in spontaneous splitting of an NO group accompanied by the energy release. Intramolecular hydrogen transfer is found to be a rare event in FOX-7 unless free electrons are available in the vicinity of the molecule, in which case HONO formation is a feasible exothermic reaction with a relatively low energy barrier. The effect of charged and excited states on other possible reactions is also studied. Implications of the obtained results to FOX-7 decomposition in condensed state are discussed.

OSTI ID:
20991285
Journal Information:
Journal of Chemical Physics, Vol. 126, Issue 23; Other Information: DOI: 10.1063/1.2741530; (c) 2007 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English

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