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Título

New Insight into the Gas-Phase Bimolecular Self-Reaction of the HOO Radical

AutorAnglada Rull, Josep M.; Olivella, Santiago; Sol, Albert
Palabras claveAtmospherical chemistry
Theorical chemistry
Hidroperoxil radical
Gas-phase chemistry
Fecha de publicación2-oct-2007
EditorAmerican Chemical Society
CitaciónThe Journal of Physical Chemistry 111(9): 1695-1704 (2007)
ResumenThe singlet and triplet potential energy surfaces (PESs) for the gas-phase bimolecular self-reaction of HOO·, a key reaction in atmospheric environments, have been investigated by means of quantum-mechanical electronic structure methods (CASSCF and CASPT2). All the reaction pathways on both PESs consist of a first step involving the barrierless formation of a prereactive doubly hydrogen-bonded complex, which is a diradical species lying about 8 kcal/mol below the energy of the reactants at 0 K. The lowest energy reaction pathway on both PESs is the degenerate double hydrogen exchange between the HOO· moieties of the prereactive complex via a double proton transfer mechanism involving an energy barrier of only 1.1 kcal/mol for the singlet and 3.3 kcal/mol for the triplet at 0 K. The single H-atom transfer between the two HOO· moieties of the prereactive complex (yielding HOOH + O2) through a pathway keeping a planar arrangement of the six atoms involves a conical intersection between either two singlet or two triplet states of A´ and A´´ symmetries. Thus, the lowest energy reaction pathway occurs via a nonplanar cisoid transition structure with an energy barrier of 5.8 kcal/mol for the triplet and 17.5 kcal/mol for the singlet at 0 K. The simple addition between the terminal oxygen atoms of the two HOO· moieties of the prereactive complex, leading to the straight chain H2O4 intermediate on the singlet PES, involves an energy barrier of 7.3 kcal/mol at 0 K. Because the decomposition of such an intermediate into HOOH + O2 entails an energy barrier of 45.2 kcal/mol at 0 K, it is concluded that the single H-atom transfer on the triplet PES is the dominant pathway leading to HOOH + O2. Finally, the strong negative temperature dependence of the rate constant observed for this reaction is attributed to the reversible formation of the prereactive complex in the entrance channel rather than to a short-lived tetraoxide intermediate.
Descripción10 pages, 8 figures.-- PMID: 17290977 [PubMed].
Supporting information (cartesian coordinates of the CASSCF/6-311+G(3d,2p)-optimized geometries, tables S1-S2, figures S1-S4, 9 pages) available at: http://pubs.acs.org/doi/suppl/10.1021/jp066823d/suppl_file/jp066823dsi20070104_064851.pdf
Versión del editorhttp://dx.doi.org/10.1021/jp066823d
URIhttp://hdl.handle.net/10261/9329
DOI10.1021/jp066823d
ISSN1520-5215
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