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dc.contributor.authorZhu, R. S.en_US
dc.contributor.authorLin, M. C.en_US
dc.date.accessioned2019-04-02T06:00:09Z-
dc.date.available2019-04-02T06:00:09Z-
dc.date.issued2009-08-17en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2009.07.034en_US
dc.identifier.urihttp://hdl.handle.net/11536/149816-
dc.description.abstractThe low-lying energy pathways for the decomposition/isomerization of nitromethane (NM) have been investigated using different molecular orbital methods. Our results show that in addition to the commonly known CH3 + NO2 products formed by direct C-N bond breaking and the trans-CH3ONO formed by nitro-nitrite isomerization, NM can also isomerize to cis-CH3ONO via a very loose transition state (TS) lying 59.2 kcal/mol above CH3NO2 or 0.6 kcal/mol below the CH3 + NO2 asymptote predicted at the UCCSD(T)/CBS level of theory. Kinetic results indicate that in the energy range of 59 +/- 1 kcal/mol, production of CH3O + NO is dominant, whereas above the C-N bond breaking threshold, the formation of CH3 + NO2 sharply increases and becomes dominant. The k(E) values predicted at different energies clearly indicate that CH3O + NO could be detected in an infrared multi-photon dissociation study, whereas in UV dissociation experiments with energies high above the C-N bond breaking threshold the CH3 + NO2 products are generated predominantly. (C) 2009 Elsevier B. V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleCH3NO2 decomposition/isomerization mechanism and product branching ratios: An ab initio chemical kinetic studyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2009.07.034en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume478en_US
dc.citation.spage11en_US
dc.citation.epage16en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.identifier.wosnumberWOS:000268767500002en_US
dc.citation.woscount57en_US
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