Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/10298
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dc.contributor.authorVarandas, A. J. C.-
dc.contributor.authorBrandão, J.-
dc.contributor.authorQuintales, L. A. M.-
dc.date.accessioned2009-06-24T10:59:23Z-
dc.date.available2009-06-24T10:59:23Z-
dc.date.issued1988-06-
dc.identifier.citationThe Journal of Physical Chemistry. 92:13 (1988) 3732-3742en_US
dc.identifier.urihttp://hdl.handle.net/10316/10298-
dc.description.abstractA double many-body expansion potential energy surface reported previously for H02(R2A”) and referred to here as DMBE I is modified to produce thermal rate coefficients for the reaction 0 + OH - O2 + H in good agreement with experiment. This new potential energy surface will be referred to as DMBE 11. By the further imposition that the potential function should reproduce the experimental spectroscopic force field data for the hydroperoxyl radical, another potential energy surface has been obtained, DMBE 111. Both of these improved DMBE I1 and DMBE 111 potential energy surfaces preserve the functional form used previously for DMBE I except for the long-range 0. -.OH electrostatic interaction, which is defined in the spirit of a more satisfactory adiabatic theory.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsopenAccesseng
dc.titleA realistic hydroperoxo(~X2A") potential energy surface from the double many-body expansion methoden_US
dc.typearticleen_US
dc.identifier.doi10.1021/j100324a010-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.deptFaculty of Sciences and Technology-
crisitem.author.parentdeptUniversity of Coimbra-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-1501-3317-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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