dc.creatorGerli Candia, Lorena
dc.creatorOrtiz, Nahara
dc.creatorSalgado, Guillermo
dc.creatorGlossman, Daniel
dc.date2015-11-19T18:27:52Z
dc.date2015-11-19T18:27:52Z
dc.date2013
dc.identifierInternational journal of pharma and bio sciences
dc.identifier0975-6299
dc.identifierhttp://repositoriodigital.ucsc.cl/handle/25022009/324
dc.descriptionArtículo de publicación SCOPUS
dc.descriptionAtmospheric temperature affects both the absorption spectrum and the concentration of atmospheric gases. Gases with larger abundances and stronger absorption band intensities in the infrared region have a greater influence on the greenhouse effect. The purpose of this work is to provide an ab initio theoretical conformational model of the reaction between the OH radical and CO, which is used to model common environmental reactions. The geometric optimization of the studied structures was performed using Hartree-Fock (HF) methodology, B3LYP (Becke, three-parameter, Lee-Yang-Par) and the Moller- Plesset perturbation theory to the 2nd order (MP2), using the 6-311++G** basis set and Gaussian 09W software for all calculations. Three stationary structures and six transition structures were found and were characterized by their normal modes of vibration. Using this methodology, we discovered two possible paths for the studied reaction, which were characterized by their potential energy hypersurface. These paths are the geometric isomers cis and trans HOCO radicals that yield a ΔH for the general reaction of -34.51 kcal/mol. According to the Hammond postulate, which relates the similarity in transition states with the reactants or products, the transition states participating in the studied reaction have a similar energetic character to the reactants, which is generally observed in exothermic reactions.
dc.languageen
dc.publisherResearchGate
dc.rightsAtribucion-Nocomercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.sourcehttp://goo.gl/oU4ZtB
dc.subjectChemistry
dc.subjectTheory
dc.subjectEnvironmental Reaction
dc.titleAB initio theoretical study of the HO + CO → CO 2 + H environmental chemical reaction
dc.typeArtículos de revistas


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