Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path
Substantial non-Arrhenius behavior has been previously observed in the low temperature reaction between the hydroxyl radical and methanol. This behavior can be rationalized assuming the stabilization of an association adduct in the entrance channel of the reaction, from which barrier penetration via...
| Autores: | , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2015 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/47174 |
| Acceso en línea: | http://hdl.handle.net/11336/47174 |
| Access Level: | acceso abierto |
| Palabra clave: | Espectroscopia Laser Agregados Moleculares Espectroscopia Infrarroja https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
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Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction pathHernández, Federico JavierBrice, JosephLeavitt, Christopher M.Pino, Gustavo ArielDouberly, Gary E.Espectroscopia LaserAgregados MolecularesEspectroscopia Infrarrojahttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Substantial non-Arrhenius behavior has been previously observed in the low temperature reaction between the hydroxyl radical and methanol. This behavior can be rationalized assuming the stabilization of an association adduct in the entrance channel of the reaction, from which barrier penetration via quantum mechanical tunneling produces the CH3O radical and H2O. Helium nanodroplet isolation and a serial pick-up technique are used to stabilize the hydrogen bonded prereactive OH··CH3OH complex. Mass spectrometry and infrared spectroscopy are used to confirm its production and probe the OH stretch vibrations. Stark spectroscopy reveals the magnitude of the permanent electric dipole moment, which is compared to ab initio calculations that account for wide-amplitude motion in the complex. The vibrationally averaged structure has Cs symmetry with the OH moiety hydrogen bonded to the hydroxyl group of methanol. Nevertheless, the zero-point level of the complex exhibits a wave function significantly delocalized over a bending coordinate leading to the transition state of the CH3O producing reaction.Fil: Hernández, Federico Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Brice, Joseph. University of Georgia; Estados UnidosFil: Leavitt, Christopher M.. University of Georgia; Estados UnidosFil: Pino, Gustavo Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Douberly, Gary E.. University of Georgia; Estados UnidosAmerican Chemical Society2015-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/47174Hernández, Federico Javier; Brice, Joseph; Leavitt, Christopher M.; Pino, Gustavo Ariel; Douberly, Gary E.; Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path; American Chemical Society; Journal of Physical Chemistry A; 119; 29; 7-2015; 8125-81321089-56391520-5215CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jpca.5b04875info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpca.5b04875info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T14:27:26Zoai:ri.conicet.gov.ar:11336/47174instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982024-05-08 14:27:26.979CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| title |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| spellingShingle |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path Hernández, Federico Javier Espectroscopia Laser Agregados Moleculares Espectroscopia Infrarroja https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| title_short |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| title_full |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| title_fullStr |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| title_full_unstemmed |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| title_sort |
Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path |
| dc.creator.none.fl_str_mv |
Hernández, Federico Javier Brice, Joseph Leavitt, Christopher M. Pino, Gustavo Ariel Douberly, Gary E. |
| author |
Hernández, Federico Javier |
| author_facet |
Hernández, Federico Javier Brice, Joseph Leavitt, Christopher M. Pino, Gustavo Ariel Douberly, Gary E. |
| author_role |
author |
| author2 |
Brice, Joseph Leavitt, Christopher M. Pino, Gustavo Ariel Douberly, Gary E. |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Espectroscopia Laser Agregados Moleculares Espectroscopia Infrarroja https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| topic |
Espectroscopia Laser Agregados Moleculares Espectroscopia Infrarroja https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
| description |
Substantial non-Arrhenius behavior has been previously observed in the low temperature reaction between the hydroxyl radical and methanol. This behavior can be rationalized assuming the stabilization of an association adduct in the entrance channel of the reaction, from which barrier penetration via quantum mechanical tunneling produces the CH3O radical and H2O. Helium nanodroplet isolation and a serial pick-up technique are used to stabilize the hydrogen bonded prereactive OH··CH3OH complex. Mass spectrometry and infrared spectroscopy are used to confirm its production and probe the OH stretch vibrations. Stark spectroscopy reveals the magnitude of the permanent electric dipole moment, which is compared to ab initio calculations that account for wide-amplitude motion in the complex. The vibrationally averaged structure has Cs symmetry with the OH moiety hydrogen bonded to the hydroxyl group of methanol. Nevertheless, the zero-point level of the complex exhibits a wave function significantly delocalized over a bending coordinate leading to the transition state of the CH3O producing reaction. |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015-07 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/47174 Hernández, Federico Javier; Brice, Joseph; Leavitt, Christopher M.; Pino, Gustavo Ariel; Douberly, Gary E.; Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path; American Chemical Society; Journal of Physical Chemistry A; 119; 29; 7-2015; 8125-8132 1089-5639 1520-5215 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/47174 |
| identifier_str_mv |
Hernández, Federico Javier; Brice, Joseph; Leavitt, Christopher M.; Pino, Gustavo Ariel; Douberly, Gary E.; Infrared spectroscopy of OH··CH3OH: Hydrogen-bonded intermediate along the hydrogen abstraction reaction path; American Chemical Society; Journal of Physical Chemistry A; 119; 29; 7-2015; 8125-8132 1089-5639 1520-5215 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jpca.5b04875 info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpca.5b04875 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
American Chemical Society |
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American Chemical Society |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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