Confinement effects in protonation reactions catalyzed by zeolites with large void structures

Autores
Zalazar, María Fernanda; Cabral, Néstor Damián; Romero Ojeda, Gonzalo David; Alegre, Clara Iris Aymará; Peruchena, Nélida María
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil: Zalazar, María Fernanda. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Zalazar, María Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Cabral, Néstor Damián. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.
Fil: Romero Ojeda, Gonzalo David. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.
Fil: Alegre, Clara Iris Aymará. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Alegre, Clara Iris Aymará. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Peruchena, Nélida María. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Peruchena, Nélida María. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Procesos Biotecnológicos y Químicos; Argentina.
In the present work, we studied the protonation reaction of styrene inside the cavity of acidic H-Y zeolite. Density functional theory calculation using M06-2X functional and analysis of quantum theory of atoms in molecules are used to investigate the confinement effects of zeolite framework on species involved on the reaction. A detailed analysis of the topology of the electron density of interactions among reactants, transition state, and intermediate products with the cavity of H-Y zeolite is performed, extracting conclusions about adsorption, catalysis, and confinement effects. Identification and quantification of host−guest interactions between zeolite framework and styryl cation support the larger contribution of weak closed-shell interactions in stabilization of the formed carbenium ion. Our results clearly show that reaction energies for all formed species inside a zeolite with large void structure are also significantly governed by the confinement effects related to weak host−guest interactions. In other words, zeolite confinement effect is a crucial factor that may affect the catalytic activity even on zeolites with large pore size and void structure as H-Y.
Fuente
Journal of Physical Chemistry A, 2018, vol. 122, no. 48, p. 27350-27359.
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)
Institución
Universidad Nacional del Nordeste
OAI Identificador
oai:repositorio.unne.edu.ar:123456789/59349

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network_name_str Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)
spelling Confinement effects in protonation reactions catalyzed by zeolites with large void structuresZalazar, María FernandaCabral, Néstor DamiánRomero Ojeda, Gonzalo DavidAlegre, Clara Iris AymaráPeruchena, Nélida MaríaFil: Zalazar, María Fernanda. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.Fil: Zalazar, María Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.Fil: Cabral, Néstor Damián. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.Fil: Romero Ojeda, Gonzalo David. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.Fil: Alegre, Clara Iris Aymará. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.Fil: Alegre, Clara Iris Aymará. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.Fil: Peruchena, Nélida María. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.Fil: Peruchena, Nélida María. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Procesos Biotecnológicos y Químicos; Argentina.In the present work, we studied the protonation reaction of styrene inside the cavity of acidic H-Y zeolite. Density functional theory calculation using M06-2X functional and analysis of quantum theory of atoms in molecules are used to investigate the confinement effects of zeolite framework on species involved on the reaction. A detailed analysis of the topology of the electron density of interactions among reactants, transition state, and intermediate products with the cavity of H-Y zeolite is performed, extracting conclusions about adsorption, catalysis, and confinement effects. Identification and quantification of host−guest interactions between zeolite framework and styryl cation support the larger contribution of weak closed-shell interactions in stabilization of the formed carbenium ion. Our results clearly show that reaction energies for all formed species inside a zeolite with large void structure are also significantly governed by the confinement effects related to weak host−guest interactions. In other words, zeolite confinement effect is a crucial factor that may affect the catalytic activity even on zeolites with large pore size and void structure as H-Y.American Chemical Society2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfp. 27350-27359application/pdfZalazar, María Fernanda, et al., 2018. Confinement effects in protonation reactions catalyzed by zeolites with large void structures. Journal of Physical Chemistry A. Washington: American Chemical Society, vol. 122, no. 48, p. 27350-27359. E-ISSN 1520-5215.1089-5639http://repositorio.unne.edu.ar/handle/123456789/59349Journal of Physical Chemistry A, 2018, vol. 122, no. 48, p. 27350-27359.reponame:Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)instname:Universidad Nacional del Nordesteenghttps://pubs.acs.org/doi/10.1021/acs.jpcc.8b07357info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/2.5/ar/Atribución-NoComercial-SinDerivadas 2.5 Argentina2026-01-08T11:17:35Zoai:repositorio.unne.edu.ar:123456789/59349instacron:UNNEInstitucionalhttp://repositorio.unne.edu.ar/Universidad públicaNo correspondehttp://repositorio.unne.edu.ar/oaiososa@bib.unne.edu.ar;sergio.alegria@unne.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:48712026-01-08 11:17:36.25Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) - Universidad Nacional del Nordestefalse
dc.title.none.fl_str_mv Confinement effects in protonation reactions catalyzed by zeolites with large void structures
title Confinement effects in protonation reactions catalyzed by zeolites with large void structures
spellingShingle Confinement effects in protonation reactions catalyzed by zeolites with large void structures
Zalazar, María Fernanda
title_short Confinement effects in protonation reactions catalyzed by zeolites with large void structures
title_full Confinement effects in protonation reactions catalyzed by zeolites with large void structures
title_fullStr Confinement effects in protonation reactions catalyzed by zeolites with large void structures
title_full_unstemmed Confinement effects in protonation reactions catalyzed by zeolites with large void structures
title_sort Confinement effects in protonation reactions catalyzed by zeolites with large void structures
dc.creator.none.fl_str_mv Zalazar, María Fernanda
Cabral, Néstor Damián
Romero Ojeda, Gonzalo David
Alegre, Clara Iris Aymará
Peruchena, Nélida María
author Zalazar, María Fernanda
author_facet Zalazar, María Fernanda
Cabral, Néstor Damián
Romero Ojeda, Gonzalo David
Alegre, Clara Iris Aymará
Peruchena, Nélida María
author_role author
author2 Cabral, Néstor Damián
Romero Ojeda, Gonzalo David
Alegre, Clara Iris Aymará
Peruchena, Nélida María
author2_role author
author
author
author
dc.description.none.fl_txt_mv Fil: Zalazar, María Fernanda. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Zalazar, María Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Cabral, Néstor Damián. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.
Fil: Romero Ojeda, Gonzalo David. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura Universidad Nacional del Nordeste; Argentina.
Fil: Alegre, Clara Iris Aymará. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Alegre, Clara Iris Aymará. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Peruchena, Nélida María. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Peruchena, Nélida María. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Procesos Biotecnológicos y Químicos; Argentina.
In the present work, we studied the protonation reaction of styrene inside the cavity of acidic H-Y zeolite. Density functional theory calculation using M06-2X functional and analysis of quantum theory of atoms in molecules are used to investigate the confinement effects of zeolite framework on species involved on the reaction. A detailed analysis of the topology of the electron density of interactions among reactants, transition state, and intermediate products with the cavity of H-Y zeolite is performed, extracting conclusions about adsorption, catalysis, and confinement effects. Identification and quantification of host−guest interactions between zeolite framework and styryl cation support the larger contribution of weak closed-shell interactions in stabilization of the formed carbenium ion. Our results clearly show that reaction energies for all formed species inside a zeolite with large void structure are also significantly governed by the confinement effects related to weak host−guest interactions. In other words, zeolite confinement effect is a crucial factor that may affect the catalytic activity even on zeolites with large pore size and void structure as H-Y.
description Fil: Zalazar, María Fernanda. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
publishDate 2018
dc.date.none.fl_str_mv 2018
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 Zalazar, María Fernanda, et al., 2018. Confinement effects in protonation reactions catalyzed by zeolites with large void structures. Journal of Physical Chemistry A. Washington: American Chemical Society, vol. 122, no. 48, p. 27350-27359. E-ISSN 1520-5215.
1089-5639
http://repositorio.unne.edu.ar/handle/123456789/59349
identifier_str_mv Zalazar, María Fernanda, et al., 2018. Confinement effects in protonation reactions catalyzed by zeolites with large void structures. Journal of Physical Chemistry A. Washington: American Chemical Society, vol. 122, no. 48, p. 27350-27359. E-ISSN 1520-5215.
1089-5639
url http://repositorio.unne.edu.ar/handle/123456789/59349
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://pubs.acs.org/doi/10.1021/acs.jpcc.8b07357
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Atribución-NoComercial-SinDerivadas 2.5 Argentina
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Atribución-NoComercial-SinDerivadas 2.5 Argentina
dc.format.none.fl_str_mv application/pdf
p. 27350-27359
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv Journal of Physical Chemistry A, 2018, vol. 122, no. 48, p. 27350-27359.
reponame:Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)
instname:Universidad Nacional del Nordeste
reponame_str Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)
collection Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)
instname_str Universidad Nacional del Nordeste
repository.name.fl_str_mv Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) - Universidad Nacional del Nordeste
repository.mail.fl_str_mv ososa@bib.unne.edu.ar;sergio.alegria@unne.edu.ar
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