The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals
- Autores
- Miranda, Matias Orlando; Duarte, Darío Jorge Roberto; Rayón, Victor M.
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- This article reports a theoretical study on the halogen exchange reactions YX + CHO → Y + XCHO (with Y = F, Cl, Br; X = Cl, Br, I) carried out at a high level of accuracy using coupled-cluster based methodologies including CCSD(T)-F12, CCSD(T)/CBS and CCSDT(Q)Λ. Most of the reactions are exothermic at room temperature, with the exception of the reactions FI + CHO → F + ICHO and ClI + CHO → Cl + ICHO. Exothermicity follows two concurrent trends established by the strength of the bonds being cleaved and formed: Y = F < Cl < Br (X–Y bond strength) and X = Cl > Br > I (C–X bond strength). Regarding the topology of the potential energy surfaces, we find that at the CCSD level of theory only some processes present the expected reaction profile: a pre-reactive complex (preRC) followed by a transition state (TS) and a post-reactive complex (postRC). However, when triple excitations are taken into account, all reactions become barrierless with no preRC/TS along the reaction profile. We propose that halogen-mediated interactions through the σ-hole, which represent the driving force in the early stages of the title reactions, are responsible for the absence of a tight transition state. We suggest that the strength of these interactions formed during these processes triggers the onset of the halogen atom exchange, before the preRC is formed. Therefore, this study aims to show the relevant role of halogen-mediated interactions in the mechanism of reactions in which a halogen atom is abstracted by the formyl radical (CHO).
Fil: Miranda, Matias Orlando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina
Fil: Duarte, Darío Jorge Roberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina
Fil: Rayón, Victor M.. Universidad de Valladolid. Facultad de Ciencias; España - Materia
-
Molecule-radical reactions
Potential Energy Surface
Coupled-Cluster methods
Computational Chemistry - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/279131
Ver los metadatos del registro completo
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The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicalsMiranda, Matias OrlandoDuarte, Darío Jorge RobertoRayón, Victor M.Molecule-radical reactionsPotential Energy SurfaceCoupled-Cluster methodsComputational Chemistryhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1This article reports a theoretical study on the halogen exchange reactions YX + CHO → Y + XCHO (with Y = F, Cl, Br; X = Cl, Br, I) carried out at a high level of accuracy using coupled-cluster based methodologies including CCSD(T)-F12, CCSD(T)/CBS and CCSDT(Q)Λ. Most of the reactions are exothermic at room temperature, with the exception of the reactions FI + CHO → F + ICHO and ClI + CHO → Cl + ICHO. Exothermicity follows two concurrent trends established by the strength of the bonds being cleaved and formed: Y = F < Cl < Br (X–Y bond strength) and X = Cl > Br > I (C–X bond strength). Regarding the topology of the potential energy surfaces, we find that at the CCSD level of theory only some processes present the expected reaction profile: a pre-reactive complex (preRC) followed by a transition state (TS) and a post-reactive complex (postRC). However, when triple excitations are taken into account, all reactions become barrierless with no preRC/TS along the reaction profile. We propose that halogen-mediated interactions through the σ-hole, which represent the driving force in the early stages of the title reactions, are responsible for the absence of a tight transition state. We suggest that the strength of these interactions formed during these processes triggers the onset of the halogen atom exchange, before the preRC is formed. Therefore, this study aims to show the relevant role of halogen-mediated interactions in the mechanism of reactions in which a halogen atom is abstracted by the formyl radical (CHO).Fil: Miranda, Matias Orlando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; ArgentinaFil: Duarte, Darío Jorge Roberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; ArgentinaFil: Rayón, Victor M.. Universidad de Valladolid. Facultad de Ciencias; EspañaRoyal Society of Chemistry2025-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/279131Miranda, Matias Orlando; Duarte, Darío Jorge Roberto; Rayón, Victor M.; The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 27; 6; 1-2025; 3330-33401463-9076CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://xlink.rsc.org/?DOI=D4CP03882Ginfo:eu-repo/semantics/altIdentifier/doi/10.1039/D4CP03882Ginfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-06T12:28:52Zoai:ri.conicet.gov.ar:11336/279131instacron: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:34982026-02-06 12:28:52.327CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| title |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| spellingShingle |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals Miranda, Matias Orlando Molecule-radical reactions Potential Energy Surface Coupled-Cluster methods Computational Chemistry |
| title_short |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| title_full |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| title_fullStr |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| title_full_unstemmed |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| title_sort |
The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals |
| dc.creator.none.fl_str_mv |
Miranda, Matias Orlando Duarte, Darío Jorge Roberto Rayón, Victor M. |
| author |
Miranda, Matias Orlando |
| author_facet |
Miranda, Matias Orlando Duarte, Darío Jorge Roberto Rayón, Victor M. |
| author_role |
author |
| author2 |
Duarte, Darío Jorge Roberto Rayón, Victor M. |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Molecule-radical reactions Potential Energy Surface Coupled-Cluster methods Computational Chemistry |
| topic |
Molecule-radical reactions Potential Energy Surface Coupled-Cluster methods Computational Chemistry |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
This article reports a theoretical study on the halogen exchange reactions YX + CHO → Y + XCHO (with Y = F, Cl, Br; X = Cl, Br, I) carried out at a high level of accuracy using coupled-cluster based methodologies including CCSD(T)-F12, CCSD(T)/CBS and CCSDT(Q)Λ. Most of the reactions are exothermic at room temperature, with the exception of the reactions FI + CHO → F + ICHO and ClI + CHO → Cl + ICHO. Exothermicity follows two concurrent trends established by the strength of the bonds being cleaved and formed: Y = F < Cl < Br (X–Y bond strength) and X = Cl > Br > I (C–X bond strength). Regarding the topology of the potential energy surfaces, we find that at the CCSD level of theory only some processes present the expected reaction profile: a pre-reactive complex (preRC) followed by a transition state (TS) and a post-reactive complex (postRC). However, when triple excitations are taken into account, all reactions become barrierless with no preRC/TS along the reaction profile. We propose that halogen-mediated interactions through the σ-hole, which represent the driving force in the early stages of the title reactions, are responsible for the absence of a tight transition state. We suggest that the strength of these interactions formed during these processes triggers the onset of the halogen atom exchange, before the preRC is formed. Therefore, this study aims to show the relevant role of halogen-mediated interactions in the mechanism of reactions in which a halogen atom is abstracted by the formyl radical (CHO). Fil: Miranda, Matias Orlando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina Fil: Duarte, Darío Jorge Roberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Química Básica y Aplicada del Nordeste Argentino. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina Fil: Rayón, Victor M.. Universidad de Valladolid. Facultad de Ciencias; España |
| description |
This article reports a theoretical study on the halogen exchange reactions YX + CHO → Y + XCHO (with Y = F, Cl, Br; X = Cl, Br, I) carried out at a high level of accuracy using coupled-cluster based methodologies including CCSD(T)-F12, CCSD(T)/CBS and CCSDT(Q)Λ. Most of the reactions are exothermic at room temperature, with the exception of the reactions FI + CHO → F + ICHO and ClI + CHO → Cl + ICHO. Exothermicity follows two concurrent trends established by the strength of the bonds being cleaved and formed: Y = F < Cl < Br (X–Y bond strength) and X = Cl > Br > I (C–X bond strength). Regarding the topology of the potential energy surfaces, we find that at the CCSD level of theory only some processes present the expected reaction profile: a pre-reactive complex (preRC) followed by a transition state (TS) and a post-reactive complex (postRC). However, when triple excitations are taken into account, all reactions become barrierless with no preRC/TS along the reaction profile. We propose that halogen-mediated interactions through the σ-hole, which represent the driving force in the early stages of the title reactions, are responsible for the absence of a tight transition state. We suggest that the strength of these interactions formed during these processes triggers the onset of the halogen atom exchange, before the preRC is formed. Therefore, this study aims to show the relevant role of halogen-mediated interactions in the mechanism of reactions in which a halogen atom is abstracted by the formyl radical (CHO). |
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2025 |
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2025-01 |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/279131 Miranda, Matias Orlando; Duarte, Darío Jorge Roberto; Rayón, Victor M.; The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 27; 6; 1-2025; 3330-3340 1463-9076 CONICET Digital CONICET |
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http://hdl.handle.net/11336/279131 |
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Miranda, Matias Orlando; Duarte, Darío Jorge Roberto; Rayón, Victor M.; The influence of halogen-mediated interactions on halogen abstraction reactions by formyl radicals; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 27; 6; 1-2025; 3330-3340 1463-9076 CONICET Digital CONICET |
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eng |
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eng |
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Royal Society of Chemistry |
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Royal Society of Chemistry |
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