Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts

Autores
Iramain, Maximiliano Alberto; Brandan, Silvia Antonia
Año de publicación
2019
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In this work, the role of halogen F---H bonds in potassium 3-furoyl-trifluoroborate (FTFB), 2-isonicotinoyl-trifluoroborate (ITFB), 5-hydroxypentanoyl-trifluoroborate (HTFB), 5-Br-2-isonicotinoyl-trifluoroborate (Br-ITFB), 6-chloro-2-isonicotinoyl-trifluoroborate (Cl-ITFB), 4-fluorobenzoyl-trifluoroborate (FBTFB) and 2-phenylacetyl-trifluoroborate (PTFB) salts have been studied in gas phase and in aqueous solution by using NBO and AIM calculations with the hybrid B3LYP/6-311++G** method and the SCRF and SM models. In addition, the corrected solvation energy by using ZPVE and non electrostatic terms, volumes and gap values were evaluated as function of molecular weights of salts by using the same level of theory. The AIM calculations show that the IFTB salt present the lower F---H distances in the two media. Evidently, the presence of a pyridine ring linked to C of C=O groups in IFTB favors the formation of halogen interaction, as compared with furyl and phenyl rings. NBO studies show that the higher delocalizations energies of halogen F---H interactions are observed in the Br-ITFB salt in both media together with the ITFB and Cl-ITFB salts. This study evidence clearly that the halogen F---H interaction play a important role in the reactivity and properties of trifluoroborate salts showing that the FTFB salt has lower volume, low corrected solvation energy and is the less reactive while the most reactive Br-ITFB, Cl-ITFB and IFTB salts present high stabilization energies of halogen F---H interactions and high corrected solvation energies. The analyses of the geometrical C-C, C-B, C=O, C-C-B, C-C-O and O-C-B parameters commons at all salts have showed notable influence on the halogen F---H interactions and on the properties of trifluoroborate salts
Fil: Iramain, Maximiliano Alberto. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina
Fil: Brandan, Silvia Antonia. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; Argentina
Materia
Potassium trifluoroborate salt
DFT calculations
Vibrational spectra
molecular structure
NBO
AIM
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/141566

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oai_identifier_str oai:ri.conicet.gov.ar:11336/141566
network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling Role of Halogen F---H Bonds in Potassium Trifluoroborate SaltsIramain, Maximiliano AlbertoBrandan, Silvia AntoniaPotassium trifluoroborate saltDFT calculationsVibrational spectramolecular structureNBOAIMhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1In this work, the role of halogen F---H bonds in potassium 3-furoyl-trifluoroborate (FTFB), 2-isonicotinoyl-trifluoroborate (ITFB), 5-hydroxypentanoyl-trifluoroborate (HTFB), 5-Br-2-isonicotinoyl-trifluoroborate (Br-ITFB), 6-chloro-2-isonicotinoyl-trifluoroborate (Cl-ITFB), 4-fluorobenzoyl-trifluoroborate (FBTFB) and 2-phenylacetyl-trifluoroborate (PTFB) salts have been studied in gas phase and in aqueous solution by using NBO and AIM calculations with the hybrid B3LYP/6-311++G** method and the SCRF and SM models. In addition, the corrected solvation energy by using ZPVE and non electrostatic terms, volumes and gap values were evaluated as function of molecular weights of salts by using the same level of theory. The AIM calculations show that the IFTB salt present the lower F---H distances in the two media. Evidently, the presence of a pyridine ring linked to C of C=O groups in IFTB favors the formation of halogen interaction, as compared with furyl and phenyl rings. NBO studies show that the higher delocalizations energies of halogen F---H interactions are observed in the Br-ITFB salt in both media together with the ITFB and Cl-ITFB salts. This study evidence clearly that the halogen F---H interaction play a important role in the reactivity and properties of trifluoroborate salts showing that the FTFB salt has lower volume, low corrected solvation energy and is the less reactive while the most reactive Br-ITFB, Cl-ITFB and IFTB salts present high stabilization energies of halogen F---H interactions and high corrected solvation energies. The analyses of the geometrical C-C, C-B, C=O, C-C-B, C-C-O and O-C-B parameters commons at all salts have showed notable influence on the halogen F---H interactions and on the properties of trifluoroborate saltsFil: Iramain, Maximiliano Alberto. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; ArgentinaFil: Brandan, Silvia Antonia. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; ArgentinaIJCAR2019-06info: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/11336/141566Iramain, Maximiliano Alberto; Brandan, Silvia Antonia; Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts; IJCAR; International Journal of Current Advanced Research; 8; 6; 6-2019; 18527-185292319-6475CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.journalijcar.org/sites/default/files/issue-files/9614-A-2019_0.pdfinfo:eu-repo/semantics/altIdentifier/doi/10.24327/ijcar.2019.19253.3703info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:53:06Zoai:ri.conicet.gov.ar:11336/141566instacron: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:34982025-09-03 09:53:06.648CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
title Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
spellingShingle Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
Iramain, Maximiliano Alberto
Potassium trifluoroborate salt
DFT calculations
Vibrational spectra
molecular structure
NBO
AIM
title_short Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
title_full Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
title_fullStr Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
title_full_unstemmed Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
title_sort Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts
dc.creator.none.fl_str_mv Iramain, Maximiliano Alberto
Brandan, Silvia Antonia
author Iramain, Maximiliano Alberto
author_facet Iramain, Maximiliano Alberto
Brandan, Silvia Antonia
author_role author
author2 Brandan, Silvia Antonia
author2_role author
dc.subject.none.fl_str_mv Potassium trifluoroborate salt
DFT calculations
Vibrational spectra
molecular structure
NBO
AIM
topic Potassium trifluoroborate salt
DFT calculations
Vibrational spectra
molecular structure
NBO
AIM
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv In this work, the role of halogen F---H bonds in potassium 3-furoyl-trifluoroborate (FTFB), 2-isonicotinoyl-trifluoroborate (ITFB), 5-hydroxypentanoyl-trifluoroborate (HTFB), 5-Br-2-isonicotinoyl-trifluoroborate (Br-ITFB), 6-chloro-2-isonicotinoyl-trifluoroborate (Cl-ITFB), 4-fluorobenzoyl-trifluoroborate (FBTFB) and 2-phenylacetyl-trifluoroborate (PTFB) salts have been studied in gas phase and in aqueous solution by using NBO and AIM calculations with the hybrid B3LYP/6-311++G** method and the SCRF and SM models. In addition, the corrected solvation energy by using ZPVE and non electrostatic terms, volumes and gap values were evaluated as function of molecular weights of salts by using the same level of theory. The AIM calculations show that the IFTB salt present the lower F---H distances in the two media. Evidently, the presence of a pyridine ring linked to C of C=O groups in IFTB favors the formation of halogen interaction, as compared with furyl and phenyl rings. NBO studies show that the higher delocalizations energies of halogen F---H interactions are observed in the Br-ITFB salt in both media together with the ITFB and Cl-ITFB salts. This study evidence clearly that the halogen F---H interaction play a important role in the reactivity and properties of trifluoroborate salts showing that the FTFB salt has lower volume, low corrected solvation energy and is the less reactive while the most reactive Br-ITFB, Cl-ITFB and IFTB salts present high stabilization energies of halogen F---H interactions and high corrected solvation energies. The analyses of the geometrical C-C, C-B, C=O, C-C-B, C-C-O and O-C-B parameters commons at all salts have showed notable influence on the halogen F---H interactions and on the properties of trifluoroborate salts
Fil: Iramain, Maximiliano Alberto. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina
Fil: Brandan, Silvia Antonia. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; Argentina
description In this work, the role of halogen F---H bonds in potassium 3-furoyl-trifluoroborate (FTFB), 2-isonicotinoyl-trifluoroborate (ITFB), 5-hydroxypentanoyl-trifluoroborate (HTFB), 5-Br-2-isonicotinoyl-trifluoroborate (Br-ITFB), 6-chloro-2-isonicotinoyl-trifluoroborate (Cl-ITFB), 4-fluorobenzoyl-trifluoroborate (FBTFB) and 2-phenylacetyl-trifluoroborate (PTFB) salts have been studied in gas phase and in aqueous solution by using NBO and AIM calculations with the hybrid B3LYP/6-311++G** method and the SCRF and SM models. In addition, the corrected solvation energy by using ZPVE and non electrostatic terms, volumes and gap values were evaluated as function of molecular weights of salts by using the same level of theory. The AIM calculations show that the IFTB salt present the lower F---H distances in the two media. Evidently, the presence of a pyridine ring linked to C of C=O groups in IFTB favors the formation of halogen interaction, as compared with furyl and phenyl rings. NBO studies show that the higher delocalizations energies of halogen F---H interactions are observed in the Br-ITFB salt in both media together with the ITFB and Cl-ITFB salts. This study evidence clearly that the halogen F---H interaction play a important role in the reactivity and properties of trifluoroborate salts showing that the FTFB salt has lower volume, low corrected solvation energy and is the less reactive while the most reactive Br-ITFB, Cl-ITFB and IFTB salts present high stabilization energies of halogen F---H interactions and high corrected solvation energies. The analyses of the geometrical C-C, C-B, C=O, C-C-B, C-C-O and O-C-B parameters commons at all salts have showed notable influence on the halogen F---H interactions and on the properties of trifluoroborate salts
publishDate 2019
dc.date.none.fl_str_mv 2019-06
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/11336/141566
Iramain, Maximiliano Alberto; Brandan, Silvia Antonia; Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts; IJCAR; International Journal of Current Advanced Research; 8; 6; 6-2019; 18527-18529
2319-6475
CONICET Digital
CONICET
url http://hdl.handle.net/11336/141566
identifier_str_mv Iramain, Maximiliano Alberto; Brandan, Silvia Antonia; Role of Halogen F---H Bonds in Potassium Trifluoroborate Salts; IJCAR; International Journal of Current Advanced Research; 8; 6; 6-2019; 18527-18529
2319-6475
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://www.journalijcar.org/sites/default/files/issue-files/9614-A-2019_0.pdf
info:eu-repo/semantics/altIdentifier/doi/10.24327/ijcar.2019.19253.3703
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv IJCAR
publisher.none.fl_str_mv IJCAR
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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