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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/141566
Ver los metadatos del registro completo
id |
CONICETDig_ca10a298057600c78b0aaf4ab1de2d0b |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/141566 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
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 |
_version_ |
1842269201476091904 |
score |
13.13397 |