Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution

Autores
Ruiz Hidalgo, José; Brandan, Silvia Antonia
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Theoretical studies based on the density functional theory (DFT) have been performed to study structural and vibrational properties of the free base, cationic, and hydrochloride species of narcotic tramadol agent in the gas phase and aqueous solution. In both media, B3LYP/6-31G* calculations were used while in solution, the self-consistent reaction field (SCRF) method together with the integral equation formalism variant polarised continuum (IEFPCM) and universal solvation model density (SMD) models have been employed because these models consider the solvent effects. The vibrational studies have revealed that the species cationic is present in the solid phase because the most intense band predicted for the hydrochloride in infrared and Raman spectra is not observed in the experimental spectra. The harmonic force fields, together with the normal internal coordinates and scaling factors, have allowed the complete vibrational assignments of 126, 129, and 132 vibration modes expected for the free base, cationic, and hydrochloride species, respectively, by using the SQMFF methodology. The cationic species evidence the most negative solvation energy and higher hydration in solution in agreement with its lower stability, while the hydrochloride species is the most reactive in solution. MK charges and NBO and AIM studies support cationic species' instability due to the positive charge on N atom. Comparisons of the experimental UV spectrum of hydrochloride tramadol with the predicted for the three species suggest that the free base, cationic, and hydrochloride species can be present in solution. Comparisons of predicted infrared, Raman,1H, and13 C NMR and electronic spectra for the free base, cationic, and hydrochloride species of tramadol with the corresponding experimental ones have evidenced reasonable correlations for the cationic species showing that this species present in the solid phase and in solution.
Fil: Ruiz Hidalgo, José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; 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
DFT CALCULATIONS
MOLECULAR STRUCTURE
TRAMADOL
VIBRATIONAL SPECTRA
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/171003

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network_name_str CONICET Digital (CONICET)
spelling Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solutionRuiz Hidalgo, JoséBrandan, Silvia AntoniaDFT CALCULATIONSMOLECULAR STRUCTURETRAMADOLVIBRATIONAL SPECTRAhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Theoretical studies based on the density functional theory (DFT) have been performed to study structural and vibrational properties of the free base, cationic, and hydrochloride species of narcotic tramadol agent in the gas phase and aqueous solution. In both media, B3LYP/6-31G* calculations were used while in solution, the self-consistent reaction field (SCRF) method together with the integral equation formalism variant polarised continuum (IEFPCM) and universal solvation model density (SMD) models have been employed because these models consider the solvent effects. The vibrational studies have revealed that the species cationic is present in the solid phase because the most intense band predicted for the hydrochloride in infrared and Raman spectra is not observed in the experimental spectra. The harmonic force fields, together with the normal internal coordinates and scaling factors, have allowed the complete vibrational assignments of 126, 129, and 132 vibration modes expected for the free base, cationic, and hydrochloride species, respectively, by using the SQMFF methodology. The cationic species evidence the most negative solvation energy and higher hydration in solution in agreement with its lower stability, while the hydrochloride species is the most reactive in solution. MK charges and NBO and AIM studies support cationic species' instability due to the positive charge on N atom. Comparisons of the experimental UV spectrum of hydrochloride tramadol with the predicted for the three species suggest that the free base, cationic, and hydrochloride species can be present in solution. Comparisons of predicted infrared, Raman,1H, and13 C NMR and electronic spectra for the free base, cationic, and hydrochloride species of tramadol with the corresponding experimental ones have evidenced reasonable correlations for the cationic species showing that this species present in the solid phase and in solution.Fil: Ruiz Hidalgo, José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; ArgentinaFil: Brandan, Silvia Antonia. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; ArgentinaAMG Transcend Association2021-02info: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/11336/171003Ruiz Hidalgo, José; Brandan, Silvia Antonia; Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution; AMG Transcend Association; Biointerface Research in Applied Chemistry; 11; 5; 2-2021; 13064-130882069-5837CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://biointerfaceresearch.com/?page_id=7490info:eu-repo/semantics/altIdentifier/doi/10.33263/BRIAC115.1306413088info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:57:46Zoai:ri.conicet.gov.ar:11336/171003instacron: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 09:57:46.378CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
title Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
spellingShingle Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
Ruiz Hidalgo, José
DFT CALCULATIONS
MOLECULAR STRUCTURE
TRAMADOL
VIBRATIONAL SPECTRA
title_short Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
title_full Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
title_fullStr Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
title_full_unstemmed Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
title_sort Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution
dc.creator.none.fl_str_mv Ruiz Hidalgo, José
Brandan, Silvia Antonia
author Ruiz Hidalgo, José
author_facet Ruiz Hidalgo, José
Brandan, Silvia Antonia
author_role author
author2 Brandan, Silvia Antonia
author2_role author
dc.subject.none.fl_str_mv DFT CALCULATIONS
MOLECULAR STRUCTURE
TRAMADOL
VIBRATIONAL SPECTRA
topic DFT CALCULATIONS
MOLECULAR STRUCTURE
TRAMADOL
VIBRATIONAL SPECTRA
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Theoretical studies based on the density functional theory (DFT) have been performed to study structural and vibrational properties of the free base, cationic, and hydrochloride species of narcotic tramadol agent in the gas phase and aqueous solution. In both media, B3LYP/6-31G* calculations were used while in solution, the self-consistent reaction field (SCRF) method together with the integral equation formalism variant polarised continuum (IEFPCM) and universal solvation model density (SMD) models have been employed because these models consider the solvent effects. The vibrational studies have revealed that the species cationic is present in the solid phase because the most intense band predicted for the hydrochloride in infrared and Raman spectra is not observed in the experimental spectra. The harmonic force fields, together with the normal internal coordinates and scaling factors, have allowed the complete vibrational assignments of 126, 129, and 132 vibration modes expected for the free base, cationic, and hydrochloride species, respectively, by using the SQMFF methodology. The cationic species evidence the most negative solvation energy and higher hydration in solution in agreement with its lower stability, while the hydrochloride species is the most reactive in solution. MK charges and NBO and AIM studies support cationic species' instability due to the positive charge on N atom. Comparisons of the experimental UV spectrum of hydrochloride tramadol with the predicted for the three species suggest that the free base, cationic, and hydrochloride species can be present in solution. Comparisons of predicted infrared, Raman,1H, and13 C NMR and electronic spectra for the free base, cationic, and hydrochloride species of tramadol with the corresponding experimental ones have evidenced reasonable correlations for the cationic species showing that this species present in the solid phase and in solution.
Fil: Ruiz Hidalgo, José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina. Universidad Nacional de Tucuman. Facultad de Bioquimica, Quimica y Farmacia. Instituto de Quimica Inorganica. Cátedra de Química General.; 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 Theoretical studies based on the density functional theory (DFT) have been performed to study structural and vibrational properties of the free base, cationic, and hydrochloride species of narcotic tramadol agent in the gas phase and aqueous solution. In both media, B3LYP/6-31G* calculations were used while in solution, the self-consistent reaction field (SCRF) method together with the integral equation formalism variant polarised continuum (IEFPCM) and universal solvation model density (SMD) models have been employed because these models consider the solvent effects. The vibrational studies have revealed that the species cationic is present in the solid phase because the most intense band predicted for the hydrochloride in infrared and Raman spectra is not observed in the experimental spectra. The harmonic force fields, together with the normal internal coordinates and scaling factors, have allowed the complete vibrational assignments of 126, 129, and 132 vibration modes expected for the free base, cationic, and hydrochloride species, respectively, by using the SQMFF methodology. The cationic species evidence the most negative solvation energy and higher hydration in solution in agreement with its lower stability, while the hydrochloride species is the most reactive in solution. MK charges and NBO and AIM studies support cationic species' instability due to the positive charge on N atom. Comparisons of the experimental UV spectrum of hydrochloride tramadol with the predicted for the three species suggest that the free base, cationic, and hydrochloride species can be present in solution. Comparisons of predicted infrared, Raman,1H, and13 C NMR and electronic spectra for the free base, cationic, and hydrochloride species of tramadol with the corresponding experimental ones have evidenced reasonable correlations for the cationic species showing that this species present in the solid phase and in solution.
publishDate 2021
dc.date.none.fl_str_mv 2021-02
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/11336/171003
Ruiz Hidalgo, José; Brandan, Silvia Antonia; Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution; AMG Transcend Association; Biointerface Research in Applied Chemistry; 11; 5; 2-2021; 13064-13088
2069-5837
CONICET Digital
CONICET
url http://hdl.handle.net/11336/171003
identifier_str_mv Ruiz Hidalgo, José; Brandan, Silvia Antonia; Theoretical DFT studies on free base, cationic and hydrochloride species of narcotic tramadol agent in gas phase and aqueous solution; AMG Transcend Association; Biointerface Research in Applied Chemistry; 11; 5; 2-2021; 13064-13088
2069-5837
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://biointerfaceresearch.com/?page_id=7490
info:eu-repo/semantics/altIdentifier/doi/10.33263/BRIAC115.1306413088
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv AMG Transcend Association
publisher.none.fl_str_mv AMG Transcend Association
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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