Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids

Autores
Tarzi, Olga Inés; Erra Balsells, Rosa
Año de publicación
2006
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The UV-absorption, fluorescence excitation and emission spectra of the 6-chloro-, 8-chloro-, 6,8-dichloro-derivatives of nor-harmane, harmane and harmine and the 8-chloro-derivative of harmol were studied. These studies were performed in EtOH and in EtOH + 1% perchloric acid solutions (pa). Furthermore, fluorescence quantum yields (ϕf) in both media and in acetonitrile and acetonitrile + 1% perchloric acid solutions at 298 K were measured. The HOMO and LUMO energy, the positions (λmax) and oscillator strength (f) of the 1S1 ← 1S0 band for all the neutral and protonated β-carbolines studied were calculated and compared with the experimental data. The pKa values in aqueous solution for for 6-chloro-, 8-chloro- and 6,8-dichloro-nor-harmane, harmane and harmine and 8-chloro-harmol were spectrophotometrically measured . The change of the acid–base character of these compounds on going from the ground state (pKa) to the first electronic excited singlet state as , in ethanol solution at 298 K were calculated (ΔpKa(EtOH)). Ground-state proton affinity (PA) for all the compounds studied defined as minus the enthalpy change of the reaction M + H+ → MH+ (gas state) were calculated. Basicity relative to pyridine (ΔHrPy) defined as the enthalpy change of the isodesmic reaction MH+ + Py → M + PyH+ in gas state and in water solution, were also calculated (ab initio calculations). The effect of chlorine as substituent on the photochemistry and acid–base properties of the β-carboline alkaloids is discussed.
Fil: Tarzi, Olga Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina
Fil: Erra Balsells, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina
Materia
carbolines
chloro-carbolines
UV
Absroption
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:11336/279573

id CONICETDig_aa8ca9d8c9d5093dcb868ed87eaccb75
oai_identifier_str oai:ri.conicet.gov.ar:11336/279573
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloidsTarzi, Olga InésErra Balsells, Rosacarbolineschloro-carbolinesUVAbsroptionhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The UV-absorption, fluorescence excitation and emission spectra of the 6-chloro-, 8-chloro-, 6,8-dichloro-derivatives of nor-harmane, harmane and harmine and the 8-chloro-derivative of harmol were studied. These studies were performed in EtOH and in EtOH + 1% perchloric acid solutions (pa). Furthermore, fluorescence quantum yields (ϕf) in both media and in acetonitrile and acetonitrile + 1% perchloric acid solutions at 298 K were measured. The HOMO and LUMO energy, the positions (λmax) and oscillator strength (f) of the 1S1 ← 1S0 band for all the neutral and protonated β-carbolines studied were calculated and compared with the experimental data. The pKa values in aqueous solution for for 6-chloro-, 8-chloro- and 6,8-dichloro-nor-harmane, harmane and harmine and 8-chloro-harmol were spectrophotometrically measured . The change of the acid–base character of these compounds on going from the ground state (pKa) to the first electronic excited singlet state as , in ethanol solution at 298 K were calculated (ΔpKa(EtOH)). Ground-state proton affinity (PA) for all the compounds studied defined as minus the enthalpy change of the reaction M + H+ → MH+ (gas state) were calculated. Basicity relative to pyridine (ΔHrPy) defined as the enthalpy change of the isodesmic reaction MH+ + Py → M + PyH+ in gas state and in water solution, were also calculated (ab initio calculations). The effect of chlorine as substituent on the photochemistry and acid–base properties of the β-carboline alkaloids is discussed.Fil: Tarzi, Olga Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; ArgentinaFil: Erra Balsells, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; ArgentinaElsevier Science SA2006-12info: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/11336/279573Tarzi, Olga Inés; Erra Balsells, Rosa; Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids; Elsevier Science SA; Journal of Photochemistry and Photobiology B: Biology; 82; 2; 12-2006; 79-931011-1344CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1011134405001806info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotobiol.2005.09.001info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-06T12:29:12Zoai:ri.conicet.gov.ar:11336/279573instacron: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 12:29:13.139CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
title Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
spellingShingle Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
Tarzi, Olga Inés
carbolines
chloro-carbolines
UV
Absroption
title_short Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
title_full Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
title_fullStr Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
title_full_unstemmed Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
title_sort Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids
dc.creator.none.fl_str_mv Tarzi, Olga Inés
Erra Balsells, Rosa
author Tarzi, Olga Inés
author_facet Tarzi, Olga Inés
Erra Balsells, Rosa
author_role author
author2 Erra Balsells, Rosa
author2_role author
dc.subject.none.fl_str_mv carbolines
chloro-carbolines
UV
Absroption
topic carbolines
chloro-carbolines
UV
Absroption
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The UV-absorption, fluorescence excitation and emission spectra of the 6-chloro-, 8-chloro-, 6,8-dichloro-derivatives of nor-harmane, harmane and harmine and the 8-chloro-derivative of harmol were studied. These studies were performed in EtOH and in EtOH + 1% perchloric acid solutions (pa). Furthermore, fluorescence quantum yields (ϕf) in both media and in acetonitrile and acetonitrile + 1% perchloric acid solutions at 298 K were measured. The HOMO and LUMO energy, the positions (λmax) and oscillator strength (f) of the 1S1 ← 1S0 band for all the neutral and protonated β-carbolines studied were calculated and compared with the experimental data. The pKa values in aqueous solution for for 6-chloro-, 8-chloro- and 6,8-dichloro-nor-harmane, harmane and harmine and 8-chloro-harmol were spectrophotometrically measured . The change of the acid–base character of these compounds on going from the ground state (pKa) to the first electronic excited singlet state as , in ethanol solution at 298 K were calculated (ΔpKa(EtOH)). Ground-state proton affinity (PA) for all the compounds studied defined as minus the enthalpy change of the reaction M + H+ → MH+ (gas state) were calculated. Basicity relative to pyridine (ΔHrPy) defined as the enthalpy change of the isodesmic reaction MH+ + Py → M + PyH+ in gas state and in water solution, were also calculated (ab initio calculations). The effect of chlorine as substituent on the photochemistry and acid–base properties of the β-carboline alkaloids is discussed.
Fil: Tarzi, Olga Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina
Fil: Erra Balsells, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina
description The UV-absorption, fluorescence excitation and emission spectra of the 6-chloro-, 8-chloro-, 6,8-dichloro-derivatives of nor-harmane, harmane and harmine and the 8-chloro-derivative of harmol were studied. These studies were performed in EtOH and in EtOH + 1% perchloric acid solutions (pa). Furthermore, fluorescence quantum yields (ϕf) in both media and in acetonitrile and acetonitrile + 1% perchloric acid solutions at 298 K were measured. The HOMO and LUMO energy, the positions (λmax) and oscillator strength (f) of the 1S1 ← 1S0 band for all the neutral and protonated β-carbolines studied were calculated and compared with the experimental data. The pKa values in aqueous solution for for 6-chloro-, 8-chloro- and 6,8-dichloro-nor-harmane, harmane and harmine and 8-chloro-harmol were spectrophotometrically measured . The change of the acid–base character of these compounds on going from the ground state (pKa) to the first electronic excited singlet state as , in ethanol solution at 298 K were calculated (ΔpKa(EtOH)). Ground-state proton affinity (PA) for all the compounds studied defined as minus the enthalpy change of the reaction M + H+ → MH+ (gas state) were calculated. Basicity relative to pyridine (ΔHrPy) defined as the enthalpy change of the isodesmic reaction MH+ + Py → M + PyH+ in gas state and in water solution, were also calculated (ab initio calculations). The effect of chlorine as substituent on the photochemistry and acid–base properties of the β-carboline alkaloids is discussed.
publishDate 2006
dc.date.none.fl_str_mv 2006-12
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/11336/279573
Tarzi, Olga Inés; Erra Balsells, Rosa; Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids; Elsevier Science SA; Journal of Photochemistry and Photobiology B: Biology; 82; 2; 12-2006; 79-93
1011-1344
CONICET Digital
CONICET
url http://hdl.handle.net/11336/279573
identifier_str_mv Tarzi, Olga Inés; Erra Balsells, Rosa; Effect of chlorine as substituent on the photochemistry and acid–base properties of β-carboline alkaloids; Elsevier Science SA; Journal of Photochemistry and Photobiology B: Biology; 82; 2; 12-2006; 79-93
1011-1344
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.sciencedirect.com/science/article/abs/pii/S1011134405001806
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jphotobiol.2005.09.001
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 Elsevier Science SA
publisher.none.fl_str_mv Elsevier Science SA
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_ 1856403122011766784
score 13.106097