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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/279573
Ver los metadatos del registro completo
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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 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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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 |
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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 |
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eng |
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eng |
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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 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf application/pdf |
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Elsevier Science SA |
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Elsevier Science SA |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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