Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects

Autores
Thomas, Andrés Héctor; Lorente, Carolina; Capparelli, Alberto Luis; Pokhrel, Megh Raj; Braun, André M.; Oliveros, Esther
Año de publicación
2002
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Steady-state and time-resolved studies have been performed on four compounds of the pterin family (pterin, 6-carboxypterin, 6-formylpterin and folic acid) in aqueous solution, using the single photon counting technique. The fluorescence characteristics (spectra, quantum yields, lifetimes) of these compounds and their dependence on the pH have been investigated. Most pterins can exist in two acid–base forms over the pH range between 3 and 13. Emission spectra and excitation spectra were obtained for both forms of each compound studied. Fluorescence quantum yields (ΦF) in acidic and basic media were measured. The ΦF of folic acid (<0.005 in both media) is very low compared to those of pterin (0.27 in basic media and 0.33 in acidic media), 6-carboxypterin (0.18 in basic media and 0.28 in acidic media) and 6-formylpterin (0.07 in basic media and 0.12 in acidic; media). The variation in integrated fluorescence intensity and fluorescence lifetimes (τF) was analysed as a function of pH. Dynamic quenching by OH⁻ was observed and the corresponding bimolecular rate constants for quenching of fluorescence (kq) were calculated. The reported values for kq; (M⁻¹ s⁻¹) are 3.6 × 10⁹, 1.9 × 10⁹ and 1.1 × 10¹⁰ M⁻¹ s⁻¹ for pterin, 6-carboxypterin and 6-formylpterin, respectively.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Materia
Física
Química
steady-state studies
time-resolved studies
pterin family
photon counting technique
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/146538

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network_name_str SEDICI (UNLP)
spelling Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effectsThomas, Andrés HéctorLorente, CarolinaCapparelli, Alberto LuisPokhrel, Megh RajBraun, André M.Oliveros, EstherFísicaQuímicasteady-state studiestime-resolved studiespterin familyphoton counting techniqueSteady-state and time-resolved studies have been performed on four compounds of the pterin family (pterin, 6-carboxypterin, 6-formylpterin and folic acid) in aqueous solution, using the single photon counting technique. The fluorescence characteristics (spectra, quantum yields, lifetimes) of these compounds and their dependence on the pH have been investigated. Most pterins can exist in two acid–base forms over the pH range between 3 and 13. Emission spectra and excitation spectra were obtained for both forms of each compound studied. Fluorescence quantum yields (Φ<sub>F</sub>) in acidic and basic media were measured. The Φ<sub>F</sub> of folic acid (<0.005 in both media) is very low compared to those of pterin (0.27 in basic media and 0.33 in acidic media), 6-carboxypterin (0.18 in basic media and 0.28 in acidic media) and 6-formylpterin (0.07 in basic media and 0.12 in acidic; media). The variation in integrated fluorescence intensity and fluorescence lifetimes (τ<sub>F</sub>) was analysed as a function of pH. Dynamic quenching by OH⁻ was observed and the corresponding bimolecular rate constants for quenching of fluorescence (k<sub>q</sub>) were calculated. The reported values for k<sub>q</sub>; (M⁻¹ s⁻¹) are 3.6 × 10⁹, 1.9 × 10⁹ and 1.1 × 10¹⁰ M⁻¹ s⁻¹ for pterin, 6-carboxypterin and 6-formylpterin, respectively.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas2002-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf421-426http://sedici.unlp.edu.ar/handle/10915/146538enginfo:eu-repo/semantics/altIdentifier/issn/1474-905Xinfo:eu-repo/semantics/altIdentifier/issn/1474-9092info:eu-repo/semantics/altIdentifier/doi/10.1039/b202114einfo:eu-repo/semantics/altIdentifier/pmid/12856711info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:24:25Zoai:sedici.unlp.edu.ar:10915/146538Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:24:26.045SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
title Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
spellingShingle Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
Thomas, Andrés Héctor
Física
Química
steady-state studies
time-resolved studies
pterin family
photon counting technique
title_short Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
title_full Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
title_fullStr Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
title_full_unstemmed Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
title_sort Fluorescence of pterin, 6-formylpterin, 6-carboxypterin and folic acid in aqueous solution: pH effects
dc.creator.none.fl_str_mv Thomas, Andrés Héctor
Lorente, Carolina
Capparelli, Alberto Luis
Pokhrel, Megh Raj
Braun, André M.
Oliveros, Esther
author Thomas, Andrés Héctor
author_facet Thomas, Andrés Héctor
Lorente, Carolina
Capparelli, Alberto Luis
Pokhrel, Megh Raj
Braun, André M.
Oliveros, Esther
author_role author
author2 Lorente, Carolina
Capparelli, Alberto Luis
Pokhrel, Megh Raj
Braun, André M.
Oliveros, Esther
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Física
Química
steady-state studies
time-resolved studies
pterin family
photon counting technique
topic Física
Química
steady-state studies
time-resolved studies
pterin family
photon counting technique
dc.description.none.fl_txt_mv Steady-state and time-resolved studies have been performed on four compounds of the pterin family (pterin, 6-carboxypterin, 6-formylpterin and folic acid) in aqueous solution, using the single photon counting technique. The fluorescence characteristics (spectra, quantum yields, lifetimes) of these compounds and their dependence on the pH have been investigated. Most pterins can exist in two acid–base forms over the pH range between 3 and 13. Emission spectra and excitation spectra were obtained for both forms of each compound studied. Fluorescence quantum yields (Φ<sub>F</sub>) in acidic and basic media were measured. The Φ<sub>F</sub> of folic acid (<0.005 in both media) is very low compared to those of pterin (0.27 in basic media and 0.33 in acidic media), 6-carboxypterin (0.18 in basic media and 0.28 in acidic media) and 6-formylpterin (0.07 in basic media and 0.12 in acidic; media). The variation in integrated fluorescence intensity and fluorescence lifetimes (τ<sub>F</sub>) was analysed as a function of pH. Dynamic quenching by OH⁻ was observed and the corresponding bimolecular rate constants for quenching of fluorescence (k<sub>q</sub>) were calculated. The reported values for k<sub>q</sub>; (M⁻¹ s⁻¹) are 3.6 × 10⁹, 1.9 × 10⁹ and 1.1 × 10¹⁰ M⁻¹ s⁻¹ for pterin, 6-carboxypterin and 6-formylpterin, respectively.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
description Steady-state and time-resolved studies have been performed on four compounds of the pterin family (pterin, 6-carboxypterin, 6-formylpterin and folic acid) in aqueous solution, using the single photon counting technique. The fluorescence characteristics (spectra, quantum yields, lifetimes) of these compounds and their dependence on the pH have been investigated. Most pterins can exist in two acid–base forms over the pH range between 3 and 13. Emission spectra and excitation spectra were obtained for both forms of each compound studied. Fluorescence quantum yields (Φ<sub>F</sub>) in acidic and basic media were measured. The Φ<sub>F</sub> of folic acid (<0.005 in both media) is very low compared to those of pterin (0.27 in basic media and 0.33 in acidic media), 6-carboxypterin (0.18 in basic media and 0.28 in acidic media) and 6-formylpterin (0.07 in basic media and 0.12 in acidic; media). The variation in integrated fluorescence intensity and fluorescence lifetimes (τ<sub>F</sub>) was analysed as a function of pH. Dynamic quenching by OH⁻ was observed and the corresponding bimolecular rate constants for quenching of fluorescence (k<sub>q</sub>) were calculated. The reported values for k<sub>q</sub>; (M⁻¹ s⁻¹) are 3.6 × 10⁹, 1.9 × 10⁹ and 1.1 × 10¹⁰ M⁻¹ s⁻¹ for pterin, 6-carboxypterin and 6-formylpterin, respectively.
publishDate 2002
dc.date.none.fl_str_mv 2002-06
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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://sedici.unlp.edu.ar/handle/10915/146538
url http://sedici.unlp.edu.ar/handle/10915/146538
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1474-905X
info:eu-repo/semantics/altIdentifier/issn/1474-9092
info:eu-repo/semantics/altIdentifier/doi/10.1039/b202114e
info:eu-repo/semantics/altIdentifier/pmid/12856711
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
421-426
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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