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dc.contributor.author
Denofrio, Maria Paula

dc.contributor.author
Thomas, Andrés Héctor

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Braun, André M.
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Oliveros, Esther
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Lorente, Carolina

dc.date.available
2025-02-06T13:22:09Z
dc.date.issued
2010-07
dc.identifier.citation
Denofrio, Maria Paula; Thomas, Andrés Héctor; Braun, André M.; Oliveros, Esther; Lorente, Carolina; Comment on “Excited-State Intermolecular Proton Transfer of Lumazine”; American Chemical Society; Journal of Physical Chemistry C; 114; 33; 7-2010; 14307-14308
dc.identifier.issn
1932-7447
dc.identifier.uri
http://hdl.handle.net/11336/253692
dc.description.abstract
A critical comment on excited-state intermolar proton transfer of lumazine was discussed. In their article, Hupper and co-researchers reported the emission properties of lumazine (Lum) using steady-state and time-resolved emission techniques. They also reported the absorption spectra at different pH and they evaluated the pKa value in water to be about 10.5. Hupper do not mention how the pH was measured. The critic´s results on emission of Lum indicate that the fluorescence of Lum is quenched by hydroxide anions, and consequently, a decrease of the fluorescence is observed at pH higher than 10.5. Hupper and co-researchers did not refer the tautomerism of Lum, which implies different atoms participating in proton transfer they also postulate. Indeed, they discuss the inter-molecular proton transfer in the excited state of Lum, but they analyzed the tautomeric forms of Lum neither in the ground state nor in the excited state.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society

dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Lumazine
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Photochemistry
dc.subject.classification
Físico-Química, Ciencia de los Polímeros, Electroquímica

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Ciencias Químicas

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CIENCIAS NATURALES Y EXACTAS

dc.title
Comment on “Excited-State Intermolecular Proton Transfer of Lumazine”
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2024-08-19T11:41:17Z
dc.journal.volume
114
dc.journal.number
33
dc.journal.pagination
14307-14308
dc.journal.pais
Estados Unidos

dc.description.fil
Fil: Denofrio, Maria Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
dc.description.fil
Fil: Thomas, Andrés Héctor. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
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Fil: Braun, André M.. Karlsruhe Institute of Technology; Alemania
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Fil: Oliveros, Esther. Université Paul Sabatier; Francia
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Fil: Lorente, Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
dc.journal.title
Journal of Physical Chemistry C

dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/jp103900j
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1021/jp103900j
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