Triplet Excited State Behavior of Naphthalene-Based Pseudopeptides in the Presence of Energy Donors
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Otros documentos de la autoría: Bonancía, Paula; Vigara, Laura; Galindo, Francisco; Luis, Santiago V.; Jiménez, M. Consuelo; Miranda, Miguel A.
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
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http://dx.doi.org/10.1021/jp304883u |
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Título
Triplet Excited State Behavior of Naphthalene-Based Pseudopeptides in the Presence of Energy DonorsAutoría
Fecha de publicación
2012Editor
American Chemical SocietyISSN
1520-6106Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://pubs.acs.org/doi/abs/10.1021/jp304883uPalabras clave / Materias
Resumen
In this work, the triplet state behavior of naphthalene-based pseudopeptides with amide-based macrocyclic or lateral chain substructures has been investigated in the presence of benzophenone and/or biphenyl, as suitable ... [+]
In this work, the triplet state behavior of naphthalene-based pseudopeptides with amide-based macrocyclic or lateral chain substructures has been investigated in the presence of benzophenone and/or biphenyl, as suitable energy-donating chromophores. Their behavior has been compared with that of 1,4-dimethylnaphthalene as model compound. In all the cases, the triplet–triplet absorption of naphthalene is detected by transient absorption spectroscopy, upon selective excitation of benzophenone at 355 nm. The kinetics of formation and decay of this species is markedly slower in the pseudopeptides, due to retardation of triplet–triplet energy transfer and exciplex formation. Finally, the delayed fluorescence detected in the model naphthalene is absent in the pseudopeptides. The concept can, in principle, be exploited for the study of excited-state interactions in supramolecular systems. [-]
Publicado en
The Journal of Physical Chemistry B, 116, 33Derechos de acceso
Copyright © 2012 American Chemical Society
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