Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/7789
DC FieldValueLanguage
dc.contributor.authorBurrows, H.-
dc.contributor.authorFonseca, S.-
dc.contributor.authorGigante, B.-
dc.contributor.authorEsteves, M.-
dc.contributor.authorGuerreiro, A.-
dc.date.accessioned2009-02-17T10:33:53Z-
dc.date.available2009-02-17T10:33:53Z-
dc.date.issued2006en_US
dc.identifier.citationJournal of Fluorescence. 16:2 (2006) 227-231en_US
dc.identifier.urihttps://hdl.handle.net/10316/7789-
dc.description.abstractThe absorption and fluorescence spectra, lifetimes and quantum yields of a series of triarylaminequinoxaline bipolar compounds, with and without the bulky dehydroabietic acid group, have been studied in toluene solution. This bulky group is introduced to improve solubility and thermal properties of these systems. It is shown that this does not affect their spectral or photophysical behavior. The compounds show relatively strong fluorescence, with the emission maximum strongly dependent upon the substituents present. Oxidation potentials have also been determined in acetonitrile solution, and again indicate that introduction of the resin acid moiety has no effect on these properties.en_US
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleFluorescence Study of Dehydroabietic Acid-Based Bipolar Arylamine-Quinoxalinesen_US
dc.typearticleen_US
dc.identifier.doi10.1007/s10895-005-0048-6en_US
uc.controloAutoridadeSim-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-3127-2298-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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