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dc.contributor.authorYousaf M.
dc.contributor.authorZarate X.
dc.contributor.authorSchott E.
dc.contributor.authorLough A.J.
dc.contributor.authorKoivisto B.D.
dc.date.accessioned2020-09-02T22:30:37Z
dc.date.available2020-09-02T22:30:37Z
dc.date.issued2018
dc.identifier10.1039/c8ra03384f
dc.identifier.citation8, 50, 28533-28537
dc.identifier.issn20462069
dc.identifier.urihttps://hdl.handle.net/20.500.12728/6652
dc.descriptionThe synthesis and study of a family of BODIPY-phenylacetylene macrocycles where donor groups have been added to the macrocycle in order to tune the physicochemical properties and absorption profile is reported. Energy transfer is observed between this phenylacetylene antennae and BODIPY core and fluorescence emission from the BODIPY, at any excitation wavelength, is consistent with energy transfer from the macrocycle. © The Royal Society of Chemistry.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.titlePhotophysical behaviour of BODIPY-phenylacetylene macrocyclic dyads for light-harvesting applications
dc.typeArticle


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