Revealing competitive Förster-type resonance energy-transfer pathways in single bichromophoric molecules

Johan Hofkens(Heidelberg University), Mircea Cotlet(University of Arizona), Tom Vosch(University of Arizona), Philip Tinnefeld(Heidelberg University), Kenneth D. Weston(Heidelberg University), Christophe Ego(Heidelberg University), Andrew C. Grimsdale(Heidelberg University), Kläus Müllen(Heidelberg University), David Beljonne(Heidelberg University), Jean Luc Brédas(Heidelberg University), Sven Jordens(University of Arizona), Gerd Schweitzer(University of Arizona), Markus Sauer(Heidelberg University), Frans De Schryver(University of Arizona)
Proceedings of the National Academy of Sciences
October 28, 2003
Cited by 178Open Access
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Abstract

We demonstrate measurements of the efficiency of competing Förster-type energy-transfer pathways in single bichromophoric systems by monitoring simultaneously the fluorescence intensity, fluorescence lifetime, and the number of independent emitters with time. Peryleneimide end-capped fluorene trimers, hexamers, and polymers with interchromophore distances of 3.4, 5.9, and on average 42 nm, respectively, served as bichromophoric systems. Because of different energy-transfer efficiencies, variations in the interchromophore distance enable the switching between homo-energy transfer (energy hopping), singlet-singlet annihilation, and singlet-triplet annihilation. The data suggest that similar energy-transfer pathways have to be considered in the analysis of single-molecule trajectories of donor/acceptor pairs as well as in natural and synthetic multichromophoric systems such as light-harvesting antennas, oligomeric fluorescent proteins, and dendrimers. Here we report selectively visualization of different energy-transfer pathways taking place between identical fluorophores in individual bichromophoric molecules.


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