A switchable self-assembling and disassembling chiral system based on a porphyrin-substituted phenylalanine–phenylalanine motif

Artificial light-harvesting systems have until now not been able to self-assemble into structures with a large photon capture cross-section that upon a stimulus reversibly can switch into an inactive state. Here we describe a simple and robust F L F L -dipeptide construct to which a meso -tetrapheny...

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Veröffentlicht in:Nature communications 2016-09, Vol.7 (1), p.12657-11, Article 12657
Hauptverfasser: Charalambidis, Georgios, Georgilis, Evangelos, Panda, Manas K., Anson, Christopher E., Powell, Annie K., Doyle, Stephen, Moss, David, Jochum, Tobias, Horton, Peter N., Coles, Simon J., Linares, Mathieu, Beljonne, David, Naubron, Jean-Valère, Conradt, Jonas, Kalt, Heinz, Mitraki, Anna, Coutsolelos, Athanassios G., Balaban, Teodor Silviu
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Sprache:eng
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Zusammenfassung:Artificial light-harvesting systems have until now not been able to self-assemble into structures with a large photon capture cross-section that upon a stimulus reversibly can switch into an inactive state. Here we describe a simple and robust F L F L -dipeptide construct to which a meso -tetraphenylporphyrin has been appended and which self-assembles to fibrils, platelets or nanospheres depending on the solvent composition. The fibrils, functioning as quenched antennas, give intense excitonic couplets in the electronic circular dichroism spectra which are mirror imaged if the unnatural F D F D -analogue is used. By slightly increasing the solvent polarity, these light-harvesting fibres disassemble to spherical structures with silent electronic circular dichroism spectra but which fluoresce. Upon further dilution with the nonpolar solvent, the intense Cotton effects are recovered, thus proving a reversible switching. A single crystal X-ray structure shows a head-to-head arrangement of porphyrins that explains both their excitonic coupling and quenched fluorescence. Artificial light-harvesting systems cannot self-assemble into photon-capturing structures that can reversibly switch into an inactive state. Here, the authors describe a simple and robust dipeptide construct which self-assembles to fibrils, platelets or nanospheres with varying optical properties.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms12657