Design principles of chiral carbon nanodots help convey chirality from molecular to nanoscale level

The chirality of (nano)structures is paramount in many phenomena, including biological processes, self-assembly, enantioselective reactions, and light or electron spin polarization. In the quest for new chiral materials, metallo-organic hybrids have been attractive candidates for exploiting the afor...

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Veröffentlicht in:Nature communications 2018-08, Vol.9 (1), p.3442-8, Article 3442
Hauptverfasser: Ðorđević, Luka, Arcudi, Francesca, D’Urso, Alessandro, Cacioppo, Michele, Micali, Norberto, Bürgi, Thomas, Purrello, Roberto, Prato, Maurizio
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Sprache:eng
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Zusammenfassung:The chirality of (nano)structures is paramount in many phenomena, including biological processes, self-assembly, enantioselective reactions, and light or electron spin polarization. In the quest for new chiral materials, metallo-organic hybrids have been attractive candidates for exploiting the aforementioned scientific fields. Here, we show that chiral carbon nanoparticles, called carbon nanodots, can be readily prepared using hydrothermal microwave-assisted synthesis and easily purified. These particles, with a mean particle size around 3 nm, are highly soluble in water and display mirror-image profile both in the UV–Vis and in the infrared regions, as detected by electronic and vibrational circular dichroism, respectively. Finally, the nanoparticles are used as templates for the formation of chiral supramolecular porphyrin assemblies, showing that it is possible to use and transfer the chiral information. This simple (and effective) methodology opens up exciting opportunities for developing a variety of chiral composite materials and applications. A promising and efficient route to chiral materials involves the transfer of chirality across length scales. Here, the authors use chiral molecular precursors to synthesize chiral carbon nanodots, which in turn can template the formation of chiral supramolecular assemblies.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-05561-2