Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 28, Pages 15276-15280Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202103710
Keywords
chirality; helicenes; organic radicals; spinterfaces; X-ray natural circular dichroism
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Funding
- Italian MIUR, through PRIN Project [2017CR5WCH]
- Dipartimenti di Eccellenza [B96C1700020008]
- Fondazione Cassa di Risparmio di Firenze (through the CeTeCS initiative) [2020.1634]
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The study presents a novel strategy for depositing a sub-monolayer of enantiopure thia[4]helicene radical cations on a pre-functionalized Au(111) substrate, maintaining both the paramagnetic character and the chemical structure of these molecules at the nanoscale. Synchrotron-based X-ray natural circular dichroism confirms the preservation of the handedness of the thia[4]helicene on the surface.
In the past few years, the chirality and magnetism of molecules have received notable interest for the development of novel molecular devices. Chiral helicenes combine both these properties, and thus their nanostructuration is the first step toward developing new multifunctional devices. Here, we present a novel strategy to deposit a sub-monolayer of enantiopure thia[4]helicene radical cations on a pre-functionalized Au(111) substrate. This approach results in both the paramagnetic character and the chemical structure of these molecules being maintained at the nanoscale, as demonstrated by in-house characterizations. Furthermore, synchrotron-based X-ray natural circular dichroism confirmed that the handedness of the thia[4]helicene is preserved on the surface.
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