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Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)

Helicene is a functional material with chirality caused by its characteristic helical geometry. The inversion of its helicity by external stimuli is a challenging task in the advanced control of the molecular chirality. This study fabricated a novel helical molecule, specifically a pentahelicene-ana...

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Detalles Bibliográficos
Autores principales: Ishii, Ayumu, Shiotari, Akitoshi, Sugimoto, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528025/
https://www.ncbi.nlm.nih.gov/pubmed/34777748
http://dx.doi.org/10.1039/d1sc03976h
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author Ishii, Ayumu
Shiotari, Akitoshi
Sugimoto, Yoshiaki
author_facet Ishii, Ayumu
Shiotari, Akitoshi
Sugimoto, Yoshiaki
author_sort Ishii, Ayumu
collection PubMed
description Helicene is a functional material with chirality caused by its characteristic helical geometry. The inversion of its helicity by external stimuli is a challenging task in the advanced control of the molecular chirality. This study fabricated a novel helical molecule, specifically a pentahelicene-analogue twisted aromatic hydrocarbon fused with a graphene nanoribbon, via on-surface synthesis using multiple precursors. Noncontact atomic force microscopy imaging with high spatial resolution confirmed the helicity of the reaction products. The helicity was geometrically converted by pushing a CO-terminated tip into the twisted framework, which is the first demonstration of helicity switching at the single-molecule scale.
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spelling pubmed-85280252021-11-12 Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111) Ishii, Ayumu Shiotari, Akitoshi Sugimoto, Yoshiaki Chem Sci Chemistry Helicene is a functional material with chirality caused by its characteristic helical geometry. The inversion of its helicity by external stimuli is a challenging task in the advanced control of the molecular chirality. This study fabricated a novel helical molecule, specifically a pentahelicene-analogue twisted aromatic hydrocarbon fused with a graphene nanoribbon, via on-surface synthesis using multiple precursors. Noncontact atomic force microscopy imaging with high spatial resolution confirmed the helicity of the reaction products. The helicity was geometrically converted by pushing a CO-terminated tip into the twisted framework, which is the first demonstration of helicity switching at the single-molecule scale. The Royal Society of Chemistry 2021-09-14 /pmc/articles/PMC8528025/ /pubmed/34777748 http://dx.doi.org/10.1039/d1sc03976h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Ishii, Ayumu
Shiotari, Akitoshi
Sugimoto, Yoshiaki
Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title_full Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title_fullStr Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title_full_unstemmed Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title_short Mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on Au(111)
title_sort mechanically induced single-molecule helicity switching of graphene-nanoribbon-fused helicene on au(111)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528025/
https://www.ncbi.nlm.nih.gov/pubmed/34777748
http://dx.doi.org/10.1039/d1sc03976h
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AT sugimotoyoshiaki mechanicallyinducedsinglemoleculehelicityswitchingofgraphenenanoribbonfusedheliceneonau111