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Cationic [6]Helicenes: Tuning (Chir)Optical Properties up to the Near Infra-Red

Published inMaterials today: proceedings, vol. 62, no. East West Chemistry Conference 2021 / edited by Mustafa Culha, Onder Metin, Georgii Sokolsky, Olena Chyhyrynets, Vitaliy Prokopenko, p. 7751-7753
Publication date2022-06-24
First online date2022-06-02
Abstract

The intramolecular condensation of ortho substituents of triaryl carbenium ions can lead to the formation of cationic helicenes. These chiral and configurationally stable molecules exhibit extended optical properties reminiscent of their parent methylium ions. Among them, cationic [6]helicenes are particularly interesting as orthogonal late-stage functionalization strategies allow the introduction of a variety of auxochromes with different regiochemistry. Intense chiroptical properties can thus be tailored in the far red and up to the near infra-red (NIR) spectral windows. A wealth of applications can be foreseen, in particular in material sciences.

Keywords
  • Cationic helicene
  • Chromophore / fluorophore
  • Near infra-red
  • ECD / CPL
  • Cyanine
Research groups
Citation (ISO format)
BOSSON, Johann et al. Cationic [6]Helicenes: Tuning (Chir)Optical Properties up to the Near Infra-Red. In: Materials today: proceedings, 2022, vol. 62, p. 7751–7753. doi: 10.1016/j.matpr.2022.05.098
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Article (Published version)
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Journal ISSN2214-7853
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Creation13/07/2022 10:56:00
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