Triple Regioselective Functionalization of Cationic (4) Helicenes via Iridium‐Catalyzed Borylation and Suzuki Cross‐Coupling Reactivity

Abstract: In essentially one‐pot, using Ir‐ and Pd‐catalysis, tris (arene)‐functionalized cationic [4]helicenes are synthesized with full regioselectivity and enantiospecificity starting from a trivial precursor (17 examples). This poly‐addition of aryl groups improves key optical properties, that is, fluorescence quantum yields and lifetimes. Electronic circular dichroism and circularly polarized luminescence signatures are observed up to the far‐red domain, in particular with additional arenes prone to aggregation.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Triple Regioselective Functionalization of Cationic (4) Helicenes via Iridium‐Catalyzed Borylation and Suzuki Cross‐Coupling Reactivity ; day:18 ; month:08 ; year:2022 ; extent:1
Chemistry - a European journal ; (18.08.2022) (gesamt 1)

Creator
Frédéric, Lucas
Fabri, Bibiana
Guénée, Laure
Zinna, Francesco
Di Bari, Lorenzo
Lacour, Jérôme

DOI
10.1002/chem.202201853
URN
urn:nbn:de:101:1-2022081915055259404426
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:22 AM CEST

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