Chiral π-extended diindenoperylenes featuring dithia[7]helicenes

Helically chiral π-expanded diindenoperylenes were synthesized and their chiroptical properties were characterized. The enantiopure synthesis of the perylene framework was achieved by two-fold Yamamoto coupling of π-expanded dibromofluoranthenes, each comprising one dithia[7]helicene unit. Oxidation...

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Autores principales: Berger, Georg (Autor) , Borstelmann, Jan (Autor) , Rominger, Frank (Autor) , Kivala, Milan (Autor)
Formato: Article (Journal)
Lenguaje:inglés
Publicado: 20 January 2026
In: Organic chemistry frontiers
Year: 2026, Volumen: 13, Número: 6, Pages: 1761-1767
ISSN:2052-4129
DOI:10.1039/D5QO01701G
Acceso en línea:Verlag, kostenfrei, Volltext: https://doi.org/10.1039/D5QO01701G
Verlag, kostenfrei, Volltext: https://pubs.rsc.org/en/content/articlelanding/2026/qo/d5qo01701g
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Notas de Autor:Georg Berger, Jan Borstelmann, Frank Rominger and Milan Kivala
Descripción
Sumario:Helically chiral π-expanded diindenoperylenes were synthesized and their chiroptical properties were characterized. The enantiopure synthesis of the perylene framework was achieved by two-fold Yamamoto coupling of π-expanded dibromofluoranthenes, each comprising one dithia[7]helicene unit. Oxidation of the thiophene units to the corresponding sulfones allowed late-stage modification of the chiroptical and electrochemical properties.
Notas:Gesehen am 18.03.2026
Descripción Física:Online Resource
ISSN:2052-4129
DOI:10.1039/D5QO01701G