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Carbon Origami via an Alumina-Assisted Cyclodehydrofluorination Strategy

Steiner, Ann-Kristin; Sharapa, Dmitry I. 1; Troyanov, Sergey I.; Nuss, Jürgen; Amsharov, Konstantin
1 Institut für Katalyseforschung und -technologie (IKFT), Karlsruher Institut für Technologie (KIT)

Abstract:
The synthesis of pristine non‐planar nanographenes (NGs) via a cyclodehydrofluorination strategy is reported and the creation of highly strained systems via alumina‐assisted C−F bond activation is shown. Steric hindrance could execute an alternative coupling program leading to rare octagon formation offering access to elusive non‐classical NGs. The combination of two alternative ways of folding could lead to the formation of various 3D NG objects, resembling the Japanese art of origami. The power of the presented “origami” approach is proved by the assembly of 12 challenging nanographenes that are π‐isoelectronic to planar hexabenzocoronene but forced out of planarity.


Verlagsausgabe §
DOI: 10.5445/IR/1000131078
Veröffentlicht am 01.04.2021
Originalveröffentlichung
DOI: 10.1002/chem.202003448
Scopus
Zitationen: 1
Web of Science
Zitationen: 1
Dimensions
Zitationen: 1
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Katalyseforschung und -technologie (IKFT)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2020
Sprache Englisch
Identifikator ISSN: 0947-6539, 1521-3765
KITopen-ID: 1000131078
Erschienen in Chemistry - A European Journal
Verlag John Wiley and Sons
Band 2021
Heft 27
Seiten 1-8
Schlagwörter aryl–aryl coupling; carbon origami; C−F bond activation; cyclodehydrofluorination; multihelical nanographenes
Nachgewiesen in Scopus
Web of Science
Dimensions
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