Symmetric C <sub>66</sub> H <sub>36</sub> multihelicenes

The relative stability and the conformational behavior of symmetric multihelicene isomers of formula C 66 H 36 are analyzed by computational means. Our efforts to synthesize some of these molecules are also reported, in particular, the observation of unexpected debromination when attempting to synthesize 13,14-dibromo[5]phenacene, and of unexpected reactivity of 13,14-dibromo[5]aphene when attempting its cyclotrimerization promoted by a nickel(0) complex.

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Publication Details

Journal
Canadian Journal of Chemistry
Published
2025-02-26
DOI
https://doi.org/10.1139/cjc-2024-0234
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Symmetric C 66 H 36 multihelicenes

Guillaume Dauvergne, Albert Artigas, Mohammed Bin Jassar, Yannick Carissan et al.
Canadian Journal of Chemistry
Synthesis and Properties of Aromatic Compounds
article

Symmetric C 66 H 36 multihelicenes

Guillaume Dauvergne, Albert Artigas, Mohammed Bin Jassar, Yannick Carissan, Florian Rigoulet, Yoann Coquerel, Denis Hagebaum‐Reignier
article en

Abstract

The relative stability and the conformational behavior of symmetric multihelicene isomers of formula C 66 H 36 are analyzed by computational means. Our efforts to synthesize some of these molecules are also reported, in particular, the observation of unexpected debromination when attempting to synthesize 13,14-dibromo[5]phenacene, and of unexpected reactivity of 13,14-dibromo[5]aphene when attempting its cyclotrimerization promoted by a nickel(0) complex.

Canadian Journal of ChemistryVol. 104(2)
Aix-Marseille Université (FR)
Aix-Marseille Université, Agence Nationale de la Recherche, Centre National de la Recherche Scientifique
Openalex Percentile: Top 97%
Synthesis and Properties of Aromatic Compounds
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