Outside Front Cover: Helically Chiral Mixed‐Valence Systems Comprising N Heterotriangulenes: Stabilization of the Cationic Species by π Expansion (Angew. Chem. Int. Ed. 16/2025)

The cover artwork visualizes the dimeric N-heterotriangulene in front of a spiral staircase reflecting its helical chirality. The blue spheres represent the redox-active nitrogens, the connecting vibrant pathway symbolizes the charge transfer leading to a mixed-valence state enabled by the p-conjugated helicene backbone. The glowing orange helix illustrates the compound's ability to emit circularly polarized light, a property relevant to future chiroptical applications with low environmental impact. Read more in the Research Article (e202423516) by Dirk M. Guldi, Milan Kivala et al.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-27
DOI
https://doi.org/10.1002/anie.202506101
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00
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Outside Front Cover: Helically Chiral Mixed‐Valence Systems Comprising N Heterotriangulenes: Stabilization of the Cationic Species by π Expansion (Angew. Chem. Int. Ed. 16/2025)

Frederik Gnannt, Jan Borstelmann, Timothy Clark, Georg Gescheidt et al.
Angewandte Chemie International Edition
Synthesis and Properties of Aromatic Compounds
article

Outside Front Cover: Helically Chiral Mixed‐Valence Systems Comprising N Heterotriangulenes: Stabilization of the Cationic Species by π Expansion (Angew. Chem. Int. Ed. 16/2025)

Frederik Gnannt, Jan Borstelmann, Timothy Clark, Georg Gescheidt, Milan Kivala, Nina Fröhlich, Lars Schneider, Felix Deschler, Dirk M. Guldi, Marcel Krug, Simon Zank, Frank Röminger, Gabriel Glotz, Georg Berger
article en

Abstract

The cover artwork visualizes the dimeric N-heterotriangulene in front of a spiral staircase reflecting its helical chirality. The blue spheres represent the redox-active nitrogens, the connecting vibrant pathway symbolizes the charge transfer leading to a mixed-valence state enabled by the p-conjugated helicene backbone. The glowing orange helix illustrates the compound's ability to emit circularly polarized light, a property relevant to future chiroptical applications with low environmental impact. Read more in the Research Article (e202423516) by Dirk M. Guldi, Milan Kivala et al.

Angewandte Chemie International EditionVol. 64(16)
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Heidelberg University (DE), Graz University of Technology (AT)
Life in Land
Openalex Percentile: Top 96%
Synthesis and Properties of Aromatic Compounds
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Outside Front Cover: Helically Chiral Mixed‐Valence Systems Comprising N Heterotriangulenes: Stabilization of the Cationic Species by π Expansion (Angew. Chem. Int. Ed. 16/2025) — Frederik Gnannt, Jan Borstelmann, et al. · Angewandte Chemie International Edition (2025) | TGRS Research Map | TGRS