Issue 14, 2026

Nitrogen-centred helical acridiniums with a 6–7–6–6 fused ring skeleton

Abstract

Helical 6–7–6–6 fused acridiniums were synthesised via oxidative ring contraction of a helical azaheptalene. X-ray, spectroscopic, and theoretical studies revealed highly distorted, configurationally stable helicity with long-wavelength absorption and chiroptical properties. These findings provide a new π-conjugated helical framework for functional chiral materials.

Graphical abstract: Nitrogen-centred helical acridiniums with a 6–7–6–6 fused ring skeleton

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Article information

Article type
Communication
Submitted
23 Oct 2025
Accepted
22 Jan 2026
First published
22 Jan 2026
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026,62, 4268-4271

Nitrogen-centred helical acridiniums with a 6–7–6–6 fused ring skeleton

S. Nakamura, S. Kawaguchi, Y. Nishimura, T. Harimoto, J. Hasegawa, T. Suzuki and Y. Ishigaki, Chem. Commun., 2026, 62, 4268 DOI: 10.1039/D5CC06029J

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