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.

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