ReviewChemistry (Weinheim an der Bergstrasse, Germany)2025
Expanding Chemistry of Expanded Helicenes.
Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Late-Stage Functionalization of a Hexa-ACS physical chemistry Au · 2026Article
- Synthesis and Structure of an S-Shaped Double Expanded Helicene With Seven Fused Anthracene Units.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- A Negatively Curved Pyrene-Fused Azaacene.Angewandte Chemie (International ed. in English) · 2026Article
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1 author.
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Abstract
Expanded helicenes are interesting compounds created by modifying the original helicene structure through the incorporation of linearly fused benzene rings, enlarging the helical diameter. Motivated by Tilley et al.'s report of a key expanded helicene structure in 2017, several research groups have synthesized such nonplanar aromatic compounds, aiming to explore their impressive structures, properties, and chiroptical performance. This review highlights recent advances in the expanded helicene chemistry through experimental and theoretical studies. The shape and length of helical structures depend on the number and combination of angularly and linearly fused benzene rings. Helical structures are classified using notations, and specific compounds corresponding to each structural form, namely, hexagonal, triangular, rhombic, or others, are introduced herein. As an extension of the molecular design, examples of nonhexagonal and heteroaromatic ring-embedded expanded helicenes are presented. Specifically, this review focuses on how the diameters, lengths, and turn numbers of helical structures depend on dynamic processes involving helical inversion and chiroptical properties (circular dichroism (CD) and circularly polarized luminescence (CPL)). The characteristics and perspectives of this molecular design are also discussed.
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