Synthesis and Chiroptical Properties of a Saddle-Shaped Quadruple Helicene with a Cyclooctatetrapyrrole Core

A quadruple helicene with a cyclooctatetrapyrrole core was synthesized via a simple Ullmann reaction. Its single-crystal structure exhibits a saddle shape. The compound shows fluorescence emission with λ<sub>em</sub> = 575 nm and good chiroptical properties, including a dissymmetric absorption factor (|<i>g</i><sub>abs</sub>|) of 5.84 × 10<sup>-3</sup> and a dissymmetric emission factor (|<i>g</i><sub>lum</sub>|) of 1.21 × 10<sup>-2</sup>.

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Publication Details

Journal
Organic Letters
Published
2025-03-28
DOI
https://doi.org/10.1021/acs.orglett.5c00294
Citations
3
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
2.81

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article

Synthesis and Chiroptical Properties of a Saddle-Shaped Quadruple Helicene with a Cyclooctatetrapyrrole Core

Han‐Yuan Gong, Ziming Cheng, Jiaqi Liang, Xiaohuan Huang et al.
3 citations
Organic Letters
Synthesis and Properties of Aromatic Compounds
2.81
article

Synthesis and Chiroptical Properties of a Saddle-Shaped Quadruple Helicene with a Cyclooctatetrapyrrole Core

Han‐Yuan Gong, Ziming Cheng, Jiaqi Liang, Xiaohuan Huang, Xu‐Lang Chen, Si-Qian Yu, Zhaoliang Zheng, An‐Na Chen, Jinku Bai
article en
3 citations

Abstract

A quadruple helicene with a cyclooctatetrapyrrole core was synthesized via a simple Ullmann reaction. Its single-crystal structure exhibits a saddle shape. The compound shows fluorescence emission with λ<sub>em</sub> = 575 nm and good chiroptical properties, including a dissymmetric absorption factor (|<i>g</i><sub>abs</sub>|) of 5.84 × 10<sup>-3</sup> and a dissymmetric emission factor (|<i>g</i><sub>lum</sub>|) of 1.21 × 10<sup>-2</sup>.

Organic LettersVol. 27(14)
Beijing Normal University (CN), CAS Key Laboratory of Urban Pollutant Conversion (CN), Hubei Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 11%
Synthesis and Properties of Aromatic Compounds
2.81
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