Double [8]Helicene Featuring a Dibenzo[<i>g</i>,<i>p</i>]chrysene Core: Synthesis and Chiroptical Response

Double [8]helicene <b>1</b>, featuring a dibenzo[<i>g</i>,<i>p</i>]chrysene core, was synthesized via the Scholl reaction, and its structure was unambiguously confirmed by single-crystal X-ray diffraction analysis of its dicationic salt [<b>1</b>-Cl]<sup>2+</sup>·(SbCl<sub>6</sub><sup>-</sup>)<sub>2</sub>. The compound exhibits red fluorescence with an emission maximum at 618 nm (λ<sub>em</sub>) and a quantum yield of 16.2%, highlighting its potential in optoelectronic applications. Furthermore, circular dichroism (CD) and circularly polarized luminescence (CPL) measurements reveal notable chiroptical activity, with absorption and emission dissymmetry factors of |<i>g</i><sub>abs</sub>| = 5.11 × 10<sup>-3</sup> and |<i>g</i><sub>lum</sub>| = 7.1 × 10<sup>-4</sup>, respectively.

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Publication Details

Journal
Organic Letters
Published
2025-05-02
DOI
https://doi.org/10.1021/acs.orglett.5c01261
Citations
4
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
3.74

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article

Double [8]Helicene Featuring a Dibenzo[g,p]chrysene Core: Synthesis and Chiroptical Response

Han‐Yuan Gong, Ziming Cheng, Baixue Liu, Xiaohuan Huang et al.
4 citations
Organic Letters
Synthesis and Properties of Aromatic Compounds
3.74
article

Double [8]Helicene Featuring a Dibenzo[g,p]chrysene Core: Synthesis and Chiroptical Response

Han‐Yuan Gong, Ziming Cheng, Baixue Liu, Xiaohuan Huang, Xu‐Lang Chen, Si-Qian Yu, Zhaoliang Zheng, Chuanyu Zhao, Jiaqi Liang, Chunyang Zheng
article en
4 citations

Abstract

Double [8]helicene <b>1</b>, featuring a dibenzo[<i>g</i>,<i>p</i>]chrysene core, was synthesized via the Scholl reaction, and its structure was unambiguously confirmed by single-crystal X-ray diffraction analysis of its dicationic salt [<b>1</b>-Cl]<sup>2+</sup>·(SbCl<sub>6</sub><sup>-</sup>)<sub>2</sub>. The compound exhibits red fluorescence with an emission maximum at 618 nm (λ<sub>em</sub>) and a quantum yield of 16.2%, highlighting its potential in optoelectronic applications. Furthermore, circular dichroism (CD) and circularly polarized luminescence (CPL) measurements reveal notable chiroptical activity, with absorption and emission dissymmetry factors of |<i>g</i><sub>abs</sub>| = 5.11 × 10<sup>-3</sup> and |<i>g</i><sub>lum</sub>| = 7.1 × 10<sup>-4</sup>, respectively.

Organic LettersVol. 27(19)
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 8%
Synthesis and Properties of Aromatic Compounds
3.74
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Double [8]Helicene Featuring a Dibenzo[<i>g</i>,<i>p</i>]chrysene Core: Synthesis and Chiroptical Response — Han‐Yuan Gong, Ziming Cheng, et al. · Organic Letters (2025) | TGRS Research Map | TGRS