Solvent‐Induced Chirality Inversion in Propeller‐Shaped PDI Oligomers with Bright Circularly Polarized Luminescence

Abstract Circularly polarized luminescence (CPL) has the potential for next‐generation optoelectronic applications. One of the major challenges in this field is the development of CPL emitters, whose emission properties can be modulated by external stimuli, such as solvents. However, CPL‐active materials are often synthetically demanding and typically require chiral separation. To address these limitations, we have synthesized a propeller‐shaped molecule, ( R / S )‐Bz‐6PDI 1 , via a one‐pot nucleophilic aromatic substitution reaction, using a chiral pyrrole‐fused perylene diimide (PDI) 4 as the blade. The introduction of a chiral auxiliary into the blade enabled the induction of propeller chirality without the need for chiral chromatographic separation. ( R )‐Bz‐6PDI 1 exhibited high CPL brightness in solution ( B CPL = 103–369 M −1 cm −1 ). Furthermore, the propeller chirality proved highly sensitive to the solvent environment, leading to significant modulation of both the sign and intensity of the CD and CPL signals, including complete signal inversion in CH 2 Cl 2 and CHCl 3 . CD spectral analysis combined with DFT calculations revealed that the propeller chirality is governed by the orientation of the hydrogen atom in the chiral auxiliary.

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Publication Details

Journal
Angewandte Chemie
Published
2025-05-29
DOI
https://doi.org/10.1002/ange.202509190
Citations
3
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
2.81

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article

Solvent‐Induced Chirality Inversion in Propeller‐Shaped PDI Oligomers with Bright Circularly Polarized Luminescence

Shigeki Mori, Masayoshi Takase, Shogo Hata, Masahiro Higashi et al.
3 citations
Angewandte Chemie
Synthesis and Properties of Aromatic Compounds
2.81
article

Solvent‐Induced Chirality Inversion in Propeller‐Shaped PDI Oligomers with Bright Circularly Polarized Luminescence

Shigeki Mori, Masayoshi Takase, Shogo Hata, Masahiro Higashi, Hirofumi Sato, Yuma Tanioka, Yukihide Ishibashi, Hidemitsu Uno, Tetsuo Okujima, Kohei Hashimoto, Yuki Nukumi, Mashiro Hamasu
article en
3 citations

Abstract

Abstract Circularly polarized luminescence (CPL) has the potential for next‐generation optoelectronic applications. One of the major challenges in this field is the development of CPL emitters, whose emission properties can be modulated by external stimuli, such as solvents. However, CPL‐active materials are often synthetically demanding and typically require chiral separation. To address these limitations, we have synthesized a propeller‐shaped molecule, ( R / S )‐Bz‐6PDI 1 , via a one‐pot nucleophilic aromatic substitution reaction, using a chiral pyrrole‐fused perylene diimide (PDI) 4 as the blade. The introduction of a chiral auxiliary into the blade enabled the induction of propeller chirality without the need for chiral chromatographic separation. ( R )‐Bz‐6PDI 1 exhibited high CPL brightness in solution ( B CPL = 103–369 M −1 cm −1 ). Furthermore, the propeller chirality proved highly sensitive to the solvent environment, leading to significant modulation of both the sign and intensity of the CD and CPL signals, including complete signal inversion in CH 2 Cl 2 and CHCl 3 . CD spectral analysis combined with DFT calculations revealed that the propeller chirality is governed by the orientation of the hydrogen atom in the chiral auxiliary.

Angewandte ChemieVol. 137(32)
Kyoto University (JP), Matsuyama University (JP), Kyoto University of Education (JP), Ehime University (JP), Nagoya University (JP)
Takahashi Industrial and Economic Research Foundation, Nagase Science Technology Foundation
Openalex Percentile: Top 10%
Synthesis and Properties of Aromatic Compounds
2.81
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