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

Y Yuma Tanioka (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan) M Masayoshi Takase (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan) M Mashiro Hamasu (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan) S Shogo Hata (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan) K Kohei Hashimoto S Shigeki Mori (Advanced Research Support Center (ADRES) Ehime University Matsuyama Japan) Y Yukihide Ishibashi (Department of Applied Chemistry, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan) Y Yuki Nukumi (Department of Molecular Engineering, Graduate School of Engineering Kyoto University Nishikyo‐ku Kyoto 615‐8510 Japan) M Masahiro Higashi (Department of Complex Systems Science, Graduate School of Informatics, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan) H Hirofumi Sato (Department of Molecular Engineering, Graduate School of Engineering, Kyoto University 1 , Kyoto 615-8510,) T Tetsuo Okujima (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan) H Hidemitsu Uno (Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan)

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.

Article Details

Volume / Issue Vol. 64, Issue 32
Published August 04, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

Y

Yuma Tanioka

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan

M

Masayoshi Takase

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan

M

Mashiro Hamasu

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan

S

Shogo Hata

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan

K

Kohei Hashimoto

S

Shigeki Mori

Advanced Research Support Center (ADRES) Ehime University Matsuyama Japan

Y

Yukihide Ishibashi

Department of Applied Chemistry, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan

Y

Yuki Nukumi

Department of Molecular Engineering, Graduate School of Engineering Kyoto University Nishikyo‐ku Kyoto 615‐8510 Japan

M

Masahiro Higashi

Department of Complex Systems Science, Graduate School of Informatics, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan

H

Hirofumi Sato

Department of Molecular Engineering, Graduate School of Engineering, Kyoto University 1 , Kyoto 615-8510,

T

Tetsuo Okujima

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan

H

Hidemitsu Uno

Graduate School of Science and Engineering Ehime University Matsuyama 790‐8577 Japan