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具有明亮圆偏振发光的螺旋桨状苝二酰亚胺低聚物中的溶剂诱导手性反转

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

作者信息

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

机构信息

Graduate School of Science and Engineering, Ehime University, Matsuyama, 790-8577, Japan.

Research Unit on Molecular Materials Science for Toroidal π-Electron Systems, Ehime University, Matsuyama, 790-8577, Japan.

出版信息

Angew Chem Int Ed Engl. 2025 Aug 4;64(32):e202509190. doi: 10.1002/anie.202509190. Epub 2025 Jun 4.

DOI:10.1002/anie.202509190
PMID:40437833
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 = 103-369 M cm). 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 CHCl and CHCl. 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.

摘要

圆偏振发光(CPL)在下一代光电子应用中具有潜力。该领域的主要挑战之一是开发CPL发射体,其发射特性可由外部刺激(如溶剂)调节。然而,具有CPL活性的材料通常合成要求高,且通常需要手性分离。为解决这些局限性,我们通过一锅法亲核芳香取代反应合成了一种螺旋桨状分子(R/S)-Bz-6PDI 1,使用手性吡咯稠合苝二酰亚胺(PDI)4作为叶片。将手性助剂引入叶片可诱导螺旋桨手性,而无需手性色谱分离。(R)-Bz-6PDI 1在溶液中表现出高CPL亮度(B = 103 - 369 M cm)。此外,螺旋桨手性对溶剂环境高度敏感,导致CD和CPL信号的符号和强度都有显著调制,包括在CHCl和CHCl中信号完全反转。CD光谱分析结合DFT计算表明,螺旋桨手性由手性助剂中氢原子的取向决定。

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