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<p>Chiral organic chromophores are foundational for advanced optical and electronic devices. Despite the widespread use of <i>N</i>-aryl carbazoles in visible-luminescent materials, chiroptical applications of their atropisomers have remained underdeveloped due to the synthetic challenge of achieving remote atroposelectivity necessitated by extended π-systems. Here, we present a unified strategy for the efficient synthesis of enantioenriched N–C and N–N carbazole atropisomers. By integrating <sup>13</sup>C NMR-based ligand parameterization, we achieve enantiotopic-group-selective coupling reactions that simultaneously incorporate tailored π-functionalities and establish axial chirality (up to &gt;99:1 er) using synthetic pathways established in carbazole chemistry. Through covalent modulation and noncovalent complexation, we investigate novel chiroptical functions of carbazole atropisomers, including circular dichroism (CD), circularly polarized luminescence (CPL), charge-transfer CPL (CT-CPL), and circularly polarized thermally activated delayed fluorescence (CP-TADF). By establishing an electrostatic steering strategy for remote atroposelectivity, our work paves the way for integrating multifunctional carbazoles into advanced optical and optoelectronic technologies.</p>

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Enantiotopic-group-selective coupling for unified access to carbazole atropisomers as versatile chiral chromophores

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月21日

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  • Junqiang Wei,
  • Zhuoer Wang,
  • Pengyao Xing,
  • Ye Zhu

摘要

Chiral organic chromophores are foundational for advanced optical and electronic devices. Despite the widespread use of N-aryl carbazoles in visible-luminescent materials, chiroptical applications of their atropisomers have remained underdeveloped due to the synthetic challenge of achieving remote atroposelectivity necessitated by extended π-systems. Here, we present a unified strategy for the efficient synthesis of enantioenriched N–C and N–N carbazole atropisomers. By integrating 13C NMR-based ligand parameterization, we achieve enantiotopic-group-selective coupling reactions that simultaneously incorporate tailored π-functionalities and establish axial chirality (up to >99:1 er) using synthetic pathways established in carbazole chemistry. Through covalent modulation and noncovalent complexation, we investigate novel chiroptical functions of carbazole atropisomers, including circular dichroism (CD), circularly polarized luminescence (CPL), charge-transfer CPL (CT-CPL), and circularly polarized thermally activated delayed fluorescence (CP-TADF). By establishing an electrostatic steering strategy for remote atroposelectivity, our work paves the way for integrating multifunctional carbazoles into advanced optical and optoelectronic technologies.