Recent advances in novel chiral macrocyclic arenes.

Chem Commun (Camb)

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

Published: November 2024

AI Article Synopsis

  • - Chiral macrocyclic arenes are unique compounds with three-dimensional asymmetric cavities that have interesting properties like electron-rich structures and chiral luminescence, making them important in macrocyclic and supramolecular chemistry.
  • - Recent interest has grown around creating new chiral macrocyclic arenes for applications in areas such as enantioselective recognition, chiral sorting, and creating chiral luminescent materials, distinguished by their types of chirality (central, axial, planar, and inherent).
  • - This review aims to provide insights into the construction and functions of these novel materials, supporting advancements in supramolecular chemistry as well as synthetic, materials, and biochemistry fields.

Article Abstract

Chiral macrocyclic arenes possess confined three-dimensional asymmetric cavities, electron-rich structures, chiral luminescence properties and excellent enantioselective recognition properties and have become a frontier and hotspot of macrocyclic chemistry and supramolecular chemistry. In recent years, there has been growing interest in the development of novel chiral macrocyclic arenes, which have found applications in various research areas. In this review, the construction, properties and functional applications of novel chiral macrocyclic arenes in enantioselective recognition, chiral sorting and construction of chiral luminescent materials according to their chiral types, including central, axial, planar, and inherent chiralities, are summarized. It is expected that this review will be helpful for research on supramolecular chemistry and for promoting the development of synthetic chemistry, materials chemistry and biochemistry.

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Source
http://dx.doi.org/10.1039/d4cc05084cDOI Listing

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