Abstract
Pillar[n]arenes are a class of emerging supramolecular macrocyclic hosts that have attracted significant attention due to their intriguing dynamic planar chirality and unique cavity structures. In particular, the conformation of pillar[5]arenes can be locked by the introduction of bulky substituents or π-conjugated units at both rims, resulting in stable planar chirality. This strategy paves the way for the application of planar chiral pillar[5]arenes as versatile chiral molecular platforms. In recent years, planar chiral pillar[5]arenes have been widely applied in various research fields, such as chiral porous materials, chiral luminescent materials, and molecular machines. However, obtaining planar chiral pillar[5]arenes in enantiomeric forms remains a significant challenge. Recently, asymmetric catalytic synthesis via dynamic kinetic resolution (DKR) has proven to serve as a powerful tool for the efficient preparation of planar chiral pillar[5]arenes, which allows for achieving high levels of enantioinduction while producing a series of functionalized planar chiral pillar[5]arenes. This concept summarizes these achievements and highlights the design principles and key challenges, aiming to provide valuable insights for future research.
| Original language | English |
|---|---|
| Article number | e202501185 |
| Journal | Chemistry - A European Journal |
| Volume | 31 |
| Issue number | 38 |
| DOIs | |
| State | Published - 8 Jul 2025 |
Keywords
- asymmetric catalysis
- circularly polarized luminescence
- dynamic kinetic resolution
- pillar[5]arenes
- planar chirality
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