Litcius/Paper detail

Pillararenes: fascinating planar chiral macrocyclic arenes

Jin-Fa Chen, Jin-Dong Ding, Tai‐Bao Wei

2021Chemical Communications119 citationsDOI

Abstract

Chiral macrocycles possess significant value in chiral science and supramolecular chemistry. Pillararenes, as a class of relatively young supramolecular macrocyclic hosts, have been widely used for host-guest recognition and self-assembly. Since the position of substituents on the benzene rings breaks the molecular symmetry (symmetric plane and symmetric center), pillararenes possess planar chirality. However, it is a great challenge to synthesize stable and resolvable enantiomers because of the easy rotation of the phenylene group. In this review, we summarize the construction methods of resolvable chiral pillararenes. We also focus on their applications in enantioselective recognition, chiral switches, chirality sensing, asymmetric catalysis, circularly polarized luminescence, metal-organic frameworks, and highly permeable membranes. Finally, we discuss the future research perspectives in this field of pillararene-based planar chiral materials. We hope that this review will encourage more researchers to work in this exciting field.

Topics & Concepts

Supramolecular chemistryEnantioselective synthesisPlanar chiralityChirality (physics)EnantiomerPhenyleneCombinatorial chemistryNanotechnologySupramolecular chiralityMaterials sciencePlanarChemistryStereochemistryCrystallographyCatalysisSymmetry breakingComputer scienceChiral symmetry breakingPhysicsOrganic chemistryCrystal structureQuantum mechanicsNambu–Jona-Lasinio modelComputer graphics (images)PolymerSupramolecular Chemistry and ComplexesMolecular Sensors and Ion DetectionLuminescence and Fluorescent Materials