BINOL‐Based Chiral Macrocycles and Cages

Author:

Yu Yabing1,Hu Yaning1,Ning Chengbing1,Shi Wudi1,Yang Ao1,Zhao Yibo1,Cao Zhong‐Yan1,Xu Youzhi1ORCID,Du Pingwu12ORCID

Affiliation:

1. College of Chemistry and Molecular Sciences Henan University Kaifeng, Henan Province 475004 China.

2. Hefei National Research Center for Physical Sciences at the Microscale Anhui Laboratory of Advanced Photon Science and Technology CAS Key Laboratory of Materials for Energy Conversion Department of Materials Science and Engineering University of Science and Technology of China 96 Jinzhai Road, Hefei Anhui Province 230026 China

Abstract

AbstractChirality, a fundamental principle in chemistry, biology, and medicine, is prevalent in nature and in organisms. Chiral molecules, such as DNA, RNA, and proteins, are crucial in biomolecular synthesis, as well as in the development of functional materials. Among these, 1,1′‐binaphthyl‐2,2′‐diol (BINOL) stands out for its stable chiral configuration, versatile functionality, and commercial availability. BINOL is widely employed in asymmetric catalysis and chiral materials. This review mainly focuses on recent research over the past five years concerning the use of BINOL derivatives for constructing chiral macrocycles and cages. Their contributions to chiral luminescence, enantiomeric separation, transmembrane transport, and asymmetric catalysis were examined.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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