Related Experiment Video
Updated: Nov 30, 2025

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
Published on: January 17, 2020
Induction of Chirality in a Metal-Organic Framework Built from Achiral Precursors
Dong Wu1,2, Kang Zhou1, Jindou Tian1,2
1State Key Laboratory of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, China.
Abstract:
Induction of chirality from an achiral assembly system remains a huge challenge related to the origin of life. Here, induction of chirality in a metal-organic framework (MOF) built from achiral precursors has been realized. Assembling achiral H3 BTB ligands and ZnII /CdII clusters leads to a 2D coordination polymer (FJI-H16), while introduction of achiral pyridine into such assembly system leads to a 3D chiral MOF (FJI-H27 (M) or (P)). The driven force for chiral generation has been proved to be a pyridine participated kinetic-control assembly process, which can be controlled by changing the amount of pyridine and temperature, from no induction to partial induction to complete induction. The chiral generation process has been identified in detail through a pyridine-involved key intermediate (FJI-H28). The targeted modification of pyridine can selectively lead to FJI-H27 (M) or FJI-H27 (P), making the chiral orientation and distribution of bulk FJI-H27 samples can be controlled. Our work not only represents a new chiral induction process that may relate to the chiral origin in nature, but also firstly reveals how achiral external stimuli generate chirality from achiral precursors, and offers a guide for rational preparation of chiral MOFs.
Related Concept Videos
Prochirality
Molecules with Multiple Chiral Centers
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
Chirality in Nature
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

