Affiliation:
1. Beijing National Laboratory for Molecular Sciences (BNLMS) CAS Key Laboratory of Photochemistry CAS Research/Education Center for Excellence in Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
2. School of Chemical Sciences University of Chinese Academy of Sciences Beijing 100049 China
3. Department of Chemistry Carnegie Mellon University Pittsburgh Pennsylvania 15213 United States of America
Abstract
AbstractRecently, chiral metal‐organic coordination materials have emerged as promising candidates for a wide range of applications in chiroptoelectronics, chiral catalysis, and information encryption, etc. Notably, the chiroptical effect of coordination chromophores makes them appealing for applications such as photodetectors, OLEDs, 3D displays, and bioimaging. The direct synthesis of chiral coordination materials using chiral organic ligands or complexes with metal‐centered chirality is very often tedious and costly. In the case of ionic coordination materials, the combination of chiral anions with cationic, achiral coordination compounds through noncovalent interactions may endow molecular materials with desirable chiroptical properties. The use of such a simple chiral strategy has been proven effective in inducing promising circular dichroism and/or circularly polarized luminescence signals. This concept article mainly delves into the latest advances in exploring the efficacy of such a chiral anion strategy for transforming achiral coordination materials into chromophores with superb photo‐ or electro‐chiroptical properties. In particular, ionic small‐molecular metal complexes, metal clusters, coordination supramolecular assemblies, and metal‐organic frameworks containing chiral anions are discussed. A perspective on the future opportunities on the preparation of chiroptical materials with the chiral anion strategy is also presented.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
National Science Foundation
Cited by
1 articles.
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