Design and Synthesis of New Type of Macrocyclic Architectures Used for Optoelectronic Materials and Supramolecular Chemistry

Author:

Li Pengfei1,Jia Yawei2,Chen Pangkuan2ORCID

Affiliation:

1. School of Chemistry and Material Engineering Henan University of Urban Construction Pingdingshan 467036 Henan Province P. R. China

2. Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials Key Laboratory of Cluster Science of the Ministry of Education School of Chemistry and Chemical Engineering Beijing Institute of Technology Beijing 102488 P. R. China

Abstract

AbstractSupramolecular chemistry has received much attention for decades. Macrocyclic architectures as representative receptors play a vital role in supramolecular chemistry and are applied in many fields such as supramolecular assembly and host‐guest recognition. However, the classical macrocycles generally lack functional groups in the scaffolds, which limit their further applications, especially in optoelectronic materials. Therefore, developing a new design principle is not only essential to better understand macrocyclic chemistry and the supramolecular behaviors, but also further expand their applications in many research fields. In recent years, the doping compounds with main‐group heteroatoms (B, N, S, O, P) into the carbon‐based π‐conjugated macrocycles offered a new strategy to build macrocyclic architectures with unique optoelectronic properties. In particular, the energy gaps and redox behavior can be effectively tuned by incorporating heteroatoms into the macrocyclic scaffolds. In this Minireview, we briefly summarize the design and synthesis of new macrocycles, and further discuss the related applications in optoelectronic materials and supramolecular chemistry.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference236 articles.

1.  

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4. Host-Guest Chemistry

5. Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes

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