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通过间环对亚苯基的后官能化合成全苯多环纳米碳。

Synthesis of All-Benzene Multi-Macrocyclic Nanocarbons by Post-Functionalization of meta-Cycloparaphenylenes.

作者信息

Gao Jia-Nan, Bu An, Chen Yiming, Huang Mianling, Chen Zhi, Li Xiaopeng, Tung Chen-Ho, Wu Li-Zhu, Cong Huan

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials, CAS-HKU Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry; School of Future Technology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, 100190, China.

College of Chemistry and Environmental Engineering, Shenzhen University, Guangdong, 518060, China.

出版信息

Angew Chem Int Ed Engl. 2024 Aug 12;63(33):e202408016. doi: 10.1002/anie.202408016. Epub 2024 Jul 17.

Abstract

Expanding the diversity of multi-macrocyclic nanocarbons, particularly those with all-benzene scaffolds, represents intriguing yet challenging synthetic tasks. Complementary to the existing synthetic approaches, here we report an efficient and modular post-functionalization strategy that employs iridium-catalyzed C-H borylation of the highly strained meta-cycloparaphenylenes (mCPPs) and an mCPP-derived catenane. Based on the functionalized macrocyclic synthons, a number of novel all-benzene topological structures including linear and cyclic chains, polycatenane, and pretzelane have been successfully prepared and characterized, thereby showcasing the synthetic utility and potential of the post-functionalization strategy.

摘要

拓展多大环纳米碳的多样性,尤其是那些具有全苯骨架的纳米碳,是既有趣又具有挑战性的合成任务。作为现有合成方法的补充,我们在此报告一种高效且模块化的后功能化策略,该策略采用铱催化的高度张力间环对亚苯基(mCPPs)和一种源自mCPP的索烃的C-H硼化反应。基于功能化的大环合成子,已成功制备并表征了许多新型的全苯拓扑结构,包括线性和环状链、多索烃和扭结烷,从而展示了后功能化策略的合成效用和潜力。

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