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

Jia-Nan GaoAn BuYiming ChenMianling HuangZhi ChenXiaopeng LiChen-Ho TungLi-Zhu WuHuan Cong
Published in: Angewandte Chemie (International ed. in English) (2024)
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.
Keyphrases
  • high resolution
  • working memory
  • room temperature
  • mass spectrometry
  • liquid chromatography