表面改性
合成子
硼酸化
组合化学
苯
铱
化学
纳米技术
材料科学
催化作用
有机化学
物理化学
烷基
芳基
作者
Jia‐Nan Gao,An Bu,Yi‐Ming Chen,Mianling Huang,Zhi Chen,Xiaopeng Li,Chen‐Ho Tung,Li‐Zhu Wu,Huan Cong
标识
DOI:10.1002/anie.202408016
摘要
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.
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