摘要
On-surface synthesis recently enabled access to generate a series of cyclo[ n ]carbons (C n , up to C 26 ) via delicately designed precursors. However, for larger cyclocarbons, synthesis of the corresponding precursors is being challenged. Here, we report another strategy for synthesizing larger cyclocarbons via the coupling and ring-opening reactions from smaller ones. We chose C 10 as the precursor, and induce the coupling and ring-opening reactions via tip manipulation to successfully generate C 20 and C 30 . Bond-resolved atomic force microscopy imaging unambiguously reveals the polyynic structure of C 30 , aligning with theoretical prediction. This approach establishes a new pathway to access larger cyclocarbons, and potentially enables controlled polymerization of cyclocarbons.
危险品化学品经营许可证(带存储)