Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, 215123, China.
School of Physics and Information Technology, Shaanxi Normal University, Xi'an, 710062, China.
Nat Commun. 2018 Aug 6;9(1):3113. doi: 10.1038/s41467-018-05472-2.
The synthetic challenges of radialenes have precluded their practical applications. Here, we report a one-step synthetic protocol of [4]radialene on a copper surface. High-resolution scanning tunneling microscopy measurements reveal that such catalytic reaction proceeds readily with high selectivity at the temperature below 120 K. First-principles calculations show that the reaction pathway is characterized by firstly the cooperative inter-molecular hydrogen tautomerization and then the C-C bond formation. The feasibility of such cyclotetramerization reaction can be interpreted by the surface effect of Cu(100), which firstly plays an important role in directing the molecular assembly and then serves as an active catalyst in the hydrogen tautomerization and C-C coupling processes. This work presents not only a novel strategy to the scant number of synthetic methods to produce [4]radialenes via a novel [1 + 1 + 1 + 1] reaction pathway, but also a successful example of C-C bond coupling reactions guided by the surface-induced C-H/π assembly.
轮烯的合成挑战使其无法实际应用。在这里,我们在铜表面上报告了一种[4]轮烯的一步合成方案。高分辨率扫描隧道显微镜测量表明,在低于 120 K 的温度下,这种催化反应很容易进行,具有高选择性。第一性原理计算表明,反应途径的特征是首先是分子间协同氢互变异构,然后是 C-C 键形成。这种环四聚化反应的可行性可以通过 Cu(100)的表面效应来解释,它首先在指导分子组装方面起着重要作用,然后在氢互变异构和 C-C 偶联过程中充当活性催化剂。这项工作不仅为通过新颖的[1+1+1+1]反应途径生产[4]轮烯的少数几种合成方法提供了一种新策略,而且为表面诱导的 C-H/π组装指导的 C-C 键偶联反应提供了一个成功的范例。