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Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces

Author

Listed:
  • Qing Li

    (Soochow University)

  • Jianzhi Gao

    (Shaanxi Normal University)

  • Youyong Li

    (Soochow University)

  • Miguel Fuentes-Cabrera

    (Oak Ridge National Laboratory
    Oak Ridge National Laboratory)

  • Mengxi Liu

    (CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology)

  • Xiaohui Qiu

    (CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology
    University of Chinese Academy of Sciences)

  • Haiping Lin

    (Soochow University)

  • Lifeng Chi

    (Soochow University)

  • Minghu Pan

    (Huazhong University of Science and Technology)

Abstract

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.

Suggested Citation

  • Qing Li & Jianzhi Gao & Youyong Li & Miguel Fuentes-Cabrera & Mengxi Liu & Xiaohui Qiu & Haiping Lin & Lifeng Chi & Minghu Pan, 2018. "Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces," Nature Communications, Nature, vol. 9(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05472-2
    DOI: 10.1038/s41467-018-05472-2
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