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Synthesis and X-ray characterization of 15- and 16-vertex closo-carboranes

Author

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  • Fangrui Zheng

    (The Chinese University of Hong Kong, Shatin, New Territories)

  • Tsz Hin Yui

    (The Chinese University of Hong Kong, Shatin, New Territories)

  • Jiji Zhang

    (The Chinese University of Hong Kong, Shatin, New Territories)

  • Zuowei Xie

    (The Chinese University of Hong Kong, Shatin, New Territories)

Abstract

Carboranes are a class of carbon-boron molecular clusters with three-dimensional aromaticity, and inherent robustness. These endowments enable carboranes as valuable building blocks for applications ranging from functional materials to pharmaceuticals. Thus, the chemistry of carboranes has received tremendous research interest, and significant progress has been made in the past decades. However, many attempts to the synthesis of carboranes with more than 14 vertices had been unsuccessful since the report of a 14-vertex carborane in 2005. The question arises as to whether these long sought-after molecules exist. We describe in this article the synthesis and structural characterization of 15- and 16-vertex closo-carboranes as well as 16-vertex ruthenacarborane. Such a success relies on the introduction of silyl groups to both cage carbons, stabilizing the corresponding nido-carborane dianions and promoting the capitation reaction with HBBr2·SMe2. This work would shed some light on the preparation of carboranes with 17 vertices or more, and open the door for studying supercarborane chemistry.

Suggested Citation

  • Fangrui Zheng & Tsz Hin Yui & Jiji Zhang & Zuowei Xie, 2020. "Synthesis and X-ray characterization of 15- and 16-vertex closo-carboranes," Nature Communications, Nature, vol. 11(1), pages 1-5, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19661-5
    DOI: 10.1038/s41467-020-19661-5
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    Cited by:

    1. Ruofei Cheng & Jie Zhang & Huifang Zhang & Zaozao Qiu & Zuowei Xie, 2021. "Ir-catalyzed enantioselective B−H alkenylation for asymmetric synthesis of chiral-at-cage o‑carboranes," Nature Communications, Nature, vol. 12(1), pages 1-9, December.

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