Citation: Liao Gang, Wu Yong-Jie, Shi Bing-Feng. Noncovalent Interaction in Transition Metal-Catalyzed Selective C-H Activation[J]. Acta Chimica Sinica, ;2020, 78(4): 289-298. doi: 10.6023/A20020027 shu

Noncovalent Interaction in Transition Metal-Catalyzed Selective C-H Activation

  • Corresponding author: Shi Bing-Feng, bfshi@zju.edu.cn
  • Received Date: 8 February 2020
    Available Online: 12 March 2020

    Fund Project: the National Natural Science Foundation of China 21772170the Natural Science Foundation of Zhejiang Province LR17B020001Project supported by the National Natural Science Foundation of China (Nos. 21901228, 21772170), the China Postdoctoral Science Foundation (No. 2019M650135), the Outstanding Young Talents of Zhejiang Province High-level Personnel of Special Support (No. ZJWR0108) and the Natural Science Foundation of Zhejiang Province (No. LR17B020001)the National Natural Science Foundation of China 21901228the China Postdoctoral Science Foundation 2019M650135the Outstanding Young Talents of Zhejiang Province High-level Personnel of Special Support ZJWR0108

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  • Transition metal-catalyzed direct C-H functionalization is one of the most efficient and powerful tools for the rapid synthesis of organic molecules. The use of functional groups in the molecules or covalently attached coordinating groups as directing groups has been realized as a major strategy to control the selectivity. Noncovalent interactions are of great importance in the field of molecular biology, supramolecular chemistry, material science and drug discovery. More recently, the use of well-designed ligands to enable the site-selective C-H functionalization via noncovalent interactions has emerged as a highly promising yet relatively less explored strategy. In this perspective, recent advances in this cutting-edge area are summarized. The perspective was classified into four sections according to the type of noncovalent interactions, including hydrogen bonding, ion pair, Lewis acid-base interaction and electrostatic interaction. Emphasis is placed on the mode of noncovalent interactions among the transition metals, ligands and substrates. The limitation of current research and the prospect of future work will also be discussed. We anticipate that this strategy might become a promising complementary strategy to control the positional selectivity in C-H functionalization reactions.
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