Citation: Liu Chuan-Zhi, Wang Hui, Zhang Dan-Wei, Zhao Xin, Li Zhan-Ting. Study on Halogen Bonding of Organofluorine Compounds in China[J]. Chinese Journal of Organic Chemistry, ;2019, 39(1): 28-37. doi: 10.6023/cjoc201812026 shu

Study on Halogen Bonding of Organofluorine Compounds in China

a.
Department of Chemistry, Fudan University, Shanghai 200438
b.
Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032

Corresponding author: Zhang Dan-Wei, zhangdw@fudan.edu.cn Li Zhan-Ting, ztli@fudan.edu.cn
Received Date: 14 December 2018
Revised Date: 19 December 2018
Available Online: 21 January 2018
Fund Project: Project supported by the National Natural Science Foundation of China (Nos. 21772026, 21432004)the National Natural Science Foundation of China 21772026the National Natural Science Foundation of China 21432004

Figures(18)

This review summarizes studies on halogen bonding of fluorine-containing alkyl and aryl iodides in China. From 1987 to 1993, Chen et al. found that there existed donor-acceptor interaction between fluorinated organic (di)iodides, as Lewis acids, and organic Lewis bases such as amines and ethers, which represented early important advances for the research on the non-covalent force currently called as halogen bonding. From 2001 to now, several groups have used halogen bonding as driving force to conduct researches on crystal engineering. In this catogery, Zhu et al. investigated the one-dimensional self-assembly between perfluoro-α, ϖ-diioodalkanes and amines, ethers, and hexamethylphosphamide. Jin et al. studied the complexation between fluorinated aryl iodides and various N-heterocycles, whereas Zhang and Li et al. constructed supramolecular double and quadruple helices from one or two molecular components. Jin et al. conducted extensive studies on C—I…π halogen bonding and its applications in crystal engineering. Wang and Wan et al. utilized halogen bonding to induce trianglular aromatic molecules to co-assemble into two-dimensional honeycomb arrays on surface, whereas Wang et al. utilized halogen bond to induce mono-layer and layer-by-layer self-assembly of two polymers or organic molecules. Zhao and Li et al. developed the applications of halogen bonding in solution-phase multi-site molecular recognition of foldamer receptors for ICF₂-incorporated tri-armed guests. Hu, Gong, Liao et al. utilized halogen bonding to improve the material properties of a variety of organic aromatic molecules. Several groups have also used halogen bonding to increase the selectivity of a number of organic reactions. Representative examples are described, which highlight the utility of halogen bonding.
- halogen bond,
- organofluorine compounds,
- crystal engineering,
- molecular recognition,
- self-assembly,
- helix,
- foldamer,
- electron-transfer reaction
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