Citation: Wei Zheyu, Chang Yalin, Yu Han, Han Sheng, Wei Yongge. Application of Anderson Type Heteropoly Acids as Catalysts in Organic Synthesis[J]. Acta Chimica Sinica, ;2020, 78(8): 725-732. doi: 10.6023/A20050187 shu

Application of Anderson Type Heteropoly Acids as Catalysts in Organic Synthesis

  • Corresponding author: Yu Han, hanyu0220@tsinghua.edu.cn Han Sheng, hansheng654321@sina.com Wei Yongge, yonggewei@tsinghua.edu.cn
  • Received Date: 26 May 2020
    Available Online: 29 June 2020

    Fund Project: the National Natural Science Foundation of China 21971134the National Natural Science Foundation of China 21631007Project supported by the National Natural Science Foundation of China (Nos. 21971134, 21631007, 21225103)the National Natural Science Foundation of China 21225103

Figures(11)

  • Anderson type heteropoly acids, also known as Anderson type polyoxometalates, are a kind of important structures in polyoxometalates. Their general structural formula can be expressed as [XM6O24]n, in which the core heteroatom X can almost be replaced by almost any metal or nonmetal element in the periodic table. Due to unique structure easy to be modified with organic ligands and designability, as well as their potential applications in materials, catalysis and medicines, Anderson type heteropoly acids have been widely concerned by researchers. In recent years, the application of Anderson type heteropoly acids in organic synthesis has gradually shown great significance for the study of green catalytic process. In this paper, the catalytic application of Anderson type heteropoly acids in organic synthesis has been reviewed and summarized according to the structure classification of Anderson type polyoxometalates. This will be helpful for the researchers to further study the catalytic application of Anderson heteropoly acids and provides new ideas for the research of green catalysis.
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    1. [1]

      Chen, W. L.; Wang, E. B. Polyoxometalate Chemistry, Science Press, Beijing, 2013, p. 38.

    2. [2]

      Wang, N. J. Changchun Normal Univ. 2015, 34, 58.

    3. [3]

      Wang, F. Ph.D. Dissertation, Northeast Normal University, Shenyang, 2007 (in Chinese).

    4. [4]

      Qin, Z. X.; Li, Q.; Huang, Y. C.; Zhang, J. W.; Li, G.; Wei, Y. G. Chin. Sci. Bull. 2018, 63, 3263.  doi: 10.1360/N972018-00853

    5. [5]

      Zhang, J. W.; Huang, Y. C.; Hao, J.; Wei, Y. G. Inorg. Chem. Front. 2017, 4, 1215.

    6. [6]

      Wei, Z. Y.; Wei, Y. G. CN 104152980A, 2014 [Chem. Abstr. 2014, 9, 60].

    7. [7]

      Hu, C. W.; Zhen, H.; Xu, L.; Wang, E. B. J. Mol. Sci. 1997, (1), 45 (in Chinese).
       

    8. [8]

      Wu, P. S.; Zhang, H. Y.; Xu, L; De, G. J. R. H.; Hu, C. W.; Wang, E. B. J. Northeast Normal Univ. (Nat. Sci.) 2001, 4, 51 (in Chinese).
       

    9. [9]

      Guo, S. R.; Kong, Y. M.; Peng, J.; Wang, E. B. Chem. Bull. 2007, 10, 748 (in Chinese).
       

    10. [10]

      Wei, Y. G. New progress of Polyacid Imine Derivatives, Abstracts of the 6th annual academic meeting and member congress of China Crystal Society (functional molecular crystal branch), China Crystal Society, 2016, p. 28.

    11. [11]

      Wei, Z. Y.; Li, Q.; Wei, Y. G. J. Mol. Sci. 2017, 33, 391 (in Chinese).
       

    12. [12]

      Song, Y. F.; Wei, Y. G. Chin. Sci. Bull. 2018, 63, 3261 (in Chinese).
       

    13. [13]

      Yu, F. L.; Liu, C. Y.; Xie, P. H.; Yuan, B.; Xie, C. X.; Yu, S. T. RSC Adv. 2015, 5, 85540.  doi: 10.1039/C5RA16013H

    14. [14]

      Lei, Y.; Li, Z.; Yuan, Z.; Wang, R.; Sunee, W.; Dong, Z. L. Sep. Purif. Technol. 2015, 151, 155.  doi: 10.1016/j.seppur.2015.05.045

    15. [15]

      Li, P. C. M.S. Dissertation, Yantai University, Yantai, 2017 (in Chinese).

    16. [16]

      Yang, W.; Hou, Y. J.; An, H. Y. J. Mol. Sci. 2017, 33, 385 (in Chinese).
       

    17. [17]

      Sun, L.; Su, T.; Li, P. Catal. Lett. 2019, 149, 7.  doi: 10.1007/s10562-018-2589-8

    18. [18]

      Ji, H. B.; She, Y. B. Prog. Chem. Eng. 2007, 26, 605 (in Chinese).
       

    19. [19]

      Li, J. J.; Wu, F. Textbook of introduction to green chemistry, Wuhan University Press, WuHan, 2015, p. 8.

    20. [20]

      He, Y. M.; Sun, Y. H.; Han, B. X. Chin. Sci. Bull. 2015, 16, 1421.

    21. [21]

      Song, J. L.; Han, B. X. Natl. Sci. Rev. 2015, 3, 255.

    22. [22]

      SD, K.; Gokavi, G. S. Res. J. Chem. 2016, 6, 17.

    23. [23]

      Yu, H.; Zhai, Y. Y.; Dai, G. Y.; Ru, S.; Han, S.; Wei, Y. G. Chem.-Eur. J. 2017, 23, 13883.  doi: 10.1002/chem.201703185

    24. [24]

      Yu, H.; Ru, S.; Zhai, Y. Y.; Dai, G. Y.; Han, S.; Wei, Y. G. ChemCatChem 2018, 10, 1253.  doi: 10.1002/cctc.201701599

    25. [25]

      Zhai, Y. Y.; Zhang, M. Q.; Fang, H. B.; Ru, S.; Yu, H.; Zhao, W. S.; Wei, Y. G. Org. Chem. Front. 2018, 5, 3454.  doi: 10.1039/C8QO00833G

    26. [26]

      Zhang, M. Q.; Zhai, Y. Y.; Ru, S.; Zang, D. J.; Han, S.; Yu, H.; Wei, Y. G. Chem. Commun. 2018, 54, 10164.  doi: 10.1039/C8CC03722A

    27. [27]

      Wang, J. J.; Zhai, Y. Y.; Wang, Y.; Yu, H.; Zhao, W. S.; Wei, Y. G. Dalton Trans. 2018, 47, 13323.  doi: 10.1039/C8DT03003K

    28. [28]

      Sawant, J. D.; Patil, K. K.; Gokavi, G. S. Transition Met. Chem. 2019, 44, 153.  doi: 10.1007/s11243-018-0279-4

    29. [29]

      Wei, Z. Y.; Ru, S.; Zhao, Q. X.; Yu, H.; Zhang, G.; Wei, Y. G. Green Chem. 2019, 21, 4069.  doi: 10.1039/C9GC01248F

    30. [30]

      Zhou, Z. H.; Dai, G. Y.; Ru, S.; Yu, H.; Wei, Y. G. Dalton Trans. 2019, 48, 14201.  doi: 10.1039/C9DT02997D

    31. [31]

      Yu, H.; Wang, J. J.; Wu, Z. K.; Zhao, Q. X.; Dan, D. M.; Han, S.; Tang, J. J.; Wei, Y. G. Green Chem. 2019, 21, 4550.  doi: 10.1039/C9GC02053E

    32. [32]

      Yu, H.; Wu, Z. K.; Wei, Z. Y.; Zhai, Y. Y.; Ru, S.; Zhao, Q. X.; Wang, J. J.; Han, S.; Wei, Y. G. Commun. Chem. 2019, 2, 1.  doi: 10.1038/s42004-018-0104-1

    33. [33]

      Wu, Z. K.; Zhai, Y. Y.; Zhao, W. S.; Wei, Z. Y.; Yu, H.; Han, S.; Wei, Y. G. Green Chem. 2020, 22, 737.  doi: 10.1039/C9GC03564H

    34. [34]

      Xu, J. J.; Zhu, Z. G.; Yuan, Z. L.; Su, T.; Zhao, Y. C.; Ren, W. Z.; Zhang, Z. H.; Lu, H. Y. J. Taiwan Inst. Chem. E. 2019, 104, 8.  doi: 10.1016/j.jtice.2019.08.006

    35. [35]

      Wang, J. J.; Yu, H.; Wei, Z. Y.; Qi, L.; Xuan, W. M.; Wei, Y. G. Research, 2020, 1, 3875920.

    36. [36]

      Luo, J. H.; Huang, Y. C.; Ding, B.; Wang, P. M.; Geng, X. F.; Zhang, J. W.; Wei, Y. G. Catalysts 2018, 8, 121.  doi: 10.3390/catal8030121

    37. [37]

      Yu, H.; Ru, S.; Dai, G. Y.; Zhai, Y. Y.; Lin, H. L.; Han, S.; Wei, Y. G. Angew. Chem. Int. Ed. 2017, 56, 3867.  doi: 10.1002/anie.201612225

    38. [38]

      She, S.; Mu, L.; Li, Q.; Huang, Z. H.; Wei, Y. G.; Yin, P. C. ChemPlusChem 2019, 11, 84.

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