Citation: Tengteng Wang, Yiming Ju, Yao Cheng, Haiyang Wang, Dejin Zang. Recent advances in polyoxometalates based strategies for green synthesis of drugs[J]. Chinese Chemical Letters, ;2025, 36(5): 109871. doi: 10.1016/j.cclet.2024.109871 shu

Recent advances in polyoxometalates based strategies for green synthesis of drugs

School of Pharmacy and Pharmaceutical Sciences & Institute of Materia Medica, State Key Laboratory of Advanced Drug Delivery and Release Systems, Shandong First Medical University & Shandong Academy of Medical Sciences, NHC Key Laboratory of Biotechnology Drugs (Shandong Academy of Medical Sciences), Key Lab for Rare & Uncommon Diseases of Shandong Province, Ji’nan 250117, China

wanghaiyang@sdfmu.edu.cn

zangdejin_lm@163.com

Received Date: 15 February 2024
Revised Date: 19 March 2024
Accepted Date: 8 April 2024
Available Online: 9 April 2024

Figures(10)

Green synthesis of drugs is of paramount importance for current public health and a prerequisite to new drugs exploiting. Nowadays, novel strategies of disease diagnosis and therapies are in blooming development as remarkable advances have been achieved which are all highly depended on drug development. Under the current requirements to high production capacity and novel synthesis methods of drugs, green synthesis based on strategies with different ways of empowering, advanced catalysts and unique reaction equipment are attracting huge attention and of great challenging. Higher quality products and environmentally friendly synthesis conditions are becoming more and more important for manufacturing process which has new requirements for catalyst materials and synthesis processes. Polyoxometalates (POMs) are class of transition metals-oxygen clusters with precise molecular structures and superior physicochemical properties which have made longstanding and important applications upon research community of functional materials, catalysis and medicine. In this review, the recent advances of polyoxometalates based strategies for green synthesis of drugs are summarized including POMs based catalysts, alternative reaction equipment based novel synthesis protocols. The significance of POMs to pharmaceutical and industrial field is highlighted and the related perspective for future development are well discussed.
- Polyoxometalates,
- Drug synthesis,
- Green catalysis,
- Healthcare,
- Medicine manufacture
1. [1]
  S. Bayramzadeh, P. Aghaei, Appl. Ergon 92 (2021) 103351. doi: 10.1016/j.apergo.2020.103351
2. [2]
  D.M. Fan, Front. Med. 11 (2017) 152–159. doi: 10.1007/s11684-017-0499-6
3. [3]
  J.H. Cai, X.Z. Zhu, P.Y. Guo, et al., Front. Chem. 11 (2023) 1114970. doi: 10.3389/fchem.2023.1114970
4. [4]
  E.L. Ongey, P. Neubauer, Microb. Cell. Fact. 15 (2016) 97. doi: 10.1186/s12934-016-0502-y
5. [5]
  X. Hu, Y. Zhang, T. Ding, J. Liu, H. Zhao, Front. Bioeng. Biotech. 8 (2020), doi:10.3389/fbioe.2020.00990. doi: 10.3389/fbioe.2020.00990
6. [6]
  M.X. Liu, J.Y. Zhang, X.L. Zhang, Mate. Chem. Phys. 281 (2022) 125925. doi: 10.1016/j.matchemphys.2022.125925
7. [7]
  H.L. Wu, D.H. Bremner, H.Y. Li, et al., Mat. Sci. Eng. C: Mater. 62 (2016) 702–709. doi: 10.1016/j.msec.2016.02.026
8. [8]
  S. Chenampulli, G. Unnikrishnan, S. Thomas, et al., Cellulose 26 (2019) 1795–1809. doi: 10.1007/s10570-018-02227-6
9. [9]
  B. Huang, Z. Sun, G. Sun, eScience 2 (2022) 243–277. doi: 10.1016/j.esci.2022.04.006
10. [10]
  D. Zang, H. Wang, Polyoxometalates 1 (2022) 9140006. doi: 10.26599/pom.2022.9140006
11. [11]
  Y. Liu, G. Zeng, Y. Cheng, et al., Chin. Chem. Lett. 35 (2024) 108480. doi: 10.1016/j.cclet.2023.108480
12. [12]
  Y.F. Liu, C.W. Hu, G.P. Yang, Chin. Chem. Lett. 34 (2023) 108097. doi: 10.1016/j.cclet.2022.108097
13. [13]
  Y.F. Liu, Q.L. Hu, X.J. Chen, et al., Rare Metals 43 (2024) 1316–1322. doi: 10.1007/s12598-023-02532-5
14. [14]
  K Song, X.D Lv, Y.T Xin, et al., Solid State Sci. 136 (2023) 107103. doi: 10.1016/j.solidstatesciences.2022.107103
15. [15]
  K. Kamata, K. Sugahara, Catalysts 7 (2017) 345. doi: 10.3390/catal7110345
16. [16]
  D. Zang, Q. Li, G. Dai, et al., Appl. Catal. B: Environ. 281 (2021) 119426. doi: 10.1016/j.apcatb.2020.119426
17. [17]
  M.R. Horn, A. Singh, S. Alomari, et al., Energy Environ. Sci. 14 (2021) 1652–1700. doi: 10.1039/d0ee03407j
18. [18]
  K. Chen, G.Y. Dai, S.Q. Liu, et al., Chin. Chem. Lett. 34 (2023) 107638. doi: 10.1016/j.cclet.2022.06.061
19. [19]
  K. Chen, Y. Liu, M. Li, et al., J. Inorg. Biochem. 226 (2022) 111654. doi: 10.1016/j.jinorgbio.2021.111654
20. [20]
  K. Chen, Q. Yu, Y. Liu, P. Yin, J. Inorg. Biochem. 220 (2021) 111463. doi: 10.1016/j.jinorgbio.2021.111463
21. [21]
  D.N. Chang, Y.D. Li, Y.X. Chen, et al., Nanoscale Adv. 4 (2022) 3689–3706. doi: 10.1039/d2na00391k
22. [22]
  D. Zang, X.J. Gao, L. Li, Y. Wei, H. Wang, Nano Res. 15 (2022) 8872–8879. doi: 10.1007/s12274-022-4698-3
23. [23]
  J. Liu, M. Huang, X. Zhang, et al., Coord. Chem. Rev. 472 (2022) 214785. doi: 10.1016/j.ccr.2022.214785
24. [24]
  S.S. Shetty, B. Moosa, L. Zhang, et al., Biosens. Bioelectron. 229 (2023) 115240. doi: 10.1016/j.bios.2023.115240
25. [25]
  Y.T. Zhang, Y. Pi, Y.S. Hua, et al., Theranostics 10 (2020) 10031–10045. doi: 10.7150/thno.49008
26. [26]
  W.C. Huang, K.F. Cheng, H.W. Yang, K.H. Wu, J. Sol-Gel. Sci. Techn. 107 (2023) 629–639. doi: 10.1007/s10971-023-06141-7
27. [27]
  M. Zhao, X. Chen, G. Chi, et al., Inorg. Chem. Front. 7 (2020) 4320–4332. doi: 10.1039/d0qi00860e
28. [28]
  J. Wang, Y. Liu, K. Xu, et al., ACS Appl. Mater. Interfaces 6 (2014) 9785–9789. doi: 10.1021/am502193f
29. [29]
  L. Guo, L. He, Q. Zhuang, et al., Small 19 (2023) 2207315. doi: 10.1002/smll.202207315
30. [30]
  B. Han, X.H. He, Y.Q. Liu, et al., Chem. Soc. Rev. 50 (2021) 1522–1586. doi: 10.1039/d0cs00196a
31. [31]
  M.M. Korbekandi, M. Nasr-Esfahani, I. Mohammadpoor-Baltork, et al., Catal. Lett. 149 (2019) 1057–1066. doi: 10.1007/s10562-019-02668-z
32. [32]
  A. Nadin, C. Hattotuwagama, I. Churcher, Angew. Chem. Int. Ed. 51 (2012) 1114–1122. doi: 10.1002/anie.201105840
33. [33]
  Y. Qiao, A. Headley, Catalysts 3 (2013) 709–725. doi: 10.3390/catal3030709
34. [34]
  E. Estakhri, M. Nasr-Esfahani, I. Mohammadpoor-Baltork, et al., Appl. Organomet. Chem. 31 (2017) e3799. doi: 10.1002/aoc.3799
35. [35]
  Y.Q. Zhao, Y.Y. Liu, J.F. Ma, Cryst. Growth Des. 21 (2020) 1019–1027.
36. [36]
  A.G. Moaser, A.G. Afkham, R. Khoshnavazi, S. Rostamnia, Sci. Rep. 13 (2023) 4114. doi: 10.1038/s41598-023-31356-7
37. [37]
  E. da Silva, H. Vidal, A. Corrêa, Pharmaceuticals 14 (2021) 1125. doi: 10.3390/ph14111125
38. [38]
  M.C. Holland, R. Gilmour, Angew. Chem. Int. Ed. 54 (2015) 3862–3871. doi: 10.1002/anie.201409004
39. [39]
  E. Reyes, L. Prieto, A. Milelli, Molecules 28 (2022) 271. doi: 10.3390/molecules28010271
40. [40]
  M. Deliaval, R. Jayarajan, L. Eriksson, K.J. Szabó, J. Am. Chem. Soc. 145 (2023) 10001–10006. doi: 10.1021/jacs.3c02852
41. [41]
  A. Yadav, M. Gill, V.K. Singh, Org. Lett. 25 (2023) 4813–4818. doi: 10.1021/acs.orglett.3c01413
42. [42]
  M. Colella, L. Degennaro, R. Luisi, Molecules 25 (2020) 3242. doi: 10.3390/molecules25143242
43. [43]
  J. M.de Souza, M. Berton, D.R. Snead, D.T. McQuade, Org. Process Res. Dev. 24 (2020) 2271–2280. doi: 10.1021/acs.oprd.0c00146
44. [44]
  Y. Liu, L. Sun, H. Zhang, L. Shang, Y. Zhao, Chem. Rev. 121 (2021) 7468–7529. doi: 10.1021/acs.chemrev.0c01289
45. [45]
  Z. Duan, Y. Wang, L. Zhang, et al., Int. J. Chem. Reactor Eng. 19 (2021) 287–294. doi: 10.1515/ijcre-2020-0173
46. [46]
  C.R. Sagandira, A.Z. Khasipo, P. Watts, Chem. Eur. J. 27 (2021) 16028–16035. doi: 10.1002/chem.202103196
47. [47]
  M. Di Filippo, M. Baumann, Molecules 26 (2021) 6992. doi: 10.3390/molecules26226992
48. [48]
  H. Jin, Q. Cai, P. Liu, et al., Chin. Chem. Lett. 35 (2024) 108721. doi: 10.1016/j.cclet.2023.108721
49. [49]
  L. Cao, M. Sun, C. Liang, et al., Chin. Chem. Lett. 35 (2024) 108758. doi: 10.1016/j.cclet.2023.108758
50. [50]
  M. Tao, Y. Li, X. Zhang, et al., ChemSusChem. 12 (2019) 2550–2553. doi: 10.1002/cssc.201901057
51. [51]
  E. Tomarelli, B. Cerra, F.G. Mutti, A. Gioiello, Adv. Synth. Catal. 365 (2023) 4024–4048. doi: 10.1002/adsc.202300305
52. [52]
  N.B. Patil, R.S. Atapalkar, S.P. Chavan, A.A. Kulkarni, Chem. Eur. J. 27 (2021) 17695–17699. doi: 10.1002/chem.202103499
53. [53]
  M.G. Russell, T.F. Jamison, Angew. Chem. Int. Ed. 58 (2019) 7678–7681. doi: 10.1002/anie.201901814
54. [54]
  J. Liu, H. Ren, T. Tang, et al., ACS Catal. 13 (2023) 7730–7755. doi: 10.1021/acscatal.3c01363
55. [55]
  A. Fryszkowska, P.N. Devine, Curr. Opin. Chem. Biol. 55 (2020) 151–160. doi: 10.1016/j.cbpa.2020.01.012
56. [56]
  H. Sun, H. Zhang, E.L. Ang, H. Zhao, Bioorg. Med. Chem. 26 (2018) 1275–1284. doi: 10.1016/j.bmc.2017.06.043
57. [57]
  C.A. Denard, H. Ren, H. Zhao, Curr. Opin. Chem. Biol. 25 (2015) 55–64. doi: 10.1016/j.cbpa.2014.12.036
58. [58]
  S. Simić, E. Zukić, L. Schmermund, et al., Chem. Rev. 122 (2021) 1052–1126.
59. [59]
  S. Wu, R. Snajdrova, J.C. Moore, K. Baldenius, U.T. Bornscheuer, Angew. Chem. Int. Ed. 60 (2020) 88–119. doi: 10.1051/cocv/2020012
60. [60]
  U.T. Bornscheuer, G.W. Huisman, R.J. Kazlauskas, et al., Nature 485 (2012) 185–194. doi: 10.1038/nature11117
61. [61]
  A. Kinner, P. Nerke, R. Siedentop, et al., Biomedicines 10 (2022) 964. doi: 10.3390/biomedicines10050964
62. [62]
  T.K.N. Luong, T.T. Mihaylov, G. Absillis, et al., Inorg. Chem. 55 (2016) 9898–9911. doi: 10.1021/acs.inorgchem.6b01802
63. [63]
  B. Li, X. Xu, Y. Lv, et al., Small 20 (2023) 2305539.
64. [64]
  B. Zhang, M. Zhao, Y. Qi, et al., Sci. Rep. 9 (2019) 14832. doi: 10.1038/s41598-019-50539-9
65. [65]
  D. Li, H. Han, Y. Wang, et al., Eur. J. Inorg. Chem. 2013 (2012) 1926–1934. doi: 10.1007/s00586-012-2273-4
66. [66]
  Z. Ma, Y. Qiu, H. Yang, et al., ACS Appl. Mater. Interfaces 7 (2015) 22036–22045. doi: 10.1021/acsami.5b07046
67. [67]
  D.F. Chai, Z. Ma, H. Yan, et al., RSC Adv. 5 (2015) 78771–78779. doi: 10.1039/C5RA13265G
68. [68]
  K. Hernandez, R. Fernandez-Lafuente, Enzyme Microb. Technol. 48 (2011) 107–122. doi: 10.1016/j.enzmictec.2010.10.003
69. [69]
  W. Jiang, B. Fang, Appl. Biochem. Biotechnol. 192 (2020) 146–179. doi: 10.1007/s12010-020-03272-3
70. [70]
  D. Rossi, M. Tarantino, G. Rossino, et al., Expert Opin. Drug Discovery 12 (2017) 1253–1269. doi: 10.1080/17460441.2017.1383981
71. [71]
  G. Rossino, M.S. Robescu, E. Licastro, et al., Chirality 34 (2022) 1403–1418. doi: 10.1002/chir.23498
72. [72]
  C.A. Martinez, S. Hu, Y. Dumond, et al., Org. Process Res. Dev. 12 (2008) 392–398. doi: 10.1021/op7002248
73. [73]
  L.S.M.Miranda R.O.M.A.de Souza, U.T. Bornscheuer, Chem. Eur. J. 23 (2017) 12040–12063. doi: 10.1002/chem.201702235
74. [74]
  P.Ž. Plazl, Curr. Opin. Green Sustain. Chem. 32 (2021) 100546. doi: 10.1016/j.cogsc.2021.100546
75. [75]
  Y. Zhang, M. Luo, P. Wu, et al., Int. J. Mol. Sci. 23 (2022) 13568. doi: 10.3390/ijms232113568
76. [76]
  B. Tan, J. Zhang, C. Xiao, et al., Molecules 28 (2023) 1900. doi: 10.3390/molecules28041900
77. [77]
  F. Miljković, R. Rodríguez-Pérez, J. Bajorath, ACS Omega 6 (2021) 33293–33299. doi: 10.1021/acsomega.1c05512
78. [78]
  M. Moret, I.P. Angona, et al. L.Cotos, Nat. Commun. 14 (2023) 114.
79. [79]
  M. Lu, J. Yin, Q. Zhu, et al., Engineering 27 (2023) 37–69. doi: 10.1016/j.eng.2023.01.014
80. [80]
  L.K. Vora, A.D. Gholap, K. Jetha, et al., Pharmaceutics 15 (2023) 1916. doi: 10.3390/pharmaceutics15071916
81. [81]
  X.B. Cui, Molecules 28 (2023) 4662. doi: 10.3390/molecules28124662
82. [82]
  K. Chen, H. Jia, Y. Liu, P. Yin, Y. Wei, Adv. Biosyst. 4 (2020) 1900281. doi: 10.1002/adbi.201900281
83. [83]
  T. Sun, W. Cui, M. Yan, et al., Adv. Mater. 28 (2016) 7397–7404. doi: 10.1002/adma.201601778
84. [84]
  M. Tang, J. Ni, Z. Yue, et al., Angew. Chem. Int. Ed. 136 (2024) e202315031. doi: 10.1002/ange.202315031
85. [85]
  T. Wang, M. Xu, F. Li, Y. Li, W. Chen, Appl. Catal. B: Environ. 280 (2021) 119421. doi: 10.1016/j.apcatb.2020.119421
86. [86]
  K. Qin, D. Zang, Y. Wei, Chin. Chem. Lett. 34 (2023) 107999. doi: 10.1016/j.cclet.2022.107999
87. [87]
  S.D. Adhikary, D. Mandal, Tetrahedron 76 (2020) 131245. doi: 10.1016/j.tet.2020.131245
88. [88]
  A.P. Wang, Y. Xie, J.J. Wang, D. Shi, H. Yu, Chem. Commun. 58 (2022) 1127–1130. doi: 10.1039/d1cc05417a
89. [89]
  K. Chen, A. Bayaguud, H. Li, et al., Nano Res. 11 (2018) 1313–1321. doi: 10.1007/s12274-017-1746-5
90. [90]
  K. Chen, S. Liu, W. Zhu, P. Yin, Small 18 (2022) e2203957. doi: 10.1002/smll.202203957
91. [91]
  H. Jia, Q. Li, A. Bayaguud, et al., Dalton Trans. 47 (2018) 577–584. doi: 10.1039/C7DT03822D
92. [92]
  H.F. Shi, G. Yan, Y. Zhang, et al., ACS Appl. Mater. Inter. 9 (2016) 422–430.
93. [93]
  S. Martín, Y. Takashima, C.G. Lin, et al., Inorg. Chem. 58 (2019) 4110–4116. doi: 10.1021/acs.inorgchem.8b03013
94. [94]
  K. Chen, S. Liu, Y. Wei, Nano Res. 17 (2024) 1818–1826. doi: 10.1007/s12274-023-6366-7
95. [95]
  T. Sun, M. Tang, Y. Shi, B. Li, Chem. Rec. 22 (2022) e202200019. doi: 10.1002/tcr.202200019
96. [96]
  M.J. Firdhouse, P. Lalitha, Inorg. Chem. Commun. 143 (2022) 109800. doi: 10.1016/j.inoche.2022.109800
97. [97]
  L.S. VanRompuy, T.N. Parac-Vogt, Curr. Opin. Biotech. 58 (2023) 92–99.
98. [98]
  S.A.M. Abdelhameed, L. Vandebroek, F. de Azambuja, T.N. Parac-Vogt, Inorg. Chem. 59 (2020) 10569–10577. doi: 10.1021/acs.inorgchem.0c00993
99. [99]
  S. Lin, J. Li, F. Zhou, et al., ACS Omega 8 (2023) 33966–33974. doi: 10.1021/acsomega.3c04790
100. [100]
  Y. Guan, M. Li, K. Dong, et al., Biomaterials 98 (2016) 92–102. doi: 10.1016/j.biomaterials.2016.05.005
101. [101]
  D. Zhu, J. Hai, L. Wang, X. Long, Mol. Catal. 551 (2023) 113626. doi: 10.1016/j.mcat.2023.113626
102. [102]
  Z. Wei, J. Wang, H. Yu, S. Han, Y. Wei, Molecules 27 (2022) 5212. doi: 10.3390/molecules27165212
103. [103]
  F. de Azambuja, T.N. Parac-Vogt, ACS Catal. 9 (2019) 10245–10252. doi: 10.1021/acscatal.9b03415
104. [104]
  Z. Shi, J. Li, Q. Han, et al., Inorg. Chem. 58 (2019) 12529–12533. doi: 10.1021/acs.inorgchem.9b02056
105. [105]
  J. Jiao, H. Sun, C. Si, et al., ACS Appl. Mater. Interfaces 14 (2022) 16386–16393. doi: 10.1021/acsami.1c24911
106. [106]
  Q. Gu, X. Zhao, M. Meng, et al., Chin. Chem. Lett. 34 (2023) 107444. doi: 10.1016/j.cclet.2022.04.042
107. [107]
  I. Ahmed, X.X. Wang, N. Boualili, et al., Appl. Catal. A: Gen. 447 (2012) 89–99.
108. [108]
  L. Zeng, X.Y. Guo, C. He, C.Y. Duan, ACS Catal. 6 (2016) 7935–7947. doi: 10.1021/acscatal.6b02228
109. [109]
  P. Jin, H. Wei, L. Zhou, et al., Mol. Catal. 510 (2021) 111705. doi: 10.1016/j.mcat.2021.111705
110. [110]
  X. Huang, S. Liu, G. Liu, et al., Appl. Catal. B 323 (2023) 122134. doi: 10.1016/j.apcatb.2022.122134
111. [111]
  T. Ali, H. Wang, W. Iqbal, et al., Adv. Sci. 10 (2022) 2205077.
112. [112]
  E.C.R. McKenzie, S. Hosseini, A.G.C. Petro, et al., Chem. Rev. 122 (2021) 3292–3335.
113. [113]
  R. Francke, Curr. Opin. Electrochem. 36 (2022) 101111. doi: 10.1016/j.coelec.2022.101111
114. [114]
  A. Wiebe, T. Gieshoff, S. Möhle, et al., Angew. Chem. Int. Ed. 57 (2018) 5594–5619. doi: 10.1002/anie.201711060
115. [115]
  B.A. Frontana-Uribe, R.D. Little, J.G. Ibanez, A. Palma, R. Vasquez-Medrano, Green Chem. 12 (2010) 2099–2119. doi: 10.1039/c0gc00382d
116. [116]
  H.J. Schäfer, C.R. Chim. 14 (2011) 745–765. doi: 10.1016/j.crci.2011.01.002
117. [117]
  F. Marken, A.J. Cresswell, S.D. Bull, Chem. Rec. 21 (2021) 2585–2600. doi: 10.1002/tcr.202100047
118. [118]
  A.V. Anyushin, A. Kondinski, T.N. Parac-Vogt, Chem. Soc. Rev. 49 (2020) 382–432. doi: 10.1039/c8cs00854j
119. [119]
  K. Xia, T. Yatabe, K. Yonesato, et al., Angew. Chem. Int. Ed. 61 (2022) e202205873. doi: 10.1002/anie.202205873
120. [120]
  L.J. Xu, C.M. Wang, K. Yu, C.X. Wang, B.B. Zhou, Coordin. Chem. 481 (2023) 215044. doi: 10.1016/j.ccr.2023.215044
121. [121]
  S. Zhong, Z. Liu, C. Zhang, Y. Liu, Z. Fu, Catal. Lett. 154 (2023) 553–568.
122. [122]
  S. Aghajani, M. Mohammadikish, M. Khalaji-Verjani, Langmuir 39 (2023) 8484–8493. doi: 10.1021/acs.langmuir.3c00766
123. [123]
  A. Wang, Y. Xie, J. Wang, D. Shi, H. Yu, Chem. Commun. 58 (2022) 1127–1130. doi: 10.1039/D1CC05417A
124. [124]
  Q. Zheng, M. Kupper, W. Xuan, et al., J. Am. Chem. Soc. 141 (2019) 13479–13486. doi: 10.1021/jacs.9b04533
125. [125]
  K. Sato, K. Yonesato, T. Yatabe, K. Yamaguchi, K. Suzuki, Chem. Eur. J. 28 (2021) e202104051.
126. [126]
  H.L. Li, C. Lian, G.Y. Yang, Sci. China Chem. 65 (2022) 892–897. doi: 10.1007/s11426-022-1215-1
127. [127]
  X. Huang, Z. Wang, T. Wang, W. Wang, P. He, Chem. Res. Chin. Univ. 39 (2023) 660–665. doi: 10.1007/s40242-023-3092-3
128. [128]
  Q. Huang, E.Y. Rui, M. Cobbs, et al., J. Med. Chem. 58 (2015) 2821–2833. doi: 10.1021/acs.jmedchem.5b00043
129. [129]
  Y. Zhang, Z. Cai, C. Zhao, H. Zheng, L. Ackermann, Chem. Sci. 14 (2023) 3541–3547. doi: 10.1039/d2sc07045f
130. [130]
  H. Li, F. Han, L. Jiang, et al., Ind. Eng. Chem. Res. 60 (2021) 14134–14142. doi: 10.1021/acs.iecr.1c02881
131. [131]
  L. Yang, J. Feng, M. Qiao, Q. Zeng, Org. Chem. Front. 5 (2018) 24–28. doi: 10.1039/C7QO00766C
132. [132]
  C. Zhu, N.W.J. Ang, T.H. Meyer, Y. Qiu, L. Ackermann, ACS Cent. Sci. 7 (2021) 415–431. doi: 10.1021/acscentsci.0c01532
133. [133]
  P. Xiong, H.C. Xu, Acc. Chem. Res. 52 (2019) 3339–3350. doi: 10.1021/acs.accounts.9b00472
134. [134]
  G. Liu, Y. Chen, Y. Chen, et al., Adv. Mater. 35 (2023) 2304716. doi: 10.1002/adma.202304716
135. [135]
  S. Arndt, D. Weis, K. Donsbach, S.R. Waldvogel, Angew. Chem. Int. Ed. 59 (2020) 8036–8041. doi: 10.1002/anie.202002717
136. [136]
  M.M. Shi, D. Bao, S.J. Li, et al., Adv. Energy Mater. 8 (2018) 1800124. doi: 10.1002/aenm.201800124
137. [137]
  L. Li, H. Chen, L. Li, et al., Chin. J. Catal. 42 (2021) 1755–1762. doi: 10.1016/S1872-2067(21)63795-6
138. [138]
  T. He, S.K. Matta, A. Du, PCCP 21 (2019) 1546–1551. doi: 10.1039/c8cp06978f
139. [139]
  H.Q. Yin, L.L. Yang, H. Sun, et al., Chin. Chem. Lett. 34 (2023) 107337. doi: 10.1016/j.cclet.2022.03.060
140. [140]
  M. Zhou, L.P. Guo, F.Y. Lin, H.X. Liu, Anal. Chim. Acta 587 (2007) 124–131. doi: 10.1016/j.aca.2007.01.017
141. [141]
  Z. Weng, Y. Ren, X. Li, B. Yue, H. He, Polyhedron 195 (2021) 114974. doi: 10.1016/j.poly.2020.114974
142. [142]
  H. Zhang, W. Zhao, H. Li, et al., Polyoxometalates 1 (2022) 9140011. doi: 10.26599/pom.2022.9140011
143. [143]
  G. Dai, Q. Li, D. Zang, Y. Wei, Green Chem. 25 (2023) 6263–6269. doi: 10.1039/d3gc00951c
144. [144]
  H. Shi, R. Wang, M. Lou, et al., Electrochim. Acta 294 (2019) 93–101. doi: 10.1504/ijmic.2019.10024004
145. [145]
  Y. Liu, S.F. Zhao, S.X. Guo, et al., J. Am. Chem. Soc. 138 (2016) 2617–2628. doi: 10.1021/jacs.5b11408
146. [146]
  Y. Jiang, S. Liu, S. Li, et al., Chem. Commun. 47 (2011) 10287–10289. doi: 10.1039/c1cc13721b
147. [147]
  L. Zhang, L. Chen, S.X. Liu, et al., Dalton Trans. 47 (2018) 105–111. doi: 10.1039/C7DT03201C
148. [148]
  S. Ingavale, I. Patil, K. Prabakaran, A. Swami, Int. J. Energy Res. 45 (2020) 7366–7379.
149. [149]
  R. Liu, K. Cao, A.H. Clark, et al., Chem. Sci. 11 (2020) 1043–1051. doi: 10.1039/c9sc05469c
150. [150]
  A. Yaqub, M. Vagin, J.J. Walsh, et al., ACS Omega 7 (2022) 43381–43389. doi: 10.1021/acsomega.2c01287
151. [151]
  J.H. Li, Y.S. Wang, Y.C. Chen, C.W. Kung, Appl. Sci. Basel. 9 (2019) 2427. doi: 10.3390/app9122427
152. [152]
  L.S. Xie, G. Skorupskii, M. Dincă, Chem. Rev. 120 (2020) 8536–8580. doi: 10.1021/acs.chemrev.9b00766
153. [153]
  W.H. Ho, T.Y. Chen, K.I. Otake, et al., Chem. Commun. 56 (2020) 11763–11766. doi: 10.1039/d0cc04904b
154. [154]
  Z. Li, J. Zhang, X. Jing, et al., J. Mater. Chem. A 9 (2021) 6152–6159. doi: 10.1039/d0ta09421h
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沈阳化工大学材料科学与工程学院沈阳 110142