Citation: Shuai Tang, Zian Wang, Mengyi Zhu, Xinyun Zhao, Xiaoyun Hu, Hua Zhang. Synthesis of organoboron compounds via heterogeneous C–H and C–X borylation[J]. Chinese Chemical Letters, ;2025, 36(5): 110503. doi: 10.1016/j.cclet.2024.110503 shu

Synthesis of organoboron compounds via heterogeneous C–H and C–X borylation

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science & Key Laboratory of Analytical Chemistry of the State Ethnic Affairs Commission, School of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, China

ccnuzhao@mail.scuec.edu.cn

xyhu@mail.scuec.edu.cn

huazhang@scuec.edu.cn

Received Date: 29 May 2024
Revised Date: 13 September 2024
Accepted Date: 24 September 2024
Available Online: 24 September 2024

Figures(32)

Homogeneous C–H and C–X borylation via transition-metal-catalysis have undergone rapid development in the past decades and become one of the most practical methods for the synthesis of organoboron compounds. However, the catalysts employed in homogeneous catalysis are generally expensive, sensitive, and difficult to separate from the reaction mixture and reuse. With the rapid development of heterogeneous catalysis, heterogeneous C–H and C–X borylation have emerged as highly efficient and sustainable approaches towards the synthesis of organoboron compounds. This review aims to highlight the recent advances in the synthesis of organoboron compounds employing heterogeneous C–H and C–X borylation strategies. We endeavor to shed light on new perspectives and inspire further research and applications in this emerging area.
- Organoboron compounds,
- Heterogeneous catalysis,
- C–H borylation,
- C–X borylation,
- Heterogeneous catalysts
1. [1]
  D. Hall, Boronic Acids: Preparation and Applications, Wiley, Weinheim, 2011.
2. [2]
  D.B. Diaz, A.K. Yudin, Nat. Chem. 9 (2017) 731–742. doi: 10.1038/nchem.2814
3. [3]
  L. Ji, S. Griesbeck, T.B. Marder, Chem. Sci. 8 (2017) 846–863. doi: 10.1039/C6SC04245G
4. [4]
  S.K. Mellerup, S. Wang, Chem. Soc. Rev. 48 (2019) 3537–3549. doi: 10.1039/c9cs00153k
5. [5]
  G.F.S. Fernandes, W.A. Denny, J.L. Dos Santos, Eur. J. Med. Chem. 179 (2019) 791–804. doi: 10.1016/j.ejmech.2019.06.092
6. [6]
  T. Ishiyama, M. Murata, N. Miyaura, J. Org. Chem. 60 (1995) 7508–7510. doi: 10.1021/jo00128a024
7. [7]
  M. Murata, S. Watanabe, Y. Masuda, J. Org. Chem. 62 (1997) 6458–6459. doi: 10.1021/jo970963p
8. [8]
  W.K. Chow, O.Y. Yuen, P.Y. Choy, et al., RSC Adv 3 (2013) 12518–12539. doi: 10.1039/c3ra22905j
9. [9]
  M. Wang, Z. Shi, Chem. Rev. 120 (2020) 7348–7398. doi: 10.1021/acs.chemrev.9b00384
10. [10]
  L. Rout, T. Punniyamurthy, Coord. Chem. Rev. 431 (2021) 213675. doi: 10.1016/j.ccr.2020.213675
11. [11]
  Y.M. Tian, X.N. Guo, H. Braunschweig, U. Radius, T.B. Marder, Chem. Rev. 121 (2021) 3561–3597. doi: 10.1021/acs.chemrev.0c01236
12. [12]
  P. Nguyen, H.P. Blom, S.A. Westcott, N.J. Taylor, T.B. Marder, J. Am. Chem. Soc. 115 (1993) 9329–9330. doi: 10.1021/ja00073a075
13. [13]
  K.M. Waltz, X. He, C. Muhoro, J.F. Hartwig, J. Am. Chem. Soc. 117 (1995) 11357–11358. doi: 10.1021/ja00150a041
14. [14]
  I.A.I. Mkhalid, J.H. Barnard, T.B. Marder, J.M. Murphy, J.F. Hartwig, Chem. Rev. 110 (2010) 890–931. doi: 10.1021/cr900206p
15. [15]
  A. Ros, R. Fernandez, J.M. Lassaletta, Chem. Soc. Rev. 43 (2014) 3229–3243. doi: 10.1039/C3CS60418G
16. [16]
  L. Xu, G. Wang, S. Zhang, et al., Tetrahedron 73 (2017) 7123–7157. doi: 10.1016/j.tet.2017.11.005
17. [17]
  J.S. Wright, P.J.H. Scott, P.G. Steel, Angew. Chem. Int. Ed. 60 (2021) 2796–2821. doi: 10.1002/anie.202001520
18. [18]
  B. Su, J.F. Hartwig, Angew. Chem. Int. Ed. 61 (2022) e202113343. doi: 10.1002/anie.202113343
19. [19]
  R. Bisht, C. Haldar, M.M.M. Hassan, et al., Chem. Soc. Rev. 51 (2022) 5042–5100. doi: 10.1039/d1cs01012c
20. [20]
  I.F. Yu, J.W. Wilson, J.F. Hartwig, Chem. Rev. 123 (2023) 11619–11663. doi: 10.1021/acs.chemrev.3c00207
21. [21]
  H. Yang, Z. Zhou, C. Tang, F. Chen, Chin. Chem. Lett. 35 (2024) 109257. doi: 10.1016/j.cclet.2023.109257
22. [22]
  T. Ishiyama, K. Ishida, J. Takagi, N. Miyaura, Chem. Lett. (2001) 1082–1083.
23. [23]
  K. Maeda, K. Motokura, Synthesis 53 (2021) 3227–3234. doi: 10.1055/a-1478-6118
24. [24]
  S. Kawamorita, H. Ohmiya, K. Hara, A. Fukuoka, M. Sawamura, J. Am. Chem. Soc. 131 (2009) 5058–5059. doi: 10.1021/ja9008419
25. [25]
  S. Kawamorita, R. Murakami, T. Iwai, M. Sawamura, J. Am. Chem. Soc. 135 (2013) 2947–2950. doi: 10.1021/ja3126239
26. [26]
  R. Murakami, K. Tsunoda, T. Iwai, M. Sawamura, Chem. Eur. J. 20 (2014) 13127–13131. doi: 10.1002/chem.201404362
27. [27]
  S. Konishi, S. Kawamorita, T. Iwai, et al., Chem. Asian J. 9 (2014) 434–438. doi: 10.1002/asia.201301423
28. [28]
  H.H. Al Mamari, J. Borel, A. Hickey, et al., Chem. Eur. J. 29 (2023) e202301734. doi: 10.1002/chem.202301734
29. [29]
  S. Kawamorita, T. Miyazaki, H. Ohmiya, T. Iwai, M. Sawamura, J. Am. Chem. Soc. 133 (2011) 19310–19313. doi: 10.1021/ja208364a
30. [30]
  S. Kawamorita, T. Miyazaki, T. Iwai, H. Ohmiya, M. Sawamura, J. Am. Chem. Soc. 134 (2012) 12924–12927. doi: 10.1021/ja305694r
31. [31]
  T. Iwai, R. Murakami, T. Harada, S. Kawamorita, M. Sawamura, Adv. Synth. Catal. 356 (2014) 1563–1570. doi: 10.1002/adsc.201301147
32. [32]
  F. Wu, Y. Feng, C.W. Jones, ACS Catal. 4 (2014) 1365–1375. doi: 10.1021/cs4009539
33. [33]
  M. Waki, Y. Maegawa, K. Hara, et al., J. Am. Chem. Soc. 136 (2014) 4003–4011. doi: 10.1021/ja4131609
34. [34]
  Y. Maegawa, S. Inagaki, Dalton Trans. 44 (2015) 13007–13016. doi: 10.1039/C5DT00239G
35. [35]
  W.R. Gruening, G. Siddiqi, O.V. Safonova, C. Coperet, Adv. Synth. Catal. 356 (2014) 673–679. doi: 10.1002/adsc.201400125
36. [36]
  K. Maeda, Y. Uemura, W.J. Chun, et al., ACS Catal. 10 (2020) 14552–14559. doi: 10.1021/acscatal.0c03734
37. [37]
  S. Zhang, H. Wang, M. Li, et al., Chem. Sci. 8 (2017) 4489–4496. doi: 10.1039/C7SC00713B
38. [38]
  A.K. Cook, S.D. Schimler, A.J. Matzger, M.S. Sanford, Science 351 (2016) 1421–1424. doi: 10.1126/science.aad9289
39. [39]
  K.T. Smith, S. Berritt, M. Gonzalez-Moreiras, et al., Science 351 (2016) 1424–1427. doi: 10.1126/science.aad9730
40. [40]
  O. Staples, M.S. Ferrandon, G.P. Laurent, et al., J. Am. Chem. Soc. 145 (2023) 7992–8000. doi: 10.1021/jacs.2c13612
41. [41]
  A. Prakash, S. Saini, S. Basappa, et al., ChemCatChem 15 (2023) e202201156. doi: 10.1002/cctc.202201156
42. [42]
  K. Manna, T. Zhang, W. Lin, J. Am. Chem. Soc. 136 (2014) 6566–6569. doi: 10.1021/ja5018267
43. [43]
  K. Manna, T. Zhang, F.X. Greene, W. Lin, J. Am. Chem. Soc. 137 (2015) 2665–2673. doi: 10.1021/ja512478y
44. [44]
  T. Sawano, Z. Lin, D. Boures, et al., J. Am. Chem. Soc. 138 (2016) 9783–9786. doi: 10.1021/jacs.6b06239
45. [45]
  X. Feng, Y. Song, Z. Li, et al., J. Am. Chem. Soc. 141 (2019) 11196–11203. doi: 10.1021/jacs.9b04285
46. [46]
  T. Zhang, K. Manna, W. Lin, J. Am. Chem. Soc. 138 (2016) 3241–3249. doi: 10.1021/jacs.6b00849
47. [47]
  K. Manna, P. Ji, Z. Lin, et al., Nat. Commun. 7 (2016) 12610. doi: 10.1038/ncomms12610
48. [48]
  M.I. Gonzalez, E.D. Bloch, J.A. Mason, S.J. Teat, J.R. Long, Inorg. Chem. 54 (2015) 2995–3005. doi: 10.1021/acs.inorgchem.5b00096
49. [49]
  X. Zhang, Z. Huang, M. Ferrandon, et al., Nat. Catal. 1 (2018) 356–362. doi: 10.1038/s41929-018-0069-6
50. [50]
  Z.H. Syed, Z. Chen, K.B. Idrees, et al., Organometallics 39 (2020) 1123–1133. doi: 10.1021/acs.organomet.9b00874
51. [51]
  S. Leubner, H. Zhao, N. Van Velthoven, et al., Angew. Chem. Int. Ed. 58 (2019) 10995–11000. doi: 10.1002/anie.201905456
52. [52]
  Y. Zhang, J. Li, X. Yang, et al., Chem. Commun. 55 (2019) 2023–2026. doi: 10.1039/c8cc09491h
53. [53]
  R. Newar, W. Begum, N. Antil, et al., Inorg. Chem. 59 (2020) 10473–10481. doi: 10.1021/acs.inorgchem.0c00747
54. [54]
  R. Newar, W. Begum, N. Akhtar, et al., Eur. J. Inorg. Chem. 2022 (2022) e202101019. doi: 10.1002/ejic.202101019
55. [55]
  R. Kalita, M. Chauhan, P. Gupta, et al., Chem. Commun. 60 (2024) 6504–6507. doi: 10.1039/d4cc01568a
56. [56]
  Z. Zhuang, Y. Wang, Z. Chen, et al., Mater. Chem. Front. 4 (2020) 1158–1163. doi: 10.1039/d0qm00040j
57. [57]
  A. Dhakshinamoorthy, C.V. Garcia, P. Concepcion, H. Garcia, Catal. Today 366 (2021) 212–217. doi: 10.1016/j.cattod.2020.06.034
58. [58]
  J. Chen, H. Li, H. Wang, et al., Chem. Commun. 59 (2023) 8432–8435. doi: 10.1039/d3cc01858j
59. [59]
  S. Basappa, A. Prakash, S.S. Talekar, M.V. Mane, S.K. Bose, ACS Catal. 14 (2024) 3065–3073. doi: 10.1021/acscatal.3c05742
60. [60]
  X. Wu, X. Han, Y. Liu, Y. Liu, Y. Cui, J. Am. Chem. Soc. 140 (2018) 16124–16133. doi: 10.1021/jacs.8b08452
61. [61]
  N. Tahir, F. Muniz-Miranda, J. Everaert, et al., J. Catal. 371 (2019) 135–143. doi: 10.1016/j.jcat.2019.01.030
62. [62]
  H. Vardhan, Y. Pan, Z. Yang, et al., APL Mater. 7 (2019) 101111. doi: 10.1063/1.5122674
63. [63]
  J.H. Kim, T. Constantin, M. Simonetti, et al., Nature 595 (2021) 677. doi: 10.1038/s41586-021-03637-6
64. [64]
  A. Basak, S. Karak, R. Banerjee, J. Am. Chem. Soc. 145 (2023) 7592–7599. doi: 10.1021/jacs.3c00950
65. [65]
  M.A. Legare, M.A. Courtemanche, E. Rochette, F.G. Fontaine, Science 349 (2015) 513–516. doi: 10.1126/science.aab3591
66. [66]
  M.A. Legare, E. Rochette, J. Legare Lavergne, N. Bouchard, F.G. Fontaine, Chem. Commun. 52 (2016) 5387–5390. doi: 10.1039/C6CC01267A
67. [67]
  N. Bouchard, F.G. Fontaine, Dalton Trans. 48 (2019) 4846–4856. doi: 10.1039/c9dt00484j
68. [68]
  N.R. Bennedsen, F. Yang, F. Goodarzi, S. Kramer, S. Kegnaes, Top. Catal. 66 (2023) 1451–1456. doi: 10.1007/s11244-023-01820-9
69. [69]
  T.J. Mazzacano, N.P. Mankad, ACS Catal. 7 (2017) 146–149. doi: 10.1021/acscatal.6b02594
70. [70]
  D. Yoshii, X. Jin, N. Mizuno, K. Yamaguchi, ACS Catal. 9 (2019) 3011–3016. doi: 10.1021/acscatal.9b00761
71. [71]
  D. Yoshii, T. Yatabe, T. Yabe, K. Yamaguchi, ACS Catal. 11 (2021) 2150–2155. doi: 10.1021/acscatal.1c00185
72. [72]
  Y. Li, U. Kanbur, J. Cui, et al., Angew. Chem. Int. Ed. 61 (2022) e202117394. doi: 10.1002/anie.202117394
73. [73]
  P.K. Verma, M.L. Shegavi, S.K. Bose, K. Geetharani, Org. Biomol. Chem. 16 (2018) 857–873. doi: 10.1039/c7ob02958f
74. [74]
  Y. Zhu, C. Koh, A.T. Peng, et al., Inorg. Chem. 47 (2008) 5756–5761. doi: 10.1109/ICC.2008.1077
75. [75]
  G. Yan, Y. Jiang, C. Kuang, et al., Chem. Commun. 46 (2010) 3170–3172. doi: 10.1039/b926945b
76. [76]
  S. Kawamorita, H. Ohmiya, T. Iwai, M. Sawamura, Angew. Chem. Int. Ed. 50 (2011) 8363–8366. doi: 10.1002/anie.201103224
77. [77]
  A. Bej, D. Srimani, A. Sarkar, Green Chem. 14 (2012) 661–667. doi: 10.1039/c2gc16111g
78. [78]
  V. Pandarus, O. Marion, G. Gingras, et al., ChemCatChem 6 (2014) 1340–1348. doi: 10.1002/cctc.201301035
79. [79]
  V. Pandarus, G. Gingras, F. Beland, R. Ciriminna, M. Pagliaro, Org. Process Res. Dev. 18 (2014) 1556–1559. doi: 10.1021/op500008h
80. [80]
  Z.F. Jiao, J.X. Zhao, X.N. Guo, X.Y. Guo, Chin. J. Catal. 41 (2020) 357–363. doi: 10.1016/S1872-2067(19)63449-2
81. [81]
  J.H. Kim, Y.K. Chung, RSC Adv. 4 (2014) 39755–39758. doi: 10.1039/C4RA05999A
82. [82]
  X.F. Zhou, Y.D. Wu, J.J. Dai, et al., RSC Adv. 5 (2015) 46672–46676. doi: 10.1039/C5RA06631J
83. [83]
  M.L. Shegavi, A. Agarwal, S.K. Bose, Green Chem. 22 (2020) 2799–2803. doi: 10.1039/d0gc00677g
84. [84]
  S. Saini, D.S. Gavali, R. Bhawar, et al., Catal. Sci. Technol. 13 (2023) 147–156. doi: 10.1039/d2cy01741e
85. [85]
  M. Franco, R. Sainz, A.M. Lamsabhi, et al., Catal. Sci. Technol. 11 (2021) 3501–3513. doi: 10.1039/d1cy00104c
86. [86]
  B. Mohan, H. Kang, K.H. Park, Catal. Commun. 85 (2016) 61–65. doi: 10.1016/j.catcom.2016.07.014
87. [87]
  D. Annas, S.A. Hira, S. Song, et al., RSC Adv. 11 (2021) 32965–32972. doi: 10.1039/d1ra05586k
88. [88]
  Z.F. Jiao, Y.M. Tian, X.N. Guo, et al., J. Catal. 395 (2021) 258–265. doi: 10.1016/j.jcat.2021.01.019
89. [89]
  P. Zhang, I.A. Roundtree, J.P. Morken, Org. Lett. 14 (2012) 1416–1419. doi: 10.1021/ol3001552
90. [90]
  H. Miura, Y. Hachiya, H. Nishio, et al., ACS Catal. 11 (2021) 758–766. doi: 10.1021/acscatal.0c03771
91. [91]
  H. Miura, M. Doi, Y. Yasui, et al., J. Am. Chem. Soc. 145 (2023) 4613–4625. doi: 10.1021/jacs.2c12311
92. [92]
  H. Miura, Y. Yasui, Y. Masaki, M. Doi, T. Shishido, ACS Catal. 13 (2023) 6787–6794. doi: 10.1021/acscatal.3c00973
93. [93]
  M. Doi, H. Miura, T. Shishido, Org. Lett. 26 (2024) 2902–2907. doi: 10.1021/acs.orglett.4c00225
94. [94]
  Y. Fan, D.W. Kang, S. Labalme, J. Li, W. Lin, Angew. Chem. Int. Ed. 62 (2023) e202218908. doi: 10.1002/anie.202218908
95. [95]
  A. Prakash, S. Basappa, B. Jeebula, et al., Org. Lett. 26 (2024) 2569–2573. doi: 10.1021/acs.orglett.4c00535
96. [96]
  P. Shang, X. Yan, Y. Li, et al., Chin. Chem. Lett. 34 (2023) 107584. doi: 10.1016/j.cclet.2022.06.007
1. [1]
  Heng Yang , Zhijie Zhou , Conghui Tang , Feng Chen . Recent advances in heterogeneous hydrosilylation of unsaturated carbon-carbon bonds. Chinese Chemical Letters, 2024, 35(6): 109257-. doi: 10.1016/j.cclet.2023.109257
2. [2]
  Wen-Jing Li , Jun-Bo Wang , Yu-Heng Liu , Mo Zhang , Zhan-Hui Zhang . Molybdenum-doped carbon nitride as an efficient heterogeneous catalyst for direct amination of nitroarenes with arylboronic acids. Chinese Chemical Letters, 2025, 36(3): 110001-. doi: 10.1016/j.cclet.2024.110001
3. [3]
  Ruiying Liu , Li Zhao , Baishan Liu , Jiayuan Yu , Yujie Wang , Wanqiang Yu , Di Xin , Chaoqiong Fang , Xuchuan Jiang , Riming Hu , Hong Liu , Weijia Zhou . Modulating pollutant adsorption and peroxymonosulfate activation sites on Co3O4@N,O doped-carbon shell for boosting catalytic degradation activity. Chinese Journal of Structural Chemistry, 2024, 43(8): 100332-100332. doi: 10.1016/j.cjsc.2024.100332
4. [4]
  Uttam Pandurang Patil . Porous carbon catalysis in sustainable synthesis of functional heterocycles: An overview. Chinese Chemical Letters, 2024, 35(8): 109472-. doi: 10.1016/j.cclet.2023.109472
5. [5]
  Yu-Yao Li , Xiao-Hui Li , Zhi-Xuan An , Yang Chu , Xiu-Li Wang . Room-temperature olefin epoxidation reaction by two 2D cobalt metal-organic complexes under O₂ atmosphere: Coordination and structural regulation. Chinese Chemical Letters, 2025, 36(4): 109716-. doi: 10.1016/j.cclet.2024.109716
6. [6]
  Baokang Geng , Xiang Chu , Li Liu , Lingling Zhang , Shuaishuai Zhang , Xiao Wang , Shuyan Song , Hongjie Zhang . High-efficiency PdNi single-atom alloy catalyst toward cross-coupling reaction. Chinese Chemical Letters, 2024, 35(7): 108924-. doi: 10.1016/j.cclet.2023.108924
7. [7]
  Hao-Cong Li , Ming Zhang , Qiyan Lv , Kai Sun , Xiao-Lan Chen , Lingbo Qu , Bing Yu . Homogeneous catalysis and heterogeneous separation: Ionic liquids as recyclable photocatalysts for hydroacylation of olefins. Chinese Chemical Letters, 2025, 36(2): 110579-. doi: 10.1016/j.cclet.2024.110579
8. [8]
  Weichen Zhu , Wei Zuo , Pu Wang , Wei Zhan , Jun Zhang , Lipin Li , Yu Tian , Hong Qi , Rui Huang . Fe-N-C heterogeneous Fenton-like catalyst for the degradation of tetracycline: Fe-N coordination and mechanism studies. Chinese Chemical Letters, 2024, 35(9): 109341-. doi: 10.1016/j.cclet.2023.109341
9. [9]
  Xueyang Zhao , Bangwei Deng , Hongtao Xie , Yizhao Li , Qingqing Ye , Fan Dong . Recent process in developing advanced heterogeneous diatomic-site metal catalysts for electrochemical CO₂ reduction. Chinese Chemical Letters, 2024, 35(7): 109139-. doi: 10.1016/j.cclet.2023.109139
10. [10]
  Haoran Shi , Jiaxin Wang , Yuqin Zhu , Hongyang Li , Guodong Ju , Lanlan Zhang , Chao Wang . Highly selective α-C(sp³)-H arylation of alkenyl amides via nickel chain-walking catalysis. Chinese Chemical Letters, 2024, 35(7): 109333-. doi: 10.1016/j.cclet.2023.109333
11. [11]
  Yi Luo , Lin Dong . Multicomponent remote C(sp²)-H bond addition by Ru catalysis: An efficient access to the alkylarylation of 2H-imidazoles. Chinese Chemical Letters, 2024, 35(10): 109648-. doi: 10.1016/j.cclet.2024.109648
12. [12]
  Jinpeng Du , Junlin Chen , Yulong Shan , Tongliang Zhang , Yu Sun , Zhongqi Liu , Xiaoyan Shi , Wenpo Shan , Yunbo Yu , Hong He . Insight into the effects of C₃H₆ on fresh and hydrothermally aged Cu-SSZ-39 catalysts. Chinese Chemical Letters, 2025, 36(3): 110019-. doi: 10.1016/j.cclet.2024.110019
13. [13]
  Xiangyang Ji , Yishuang Chen , Peng Zhang , Shaojia Song , Jian Liu , Weiyu Song . Boosting the first C–H bond activation of propane on rod-like V/CeO₂ catalyst by photo-assisted thermal catalysis. Chinese Chemical Letters, 2025, 36(5): 110719-. doi: 10.1016/j.cclet.2024.110719
14. [14]
  Xiaoyu Zhang , Xin Yu . Solar-powered heterogeneous water disinfection nano-system. Chinese Journal of Structural Chemistry, 2025, 44(3): 100439-100439. doi: 10.1016/j.cjsc.2024.100439
15. [15]
  Dong-Sheng Deng , Su-Qin Tang , Yong-Tu Yuan , Ding-Xiong Xie , Zhi-Yuan Zhu , Yue-Mei Huang , Yun-Lin Liu . C-F insertion reaction sheds new light on the construction of fluorinated compounds. Chinese Chemical Letters, 2024, 35(8): 109417-. doi: 10.1016/j.cclet.2023.109417
16. [16]
  Mianying Huang , Zhiguang Xu , Xiaoming Lin . Mechanistic analysis of Co2VO4/X (X = Ni, C) heterostructures as anode materials of lithium-ion batteries. Chinese Journal of Structural Chemistry, 2024, 43(7): 100309-100309. doi: 10.1016/j.cjsc.2024.100309
17. [17]
  Xin Li , Jia-Min Lu , Bo Li , Chen Zhao , Bei-Bei Yang , Li Li . Chiroptical sensing for remote chiral amines via a C–H activation reaction. Chinese Chemical Letters, 2025, 36(5): 110310-. doi: 10.1016/j.cclet.2024.110310
18. [18]
  Hualin Jiang , Wenxi Ye , Huitao Zhen , Xubiao Luo , Vyacheslav Fominski , Long Ye , Pinghua Chen . Novel 3D-on-2D g-C₃N₄/AgI._x._y heterojunction photocatalyst for simultaneous and stoichiometric production of H₂ and H₂O₂ from water splitting under visible light. Chinese Chemical Letters, 2025, 36(2): 109984-. doi: 10.1016/j.cclet.2024.109984
19. [19]
  Ruonan Guo , Heng Zhang , Changsheng Guo , Ningqing Lv , Beidou Xi , Jian Xu . Degradation of neonicotinoids with different molecular structures in heterogeneous peroxymonosulfate activation system through different oxidation pathways. Chinese Chemical Letters, 2024, 35(9): 109413-. doi: 10.1016/j.cclet.2023.109413
20. [20]
  Ji Chen , Yifan Zhao , Shuwen Zhao , Hua Zhang , Youyu Long , Lingfeng Yang , Min Xi , Zitao Ni , Yao Zhou , Anran Chen . Heterogeneous bimetallic oxides/phosphides nanorod with upshifted d band center for efficient overall water splitting. Chinese Chemical Letters, 2024, 35(9): 109268-. doi: 10.1016/j.cclet.2023.109268

Get Citation

PDF

XML

Metrics

PDF Downloads(0)
Abstract views(24)
HTML views(4)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142