Citation: Shanghui Tian, Tian Luo, Yanping Zhu, Jie-Ping Wan. Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization[J]. Chinese Chemical Letters, ;2020, 31(12): 3073-3082. doi: 10.1016/j.cclet.2020.07.042 shu

Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization

Shanghui Tian ^a ,
Tian Luo ^a ,
Yanping Zhu ^{b, *,} ,
Jie-Ping Wan ^{a, *,}

a.
College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China
b.
School of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation, Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai 264005, China

chemzyp@foxmail.com

wanjieping@jxnu.edu.cn

Received Date: 17 June 2020
Revised Date: 10 July 2020
Accepted Date: 24 July 2020
Available Online: 26 July 2020

Figures(29)

Chromone and flavone are both central backbones of natural products and clinical medicines. Synthesis of diversely functionalized chromones and flavones constitutes significant research contents of the modern synthetic science because abundant molecular libraries of such types are crucial in providing candidate compounds for the discovery of new pharmaceuticals and functional materials. The direct C-H bond activation or functionalization on these heterocyclic backbones provides highly powerful tools for the rapid accesses to densely functionalized chromone and flavone derivatives. Considering the importance of the functionalized chromone and flavone compounds as well as the notable advances in the synthesis of such products by direct C-H activation or functionalization, we review herein the research advances in the C-H bond activation and functionalization reactions of chromone and flavones, in hope of showing the current states and promise of the research domain.
- Chromones,
- Flavones,
- C-H bond,
- Activation,
- Functionalization
1. [1]
  S.K. Sharma, S. Kumar, K. Chand, et al., Curr. Med. Chem. 18 (2011) 3825-3852. doi: 10.2174/092986711803414359
2. [2]
  M. Hadjeri, C. Beney, A. Boumendjel, Curr. Org. Chem. 7 (2003) 679-689. doi: 10.2174/1385272033486765
3. [3]
  A. Gaspar, M.J. Matos, J. Garrido, et al., Chem. Rev. 114 (2014) 4960-4992. doi: 10.1021/cr400265z
4. [4]
  D. Raffa, B. Maggio, M.V. Raimondi, et al., Eur. J. Med. Chem. 142 (2017) 213-228. doi: 10.1016/j.ejmech.2017.07.034
5. [5]
  G. Zapata-Torres, F. Opazo, C. Salgado, et al., J. Nat. Prod. 67 (2004) 416-420. doi: 10.1021/np034011s
6. [6]
  F. Yao, Q.L. Song, L. Zhang, et al., Fitoerapia 89 (2013) 200-204. doi: 10.1016/j.fitote.2013.05.020
7. [7]
  R.S. Muthyala, Y.H. Ju, S.B. Sheng, et al., Bioorg. Med. Chem. 12 (2004) 1559-1567. doi: 10.1016/j.bmc.2003.11.035
8. [8]
  H. Zhu, L. Zou, J. Tian, et al., Planta Med. 80 (2014) 262-268. doi: 10.1055/s-0033-1360340
9. [9]
  C. Li, J. He, Y. Gao, et al., Cardiovasc. Toxicol. 14 (2014) 145-152. doi: 10.1007/s12012-013-9238-7
10. [10]
  W. Li, J. Li, H. Shen, Chin. Chem. Lett. 29 (2018) 911-914. doi: 10.1016/j.cclet.2017.10.011
11. [11]
  Z. Ju, P. Shu, Z. Xie, et al., Chin. J. Org. Chem. 39 (2019) 697-702. doi: 10.6023/cjoc201808035
12. [12]
  R. Kumar, S. Chahal, S. Dahiya, et al., Corros. Rev. 35 (2017) 95-110. doi: 10.1515/corrrev-2017-0029
13. [13]
  R. Purkait, C. Patra, A. Das Mahapatra, et al., Sens. Actuators B:Chem. 257 (2018) 545-552. doi: 10.1016/j.snb.2017.10.168
14. [14]
  M. Friden-Saxin, T. Seifert, M. Malo, et al., Eur. J. Med. Chem. 114 (2016) 59-64. doi: 10.1016/j.ejmech.2016.02.046
15. [15]
  A.O. Ayt, V.A. Barachevsky, A. Duensing, et al., Opt. Quant. Electron. 49 (2017) 72. doi: 10.1007/s11082-017-0900-3
16. [16]
  A. Meydani, S. Yousefi, R. Gharibi, et al., ChemistrySelect 4 (2019) 3315-3324. doi: 10.1002/slct.201900009
17. [17]
  Y. Jia, Y. Ma, P. Zou, et al., J. Agric. Food Chem. 67 (2019) 4652-4661. doi: 10.1021/acs.jafc.8b07300
18. [18]
  W. Haider, J. Ma, X.M. Hou, et al., Chem. Nat. Compd. 56 (2020) 334-337. doi: 10.1007/s10600-020-03023-0
19. [19]
  R. Kshatriya, V.P. Jejurkar, S. Saha, Tetrahedron 74 (2018) 811-833. doi: 10.1016/j.tet.2017.12.052
20. [20]
  L. Fu, J.P. Wan, Asian J. Org. Chem. 8 (2019) 767-776. doi: 10.1002/ajoc.201900196
21. [21]
  L. Xiong, H. Hu, C.W. Wei, et al., Eur. J. Org. Chem. (2020) 1588-1597.
22. [22]
  Y. Guo, Y. Xiang, L. Wei, J.P. Wan, Org. Lett. 20 (2018) 3971-3974. doi: 10.1021/acs.orglett.8b01536
23. [23]
  C. Jiang, Z. Xiong, S. Jin, et al., Chem. Commun. 52 (2016) 11516-11519. doi: 10.1039/C6CC05391B
24. [24]
  T. Luo, J.P. Wan, Y. Liu, Org. Chem. Front. 7 (2020) 1107-1112. doi: 10.1039/D0QO00065E
25. [25]
  Y. Lin, J.P. Wan, Y. Liu, New J. Chem. 44 (2020) 8120-8124. doi: 10.1039/D0NJ00825G
26. [26]
  M. Wang, B.C. Tang, J.T. Ma, et al., Org. Biomol. Chem. 17 (2019) 1535-1541. doi: 10.1039/C8OB02994F
27. [27]
  T. Yatabe, X. Jin, K. Yamaguchi, et al., Angew. Chem. Int. Ed. 54 (2015) 13302-13306. doi: 10.1002/anie.201507134
28. [28]
  J.P. Wan, Z. Tu, Y. Wang, Chem. Eur. J. 25 (2019) 6907-6910. doi: 10.1002/chem.201901025
29. [29]
  Y. Gao, Y. Liu, J.P. Wan, J. Org. Chem. 84 (2019) 2243-2251. doi: 10.1021/acs.joc.8b02981
30. [30]
  P. Gandeepan, T. Müller, D. Zell, et al., Chem. Rev. 119 (2019) 2192-2452.
31. [31]
  D.J. Abrams, P.A. Provencher, E.J. Sorensen, Chem. Soc. Rev. 47 (2018) 8925-8967. doi: 10.1039/C8CS00716K
32. [32]
  W. Hao, Y. Liu, J. Beilstein, Org. Chem. 11 (2015) 2132-2144.
33. [33]
  J.P. Wan, Y. Jing, J. Beilstein, Org. Chem. 11 (2015) 2209-2222.
34. [34]
  J.P. Wan, L. Gan, Y. Liu, Org. Biomol. Chem. 15 (2017) 9031-9043. doi: 10.1039/C7OB02011B
35. [35]
  Y. Hu, C. Wang, ChemCatChem 11 (2019) 1167-1174. doi: 10.1002/cctc.201801787
36. [36]
  Z. Wang, P. Xie, Y. Xia, Chin. Chem. Lett. 29 (2018) 47-53. doi: 10.1016/j.cclet.2017.06.018
37. [37]
  W. Sheng, F. Lv, B. Tang, et al., Chin. Chem. Lett. 20 (2019) 1825-1833.
38. [38]
  X.L. Han, P.P. Lin, Q. Li, Chin. Chem. Lett. 30 (2019) 1495-1502. doi: 10.1016/j.cclet.2019.04.027
39. [39]
  C.H. Xu, Y. Li, J.H. Li, et al., Sci. China Chem. 62 (2019) 1463-1475. doi: 10.1007/s11426-019-9615-0
40. [40]
  X. Xu, D. Chen, Z. Wang, Chin. J. Org. Chem. 39 (2019) 3338-3352. doi: 10.6023/cjoc201904068
41. [41]
  Z. Tu, Y. Du, X. Cao, et al., Adv. Synth. Catal. 361 (2019) 4989-4997. doi: 10.1002/adsc.201900866
42. [42]
  M.M. Chen, L.Y. Shao, L.J. Lun, et al., Chin. Chem. Lett. 30 (2019) 702-706. doi: 10.1016/j.cclet.2018.09.022
43. [43]
  Y. Wang, Y. Liu, Acta Chim, Sinica 77 (2019) 418-421.
44. [44]
  D. Zhou, C. Wang, M. Li, et al., Chin. Chem. Lett. 29 (2018) 191-193. doi: 10.1016/j.cclet.2017.06.007
45. [45]
  X. Wang, Y.F. Han, X.H. Ouyang, et al., Chem. Commun. 55 (2019) 14637-14640. doi: 10.1039/C9CC07494E
46. [46]
  Y. Li, R. Pi, X.-H. Ouyang, et al., Org. Lett. 21 (2019) 397-400. doi: 10.1021/acs.orglett.8b03561
47. [47]
  H. Zou, Z.L. Wang, Y. Cao, et al., Chin. Chem. Lett. 29 (2018) 1355-1358. doi: 10.1016/j.cclet.2017.10.034
48. [48]
  Y. Wang, H. Zhou, K. Xu, et al., Chin. Chem. Lett. 28 (2017) 92-96. doi: 10.1016/j.cclet.2016.05.011
49. [49]
  Y. Li, G.A. Pan, M.J. Luo, et al., Chem. Commun. 56 (2020) 6907-6924. doi: 10.1039/D0CC02335C
50. [50]
  M.B. Zhou, Y. Li, X.H. Ouyang, et al., Sci. Chin. Chem. 63 (2020) 222-227. doi: 10.1007/s11426-019-9633-x
51. [51]
  L.Y. Xie, S. Peng, F. Liu, et al., Org. Chem. Front. 5 (2018) 2604-2609. doi: 10.1039/C8QO00661J
52. [52]
  J. Ding, Y. Guo, L.Y. Shao, et al., Chin. Chem. Lett. 27 (2016) 1617-1621. doi: 10.1016/j.cclet.2016.04.007
53. [53]
  W. Yu, W. Wu, H. Jiang, Chin. J. Chem. 37 (2019) 1158-1166. doi: 10.1002/cjoc.201900340
54. [54]
  L. Tian, J.P. Wan, S. Sheng, ChemCatChe 12 (2020) 2533-2537. doi: 10.1002/cctc.202000244
55. [55]
  Y. Dong, R.M. Gerard, J. Porter, et al., J. Am. Chem. Soc.142 (2020) 10996-11005. doi: 10.1021/jacs.0c02126
56. [56]
  A. Bose, P. Mal, Chem. Commun. 53 (2017) 11368-11371. doi: 10.1039/C7CC06267B
57. [57]
  D. Kim, K. Ham, S. Hong, Org. Biomol. Chem. 10 (2012) 7305-7312. doi: 10.1039/c2ob26061a
58. [58]
  M. Khoobi, M. Alipour, S. Zarei, et al., Chem. Commun. 48 (2012) 2985-2987. doi: 10.1039/c2cc18150a
59. [59]
  K.H. Kim, H.S. Lee, S.H. Kim, J.N. Kim, Tetrahedron Lett. 53 (2012) 2761-2764. doi: 10.1016/j.tetlet.2012.03.100
60. [60]
  H. Choi, M. Min, Q. Peng, et al., Chem. Sci. 7 (2016) 3900-3909. doi: 10.1039/C5SC04590H
61. [61]
  B. Niu, W. Zhao, Y. Ding, et al., J. Org. Chem. 80 (2015) 7251-7257. doi: 10.1021/acs.joc.5b00800
62. [62]
  C. Jin, X. Zhang, Z. Yan, et al., Synthesis 30 (2019) 1585-1591.
63. [63]
  R. Narayan, A.P. Antonchick, Chem. Eur. J. 20 (2014) 4568-4572. doi: 10.1002/chem.201400186
64. [64]
  R. Samanta, R. Narayan, J.O. Bauer, et al., Chem. Commun. 51 (2015) 925-928. doi: 10.1039/C4CC08376H
65. [65]
  R.B. Gammill, Synthesis (1979) 901-903.
66. [66]
  I. Yokoe, K. Maruyama, Y. Sugita, et al., Chem. Pharm. Bull. 42 (1994) 1697-1699. doi: 10.1248/cpb.42.1697
67. [67]
  Y.H. Joo, J.K. Kim, Synth. Commun. 28 (1998) 4287-4293. doi: 10.1080/00397919809458710
68. [68]
  Y.H. Joo, J.K. Kim, S.H. Kang, Synth. Commun. 32 (2002) 1653-1658. doi: 10.1081/SCC-120004255
69. [69]
  H.S. Rho, B.S. Ko, Y.S. Ju, Synth. Commun. 31 (2001) 2101-2106. doi: 10.1081/SCC-100104459
70. [70]
  A.M. Patil, D.A. Kamble, P.D. Lokhande, Synth. Commun. 48 (2018) 1299-1307. doi: 10.1080/00397911.2018.1440601
71. [71]
  T. Peng, G. Wang, S. Zhang, et al., Tetrahedron Lett. 61 (2020) 151511. doi: 10.1016/j.tetlet.2019.151511
72. [72]
  W. Zhao, P. Xie, Z. Bian, et al., J. Org. Chem. 80 (2015) 9167-9175. doi: 10.1021/acs.joc.5b01602
73. [73]
  W. Zhao, P. Xie, Z. Bian, et al., RSC Adv. 5 (2015) 59861-59864. doi: 10.1039/C5RA10763F
74. [74]
  Y. Ding, W. Wu, W. Zhao, et al., Org. Biomol. Chem. 14 (2016) 1428-1431. doi: 10.1039/C5OB02073E
75. [75]
  Q. Tang, Z. Bian, W. Wu, et al., J. Org. Chem. 82 (2017) 10617-10622. doi: 10.1021/acs.joc.7b01320
76. [76]
  C. Feng, J. Zhu, Q. Tang, A. Zhou, Chin. J. Org. Chem. 39 (2019) 1187-1192. doi: 10.6023/cjoc201808011
77. [77]
  J. Zhu, B. Xu, J. Yu, et al., Org. Biomol. Chem. 16 (2018) 5999-6005. doi: 10.1039/C8OB01398E
78. [78]
  T. Guo, Synth. Commun. 47 (2017) 2053-2061. doi: 10.1080/00397911.2017.1364766
79. [79]
  Y. Moon, Y. Kim, H. Hong, S. Hong, Chem. Commun. 49 (2013) 8323-8325. doi: 10.1039/c3cc44456b
80. [80]
  R. Samanta, J.O. Bauer, C. Strohmann, A.P. Antonchick, Org. Lett. 14 (2012) 5518-5521. doi: 10.1021/ol302607y
81. [81]
  D. Kim, S. Hong, Org. Lett. 13 (2011) 4466-4469. doi: 10.1021/ol2018278
82. [82]
  Y. Moon, S. Hong, Chem. Commun. 48 (2012) 7191-7193. doi: 10.1039/c2cc33204c
83. [83]
  R. Samanta, R. Narayan, A.P. Antonchick, Org. Lett. 14 (2012) 6108-6111. doi: 10.1021/ol303067f
84. [84]
  M. Min, D. Kim, S. Hong, Chem. Commun. 50 (2014) 8028-8031. doi: 10.1039/c4cc03602f
85. [85]
  S.H. Han, S. Kim, U. De, et al., J. Org. Chem. 81 (2016) 12416-12425. doi: 10.1021/acs.joc.6b02577
86. [86]
  Y. Shin, S. Han, U. De, et al., J. Org. Chem. 79 (2014) 9262-9271. doi: 10.1021/jo501709f
87. [87]
  K. Kim, H. Choe, Y. Jeong, et al., Org. Lett. 17 (2015) 2550-2553. doi: 10.1021/acs.orglett.5b01138
88. [88]
  K. Padala, M. Jeganmohan, Org. Lett. 13 (2011) 6144-6147. doi: 10.1021/ol202580e
89. [89]
  M.R. Sk, S.S. Bera, M.S. Maji, Adv. Synth. Catal. 361 (2019) 585-590. doi: 10.1002/adsc.201801385
90. [90]
  J. Kim, S.W. Park, M.H. Baik, S. Chang, J. Am. Chem. Soc. 137 (2015) 13448-13451. doi: 10.1021/jacs.5b09824
91. [91]
  G. Nacube, M.P. Huestis, Organometallics 38 (2019) 76-80. doi: 10.1021/acs.organomet.8b00327
92. [92]
  H.U. Vora, A.P. Silvestri, C.J. Engelin, Y.Q. Yu, Angew. Chem. Int. Ed. 53 (2014) 2683-2686. doi: 10.1002/anie.201310539
93. [93]
  R. Shang, L. Illies, E. Nakamura, J. Am. Chem. Soc. 138 (2016) 10132-10135. doi: 10.1021/jacs.6b06908
94. [94]
  K. Shin, Y. Park, M.H. Baik, S. Chang, Nat. Chem. 10 (2018) 218-224. doi: 10.1038/nchem.2900
95. [95]
  X. Li, G. Wu, X. Liu, et al., J. Org. Chem. 82 (2017) 13003-13011. doi: 10.1021/acs.joc.7b01489
96. [96]
  K. Sakamoto, T. Nishimura, Adv. Synth. Catal. 361 (2019) 2124-2128. doi: 10.1002/adsc.201801664
1. [1]
  Zixuan Guo , Xiaoshuai Han , Chunmei Zhang , Shuijian He , Kunming Liu , Jiapeng Hu , Weisen Yang , Shaoju Jian , Shaohua Jiang , Gaigai Duan . Activation of biomass-derived porous carbon for supercapacitors: A review. Chinese Chemical Letters, 2024, 35(7): 109007-. doi: 10.1016/j.cclet.2023.109007
2. [2]
  Tao Zhou , Jing Zhou , Yunyun Liu , Jie-Ping Wan , Fen-Er Chen . Transition metal-free tunable synthesis of 3-(trifluoromethylthio) and 3-trifluoromethylsulfinyl chromones via domino C–H functionalization and chromone annulation of enaminones. Chinese Chemical Letters, 2024, 35(11): 109683-. doi: 10.1016/j.cclet.2024.109683
3. [3]
  Hui Wang , Abdelkader Labidi , Menghan Ren , Feroz Shaik , Chuanyi Wang . 微观结构调控的g-C₃N₄在光催化NO转化中的最新进展：吸附/活化位点的关键作用. Acta Physico-Chimica Sinica, 2025, 41(5): 100039-. doi: 10.1016/j.actphy.2024.100039
4. [4]
  Peng Wang , Jianjun Wang , Ni Song , Xin Zhou , Ming Li . Radical dehydroxymethylative fluorination of aliphatic primary alcohols and diverse functionalization of α-fluoroimides via BF₃·OEt₂-catalyzed C‒F bond activation. Chinese Chemical Letters, 2025, 36(1): 109748-. doi: 10.1016/j.cclet.2024.109748
5. [5]
  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
6. [6]
  Tong Li , Leping Pan , Yan Zhang , Jihu Su , Kai Li , Kuiliang Li , Hu Chen , Qi Sun , Zhiyong Wang . Electrochemical construction of 2,5-diaryloxazoles via N–H and C(sp³)-H functionalization. Chinese Chemical Letters, 2024, 35(4): 108897-. doi: 10.1016/j.cclet.2023.108897
7. [7]
  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
8. [8]
  Yunkang Tong , Haiqiao Huang , Haolan Li , Mingle Li , Wen Sun , Jianjun Du , Jiangli Fan , Lei Wang , Bin Liu , Xiaoqiang Chen , Xiaojun Peng . Cooperative bond scission by HRP/H₂O₂ for targeted prodrug activation. Chinese Chemical Letters, 2024, 35(12): 109663-. doi: 10.1016/j.cclet.2024.109663
9. [9]
  Qiqi Li , Su Zhang , Yuting Jiang , Linna Zhu , Nannan Guo , Jing Zhang , Yutong Li , Tong Wei , Zhuangjun Fan . 前驱体机械压实制备高密度活性炭及其致密电容储能性能. Acta Physico-Chimica Sinica, 2025, 41(3): 2406009-. doi: 10.3866/PKU.WHXB202406009
10. [10]
  Guoju Guo , Xufeng Li , Jie Ma , Yongjia Shi , Jian Lv , Daoshan Yang . Photocatalyst/metal-free sequential C–N/C–S bond formation: Synthesis of S-arylisothioureas via photoinduced EDA complex activation. Chinese Chemical Letters, 2024, 35(11): 110024-. doi: 10.1016/j.cclet.2024.110024
11. [11]
  Qiao Song , Xue Peng , Zhouyu Wang , Leyong Wang . Iron-catalyzed C–H activation: A sustainable approach to efficient organic synthesis. Chinese Chemical Letters, 2025, 36(5): 110869-. doi: 10.1016/j.cclet.2025.110869
12. [12]
  Jian Han , Li-Li Zeng , Qin-Yu Fei , Yan-Xiang Ge , Rong-Hui Huang , Fen-Er Chen . Recent advances in remote C(sp³)–H functionalization via chelating group-assisted metal-catalyzed chain-walking reaction. Chinese Chemical Letters, 2024, 35(11): 109647-. doi: 10.1016/j.cclet.2024.109647
13. [13]
  Shulei Hu , Yu Zhang , Xiong Xie , Luhan Li , Kaixian Chen , Hong Liu , Jiang Wang . Rh(Ⅲ)-catalyzed late-stage C-H alkenylation and macrolactamization for the synthesis of cyclic peptides with unique Trp(C7)-alkene crosslinks. Chinese Chemical Letters, 2024, 35(8): 109408-. doi: 10.1016/j.cclet.2023.109408
14. [14]
  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
15. [15]
  Guanxiong Yu , Chengkai Xu , Huaqiang Ju , Jie Ren , Guangpeng Wu , Chengjian Zhang , Xinghong Zhang , Zhen Xu , Weipu Zhu , Hao-Cheng Yang , Haoke Zhang , Jianzhao Liu , Zhengwei Mao , Yang Zhu , Qiao Jin , Kefeng Ren , Ziliang Wu , Hanying Li . Key progresses of MOE key laboratory of macromolecular synthesis and functionalization in 2023. Chinese Chemical Letters, 2024, 35(11): 109893-. doi: 10.1016/j.cclet.2024.109893
16. [16]
  Wenling Yuan , Fengli Li , Zhe Chen , Qiaoxin Xu , Zhenhua Guan , Nanyu Yao , Zhengxi Hu , Junjun Liu , Yuan Zhou , Ying Ye , Yonghui Zhang . AbnI: An α-ketoglutarate-dependent dioxygenase involved in brassicicene CH functionalization and ring system rearrangement. Chinese Chemical Letters, 2024, 35(5): 108788-. doi: 10.1016/j.cclet.2023.108788
17. [17]
  Xiaoning Li , Quanyu Shi , Meng Li , Ningxin Song , Yumeng Xiao , Huining Xiao , Tony D. James , Lei Feng . Functionalization of cellulose carbon dots with different elements (N, B and S) for mercury ion detection and anti-counterfeit applications. Chinese Chemical Letters, 2024, 35(7): 109021-. doi: 10.1016/j.cclet.2023.109021
18. [18]
  Ningning Zhao , Yuyan Liang , Wenjie Huo , Xinyan Zhu , Zhangxing He , Zekun Zhang , Youtuo Zhang , Xianwen Wu , Lei Dai , Jing Zhu , Ling Wang , Qiaobao Zhang . Separator functionalization enables high-performance zinc anode via ion-migration regulation and interfacial engineering. Chinese Chemical Letters, 2024, 35(9): 109332-. doi: 10.1016/j.cclet.2023.109332
19. [19]
  Jie Yang , Xin-Yue Lou , Dihua Dai , Jingwei Shi , Ying-Wei Yang . Desymmetrized pillar[8]arenes: High-yield synthesis, functionalization, and host-guest chemistry. Chinese Chemical Letters, 2025, 36(1): 109818-. doi: 10.1016/j.cclet.2024.109818
20. [20]
  Limin Wang , Feiyi Huang , Xinyi Liang , Rajkumar Devasenathipathy , Xiaotian Liu , Qiulan Huang , Zhongyun Yang , Dujuan Huang , Xinglan Peng , Du-Hong Chen , Youjun Fan , Wei Chen . Photoelectric synergy induced synchronous functionalization of graphene and its applications in water splitting and desalination. Chinese Journal of Structural Chemistry, 2025, 44(2): 100501-100501. doi: 10.1016/j.cjsc.2024.100501

Get Citation

PDF

XML

Metrics

PDF Downloads(51)
Abstract views(1432)
HTML views(302)

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