Citation: Zhou Xiao-He, Fan Yu, Li Wan-Xia, Zhang Xiang, Liang Rong-Ran, Lin Feng, Zhan Tian-Guang, Cui Jiecheng, Liu Li-Juan, Zhao Xin, Zhang Kang-Da. Viologen derivatives with extended π-conjugation structures: From supra-/molecular building blocks to organic porous materials[J]. Chinese Chemical Letters, ;2020, 31(7): 1757-1767. doi: 10.1016/j.cclet.2019.12.039 shu

Viologen derivatives with extended π-conjugation structures: From supra-/molecular building blocks to organic porous materials

Zhou Xiao-He ^a ,
Fan Yu ^b,c ,
Li Wan-Xia ^a ,
Zhang Xiang ^b,d ,
Liang Rong-Ran ^b ,
Lin Feng ^b ,
Zhan Tian-Guang ^a,*, ,
Cui Jiecheng ^a ,
Liu Li-Juan ^a ,
Zhao Xin ^b,*, ,
Zhang Kang-Da ^a,*,

a.
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China
b.
Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
c.
College of Science, Department of Physics, Shanghai University, Shanghai 200444, China
d.
College of Chemical Engineering, Hunan Chemical Vocational Technology College, Zhuzhou 310027, China

tgzhan@zjnu.cn

xzhao@sioc.ac.cn

Zhang@zjnu.cn

Received Date: 23 November 2019
Revised Date: 15 December 2019
Accepted Date: 31 December 2019
Available Online: 31 December 2019

Figures(17)

Recently, increasing attention has been paid on extending the π-conjugation structures of viologens (1, 1'-disubstituted-4, 4'-bipyridylium salts) by incorporating planar aromatic units into the bipyridinium backbones. Various viologen derivatives with extended π-conjugation structures have been synthesized, including the N-termini aromatic substituted viologens, the extended π-conjugated viologens (denoted as ECVs) as well as the π-conjugated oligomeric viologens (denoted as COVs). These compounds typically exhibit interesting properties distinguished from those of an isolated viologen unit, which make them as new class of electron deficient supra-/molecular building blocks in supramolecular chemistry and materials science. In this review, we would like to highlight the recent advances of viologen derivatives with extended π-conjugation structures in versatile applications ranging from electrochromic and energy storage materials, the ECV/COV-based supramolecular self-assembly systems including the linear supramolecular polymers and 2D/3D supramolecular organic frameworks (SOFs), to the viologen-based covalent organic frameworks (COFs)/networks. We hope this review will serve as an in-time summary worthy of referring, more importantly, to provide inspiration in the rational design of novel molecules with unexplored properties and functions.
- π-Conjugated viologens,
- Self-assembly,
- Supramolecular polymers,
- Supramolecular organic frameworks,
- Ionic organic porous materials
1. [1]
  L. Michaelis, E.S. Hill, J. Gen. Physiol. 16 (1933) 859-865. doi: 10.1085/jgp.16.6.859
2. [2]
  L. Striepe, T. Baumgartner, Chem. -Eur. J. 23 (2017) 16924-16940. doi: 10.1002/chem.201703348
3. [3]
  K. Madasamy, D. Velayutham, V. Suryanarayanan, M. Kathiresan, K.C. Ho, J. Mater. Chem. C 7 (2019) 4622-4637. doi: 10.1039/C9TC00416E
4. [4]
  T. Škorjanc, D. Shetty, M.A. Olson, A. Trabolsi, ACS Appl. Mater. Interfaces 11 (2019) 6705-6716. doi: 10.1021/acsami.8b20743
5. [5]
  E.J. Dale, N.A. Vermeulen, M. Jurícek, et al., Acc. Chem. Res. 49 (2016) 2629-273.
6. [6]
  Z. Liu, S.K.M. Nalluri, J.F. Stoddart, Chem. Soc. Rev. 46 (2017) 2459-2478. doi: 10.1039/C7CS00185A
7. [7]
  B. Zheng, F. Wang, S. Dong, F. Huang, Chem. Soc. Rev. 41 (2012) 1621-1636. doi: 10.1039/C1CS15220C
8. [8]
  D. Qian, F. Yan, Progress in Chemistry 25 (2013) 46-53.
9. [9]
  Y. Liu, H. Yang, Z. Wang, X. Zhang, Chem. -Asian J. 8 (2013) 1626-1632. doi: 10.1002/asia.201300151
10. [10]
  D.W. Zhang, J. Tian, L. Chen, L. Zhang, Z.T. Li, Chem. -Asian J.10 (2015) 56-68. doi: 10.1002/asia.201402805
11. [11]
  Y. Chen, F. Huang, Z.T. Li, Y. Liu, Sci. China Chem. 8 (2018) 979-998.
12. [12]
  H.D. Correia, S. Chowdhury, A.P. Ramos, et al., Polym. Int. 68 (2019) 572-588. doi: 10.1002/pi.5709
13. [13]
  Z.J. Zhang, H.Y. Zhang, L. Chen, Y. Liu, J. Org. Chem. 76 (2011) 8270-8276. doi: 10.1021/jo201441r
14. [14]
  Y. Wang, M. Frasconi, J.F. Stoddart, ACS Cent. Sci. 3 (2017) 927-935. doi: 10.1021/acscentsci.7b00219
15. [15]
  M. Stolar, J. Borau-Garcia, M. Toonen, T. Baumgartner, J. Am. Chem. Soc. 137 (2015) 3366-3371. doi: 10.1021/ja513258j
16. [16]
  C. Reus, M. Stolar, J. Vanderkley, J. Nebauer, T. Baumgartner, J. Am. Chem. Soc. 137 (2015) 11710-11717. doi: 10.1021/jacs.5b06413
17. [17]
  W.W. Porter, T.P. Vaid, A.L. Rheingold, J. Am. Chem. Soc. 127 (2005) 16559-16566. doi: 10.1021/ja053084q
18. [18]
  A.N. Woodward, J.M. Kolesar, S.R. Hall, et al., J. Am. Chem. Soc. 139 (2017) 8467-8473. doi: 10.1021/jacs.7b01005
19. [19]
  J. Luo, B. Hu, C. Debruler, T.L. Liu, Angew. Chem. Int. Ed. 57 (2018) 231-235. doi: 10.1002/anie.201710517
20. [20]
  T.G. Zhan, T.Y. Zhou, F. Lin, et al., Org. Chem. Front. 3 (2016) 1635-1645. doi: 10.1039/C6QO00298F
21. [21]
  L. Chen, H. Willcock, C.J. Wedge, et al., Org. Biomol. Chem.14 (2016) 980-988. doi: 10.1039/C5OB02211H
22. [22]
  A. Iordache, M. Oltean, A. Milet, et al., J. Am. Chem. Soc. 134 (2012) 2653-2671. doi: 10.1021/ja209766e
23. [23]
  F. Benyettou, X. Zheng, E. Elacqua, et al., Langmuir 32 (2016) 7144-7150. doi: 10.1021/acs.langmuir.6b01433
24. [24]
  G. Wu, M. Olesinska, Y. Wu, D. Matak-Vinkovic, O.A. Scherman, J. Am. Chem. Soc. 139 (2017) 3202-3208. doi: 10.1021/jacs.6b13074
25. [25]
  Y. Yu, Y. Li, X. Wang, et al., J. Org. Chem. 82 (2017) 5590-5596. doi: 10.1021/acs.joc.7b00400
26. [26]
  A.N. Basuray, H.P.J. de Rouville, K.J. Hartlieb, et al., Angew. Chem. Int. Ed. 51 (2012) 11872-11877. doi: 10.1002/anie.201205089
27. [27]
  A.N. Basuray, H.P.J. de Rouville, K.J. Hartlieb, A.C. Fahrenbach, J.F. Stoddart, Chem. -Asian J. 8 (2013) 524-532. doi: 10.1002/asia.201200780
28. [28]
  J.C. Barnes, M. Jurícek, N.A. Vermeulen, E.J. Dale, J.F. Stoddart, J. Org. Chem. 789 (2013) 11962-11969.
29. [29]
  E.J. Dale, N.A. Vermeulen, A.A. Thomas, et al., J. Am. Chem. Soc. 136 (2014) 10669-10682. doi: 10.1021/ja5041557
30. [30]
  W.W. Porter, T.P. Vaid, J. Org. Chem. 70 (2005) 5028-5035. doi: 10.1021/jo050328g
31. [31]
  Z. Han, T.P. Vaid, A.L. Rheingold, J. Org. Chem. 73 (2008) 445-450. doi: 10.1021/jo701944c
32. [32]
  S. Sathyamoorthi, M. Kanagaraj, M. Kathiresan, V. Suryanarayanana, D. Velayutham, J. Mater. Chem. A 4 (2016) 4562-4569. doi: 10.1039/C6TA00858E
33. [33]
  B. Hu, C. DeBruler, Z. Rhodes, T.L. Liu, J. Am. Chem. Soc.139 (2017) 1207-1214. doi: 10.1021/jacs.6b10984
34. [34]
  J. Luo, B. Hu, C. Debruler, T.L. Liu, Angew. Chem. Int. Ed. 57 (2018) 231-235. doi: 10.1002/anie.201710517
35. [35]
  C. Reus, M. Stolar, J. Vanderkley, J. Nebauer, T. Baumgartner, J. Am. Chem. Soc. 137 (2015) 11710-11717. doi: 10.1021/jacs.5b06413
36. [36]
  L. Chen, F. Hartl, H.M. Colquhoun, B.W. Greenland, Tetrahedron Lett. 58 (2017) 1859-1862. doi: 10.1016/j.tetlet.2017.03.089
37. [37]
  L. Chen, E. Vivier, C.J. Eling, et al., Synth. Met. 241 (2018) 31-38. doi: 10.1016/j.synthmet.2018.03.019
38. [38]
  T.G. Zhan, B.Y. Lu, F. Lin, et al., Org. Chem. Front. 2 (2015) 1578-1583. doi: 10.1039/C5QO00244C
39. [39]
  F. Lin, R.R. Liang, Q.Y. Qi, et al., Chin. J. Chem. 35 (2017) 429-434. doi: 10.1002/cjoc.201600906
40. [40]
  Y.C. Zhang, D.W. Zhang, H. Wang, Y. Zhou, Z.T. Li, Polym.Chem. 6 (2015) 4404-4408. doi: 10.1039/C5PY00419E
41. [41]
  Q. Qi, C.G. Xi, H. Wang, D.W. Zhang, Z.T. Li, Supramol. Chem. 28 (2016) 762-767. doi: 10.1080/10610278.2016.1165348
42. [42]
  K.J. Hartlieb, A.N. Basuray, C. Ke, et al., Asian J. Org. Chem. 2 (2013) 225-229. doi: 10.1002/ajoc.201200187
43. [43]
  Y. Song, X. Huang, H. Hua, Q. Wang, Dyes Pigm. 137 (2017) 229-235. doi: 10.1016/j.dyepig.2016.10.012
44. [44]
  S.K. Samanta, K.G. Brady, L. Isaacs, Chem. Commun. (Camb.) 53 (2017) 2756-2759. doi: 10.1039/C6CC10328F
45. [45]
  Y. Yao, R. Zhao, Y. Shi, et al., Chem. Commun. (Camb.) 54 (2018) 8068-8071. doi: 10.1039/C8CC04423F
46. [46]
  B. Tang, W.L. Li, Y. Chang, et al., Angew. Chem. Int. Ed. 58 (2019) 15526-15531. doi: 10.1002/anie.201910257
47. [47]
  W. Huang, T.G. Zhan, F. Lin, X. Zhao, Prog. Chem. 28 (2016) 165-183.
48. [48]
  F. Lin, T.G. Zhan, T.Y. Zhou, et al., Chem. Commun. (Camb.) 50 (2014) 7982-7985. doi: 10.1039/C4CC02971B
49. [49]
  Y. Fan, F. Lin, X.N. Xu, J.Q. Xu, X. Zhao, Acta Polym. Sin. (2017) 80-85.
50. [50]
  Z.J. Yin, Z.Q. Wu, F. Lin, et al., Chem. Chin. Lett. 28 (2017) 1167-1171. doi: 10.1016/j.cclet.2017.03.029
51. [51]
  H.J. Kim, D.R. Whang, J. Gierschner, S.Y. Park, Angew. Chem. Int. Ed. 55 (2016) 15915-15919. doi: 10.1002/anie.201609699
52. [52]
  H.J. Kim, P.C. Nandajan, J. Gierschner, S.Y. Park, Adv. Funct. Mater. 28 (2017) 1705141.
53. [53]
  X.L. Ni, S. Chen, Y. Yang, Z. Tao, J. Am. Chem. Soc. 138 (2016) 6177-6183. doi: 10.1021/jacs.6b01223
54. [54]
  S.L. Cai, W.G. Zhang, R.N. Zuckermann, et al., Adv. Mater. 27 (2015) 5762-5770. doi: 10.1002/adma.201500124
55. [55]
  J. Zhu, C. Yang, C. Lu, et al., Acc. Chem. Res. 51 (2018) 3191-3202. doi: 10.1021/acs.accounts.8b00444
56. [56]
  X. Feng, A.D. Schlüter, Angew. Chem. Int. Ed. 57 (2018) 13748-13763. doi: 10.1002/anie.201803456
57. [57]
  R. Sakamoto, K. Takada, T. Pal, et al., Chem. Commun. (Camb.) 53 (2017) 5781-5801. doi: 10.1039/C7CC00810D
58. [58]
  L. Cao, T. Wang, C. Wang, Chin. J. Chem. 36 (2018) 754-764. doi: 10.1002/cjoc.201800144
59. [59]
  P.J. Waller, F. Gándara, O.M. Yaghi, Acc. Chem. Res. 48 (2015) 3053-3063. doi: 10.1021/acs.accounts.5b00369
60. [60]
  J. Tian, L. Chen, D.W. Zhang, Y. Liu, Z.T. Li, Chem. Commun. (Camb.) 52 (2016) 6351-6362. doi: 10.1039/C6CC02331B
61. [61]
  J. Tian, H. Wang, D.W. Zhang, Y. Liu, Z.T. Li, Natl. Sci. Rev. 4 (2017) 426-436. doi: 10.1093/nsr/nwx030
62. [62]
  S.Y. Jiang, X. Zhao, Chin. J. Polym. Sci. 37 (2019) 1-10. doi: 10.1007/s10118-019-2189-0
63. [63]
  K.D. Zhang, J. Tian, D. Hanifi, et al., J. Am. Chem. Soc.135 (2013) 17913-17918. doi: 10.1021/ja4086935
64. [64]
  L. Zhang, T.Y. Zhou, J. Tian, et al., Polym. Chem. 5 (2014) 4715-4721. doi: 10.1039/C4PY00139G
65. [65]
  L. Zhang, Y. Jia, H. Wang, et al., Polym. Chem. 7 (2016) 1861-1865. doi: 10.1039/C5PY02054A
66. [66]
  X. Zhang, C.B. Nie, T.Y. Zhou, et al., Polym. Chem. 6 (2015) 1923-1927. doi: 10.1039/C4PY01669F
67. [67]
  J. Mei, N.L.C. Leung, R.T.K. Kwok, J.W.Y. Lam, B.Z. Tang, Chem. Rev. 115 (2015) 11718-11940. doi: 10.1021/acs.chemrev.5b00263
68. [68]
  S.Q. Xu, X. Zhang, C.B. Nie, et al., Chem. Commun. (Camb.) 51 (2015) 16417-16420. doi: 10.1039/C5CC05875A
69. [69]
  X.M. Chen, Y.M. Zhang, Y. Liu, Supramol. Chem. 28 (2016) 817-824. doi: 10.1080/10610278.2016.1158406
70. [70]
  H. Liu, Q. Pan, C. Wu, et al., Mater. Chem. Front. 3 (2019) 1532-1537. doi: 10.1039/C9QM00243J
71. [71]
  Y. Li, Y. Dong, X. Miao, et al., Angew. Chem. Int. Ed. 57 (2018) 729-733. doi: 10.1002/anie.201710553
72. [72]
  H.J. Lee, H.J. Kim, E.C. Lee, J. Kim, S.Y. Park, Chem. -Asian J.13 (2018) 390-394. doi: 10.1002/asia.201800020
73. [73]
  H. Liu, Z. Zhang, Y. Zhao, et al., J. Mater. Chem. B 7 (2019) 1435-1441.
74. [74]
  J. Tian, T.Y. Zhou, S.C. Zhang, et al., Nat. Commun. 5 (2014) 5574. doi: 10.1038/ncomms6574
75. [75]
  J. Tian, C. Yao, W.L. Yang, et al., Chin. Chem. Lett. 28 (2017) 798-806. doi: 10.1016/j.cclet.2017.01.010
76. [76]
  C. Yao, J. Tian, H. Wang, et al., Chin. Chem. Lett. 28 (2017) 893-899. doi: 10.1016/j.cclet.2017.01.005
77. [77]
  B. Yang, X.D. Zhang, J. Li, et al., CCS Chem. 1 (2019) 156-165. doi: 10.31635/ccschem.019.20180011
78. [78]
  J. Tian, Z.Y. Xu, D.W. Zhang, et al., Nat. Commun. 10 (2016) 11580.
79. [79]
  Y.P. Wu, B. Yang, J. Tian, et al., Chem. Commun. (Camb.) 53 (2017) 13367-13370. doi: 10.1039/C7CC08824H
80. [80]
  Y.P. Wu, M. Yan, Z.Z. Gao, et al., Chin. Chem. Lett. 30 (2019) 1383-1386. doi: 10.1016/j.cclet.2019.03.056
81. [81]
  S.B. Yu, Q. Qi, B. Yang, et al., Small 14 (2018) 1801037.
82. [82]
  X.F. Li, S.B. Yu, B. Yang, et al., Sci. China Chem. 61 (2018) 830-835. doi: 10.1007/s11426-018-9234-2
83. [83]
  M. Yan, X.B. Liu, Z.Z. Gao, et al., Org. Chem. Front. 6 (2019) 1698-1704. doi: 10.1039/C9QO00382G
84. [84]
  Z. Xiang, D. Cao, L. Dai, Polym. Chem. 6 (2015) 1896-1911. doi: 10.1039/C4PY01383B
85. [85]
  P. Puthiaraj, Y.R. Lee, S. Zhang, W.S. Ahn, J. Mater. Chem. A 4 (2016) 16288-16311. doi: 10.1039/C6TA06089G
86. [86]
  R.R. Liang, X. Zhao, Org. Chem. Front. 5 (2018) 3341-3356. doi: 10.1039/C8QO00830B
87. [87]
  X. Chen, K. Geng, R. Liu, et al., Angew. Chem. Int. Ed. 59 (2020) 5050-5091. doi: 10.1002/anie.201904291
88. [88]
  S. Fischer, J. Schmidt, P. Strauch, A. Thomas, Angew. Chem. Int. Ed. 52 (2013) 12174-12178. doi: 10.1002/anie.201303045
89. [89]
  Y. Du, H. Yang, J.M. Whiteley, et al., Angew. Chem. Int. Ed. 55 (2016) 1737-1741. doi: 10.1002/anie.201509014
90. [90]
  H. Ma, B. Liu, B. Li, et al., J. Am. Chem. Soc. 138 (2016) 5897-5903. doi: 10.1021/jacs.5b13490
91. [91]
  N. Huang, P. Wang, M.A. Addicoat, T. Heine, D. Jiang, Angew. Chem. Int. Ed. 56 (2017) 4982-4986. doi: 10.1002/anie.201611542
92. [92]
  Z. Li, H. Li, X. Guan, et al., J. Am. Chem. Soc. 139 (2017) 17771-17774. doi: 10.1021/jacs.7b11283
93. [93]
  J. Roeser, D. Prill, M.J. Bojdys, et al., Nat. Chem. 9 (2017) 977-982. doi: 10.1038/nchem.2771
94. [94]
  A. Mal, R.K. Mishra, V.K. Praveen, et al., Angew. Chem. Int. Ed. 57 (2018) 8443-8447. doi: 10.1002/anie.201801352
95. [95]
  K. Murugavel, Polym. Chem. 5 (2014) 5873-5884. doi: 10.1039/C4PY00718B
96. [96]
  A.F. Greene, M.K. Danielson, A.O. Delawder, et al., Chem. Mater. 29 (2017) 9498-9508. doi: 10.1021/acs.chemmater.7b03635
97. [97]
  K.P. Liles, A.F. Greene, M.K. Danielson, et al., Macromol. Rapid Commun. 39 (2018) 1700781.
98. [98]
  S.B. Yu, H. Lyu, J. Tian, et al., Polym. Chem. 7 (2016) 3392-3397. doi: 10.1039/C6PY00281A
99. [99]
  G. Das, T. Skorjanc, S.K. Sharma, et al., J. Am. Chem. Soc. 139 (2017) 9558-9565. doi: 10.1021/jacs.7b02836
100. [100]
  G. Das, T. Skorjanc, S.K. Sharma, et al., ChemNanoMat 4 (2018) 61-65. doi: 10.1002/cnma.201700242
101. [101]
  L.Z. Peng, P. Liu, Q.Q. Cheng, et al., Chem. Commun. (Camb.) 54 (2018) 4433-4436. doi: 10.1039/C8CC00957K
102. [102]
  P. Samanta, P. Chandra, S. Dutta, A.V. Desaia, S.K. Ghosh, Chem. Sci. 9 (2018) 7874-7881. doi: 10.1039/C8SC02456A
103. [103]
  O. Buyukcakir, S.H. Je, S.N. Talapaneni, D. Kim, A. Coskun, ACS Appl. Mater. Interfaces 9 (2017) 7209-7216. doi: 10.1021/acsami.6b16769
104. [104]
  O. Buyukcakir, S.H. Je, D.S. Choi, et al., Chem. Commun. (Camb.) 52 (2016) 934-937. doi: 10.1039/C5CC08132G
105. [105]
  G. Chen, X. Huang, Y. Zhang, et al., Chem. Commun. (Camb.) 54 (2018) 12174-12177. doi: 10.1039/C8CC06972G
106. [106]
  G. Das, T. Prakasam, S. Nuryyeva, et al., J. Mater. Chem. A 4 (2016) 15361-15369. doi: 10.1039/C6TA06439F
107. [107]
  T. Skorjanc, D. Shetty, S.K. Sharma, et al., Chem. Eur. J. 24 (2018) 8648-8655. doi: 10.1002/chem.201800623
108. [108]
  G. Das, S.K. Sharma, T. Prakasam, et al., Commun. Chem. 2 (2019) 106.
1. [1]
  Sifan Du , Yuan Wang , Fulin Wang , Tianyu Wang , Li Zhang , Minghua Liu . Evolution of hollow nanosphere to microtube in the self-assembly of chiral dansyl derivatives and inversed circularly polarized luminescence. Chinese Chemical Letters, 2024, 35(7): 109256-. doi: 10.1016/j.cclet.2023.109256
2. [2]
  Zhenzhu Wang , Chenglong Liu , Yunpeng Ge , Wencan Li , Chenyang Zhang , Bing Yang , Shizhong Mao , Zeyuan Dong . Differentiated self-assembly through orthogonal noncovalent interactions towards the synthesis of two-dimensional woven supramolecular polymers. Chinese Chemical Letters, 2024, 35(5): 109127-. doi: 10.1016/j.cclet.2023.109127
3. [3]
  Jingqi Xin , Shupeng Han , Meichen Zheng , Chenfeng Xu , Zhongxi Huang , Bin Wang , Changmin Yu , Feifei An , Yu Ren . A nitroreductase-responsive nanoprobe with homogeneous composition and high loading for preoperative non-invasive tumor imaging and intraoperative guidance. Chinese Chemical Letters, 2024, 35(7): 109165-. doi: 10.1016/j.cclet.2023.109165
4. [4]
  Keyang Li , Yanan Wang , Yatao Xu , Guohua Shi , Sixian Wei , Xue Zhang , Baomei Zhang , Qiang Jia , Huanhua Xu , Liangmin Yu , Jun Wu , Zhiyu He . Flash nanocomplexation (FNC): A new microvolume mixing method for nanomedicine formulation. Chinese Chemical Letters, 2024, 35(10): 109511-. doi: 10.1016/j.cclet.2024.109511
5. [5]
  Xingwen Cheng , Haoran Ren , Jiangshan Luo . Boosting the self-trapped exciton emission in vacancy-ordered double perovskites via supramolecular assembly. Chinese Journal of Structural Chemistry, 2024, 43(6): 100306-100306. doi: 10.1016/j.cjsc.2024.100306
6. [6]
  Yikun Wang , Qiaomei Chen , Shijie Liang , Dongdong Xia , Chaowei Zhao , Christopher R. McNeill , Weiwei Li . Near-infrared double-cable conjugated polymers based on alkyl linkers with tunable length for single-component organic solar cells. Chinese Chemical Letters, 2024, 35(4): 109164-. doi: 10.1016/j.cclet.2023.109164
7. [7]
  Wenlong Li , Feishi Shan , Qingdong Bao , Qinghua Li , Hua Gao , Leyong Wang . Supramolecular assembly nanoparticle for trans-epithelial treatment of keratoconus. Chinese Chemical Letters, 2024, 35(10): 110060-. doi: 10.1016/j.cclet.2024.110060
8. [8]
  Weixu Li , Yuexin Wang , Lin Li , Xinyi Huang , Mengdi Liu , Bo Gui , Xianjun Lang , Cheng Wang . Promoting energy transfer pathway in porphyrin-based sp2 carbon-conjugated covalent organic frameworks for selective photocatalytic oxidation of sulfide. Chinese Journal of Structural Chemistry, 2024, 43(7): 100299-100299. doi: 10.1016/j.cjsc.2024.100299
9. [9]
  Xinyi Cao , Yucheng Jin , Hailong Wang , Xu Ding , Xiaolin Liu , Baoqiu Yu , Xiaoning Zhan , Jianzhuang Jiang . A tetraaldehyde-derived porous organic cage and covalent organic frameworks: Syntheses, structures, and iodine vapor capture. Chinese Chemical Letters, 2024, 35(9): 109201-. doi: 10.1016/j.cclet.2023.109201
10. [10]
  Conghui Wang , Lei Xu , Zhenhua Jia , Teck-Peng Loh . Recent applications of macrocycles in supramolecular catalysis. Chinese Chemical Letters, 2024, 35(4): 109075-. doi: 10.1016/j.cclet.2023.109075
11. [11]
  Xiaofei NIU , Ke WANG , Fengyan SONG , Shuyan YU . Self-assembly of [Pd₆(L)₄]⁸⁺-type macrocyclic complexes for fluorescent sensing of HSO₃^-. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1233-1242. doi: 10.11862/CJIC.20240057
12. [12]
  Zengchao Guo , Weiwei Liu , Tengfei Liu , Jinpeng Wang , Hui Jiang , Xiaohui Liu , Yossi Weizmann , Xuemei Wang . Engineered exosome hybrid copper nanoscale antibiotics facilitate simultaneous self-assembly imaging and elimination of intracellular multidrug-resistant superbugs. Chinese Chemical Letters, 2024, 35(7): 109060-. doi: 10.1016/j.cclet.2023.109060
13. [13]
  Rui Wang , Yang Liang , Julius Rebek Jr. , Yang Yu . Stabilization and detection of labile reaction intermediates in supramolecular containers. Chinese Chemical Letters, 2024, 35(6): 109228-. doi: 10.1016/j.cclet.2023.109228
14. [14]
  Yuanzhe Lu , Yuanqin Zhu , Linfeng Zhong , Dingshan Yu . Long-lifespan aqueous alkaline and acidic batteries enabled by redox conjugated covalent organic polymer anodes. Chinese Journal of Structural Chemistry, 2024, 43(3): 100249-100249. doi: 10.1016/j.cjsc.2024.100249
15. [15]
  Changhui Yu , Peng Shang , Huihui Hu , Yuening Zhang , Xujin Qin , Linyu Han , Caihe Liu , Xiaohan Liu , Minghua Liu , Yuan Guo , Zhen Zhang . Evolution of template-assisted two-dimensional porphyrin chiral grating structure by directed self-assembly using chiral second harmonic generation microscopy. Chinese Chemical Letters, 2024, 35(10): 109805-. doi: 10.1016/j.cclet.2024.109805
16. [16]
  Lihua Ma , Song Guo , Zhi-Ming Zhang , Jin-Zhong Wang , Tong-Bu Lu , Xian-Shun Zeng . Sensitizing photoactive metal–organic frameworks via chromophore for significantly boosting photosynthesis. Chinese Chemical Letters, 2024, 35(5): 108661-. doi: 10.1016/j.cclet.2023.108661
17. [17]
  Xiaoyan Peng , Xuanhao Wu , Fan Yang , Yefei Tian , Mingming Zhang , Hongye Yuan . Gas sensors based on metal-organic frameworks: challenges and opportunities. Chinese Journal of Structural Chemistry, 2024, 43(3): 100251-100251. doi: 10.1016/j.cjsc.2024.100251
18. [18]
  Deshuai Zhen , Chunlin Liu , Qiuhui Deng , Shaoqi Zhang , Ningman Yuan , Le Li , Yu Liu . A review of covalent organic frameworks for metal ion fluorescence sensing. Chinese Chemical Letters, 2024, 35(8): 109249-. doi: 10.1016/j.cclet.2023.109249
19. [19]
  Yunyu Zhao , Chuntao Yang , Yingjian Yu . A review on covalent organic frameworks for rechargeable zinc-ion batteries. Chinese Chemical Letters, 2024, 35(7): 108865-. doi: 10.1016/j.cclet.2023.108865
20. [20]
  Hong Dong , Feng-Ming Zhang . Covalent organic frameworks for artificial photosynthetic diluted CO2 reduction. Chinese Journal of Structural Chemistry, 2024, 43(7): 100307-100307. doi: 10.1016/j.cjsc.2024.100307

Get Citation

PDF

XML

Metrics

PDF Downloads(66)
Abstract views(1441)
HTML views(398)

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