Citation: Zhu Junlong, Liu Xi, Huang Junhai, Xu Lin. Our expedition in the construction of fluorescent supramolecular metallacycles[J]. Chinese Chemical Letters, ;2019, 30(10): 1767-1774. doi: 10.1016/j.cclet.2019.08.027 shu

Our expedition in the construction of fluorescent supramolecular metallacycles

Zhu Junlong ^a,1 ,
Liu Xi ^a,1 ,
Huang Junhai ^b ,
Xu Lin ^a,c,*,

a.
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China
b.
Zhangjiang Institute, China State Institute of Pharmaceutical Industry, Shanghai 201203, China
c.
State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China

lxu@chem.ecnu.edu.cn

Received Date: 12 July 2019
Revised Date: 14 August 2019
Accepted Date: 15 August 2019
Available Online: 16 October 2019

Figures(18)

During the past few years, the construction of fluorescent supramolecular metallocycles has attracted extensive attention due to their diverse applications such as sensing, photoelectric devices, and mimicking complicated natural photo-processes. In this review, we will discuss how we entered the field of fluorescent supramolecular metallacycles and what we investigated in this field. The preparation of various fluorescent supramolecular metallacycles and their applications in monitoring the dynamics of coordination-driven self-assembly, sensing, catalysts, and supramolecular gels will be summarized.
- Supramolecular chemistry,
- Fluorescent metallacycle,
- Coordination-driven self-assembly,
- Functionalized metallacycle,
- Supramolecular gel
1. [1]
  Z. Xu, L. Xu, J. Zhou, et al., Chem. Commun. 48(2012) 10871-10873. doi: 10.1039/c2cc36141h
2. [2]
  H.I. Un, S. Wu, C.B. Huang, Z. Xu, L. Xu, Chem. Commun. 51(2015) 3143-3146. doi: 10.1039/C4CC09488C
3. [3]
  Z. Xu, L. Xu, Chem. Commun. 52(2016) 1094-1119. doi: 10.1039/C5CC09248E
4. [4]
  J.L. Zhu, Z. Xu, Y. Yang, L. Xu, Chem. Commun. 55(2019) 6629-6671. doi: 10.1039/C9CC03299A
5. [5]
  L. Xu, Y.X. Wang, H.B. Yang, Dalton Trans. 44(2015) 867-890. doi: 10.1039/C4DT02996H
6. [6]
  P.J. Stang, B. Olenyuk, Acc. Chem. Res. 30(1997) 502-518. doi: 10.1021/ar9602011
7. [7]
  D. Fiedler, D.H. Leung, R.G. Bergman, K.N. Raymond, Acc. Chem. Res. 38(2005) 349-358. doi: 10.1021/ar040152p
8. [8]
  M. Fujita, M. Tominaga, A. Hori, B. Therrien, Acc. Chem. Res. 38(2005) 369-378. doi: 10.1021/ar040153h
9. [9]
  S. Liu, Y.F. Han, G.X. Jin, Chem. Soc. Rev. 36(2007) 1543-1560. doi: 10.1039/b701869j
10. [10]
  C.G. Oliver, P.A. Ulman, M.J. Wiester, C.A. Mirkin, Acc. Chem. Res. 41(2008) 1618-1629. doi: 10.1021/ar800025w
11. [11]
  B.H. Northrop, Y.R. Zheng, K.W. Chi, P.J. Stang, Acc. Chem. Res. 42(2009) 1554-1563. doi: 10.1021/ar900077c
12. [12]
  P. Thanasekaran, R.T. Liao, Y.H. Liu, et al., Coord. Chem. Rev. 249(2005) 1085-1110. doi: 10.1016/j.ccr.2004.11.006
13. [13]
  M.J. Prakash, M.S. Lah, Chem. Commun. (2009) 3326-3341.
14. [14]
  S.L. James, Chem. Soc. Rev. 38(2009) 1744-1758. doi: 10.1039/b814096k
15. [15]
  M. Fujita, J. Yazaki, K. Ogura, J. Am. Chem. Soc. 112(1990) 5645-5647. doi: 10.1021/ja00170a042
16. [16]
  P.J. Stang, D.H. Cao, J. Am. Chem. Soc. 116(1994) 4981-4982. doi: 10.1021/ja00090a051
17. [17]
  N.C. Gianneschi, M.S. Masar, C.A. Mirkin, Acc. Chem. Res. 38(2005) 825-837. doi: 10.1021/ar980101q
18. [18]
  Y.T. Chan, X. Li, M. Soler, et al., J. Am. Chem. Soc. 131(2009) 16395-16397. doi: 10.1021/ja907262c
19. [19]
  S.L. Huang, Y.J. Lin, T.S.A. Hor, G.X. Jin, J. Am. Chem. Soc. 135(2013) 8125-8128. doi: 10.1021/ja402630g
20. [20]
  A. Mishra, Y.J. Jeong, J.H. Jo, et al., Organometallics 33(2014) 1144-1151. doi: 10.1021/om401042m
21. [21]
  G.H. Ning, L.Y. Yao, L.X. Liu, et al., Inorg. Chem. 49(2010) 7783-7792. doi: 10.1021/ic100724r
22. [22]
  C.C. You, F. Würthner, J. Am. Chem. Soc. 125(2003) 9716-9725. doi: 10.1021/ja029648x
23. [23]
  J. Stahl, W. Mohr, L. de Quadras, et al., J. Am. Chem. Soc. 129(2007) 8282-8295. doi: 10.1021/ja0716103
24. [24]
  G.S. Papaefstathiou, Z. Zhong, L. Gang, L.R. MacGillivray, J. Am. Chem. Soc. 126(2004) 9158-9159. doi: 10.1021/ja047819n
25. [25]
  S. Shanmugaraju, S.A. Joshi, P.S. Mukherjee, Inorg. Chem. 50(2011) 11736-11745. doi: 10.1021/ic201745y
26. [26]
  S. Shanmugaraju, A.K. Bar, K.W. Chi, P.S. Mukherjee, Organometallics 29(2010) 2971-2980. doi: 10.1021/om100202c
27. [27]
  V. Vajpayee, Y.H. Song, M.H. Lee, et al., Chem.-Eur. J. 17(2011) 7837-7844. doi: 10.1002/chem.201100242
28. [28]
  S. Ghosh, R. Chakrabarty, P.S. Mukherjee, Inorg. Chem. 48(2009) 549-556. doi: 10.1021/ic801381p
29. [29]
  S. Shanmugaraju, V. Vajpayee, S. Lee, et al., Inorg. Chem. 51(2012) 4817-4823. doi: 10.1021/ic300199j
30. [30]
  F. Würthner, A. Sautter, Org. Biomol. Chem. 1(2003) 240-243. doi: 10.1039/b208582h
31. [31]
  X. Yan, H. Wang, C.E. Hauke, et al., J. Am. Chem. Soc. 137(2015) 15276-15286. doi: 10.1021/jacs.5b10130
32. [32]
  L.J. Chen, Y.Y. Ren, N.W. Wu, et al., J. Am. Chem. Soc. 137(2015) 11725-11735. doi: 10.1021/jacs.5b06565
33. [33]
  Y. Tian, X. Yan, M.L. Saha, Z. Niu, P.J. Stang, J. Am. Chem. Soc.138(2016) 12033-12036. doi: 10.1021/jacs.6b07402
34. [34]
  N. Thakur, M.D. Pandey, R. Pandey, New J. Chem. 42(2018) 3582-3592. doi: 10.1039/C7NJ03294C
35. [35]
  Z. Li, X. Yan, F. Huang, H. Sepehrpour, P.J. Stang, Org. Lett.19(2017) 5728-5731. doi: 10.1021/acs.orglett.7b02456
36. [36]
  L. Wang, L.J. Chen, J.Q. Ma, et al., J. Organomet. Chem. 823(2016) 1-7. doi: 10.1016/j.jorganchem.2016.09.001
37. [37]
  L. Xu, H.B. Yang, Chem. Rec. 16(2016) 1274-1297. doi: 10.1002/tcr.201500271
38. [38]
  J. Zhang, N.W. Wu, X.D. Xu, et al., RSC Adv. 4(2014) 16047-16054. doi: 10.1039/C3RA46957C
39. [39]
  J.K. Ouyang, L.J. Chen, L. Xu, C.H. Wang, H.B. Yang, Chin. Chem. Lett. 24(2013) 471-474. doi: 10.1016/j.cclet.2013.03.055
40. [40]
  Y.X. Hu, X. Zhang, L. Xu, H.B. Yang, Isr. J. Chem. 59(2019) 184-196. doi: 10.1002/ijch.201800102
41. [41]
  N.W. Wu, J. Zhang, X.D. Xu, H.B. Yang, Chem. Commun. 50(2014) 10269-10272. doi: 10.1039/C4CC04039B
42. [42]
  Z.Y. Li, L. Xu, C.H. Wang, X.L. Zhao, H.B. Yang, Chem. Commun. 49(2013) 6194-6196. doi: 10.1039/c3cc42403k
43. [43]
  X.D. Xu, J. Zhang, X. Yu, et al., Chem.-Eur. J. 18(2012) 16000-16013. doi: 10.1002/chem.201202902
44. [44]
  C.B. Huang, L.J. Chen, J. Huang, L. Xu, RSC Adv. 4(2014) 19538-19549. doi: 10.1039/c4ra02373k
45. [45]
  J. Zhang, N.W. Wu, X.D. Xu, et al., RSC Adv. 4(2014) 16047-16054. doi: 10.1039/C3RA46957C
46. [46]
  B. Shi, Y. Liu, H. Zhu, et al., J. Am. Chem. Soc. 141(2019) 6494-6498. doi: 10.1021/jacs.9b02281
47. [47]
  N.W. Wu, J. Zhang, C.H. Wang, L. Xu, H.B. Yang, Monatsh. Chem. 144(2013) 553-566. doi: 10.1007/s00706-012-0892-4
48. [48]
  N.W. Wu, J. Zhang, D. Ciren, et al., Organometallics 32(2013) 2536-2545. doi: 10.1021/om301108s
49. [49]
  Y. Qin, L.J. Chen, F. Dong, et al., J. Am. Chem. Soc. 141(2019) 8943-8950. doi: 10.1021/jacs.9b02726
50. [50]
  M. Li, L.J. Chen, Y. Cai, et al., Chem 5(2019) 634-648. doi: 10.1016/j.chempr.2018.12.006
51. [51]
  M. Han, Y. Luo, B. Damaschke, et al., Angew. Chem. Int. Ed. 55(2016) 445-449. doi: 10.1002/anie.201508307
52. [52]
  Y. Cai, Z. Guo, J. Chen, et al., J. Am. Chem. Soc. 138(2016) 2219-2224. doi: 10.1021/jacs.5b11580
53. [53]
  D.H. Qu, Q.C. Wang, Q.W. Zhang, X. Ma, H. Tian, Chem. Rev. 115(2015) 7543-7588. doi: 10.1021/cr5006342
54. [54]
  Y. Qin, Y. Zhang, G. Yin, et al., Chin. J. Chem. 37(2019) 323-329. doi: 10.1002/cjoc.201800577
55. [55]
  J. Li, A.C. Grimsdale, Chem. Soc. Rev. 39(2010) 2399-2410. doi: 10.1039/b915995a
56. [56]
  A.W. Schmidt, K.R. Reddy, H.J. Knçlker, Chem. Rev. 112(2012) 3193-3328. doi: 10.1021/cr200447s
57. [57]
  N. Blouin, M. Leclerc, Acc. Chem. Res. 41(2008) 1110-1119. doi: 10.1021/ar800057k
58. [58]
  Y. Wang, B. Chen, W. Wu, et al., Angew. Chem. Int. Ed. 53(2014) 10779-11078. doi: 10.1002/anie.201406190
59. [59]
  S. Xu, T. Liu, Y. Mu, et al., Angew. Chem. Int. Ed. 53(2014) 1-6. doi: 10.1002/anie.201310509
60. [60]
  K.R. Wee, W.S. Han, D.W. Cho, et al., Angew. Chem. Int. Ed. 51(2012) 2677-2680. doi: 10.1002/anie.201109069
61. [61]
  D. Kim, V. Coropceanu, J.L. Brédas, J. Am. Chem. Soc. 133(2011) 17895-17900. doi: 10.1021/ja207554h
62. [62]
  G.R. Newkome, C.N. Moorefield, F. Vçgtle, Dendrimers and Dendrons: Concepts, Syntheses, Applications, Wiley-VCH, New York, 2001.
63. [63]
  C.N. Moorefield, S. Perera, G.R. Newkome, Dendrimer Chemistry: Supramolecular Perspectives and Applications, Wiley, Hoboken, 2012.
64. [64]
  A.W. Bosman, H.M. Janssen, E.W. Meijer, Chem. Rev. 99(1999) 1665-1688. doi: 10.1021/cr970069y
65. [65]
  H.J. Sun, S. Zhang, V. Percec, Chem. Soc. Rev. 44(2015) 3900-3923. doi: 10.1039/C4CS00249K
66. [66]
  R. van Heerbeek, P.C.J. Kamer, P.W.N.M. van Leeuwen, J.N.H. Reek, Chem. Rev. 102(2002) 3717-3756. doi: 10.1021/cr0103874
67. [67]
  X.Q. Wang, W. Wang, W.J. Li, et al., Nat. Commun. 9(2018) 3190-3200. doi: 10.1038/s41467-018-05670-y
68. [68]
  W. Wang, L.J. Chen, X.Q. Wang, et al., Proc. Natl. Acad. Sci. U. S. A. 112(2015) 5597-5601. doi: 10.1073/pnas.1500489112
69. [69]
  Y.X. Wang, Q.F. Zhou, L.J. Chen, et al., Chem. Commun. 54(2018) 2224-2227. doi: 10.1039/C7CC08729B
70. [70]
  W.J. Fan, B. Sun, J. Ma, et al., Chem.-Eur. J. 21(2015) 12947-12959. doi: 10.1002/chem.201501282
71. [71]
  M. He, Q. Han, J. He, et al., Chin. J. Chem. 31(2013) 663-672. doi: 10.1002/cjoc.201300247
72. [72]
  W. Zheng, W. Wang, S.T. Jiang, et al., J. Am. Chem. Soc. 141(2019) 583-591. doi: 10.1021/jacs.8b11642
73. [73]
  L.J. Chen, H.B. Yang, Acc. Chem. Res. 51(2018) 2699-2710. doi: 10.1021/acs.accounts.8b00317
74. [74]
  G.Y. Wu, L.J. Chen, L. Xu, X. Zhao, H.B. Yang, Coord. Chem. Rev. 369(2018) 39-75. doi: 10.1016/j.ccr.2018.05.009
75. [75]
  L.J. Chen, H.B. Yang, M. Shionoya, Chem. Soc. Rev. 46(2017) 2555-2576. doi: 10.1039/C7CS00173H
76. [76]
  B. Jiang, J. Zhang, J.Q. Ma, et al., J. Am. Chem. Soc. 138(2016) 738-741. doi: 10.1021/jacs.5b11409
77. [77]
  C.B. Huang, L. Xu, J.L. Zhu, et al., J. Am. Chem. Soc. 139(2017) 9459-9462. doi: 10.1021/jacs.7b04659
78. [78]
  L. Zhou, Z. Jin, X. Fan, et al., Chin. Chem. Lett. 29(2018) 1500-1502. doi: 10.1016/j.cclet.2018.07.018
79. [79]
  X. Sun, Y.W. Wang, Y. Peng, Org. Lett. 14(2012) 3420-3423. doi: 10.1021/ol301390g
80. [80]
  Z. Chen, Y. Xu, X. Qian, Chin. Chem. Lett. 29(2018) 1741-1756. doi: 10.1016/j.cclet.2018.09.020
81. [81]
  H.I. Un, C.B. Huang, J. Huang, et al., Chem.-Asian J. 9(2014) 3397-3402. doi: 10.1002/asia.201402946
82. [82]
  H.I. Un, C.B. Huang, C. Huang, et al., Org. Chem. Front. 1(2014) 1083-1090. doi: 10.1039/C4QO00185K
83. [83]
  C.B. Huang, H.R. Li, Y. Luo, L. Xu, Dalton Trans. 43(2014) 8102-8108. doi: 10.1039/c4dt00014e
84. [84]
  D. Wu, Y. Shen, J. Chen, et al., Chin. Chem. Lett. 28(2017) 1979-1982. doi: 10.1016/j.cclet.2017.07.004
85. [85]
  J. Zhu, P. Jia, N. Li, et al., Chin. Chem. Lett. 29(2018) 1445-1450. doi: 10.1016/j.cclet.2018.09.002
86. [86]
  M.L. He, S. Wu, J. He, Z. Abliz, L. Xu, RSC Adv. 4(2014) 2605-2608. doi: 10.1039/C3RA46500D
87. [87]
  C.B. Huang, J. Huang, L. Xu, RSC Adv. 5(2015) 13307-13310. doi: 10.1039/C4RA08337G
88. [88]
  Z. Xu, Y.Y. Ren, X. Fan, et al., Tetrahedron 71(2015) 5055-5058. doi: 10.1016/j.tet.2015.05.111
89. [89]
  L. Xu, M.L. He, H.B. Yang, X. Qian, Dalton Trans. 42(2013) 8218-8222. doi: 10.1039/c3dt50216c
90. [90]
  P. Guo, Q. Chen, T. Liu, et al., ACS Med. Chem. Lett. 4(2013) 527-531. doi: 10.1021/ml300475m
91. [91]
  Q. Chen, P. Guo, L. Xu, et al., Biochimie 97(2014) 152-162. doi: 10.1016/j.biochi.2013.10.008
92. [92]
  Z. Xu, G. Li, Y.Y. Ren, et al., Dalton Trans. 45(2016) 12087-12093. doi: 10.1039/C6DT01398H
93. [93]
  S. De, K. Mahata, M. Schmittel, Chem. Soc. Rev. 39(2010) 1555-1575. doi: 10.1039/b922293f
94. [94]
  M. Fujita, M. Aoyagi, K. Ogura, Inorg. Chim. Acta 246(1996) 53-57. doi: 10.1016/0020-1693(96)05050-5
95. [95]
  T. Yamamoto, A.M. Arif, P.J. Stang, J. Am. Chem. Soc. 125(2003) 12309-12317. doi: 10.1021/ja0302984
96. [96]
  M.L. Saha, X. Yan, P.J. Stang, Acc. Chem. Res. 49(2016) 2527-2539. doi: 10.1021/acs.accounts.6b00416
97. [97]
  A. Chowdhury, P. Howlader, P.S. Mukherjee, Chem.-Eur. J. 22(2016) 7468-7478. doi: 10.1002/chem.201600698
98. [98]
  L.J. Chen, S. Chen, Y. Qin, et al., J. Am. Chem. Soc. 140(2018) 5049-5052. doi: 10.1021/jacs.8b02386
99. [99]
  B. Jiang, L.J. Chen, G.Q. Yin, et al., Chem. Commun. 53(2017) 172-175. doi: 10.1039/C6CC08382J
100. [100]
  Y.Y. Ren, N.W. Wu, J. Huang, et al., Chem. Commun. 51(2015) 15153-15156. doi: 10.1039/C5CC04789G
101. [101]
  G.Z. Zhao, L.J. Chen, W. Wang, et al., Chem.-Eur. J. 19(2013) 10094-10100. doi: 10.1002/chem.201301385
102. [102]
  Z.Y. Li, Y. Zhang, C.W. Zhang, et al., J. Am. Chem. Soc. 136(2014) 8577-8589. doi: 10.1021/ja413047r
103. [103]
  N.W. Wu, L.J. Chen, C. Wang, et al., Chem. Commun. 50(2014) 4231-4233. doi: 10.1039/c3cc49054h
104. [104]
  Y.Y. Ren, Z. Xu, G. Li, et al., Dalton Trans. 46(2017) 333-337. doi: 10.1039/C6DT04182E
105. [105]
  C.W. Zhang, B. Ou, S.T. Jiang, et al., Polym. Chem. 9(2018) 2021-2030. doi: 10.1039/C8PY00226F
1. [1]
  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
2. [2]
  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
3. [3]
  Chao Zhang , Ai-Feng Liu , Shihui Li , Fang-Yuan Chen , Jun-Tao Zhang , Fang-Xing Zeng , Hui-Chuan Feng , Ping Wang , Wen-Chao Geng , Chuan-Rui Ma , Dong-Sheng Guo . A supramolecular formulation of icariin@sulfonatoazocalixarene for hypoxia-targeted osteoarthritis therapy. Chinese Chemical Letters, 2025, 36(1): 109752-. doi: 10.1016/j.cclet.2024.109752
4. [4]
  Xuanyu Wang , Zhao Gao , Wei Tian . Supramolecular confinement effect enabling light-harvesting system for photocatalytic α-oxyamination reaction. Chinese Chemical Letters, 2024, 35(11): 109757-. doi: 10.1016/j.cclet.2024.109757
5. [5]
  Zhengzhong Zhu , Shaojun Hu , Zhi Liu , Lipeng Zhou , Chongbin Tian , Qingfu Sun . A cationic radical lanthanide organic tetrahedron with remarkable coordination enhanced radical stability. Chinese Chemical Letters, 2025, 36(2): 109641-. doi: 10.1016/j.cclet.2024.109641
6. [6]
  Zixi Zou , Jingyuan Wang , Yian Sun , Qian Wang , Da-Hui Qu . Controlling molecular assembly on time scale: Time-dependent multicolor fluorescence for information encryption. Chinese Chemical Letters, 2024, 35(7): 108972-. doi: 10.1016/j.cclet.2023.108972
7. [7]
  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
8. [8]
  Bingbing Shi , Yuchun Wang , Yi Zhou , Xing-Xing Zhao , Yizhou Li , Nuoqian Yan , Wen-Juan Qu , Qi Lin , Tai-Bao Wei . A supramolecular oligo[2]rotaxane constructed by orthogonal platinum(Ⅱ) metallacycle and pillar[5]arene-based host–guest interactions. Chinese Chemical Letters, 2024, 35(10): 109540-. doi: 10.1016/j.cclet.2024.109540
9. [9]
  Kang Wei , Jiayu Li , Wen Zhang , Bing Yuan , Ming-De Li , Pingwu Du . A strained π-extended [10]cycloparaphenylene carbon nanoring. Chinese Chemical Letters, 2024, 35(5): 109055-. doi: 10.1016/j.cclet.2023.109055
10. [10]
  Junying Zhang , Ruochen Li , Haihua Wang , Wenbing Kang , Xing-Dong Xu . Photo-induced tunable luminescence from an aggregated amphiphilic ethylene-pyrene derivative in aqueous media. Chinese Chemical Letters, 2024, 35(6): 109216-. doi: 10.1016/j.cclet.2023.109216
11. [11]
  Zhimin Sun , Xin-Hui Guo , Yue Zhao , Qing-Yu Meng , Li-Juan Xing , He-Lue Sun . Dynamically switchable porphyrin-based molecular tweezer for on−off fullerene recognition. Chinese Chemical Letters, 2024, 35(6): 109162-. doi: 10.1016/j.cclet.2023.109162
12. [12]
  Cheng-Da Zhao , Huan Yao , Shi-Yao Li , Fangfang Du , Li-Li Wang , Liu-Pan Yang . Amide naphthotubes: Biomimetic macrocycles for selective molecular recognition. Chinese Chemical Letters, 2024, 35(4): 108879-. doi: 10.1016/j.cclet.2023.108879
13. [13]
  Jingyu Chen , Sha Wu , Yuhao Wang , Jiong Zhou . Near-perfect separation of alicyclic ketones and alicyclic alcohols by nonporous adaptive crystals of perethylated pillar[5]arene and pillar[6]arene. Chinese Chemical Letters, 2025, 36(4): 110102-. doi: 10.1016/j.cclet.2024.110102
14. [14]
  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
15. [15]
  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
16. [16]
  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
17. [17]
  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
18. [18]
  Xiangjun Zhang , Xiaodi Yang , Yan Wang , Zhongping Xu , Sisi Yi , Tao Guo , Yue Liao , Xiyu Tang , Jianxiang Zhang , Ruibing Wang . A supramolecular nanoprodrug for prevention of gallstone formation. Chinese Chemical Letters, 2025, 36(2): 109854-. doi: 10.1016/j.cclet.2024.109854
19. [19]
  Zhu Shu , Xin Lei , Yeye Ai , Ke Shao , Jianliang Shen , Zhegang Huang , Yongguang Li . ATP-induced supramolecular assembly based on chromophoric organic molecules and metal complexes. Chinese Chemical Letters, 2024, 35(11): 109585-. doi: 10.1016/j.cclet.2024.109585
20. [20]
  Qian Ren , Xue Dai , Ran Cen , Yang Luo , Mingyang Li , Ziyun Zhang , Qinghong Bai , Zhu Tao , Xin Xiao . A cucurbit[8]uril-based supramolecular phosphorescent assembly: Cell imaging and sensing of amino acids in aqueous solution. Chinese Chemical Letters, 2024, 35(12): 110022-. doi: 10.1016/j.cclet.2024.110022

Get Citation

PDF

XML

Metrics

PDF Downloads(8)
Abstract views(1731)
HTML views(9)

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