Citation: Kaiya Wang, Qian Liu, Li Zhou, Hao Sun, Xiaoquan Yao, Xiao-Yu Hu. State-of-the-art and recent progress in resorcinarene-based cavitand^☆[J]. Chinese Chemical Letters, ;2023, 34(10): 108559. doi: 10.1016/j.cclet.2023.108559 shu

State-of-the-art and recent progress in resorcinarene-based cavitand^☆

College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China

^☆

kwang6@nuaa.edu.cn

Received Date: 2 March 2023
Revised Date: 29 April 2023
Accepted Date: 9 May 2023
Available Online: 13 May 2023

Figures(20)

Compartmentalization in the biological world brings excellent efficiency and specificity to the formation of complex compounds, inspiring supramolecular chemists to continuously search for defined spaces that can mimic such natural binding sites. Bowl-shaped cavitands built up from resorcinarenes (RA) present rigid and preorganized concave surfaces, which are capable of mimicking the molecular recognition properties of enzymes. The versatile scaffold of RA endows the cavitand with terrific variety and excellent binding behavior. This review provides a comprehensive overview over the structural modification to date in the high attention field of RA-based cavitands development. Different strategies for synthesizing diverse cavitands, such as small cavity cavitands, wider cavity cavitands, deep cavity cavitands, biscavitands, and asymmetric cavitands, are discussed in details. Furthermore, insights into their applications including catalysis, separations and sensing are provided.
- Resorcinarene,
- Cavitand,
- Supramolecular chemistry,
- Host-guest chemistry,
- Molecular recognition
1. [1]
  L. Escobar, P. Ballester, Chem. Rev. 121 (2021) 2445-2514. doi: 10.1021/acs.chemrev.0c00522
2. [2]
  K. Wang, X. Tian, J.H. Jordan, et al., Chin. Chem. Lett. 33 (2022) 89-96. doi: 10.1016/j.cclet.2021.06.026
3. [3]
  K. Wang, M. Zuo, T. Zhang, H. Yue, X.Y. Hu, Chin. Chem. Lett. 34 (2023) 107848. doi: 10.1016/j.cclet.2022.107848
4. [4]
  S. Niu, L.L. Mao, H. Xiao, et al., Chin. Chem. Lett. 33 (2022) 1970-1974. doi: 10.1016/j.cclet.2021.09.090
5. [5]
  Y.X. Yan, Y. Zhang, Y. Chen, Y. Liu, ACS Appl. Polym. Mater. 2 (2020) 5641-5645. doi: 10.1021/acsapm.0c00958
6. [6]
  J.R. Moran, S. Karbach, D.J. Cram, J. Am. Chem. Soc. 104 (1982) 5826-5828. doi: 10.1021/ja00385a064
7. [7]
  D.J. Cram, Science 219 (1983) 1177-1183. doi: 10.1126/science.219.4589.1177
8. [8]
  Q. Sun, L. Escobar, P. Ballester, Angew. Chem. Int. Ed. 60 (2021) 10359-10365. doi: 10.1002/anie.202101499
9. [9]
  L. Escobar, F.A. Arroyave, P. Ballester, Eur. J. Org. Chem. 2018 (2018) 1097-1106. doi: 10.1002/ejoc.201701602
10. [10]
  K. Hermann, D.A. Turner, C.M. Hadad, J.D. Badjic, Chem. Eur. J. 18 (2012) 8301-8305. doi: 10.1002/chem.201201153
11. [11]
  S.E. Border, R.Z. Pavlovic, L. Zhiquan, J.D. Badjic, J. Am. Chem. Soc. 139 (2017) 18496-18499. doi: 10.1021/jacs.7b11960
12. [12]
  S. Mirzaei, V.M. Espinoza Castro, R. H. Sánchez, Chem. Sci. 13 (2022) 2026-2032. doi: 10.1039/d1sc07041j
13. [13]
  H. Erdtman, S. Högberg, S. Abrahamsson, B. Nilsson, Tetrahedron Lett. 9 (1968) 1679-1682. doi: 10.1016/S0040-4039(01)99028-8
14. [14]
  A. Baeyer, Ber. Dtsch. Chem. Ges. 5 (1872) 280-282. doi: 10.1002/cber.18720050186
15. [15]
  J.M. Bourgeois, H. Stoeckli-Evans, Helv. Chim. Acta 88 (2005) 2722-2730. doi: 10.1002/hlca.200590211
16. [16]
  E.R. Abdurakhmanova, P. Cmoch, A. Szumna, Org. Biomol. Chem. 20 (2022) 5095-5103. doi: 10.1039/d2ob00880g
17. [17]
  M. Wehbie, G. Arrachart, I. Karamé, L. Ghannam, S. Pellet-Rostaing, Sep. Purif. Technol. 169 (2016) 17-24. doi: 10.1016/j.seppur.2016.06.003
18. [18]
  A. Mouradzadegun, S. Elahi, F. Abadast, RSC Adv. 4 (2014) 31239-31248. doi: 10.1039/C4RA03463E
19. [19]
  A. Pedrini, F. Bertani, E. Dalcanale, Molecules 23 (2018) 2670. doi: 10.3390/molecules23102670
20. [20]
  N.W. Wu, J. Rebek, Jr., J. Am. Chem. Soc. 138 (2016) 7512-7515. doi: 10.1021/jacs.6b04278
21. [21]
  J.L. Liu, M. Sun, Y.H. Shi, et al., J. Inclus. Phenom. Macrocycl. Chem. 102 (2022) 201-233. doi: 10.1007/s10847-021-01119-w
22. [22]
  T. Heinz, D.M. Rudkevich, J. Rebek, Jr., Nature 394 (1998) 764-766. doi: 10.1038/29501
23. [23]
  D. Ajami, J. Rebek, Jr., Acc. Chem. Res. 46 (2013) 990-999. doi: 10.1021/ar300038r
24. [24]
  J. Jiao, B. Sun, Y. Ding, et al., Org. Lett. 22 (2020) 8984-8988. doi: 10.1021/acs.orglett.0c03385
25. [25]
  M.L. Tan, Q.H. Guo, X.Y. Wang, et al., Angew. Chem. Int. Ed. 59 (2020) 23649-23658. doi: 10.1002/anie.202013149
26. [26]
  L. Turunen, F. Pan, N.K. Beyeh, et al., Cryst. Growth Des. 18 (2017) 513-520.
27. [27]
  L. Turunen, F. Pan, N.K. Beyeh, et al., CrystEngComm 19 (2017) 5223-5229. doi: 10.1039/C7CE01118K
28. [28]
  L. Turunen, N.K. Beyeh, F. Pan, A. Valkonen, K. Rissanen, Chem. Commun. 50 (2014) 15920-15923. doi: 10.1039/C4CC07771G
29. [29]
  K. Twum, K. Rissanen, N.K. Beyeh, Chem. Rec. 21 (2021) 386-395. doi: 10.1002/tcr.202000140
30. [30]
  Y.J. Zhu, Y. Gao, M.M. Tang, J. Rebek, Jr., Y. Yu, Chem. Commun. 57 (2021) 1543-1549. doi: 10.1039/d0cc07784d
31. [31]
  R. Pinalli, M. Suman, E. Dalcanale, Eur. J. Org. Chem. 2004 (2004) 451-462. doi: 10.1002/ejoc.200300430
32. [32]
  R. Pinalli, G. Brancatelli, A. Pedrini, et al., J. Am. Chem. Soc. 138 (2016) 8569-8580. doi: 10.1021/jacs.6b04372
33. [33]
  N. Bontempi, E. Biavardi, D. Bordiga, et al., Nanoscale 9 (2017) 8639-8646. doi: 10.1039/C7NR02491F
34. [34]
  J.H. Jordan, H. S. Ashbaugh, J.T. Mague, B.C. Gibb, J. Am. Chem. Soc. 143 (2021) 18605-18616. doi: 10.1021/jacs.1c08457
35. [35]
  H.R. Aziz, W. Yao, J.H. Jordan, B.C. Gibb, Supramol. Chem. 33 (2021) 226-271. doi: 10.1080/14702436.2021.1888644
36. [36]
  A. Gissot, J. Rebek, J. Am. Chem. Soc. 126 (2004) 7424-7425. doi: 10.1021/ja049074r
37. [37]
  H. Konishi, T. Nakamura, K. Ohata, K. Kobayashi, O. Morikawa, Tetrahedron Lett. 37 (1996) 7383-7386. doi: 10.1016/0040-4039(96)01683-8
38. [38]
  C. Naumann, E. Roman, C. Peinador, et al., Chem. Eur. J. 7 (2001) 1637-1645. doi: 10.1002/1521-3765(20010417)7:8<1637::AID-CHEM16370>3.0.CO;2-X
39. [39]
  C. Naumann, S. Place, J.C. Sherman, J. Am. Chem. Soc. 124 (2002) 16-17.
40. [40]
  T.H. Shi, S. Tong, M.X. Wang, Angew. Chem. Int. Ed. 59 (2020) 7700-7705. doi: 10.1002/anie.202002827
41. [41]
  Q.H. Guo, Y. Qiu, M.X. Wang, J.F. Stoddart, Nat. Chem. 13 (2021) 402-419. doi: 10.1038/s41557-021-00671-9
42. [42]
  P.D. Sala, C. Gaeta, W. Navarra, et al., J. Org. Chem. 81 (2016) 5726-5731. doi: 10.1021/acs.joc.6b00803
43. [43]
  C. Gaeta, P.D. Sala, C. Talotta, et al., Org. Chem. Front. 3 (2016) 1276-1280. doi: 10.1039/C6QO00336B
44. [44]
  M. Chwastek, A. Szumna, Org. Lett. 22 (2020) 6838-6841. doi: 10.1021/acs.orglett.0c02357
45. [45]
  M. Chwastek, P. Cmoch, A. Szumna, Angew. Chem. Int. Ed. 60 (2021) 4540-4544. doi: 10.1002/anie.202013105
46. [46]
  T. Gottschalk, B. Jaun, F. Diederich, Angew. Chem. Int. Ed. 46 (2007) 260-264. doi: 10.1002/anie.200603366
47. [47]
  I. Pochorovski, M.O. Ebert, J.P. Gisselbrecht, et al., J. Am. Chem. Soc. 134 (2012) 14702-14705. doi: 10.1021/ja306473x
48. [48]
  I. Pochorovski, F. Diederich, Acc. Chem. Res. 47 (2014) 2096-2105. doi: 10.1021/ar500104k
49. [49]
  J.V. Milic, F. Diederich, Chem. Eur. J. 25 (2019) 8440-8452. doi: 10.1002/chem.201900852
50. [50]
  V. Garcia-Lopez, M. Zalibera, N. Trapp, et al., Chem. Eur. J. 26 (2020) 11451-11461. doi: 10.1002/chem.202001788
51. [51]
  L. Pirondini, F. Bertolini, B. Cantadori, et al., Proc. Natl. Acad. Sci. U.S.A. 99 (2002) 4911-4915. doi: 10.1073/pnas.072612199
52. [52]
  R.M. Yebeutchou, E. Dalcanale, J. Am. Chem. Soc. 131 (2009) 2452-2453. doi: 10.1021/ja809614y
53. [53]
  G. Valenti, E. Rampazzo, E. Biavardi, et al., Faraday Discuss. 185 (2015) 299-309. doi: 10.1039/C5FD00096C
54. [54]
  F. Bertani, N. Riboni, F. Bianchi, et al., Chem. Eur. J. 22 (2016) 3312-3319. doi: 10.1002/chem.201504229
55. [55]
  A. Aprile, F. Ciuchi, R. Pinalli, E. Dalcanale, P. Pagliusi, J. Phys. Chem. Lett. 7 (2016) 3022-3026. doi: 10.1021/acs.jpclett.6b01300
56. [56]
  W. Zhong, R.J. Hooley, Acc. Chem. Res. 55 (2022) 1035-1046. doi: 10.1021/acs.accounts.2c00026
57. [57]
  J. Chen, B.L. Hickey, L. Wang, et al., Nat. Chem. 13 (2021) 488-495. doi: 10.1038/s41557-021-00647-9
58. [58]
  Q. Shi, D. Masseroni, J. Rebek, Jr., J. Am. Chem. Soc. 138 (2016) 10846-10848. doi: 10.1021/jacs.6b06950
59. [59]
  S. Mosca, Y. Yu, J.V. Gavette, K.D. Zhang, J. Rebek, Jr., J. Am. Chem. Soc. 137 (2015) 14582-14585. doi: 10.1021/jacs.5b10028
60. [60]
  J.M. Yang, Y. Yu, J. Rebek, Jr., J. Am. Chem. Soc. 143 (2021) 2190-2193. doi: 10.1021/jacs.0c12302
61. [61]
  Y.H. Wan, Y.J. Zhu, J. Rebek, Jr., Y. Yu, Molecules 26 (2021) 1922. doi: 10.3390/molecules26071922
62. [62]
  K. Wang, X. Cai, W. Yao, et al., J. Am. Chem. Soc. 141 (2019) 6740-6747. doi: 10.1021/jacs.9b02287
63. [63]
  K. Wang, J.H. Jordan, B.C. Gibb, Chem. Commun. 55 (2019) 11695-11698. doi: 10.1039/c9cc06501f
64. [64]
  K. Wang, B.C. Gibb, J. Org. Chem. 82 (2017) 4279-4288. doi: 10.1021/acs.joc.7b00264
65. [65]
  F.U. Rahman, D. Tzeli, I.D. Petsalakis, et al., J. Am. Chem. Soc. 142 (2020) 5876-5883. doi: 10.1021/jacs.0c01290
66. [66]
  Y. Yu, J.M. Yang, J. Rebek, Chem 6 (2020) 1265-1274. doi: 10.1016/j.chempr.2020.04.014
67. [67]
  M. Petroselli, Y.Q. Chen, M.K. Zhao, J. Rebek, Y. Yu, Chin. Chem. Lett. 34 (2023) 107834. doi: 10.1016/j.cclet.2022.107834
68. [68]
  Y. Zhu, M. Tang, H. Zhang, et al., J. Am. Chem. Soc. 143 (2021) 12397-12403. doi: 10.1021/jacs.1c06510
69. [69]
  F.U. Rahman, R. Wang, H.B. Zhang, et al., Angew. Chem. Int. Ed. 61 (2022) e202205534. doi: 10.1002/anie.202205534
70. [70]
  K. Kanagaraj, R. Wang, M.K. Zhao, et al., J. Am. Chem. Soc. 145 (2023) 5816–5823. doi: 10.1021/jacs.2c12907
71. [71]
  F.U. Rahman, Y.S. Li, I.D. Petsalakis, et al., Proc. Natl. Acad. Sci. U.S.A. 116 (2019) 17648-17653. doi: 10.1073/pnas.1909154116
72. [72]
  F.U. Rahman, J.M. Yang, Y.H. Wan, et al., Chem. Commun. 56 (2020) 6945-6948. doi: 10.1039/d0cc02778b
73. [73]
  Y.H. Wan, Faiz-Ur Rahman, J. Rebek Jr., Y. Yu, Chin. J. Chem. 39 (2021) 1498-1502. doi: 10.1002/cjoc.202000709
74. [74]
  H.B. Zhang, K. Kanagaraj, J. Rebek, Jr., Y. Yu, J. Org. Chem. 86 (2021) 8873-8881. doi: 10.1021/acs.joc.1c00794
75. [75]
  Y.Q. Chen, H.W. Guan, K. Kanagaraj, J. Rebek, Y. Yu, Chin. Chem. Lett. 33 (2022) 4908-4911. doi: 10.1016/j.cclet.2022.03.039
76. [76]
  J.M. Yang, Y.Q. Chen, Y. Yu, P. Ballester, J. Rebek, Jr., J. Am. Chem. Soc. 143 (2021) 19517-19524. doi: 10.1021/jacs.1c09226
77. [77]
  C.L.D. Gibb, B.C. Gibb, J. Am. Chem. Soc. 126 (2004) 11408-11409. doi: 10.1021/ja0475611
78. [78]
  P. Suating, T.T. Nguyen, N.E. Ernst, et al., Chem. Sci. 11 (2020) 3656-3663. doi: 10.1039/c9sc06268h
79. [79]
  J.W. Barnett, M.R. Sullivan, J.A. Long, et al., Nat. Chem. 12 (2020) 589-594. doi: 10.1038/s41557-020-0458-8
80. [80]
  P. Suating, N.E. Ernst, B.D. Alagbe, et al., J. Phys. Chem. B 126 (2022) 3150-3160. doi: 10.1021/acs.jpcb.2c00628
81. [81]
  P. Jagadesan, S.R. Samanta, R. Choudhury, V. Ramamurthy, J. Phys. Org. Chem. 30 (2017) e3728. doi: 10.1002/poc.3728
82. [82]
  S. Mirzaei, E. Castro, R.H. Sanchez, Chem. Sci. 11 (2020) 8089-8094. doi: 10.1039/d0sc03384g
83. [83]
  E. Castro, S. Mirzaei, R.H. Sanchez, Org. Lett. 23 (2021) 87-92. doi: 10.1021/acs.orglett.0c03765
84. [84]
  S. Mirzaei, E. Castro, R.H. Sanchez, Chem. Eur. J. 27 (2021) 8642-8655. doi: 10.1002/chem.202005408
85. [85]
  A. Lledó, S. Kamioka, A.C. Sather, J. Rebek, Angew. Chem. Int. Ed. 50 (2011) 1299-1301. doi: 10.1002/anie.201006166
86. [86]
  S. Ro, S.J. Rowan, A.R. Pease, D.J. Cram, J.F. Stoddart, Org. Lett. 2 (2000) 2411-2414. doi: 10.1021/ol005962p
87. [87]
  D. Shimoyama, T. Haino, Asian J. Org. Chem. 9 (2020) 1718-1725. doi: 10.1002/ajoc.202000302
88. [88]
  H. Yamada, T. Ikeda, T. Mizuta, T. Haino, Org. Lett. 14 (2012) 4510–4513. doi: 10.1021/ol301996q
89. [89]
  D. Shimoyama, T. Ikeda, R. Sekiya, T. Haino, J. Org. Chem. 82 (2017) 13220-13230. doi: 10.1021/acs.joc.7b02301
90. [90]
  D. Shimoyama, R. Sekiya, H. Kudo, T. Haino, Org. Lett. 22 (2020) 352-356. doi: 10.1021/acs.orglett.9b03693
91. [91]
  D. Shimoyama, H. Yamada, T. Ikeda, R. Sekiya, T. Haino, Eur. J. Org. Chem. 20 (2016) 3300-3303. doi: 10.1002/ejoc.201600410
92. [92]
  C.A. Hunter, H.L. Anderson, Angew. Chem. Int. Ed. 48 (2009) 7488-7499. doi: 10.1002/anie.200902490
93. [93]
  D. Shimoyama, T. Haino, J. Org. Chem. 84 (2019) 13483-13489. doi: 10.1021/acs.joc.9b01730
94. [94]
  D. Shimoyama, R. Sekiya, T. Haino, Chem. Commun. 56 (2020) 3733-3736. doi: 10.1039/d0cc00933d
95. [95]
  H. Fujimoto, D. Shimoyama, K. Katayanagi, et al., Org. Lett. 23 (2021) 6217-6221. doi: 10.1021/acs.orglett.1c01837
96. [96]
  K. Wang, J.H. Jordan, X.Y. Hu, L. Wang, Angew. Chem. Int. Ed. 59 (2020) 13712-13721. doi: 10.1002/anie.202000045
97. [97]
  S. Korom, P. Ballester, J. Am. Chem. Soc. 139 (2017) 12109-12112. doi: 10.1021/jacs.7b05458
98. [98]
  N. Natarajan, E. Brenner, D. Sémeril, D. Matt, J. Harrowfield, Eur. J. Org. Chem. 2017 (2017) 6100-6113. doi: 10.1002/ejoc.201700725
99. [99]
  M.P. Schramm, M. Kanaura, K. Ito, M. Ide, T. Iwasawa, Eur. J. Org. Chem. 2016 (2016) 813-820. doi: 10.1002/ejoc.201501426
100. [100]
  M. Inoue, K. Ugawa, T. Maruyama, T. Iwasawa, Eur. J. Org. Chem. 2018 (2018) 5304-5311. doi: 10.1002/ejoc.201800948
101. [101]
  Y. Matsumoto, Y. Taguchi, N. Yoshida, et al., Supramol. Chem. 33 (2021) 253-265. doi: 10.1080/10610278.2021.1981323
102. [102]
  N. Endo, M. Kanaura, M.P. Schramm, T. Iwasawa, Tetrahedron Lett. 57 (2016) 4754-4757. doi: 10.1016/j.tetlet.2016.09.039
103. [103]
  M. Inoue, S. Kamiguchi, K. Ugawa, et al., Eur. J. Org. Chem. 2019 (2019) 6261-6268. doi: 10.1002/ejoc.201901058
104. [104]
  I. Martin-Torres, G. Ogalla, J.M. Yang, A. Rinaldi, A.M. Echavarren, Angew. Chem. Int. Ed. 60 (2021) 9339-9344. doi: 10.1002/anie.202017035
105. [105]
  D. Vidal, M. Costas, A. Lledó, ACS Catal. 8 (2018) 3667-3672. doi: 10.1021/acscatal.7b04426
106. [106]
  M. Nakamura, K. Kishimoto, Y. Kobori, et al., J. Am. Chem. Soc. 138 (2016) 12564-12577. doi: 10.1021/jacs.6b07284
107. [107]
  N. Nishimura, K. Kobayashi, Angew. Chem. Int. Ed. 47 (2008) 6255-6258. doi: 10.1002/anie.200802293
108. [108]
  K. Kobayashi, M. Yamanaka, Chem. Soc. Rev. 44 (2015) 449-466. doi: 10.1039/C4CS00153B
109. [109]
  X. Liu, R. Warmuth, J. Am. Chem. Soc. 128 (2006) 14120-14127. doi: 10.1021/ja0644733
110. [110]
  S. Collin, A. Parrot, L. Marcelis, et al., Chem. Eur. J. 24 (2018) 17964-17974. doi: 10.1002/chem.201804768
111. [111]
  S. Collin, N. Giraud, E. Dumont, O. Reinaud, Org. Chem. Front. 6 (2019) 1627-1636. doi: 10.1039/c9qo00263d
112. [112]
  L. He, S.C. Wang, L.T. Lin, et al., J. Am. Chem. Soc. 142 (2020) 7134-7144. doi: 10.1021/jacs.0c01482
113. [113]
  R. Pinalli, E. Dalcanale, F. Ugozzoli, C. Massera, CrystEngComm 18 (2016) 5788-5802. doi: 10.1039/C6CE01010E
114. [114]
  W.Y. Pei, G. Xu, J. Yang, et al., J. Am. Chem. Soc. 139 (2017) 7648-7656. doi: 10.1021/jacs.7b03169
115. [115]
  F.F. Wang, Y.Y. Liu, W.Y. Pei, J.F. Ma, Inorg. Chem. 60 (2021) 7329-7336. doi: 10.1021/acs.inorgchem.1c00497
116. [116]
  C.X. Hu, Y.H. Xuan, Z.H. Jiang, et al., CrystEngComm 23 (2021) 7179-7185. doi: 10.1039/d1ce01069g
117. [117]
  Z. Li, Y.W. Yang, Adv. Mater. 34 (2022) e2107401. doi: 10.1002/adma.202107401
118. [118]
  R. Tang, Y. Ye, S. Zhu, et al., Chin. Chem. Lett. 34 (2023) 1007734. doi: 10.1016/j.cclet.2022.08.014
119. [119]
  L.P. Skala, A. Yang, M.J. Klemes, L. Xiao, W.R. Dichtel, J. Am. Chem. Soc. 141 (2019) 13315-13319. doi: 10.1021/jacs.9b06749
1. [1]
  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
2. [2]
  Dan Luo , Jinya Tian , Jianqiao Zhou , Xiaodong Chi . Anthracene-bridged "Texas-sized" box for the simultaneous detection and uptake of tryptophan. Chinese Chemical Letters, 2024, 35(9): 109444-. doi: 10.1016/j.cclet.2023.109444
3. [3]
  Caihong Mao , Yanfeng He , Xiaohan Wang , Yan Cai , Xiaobo Hu . Synthesis and molecular recognition characteristics of a tetrapodal benzene cage. Chinese Chemical Letters, 2024, 35(8): 109362-. doi: 10.1016/j.cclet.2023.109362
4. [4]
  Fang-Yuan Chen , Wen-Chao Geng , Kang Cai , Dong-Sheng Guo . Molecular recognition of cyclophanes in water. Chinese Chemical Letters, 2024, 35(5): 109161-. doi: 10.1016/j.cclet.2023.109161
5. [5]
  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
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]
  Yuanjiao Liu , Xiaoyang Zhao , Songyao Zhang , Yi Wang , Yutuo Zheng , Xinrui Miao , Wenli Deng . Site-selection and recognition of aromatic carboxylic acid in response to coronene and pyridine derivative. Chinese Chemical Letters, 2024, 35(8): 109404-. doi: 10.1016/j.cclet.2023.109404
8. [8]
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通讯作者: 陈斌, bchen63@163.com

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沈阳化工大学材料科学与工程学院沈阳 110142

State-of-the-art and recent progress in resorcinarene-based cavitand☆

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通讯作者: 陈斌, bchen63@163.com

State-of-the-art and recent progress in resorcinarene-based cavitand^☆