Citation: Shi Yan, Yu Youwei, Xue Lin, Wang Yanfeng. Progress of Fluorescent Probes with Perylene Tetracarboxylic Diimide as Chromophore[J]. Chinese Journal of Organic Chemistry, ;2019, 39(12): 3414-3437. doi: 10.6023/cjoc201906015 shu

Progress of Fluorescent Probes with Perylene Tetracarboxylic Diimide as Chromophore

Shi Yan ^a,, ,
Yu Youwei ^a ,
Xue Lin ^b ,
Wang Yanfeng ^b,,

a.
Collge of Food Sciences, Shanxi Normal University, Linfen, Shanxi 041004
b.
Institute of Materia Medica Shandong Academy of Medical Sciences, Jinan 250062

Corresponding author: Shi Yan, wyfshiwoya@126.com Wang Yanfeng, shiyansdu@163.com
Received Date: 13 June 2019
Revised Date: 5 July 2019
Available Online: 24 December 2019
Fund Project: the National Natural Science Foundation of China 21305079Project supported by the National Natural Science Foundation of China (No. 21305079)

Figures(13)

In recent years, molecular fluorescent probes have attracted extensive attention due to their high sensitivity, high selectivity, specificity and simplicity of design. Perylene tetracarboxylic diimide derivatives (PDIs) are well known for their excellent photothermal stability, chemical stability, high fluorescence quantum yield, large stokes shift and easy modification. Therefore, they can be used as excellent fluorophores. PDI itself has strong electron-withdrawing group and easily to be reduced but it is hard to be oxidized. However, due to their inherent structure, the poor water solubility and aggregatable ablility limited their applications in biological fields. The water solubility of PDI was improved by introducing hydrophilic groups into the structure. Therefore, the PDIs with the unique advantages will have potential application values in the field of fluorescence probe and has been developed rapidly for the past few years. The development of PDI as a chromophore in fluorescent probe for the detection of ion, gas, biomolecules, etc. is systematically summarized. Meanwhile, the design of the probes, fluorescence response mechanism and application of the probe are also discussed. Finally, a novel type of PDI fluorescent probe is proposed. The challenge of construction of the PDIs and future development are also reviewed.
- perylene tetracarboxylic diimide,
- fluorescent probe,
- ion-detection,
- gas detection,
- biomolecules detection
1. [1]
  Huang, C.; Barlow, S.; Marder, S. R. J. Org. Chem. 2011, 76, 2386. doi: 10.1021/jo2001963
2. [2]
  Jozeliunaite, A.; Striela, R.; Labanauskas, L.; Orentas, E. Synthesis 2017, 49, 5176. doi: 10.1055/s-0036-1589088
3. [3]
  Pasaogullari, N.; Icil, H.; Demuth, M. Dyes Pigm. 2006, 69, 118. doi: 10.1016/j.dyepig.2005.03.001
4. [4]
  Gao, G.; Liang, N.; Geng, H.; Jiang, W.; Fu, H.; Feng, J.; Hou, J.; Feng, X.; Wang, Z. J. Am. Chem. Soc. 2017, 139, 15914. doi: 10.1021/jacs.7b09140
5. [5]
  Wang, H.; Chen, L.; Xiao, Y. J. Mater. Chem. C 2017, 5, 12816. doi: 10.1039/C7TC04726F
6. [6]
  Liu, Y.; Cole, M. D.; Jiang, Y.; Kim, P. Y.; Nordlund, D.; Emrick, T.; Russell, T. P. Adv. Mater. 2018, 30, 1705976. doi: 10.1002/adma.201705976
7. [7]
  Villafiorita-Monteleone, F.; Kozma, E.; Giovanella, U.; Catellani, M.; Paolino, M.; Collico, V.; Colombo, M.; Cappelli, A.; Botta, C. Dyes Pigm. 2018, 149, 331. doi: 10.1016/j.dyepig.2017.10.010
8. [8]
  Türkmen, G.; Erten-Ela, S.; Icli, S. Dyes Pigm. 2009, 83, 297. doi: 10.1016/j.dyepig.2009.05.014
9. [9]
  Wang, B.; Yu, C. Angew. Chem. 2010, 122, 1527. doi: 10.1002/ange.200905237
10. [10]
  Wang, B.; Zhu, Q.; Liao, D.; Yu, C. J. Mater. Chem. 2011, 21, 4821. doi: 10.1039/c0jm04527f
11. [11]
  Wang, B.; Jiao, H.; Li, W.; Liao, D.; Wang, F.; Yu, C. Chem. Commun. 2011, 47, 10269. doi: 10.1039/c1cc13606b
12. [12]
  Würthner, F. Chem. Commun. 2004, 1564.
13. [13]
  Guo, X.; Zhang, D.; Zhu, D. Adv. Mater. 2004, 2, 125.
14. [14]
  Lin, J.; Zhu, C.; Liu, J.; Chen, B.; Zhang, Y.; Xue, J.; Liu, J. Chin. J. Chem. 2014, 32, 1116. doi: 10.1002/cjoc.201400464
15. [15]
  Wang, H.; Wang, D.; Wang, Q.; Li, X.; Schalley, C. Org. Biomol. Chem. 2010, 8, 1017. doi: 10.1039/b921342b
16. [16]
  Cheng, H.; Qian, Y. Dyes Pigm. 2015, 112, 317. doi: 10.1016/j.dyepig.2014.07.005
17. [17]
  He, X.; Liu, H.; Li, Y.; Wang, S.; Li, Y.; Wang, N.; Xiao, J.; Xu, X.; Zhu, D. Adv. Mater. 2005, 17, 2811. doi: 10.1002/adma.200501173
18. [18]
  Feng, X.; An, Y.; Yao, Z.; Li, C.; Shi, G. ACS Appl. Mater. Interfaces 2012, 4, 614. doi: 10.1021/am201616r
19. [19]
  Zhong, L.; Xing, F.; Bai, Y.; Zhao, Y.; Zhu, S. Spectrochim. Acta, Part A 2013, 115, 370. doi: 10.1016/j.saa.2013.06.039
20. [20]
  Wang, Y.; Zhang, L.; Zhang, G.; Wu, Y.; Wu, S.; Yu, J.; Wang, L. Tetrahedron Lett. 2014, 55, 3218. doi: 10.1016/j.tetlet.2014.03.137
21. [21]
  Fu, L.-N.; Qiao, Z. R.; Jin, X.; Li, L. R. Chem. Res. Appl. 2019, 31, 624 (in Chinese).
22. [22]
  Che, Y.; Yang, X.; Zang, L. Chem. Commun. 2008, 1413.
23. [23]
  Ruan, Y.; Li, A.; Zhao, J.; Shen, J.; Jiang, Y. Chem. Commun. 2010, 46, 4938. doi: 10.1039/c0cc00630k
24. [24]
  Fang, H.; Shellaiah, M.; Sinhg, A.; Raju Ramakrishnam, M. V.; Wu, Y.; Lin, H. Sens. Actuators, B 2014, 194, 229. doi: 10.1016/j.snb.2013.12.082
25. [25]
  Liu, K.; Xu, Z.; Yin, M.; Yang, W.; He, B.; Wei, W.; Shen, J. J. Mater. Chem. B 2014, 2, 2093. doi: 10.1039/C3TB21801E
26. [26]
  Han, A.; Liu, X.; Prestwich, G. D.; Zang, L. Sens. Actuators, B 2014, 198, 274. doi: 10.1016/j.snb.2014.03.033
27. [27]
  Malkongu, S.; Erdemir, S. Dyes Pigm. 2015, 113, 763. doi: 10.1016/j.dyepig.2014.10.020
28. [28]
  Erdemir, S.; Kocyigit, O.; Karakurt, S. Sens. Actuators, B 2015, 220, 381. doi: 10.1016/j.snb.2015.05.103
29. [29]
  Li, J.; Wu, Y.; Song, F.; Wei, G.; Cheng, Y.; Zhu, C. J. Mater. Chem. 2012, 22, 478. doi: 10.1039/C1JM14037J
30. [30]
  Zhao, X.; Gong, L.; Wu, Y.; Zhang, X.; Xie, J. Talanta 2016, 149, 98. doi: 10.1016/j.talanta.2015.11.038
31. [31]
  Zhou, R.; Li, B.; Wu, N.; Gao, G.; You, J.; Lan, J. Chem. Commun. 2011, 47, 6668. doi: 10.1039/c1cc11200g
32. [32]
  Wang, H.; Lang, Y.; Wang, H.; Lou, J.; Guo, H.; Li, X. Tetrahedron 2014, 70, 1997. doi: 10.1016/j.tet.2014.01.063
33. [33]
  Zhang, L.; Wang, Y.; Yu, J.; Zhang, G.; Cai, X.; Wu, Y.; Wang, L. Tetrahedron Lett. 2013, 54, 4019. doi: 10.1016/j.tetlet.2013.05.076
34. [34]
  Kumar, K.; Bhargava, G.; Kumar, S.; Singh, P. New J. Chem. 2018, 42, 1010. doi: 10.1039/C7NJ03751A
35. [35]
  Singh, P.; Mittal, L. S.; Vanita, V.; Kumar, K.; Walia, A.; Bhargava, G.; Kumar, S. J. Mater. Chem. B 2016, 4, 3750. doi: 10.1039/C6TB00512H
36. [36]
  Malkondu, S. Tetrahedron 2014, 70, 5580. doi: 10.1016/j.tet.2014.06.094
37. [37]
  Liu, X.; Zhang, N.; Zhou, J.; Chang, T.; Fang, C.; Shangguan, D. Analyst 2013, 138, 901. doi: 10.1039/C2AN36203A
38. [38]
  You, S.; Cai, Q.; Müillen, K.; Yang, W.; Yin, M. Chem. Commun. 2014, 50, 823. doi: 10.1039/C3CC48046A
39. [39]
  Wan, S.; Zheng, Y.; Shen, J.; Yang, W.; Yin, M. ACS Appl. Mater. Interfaces 2014, 6, 19515. doi: 10.1021/am506641t
40. [40]
  Shen, Y.; Ma, X.; Zhang, B.; Zhou, Z.; Sun, Q.; Jin, E.; Sui, M.; Tang, J.; Wang, J.; Fan, M. Chem.-Eur. J. 2011, 17, 5319. doi: 10.1002/chem.201003495
41. [41]
  Wu, Y.; Zhang, X.; Li, J.; Zhang, C.; Liang, H.; Mao, G.; Zhou, L.; Tan, W.; Yu, R. Anal. Chem. 2014, 86, 10389. doi: 10.1021/ac502863m
42. [42]
  Ling, J.; Naren, G.; Kelly, J.; Moody, T. S.; Prasanna de Silva, A. J. Am. Chem. Soc. 2015, 137, 3763. doi: 10.1021/jacs.5b00665
43. [43]
  Huang, L.; Chang, T. S.-W. Chem. Commun. 2011, 47, 2291. doi: 10.1039/C0CC04262E
44. [44]
  Aigner, D.; Borisov, S. M.; Petritsch, P.; Klimant, I. Chem. Commun. 2013, 49, 2139. doi: 10.1039/c3cc39151e
45. [45]
  Aigner, D.; Freunberger, S. A.; Wilkening, M.; Saf, R.; Borisov, S. M.; Klimant, I. Anal. Chem. 2014, 86, 9293. doi: 10.1021/ac502513g
46. [46]
  Ma, Y.; Li, J.; Hou, S.; Zhang, J.; Shi, Z.; Jiang, T.; Wei, X. New J. Chem. 2016, 40, 6615. doi: 10.1039/C6NJ00153J
47. [47]
  Ye, F.; Liang, X.; Wu, N.; Li, P.; Chai, Q.; Fu, Y. Spectrochim. Acta, Part A 2019, 216, 359. doi: 10.1016/j.saa.2019.03.049
48. [48]
  Georgiev, N. I.; Said, A. I.; Toshkova, R. A.; Tzoneva, D.; Bojinov, V. B, Dyes Pigm. 2019, 160, 28. doi: 10.1016/j.dyepig.2018.07.048
49. [49]
  Aigner, D.; Dmitriev, R. I.; Borisov, S. M.; Papkovsky, D. B.; Klimant, I. J. Mater. Chem. B 2014, 2, 6792. doi: 10.1039/C4TB01006J
50. [50]
  Zhang, W.; Gan, S. Y.; Li, F.; Han, D.; Zhang, Q.; Niu, L. RSC Adv. 2015, 5, 2207. doi: 10.1039/C4RA11124A
51. [51]
  Pacheco-Liňán, P.; Moral, M.; Nueda, M. L.; Cruz-Sánchez, R.; Fernández-Sainz, J.; Garzón-Ruiz, A.; Bravo, I.; Melguizo, M.; Laborda, J.; Albaladejo, J. Phys. Chem. C 2017, 121, 24786. doi: 10.1021/acs.jpcc.7b07839
52. [52]
  You, S.; Cai, Q.; Müllen, K.; Yang, W.; Yin, M. Chem. Commun. 2014, 50, 823. doi: 10.1039/C3CC48046A
53. [53]
  Roy, A.; Saha, T.; Talukdar, P. Tetrahedron Lett. 2015, 56, 4975. doi: 10.1016/j.tetlet.2015.06.086
54. [54]
  Cho, E. J.; Yeo, H. M.; Ryu, B. J.; Jeong, H. A.; Nam, K. C. Bull. Korean Chem. Soc. 2006, 27, 1967. doi: 10.5012/bkcs.2006.27.12.1967
55. [55]
  Chen, Z.; Wang, L.; Zou, G.; Zhang, L.; Zhang, G.; Cai, X.; Teng, M. Dyes Pigm. 2012, 94, 410. doi: 10.1016/j.dyepig.2012.01.024
56. [56]
  Li, G.; Zhao, Y.; Li, J.; Cao, J.; Zhu, J.; Sun, X.; Zhang, Q. J. Org. Chem. 2015, 80, 196. doi: 10.1021/jo502296z
57. [57]
  Wang, R.; Li, J.; Li, G.; Hao, C.; Zhang, Y.; Wang, S.; Zhao, J.; Liu, Q.; Shi, Z. Dyes Pigm. 2018, 156, 225. doi: 10.1016/j.dyepig.2018.04.012
58. [58]
  Maiti, D. K.; Roy, S.; Datta, A.; Banerjee, A. Chem. Phys. Lett. 2013, 588, 76. doi: 10.1016/j.cplett.2013.09.056
59. [59]
  Googson, F.; Panda, D.; Ray, S.; Mitra, A.; Guha, S.; Saha, S. Org. Biomol. Chem. 2013, 11, 4797. doi: 10.1039/c3ob40703a
60. [60]
  Du, F.; Bao, Y.; Liu, B.; Tian, J.; Li, Q.; Bai, R. Chem. Commun. 2013, 49, 4631. doi: 10.1039/c3cc40810h
61. [61]
  Gao, T.; Zhou, W.; Zhao, Y.; Chang, W.; Musendo, R.; Chen, E.; Song, Y.; Ren, X. Chem. Commun. 2019, 55, 3012. doi: 10.1039/C8CC09725A
62. [62]
  Sudhakar, P.; Neena, K.; Thilagar, P. Dalton Trans. 2019, 48, 7218. doi: 10.1039/C8DT04005B
63. [63]
  Fu, Y.; Tang, H.; Liu, Z.; Zhang, W. X.; Ren, J. Chin. J. Org. Chem. 2018, 38, 1806 (in Chinese).
64. [64]
  Liu, Y.; Wang, K.; Guo, D.; Jiang, B. Adv. Funct. Mater. 2009, 19, 2230. doi: 10.1002/adfm.200900221
65. [65]
  Peng, H.; Ding, L.; Liu, T.; Chen, X.; Li, L.; Yin, S.; Fang, Y. Chem.-Asian J. 2012, 7, 1576. doi: 10.1002/asia.201100958
66. [66]
  Zhang, J.; Liu, K.; Wang, G.; Shang, C.; Peng, H.; Liu, T.; Fang, Y. New J. Chem. 2018, 42, 12737. doi: 10.1039/C8NJ02540A
67. [67]
  Hu, J.; Kuang, W.; Deng, K.; Zou, W.; Huang, Y.; Wei, Z.; Faul, C. F. J. Adv. Funct. Mater. 2012, 22, 4149. doi: 10.1002/adfm.201200973
68. [68]
  Deng, Q.; Zhou, E.; Huang, Y.; Qing, W.; Zhai, H.; Liu, Z.; Wei, Z. Chem. Commun. 2019, 55, 4379. doi: 10.1039/C9CC01443H
69. [69]
  Ji, S.; Wang, H.; Wang, T.; Yan, D. Adv. Mater. 2013, 25, 1755. doi: 10.1002/adma.201204134
70. [70]
  Kalita, A.; Hussain, S.; Malik, A. H.; Subbarao, N. V. V.; Iyer, P. K. J. Mater. Chem. C 2015, 3, 10767.
71. [71]
  Huang, Y.; Liu, X.; Wang, Q.; Fu, J.; Zhao, L.; Liu, Z.; Jin, D. J. Mater. Chem. C 2017, 5, 7644. doi: 10.1039/C7TC02580G
72. [72]
  Wang, J.; He, E.; Liu, X.; Yu, L.; Wang, H.; Zhang, H.; Zhang, H. Sens. Actuators, B 2017, 239, 898. doi: 10.1016/j.snb.2016.08.090
73. [73]
  Wang, K.; Yang, H.; Qian, X.; Xue, Z.; Li, Y.; Liu, H.; Li, Y. Dalton Trans. 2014, 43, 11542. doi: 10.1039/C4DT00962B
74. [74]
  Liu, X.; Zhai, H.; Zhang, S.; Fu, J.; Huang, Y. Sens. Actuators, B 2017, 243, 500. doi: 10.1016/j.snb.2016.12.020
75. [75]
  Zhu, P.; Wang, Y.; Ma, P.; Li, S.; Fan, F.; Cui, K.; Ge, S.; Zhang, Y.; Yu, J. Anal. Chem. 2019, 91, 5591. doi: 10.1021/acs.analchem.8b04497
76. [76]
  Acikbas, Y.; Erdogan, M.; Capan, R.; Yukruk, F. Sens. Actuators, B 2014, 200, 61. doi: 10.1016/j.snb.2014.04.051
77. [77]
  Sun, Q.; Lü, Y.; Liu, L.; Liu, K.; Miao, R.; Fang, Y. ACS Appl. Mater. Interfaces 2016, 8, 29128. doi: 10.1021/acsami.6b08642
78. [78]
  Abdalla, M. A.; Bayer, J.; Rödler, J. O.; Müllen, K. Angew. Chem., Int. Ed. 2004, 43, 3967. doi: 10.1002/anie.200353621
79. [79]
  Aubert, Y.; Asseline, U. Org. Biomol. Chem. 2004, 2, 3496. doi: 10.1039/B410695D
80. [80]
  Rahe, N.; Rinn, C.; Carell, T. Chem. Commun. 2003, 2120.
81. [81]
  Bevers, S.; Schutte, S.; Mclaughlin, L. W. J. Am. Chem. Soc. 2000, 122, 5905. doi: 10.1021/ja0001714
82. [82]
  Zheng, Y.; Long, H.; Schatz, G. C.; Lewis, F. D. Chem. Commun. 2005, 4795.
83. [83]
  Wagner, C.; Wagenknecht, H.-A. Org Lett. 2006, 8, 4191. doi: 10.1021/ol061246x
84. [84]
  Wang, Y.; Chen, J.; Jiao, H.; Chen, Y.; Li, W.; Zhang, Q.; Yu, C. Chem.-Eur. J. 2013, 19, 12846. doi: 10.1002/chem.201203998
85. [85]
  Chen, J.; Jiao, H.; Li, W.; Liao, D.; Zhou, H.; Yu, C. Chem.-Asian J. 2013, 8, 276. doi: 10.1002/asia.201200880
86. [86]
  Chen, X.; Jou, M. J.; Yoon, J. Org. Lett. 2009, 11, 2181. doi: 10.1021/ol9004849
87. [87]
  Yan, L.; Ye, Z.; Peng, C.; Zhang, S. Tetrahedron 2012, 68, 2725. doi: 10.1016/j.tet.2012.01.028
88. [88]
  Li, Y.; Yin, S.; Hou, J.; Meng, L.; Gao, M.; Sun, Y.; Zhang, C.; Bai, S.; Ren, J.; Yu, C. Analyst 2019, 144, 2034. doi: 10.1039/C8AN02231C
89. [89]
  Wang, K.; An, H.; Rong, Z.; Cao, Z.; Li, X. Biosens. Bioelectron. 2014, 58, 27. doi: 10.1016/j.bios.2014.02.038
90. [90]
  Lin, Y.; Chapman, R.; Stevens, M. M. Anal. Chem. 2014, 86, 6410. doi: 10.1021/ac500777r
91. [91]
  D'Autréaux, B.; Toledano, M. B. J. Nat. Rev. Mol. Cell Biol. 2007, 8, 813.
92. [92]
  Weinstain, R.; Savariar, E. N.; Felsen, C N.; Tsien, R. Y. J. Am. Chem. Soc. 2014, 136, 874. doi: 10.1021/ja411547j
93. [93]
  Sundaresan, M.; Yu, Z.; Finkel, T. Science 1995, 270, 296. doi: 10.1126/science.270.5234.296
94. [94]
  Ohshima, H.; Tatemichi, M.; Sawa, T. J. Arch. Biochem. Biophys. 2003, 417, 3. doi: 10.1016/S0003-9861(03)00283-2
95. [95]
  Shah, A. M.; Channon, K. M. J. Heart 2004, 90, 486. doi: 10.1136/hrt.2003.029389
96. [96]
  Barnham, K. J.; Masters, C. L.; Bush, A. I. Nat. Rev. Drug Discovery 2004, 3, 205. doi: 10.1038/nrd1330
97. [97]
  Soh, N.; Ariyoshi, T.; Fukaminato, T.; Nakano, K.; Irie, M.; Imato, T. Bioorg. Med. Chem. Lett. 2006, 16, 2943. doi: 10.1016/j.bmcl.2006.02.078
98. [98]
  Soh, N.; Ariyoshi, T.; Fukaminato, T.; Nakajima, H.; Nakano, K.; Imato, T. Org. Biomol. Chem. 2007, 5, 3762. doi: 10.1039/b713223a
99. [99]
  Maki, T.; Soh, N.; Fukaminato, T.; Nakajima, H.; Nakano, K.; Imato, T. Anal. Chim. Acta 2009, 639, 78. doi: 10.1016/j.aca.2009.02.044
100. [100]
  Kaloyanova, S.; Zagraanyarski, Y.; Ritz, S.; Hanulová, M.; Koynov, K.; Vonderheit, A.; Müllen, K.; Peneva, K, J. Am. Chem. Soc. 2016, 138, 2881. doi: 10.1021/jacs.5b10425
101. [101]
  Ou, Z.; Feng, Z.; Liu, G.; Chen, Y.; Gao, Y.; Li, Y.; Wang, X. Chem. Lett. 2015, 44, 425. doi: 10.1246/cl.141045
102. [102]
  Gao, Y.-Y.; Cai, W. J.; Ou, Z. Z.; Ma, T. T.; Wang, Z. J.; Xu, M. H. Imaging Sci. Photochem. 2017, 35, 552 (in Chinese). doi: 10.7517/j.issn.1674-0475.2017.04.017
1. [1]
  Jinlong YAN , Weina WU , Yuan WANG . A simple Schiff base probe for the fluorescent turn-on detection of hypochlorite and its biological imaging application. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1653-1660. doi: 10.11862/CJIC.20240154
2. [2]
  Yanxi LIU , Mengjia XU , Haonan CHEN , Quan LIU , Yuming ZHANG . A fluorescent-colorimetric probe for peroxynitrite-anion-imaging in living cells. Chinese Journal of Inorganic Chemistry, 2025, 41(6): 1112-1122. doi: 10.11862/CJIC.20240423
3. [3]
  Jun LUO , Baoshu LIU , Yunchang ZHANG , Bingkai WANG , Beibei GUO , Lan SHE , Tianheng CHEN . Europium(Ⅲ) metal-organic framework as a fluorescent probe for selectively and sensitively sensing Pb²⁺ in aqueous solution. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2438-2444. doi: 10.11862/CJIC.20240240
4. [4]
  Jiakun BAI , Ting XU , Lu ZHANG , Jiang PENG , Yuqiang LI , Junhui JIA . A red-emitting fluorescent probe with a large Stokes shift for selective detection of hypochlorous acid. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1095-1104. doi: 10.11862/CJIC.20240002
5. [5]
  Yu SU , Xinlian FAN , Yao YIN , Lin WANG . From synthesis to application: Development and prospects of InP quantum dots. Chinese Journal of Inorganic Chemistry, 2024, 40(11): 2105-2123. doi: 10.11862/CJIC.20240126
6. [6]
  Jinghan ZHANG , Guanying CHEN . Progress in the application of rare-earth-doped upconversion nanoprobes in biological detection. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2335-2355. doi: 10.11862/CJIC.20240249
7. [7]
  Pingping LU , Shuguang ZHANG , Peipei ZHANG , Aiyun NI . Preparation of zinc sulfate open frameworks based probe materials and detection of Pb²⁺ and Fe³⁺ ions. Chinese Journal of Inorganic Chemistry, 2025, 41(5): 959-968. doi: 10.11862/CJIC.20240411
8. [8]
  Jia-He Li , Yu-Ze Liu , Jia-Hui Ma , Qing-Xiao Tong , Jian-Ji Zhong , Jing-Xin Jian . 洛芬碱衍生物的合成、化学发光与重金属离子检测. University Chemistry, 2025, 40(6): 230-237. doi: 10.12461/PKU.DXHX202407080
9. [9]
  Yikai Wang , Xiaolin Jiang , Haoming Song , Nan Wei , Yifan Wang , Xinjun Xu , Cuihong Li , Hao Lu , Yahui Liu , Zhishan Bo . 氰基修饰的苝二酰亚胺衍生物作为膜厚不敏感型阴极界面材料用于高效有机太阳能电池. Acta Physico-Chimica Sinica, 2025, 41(3): 2406007-. doi: 10.3866/PKU.WHXB202406007
10. [10]
  Hong LI , Xiaoying DING , Cihang LIU , Jinghan ZHANG , Yanying RAO . Detection of iron and copper ions based on gold nanorod etching colorimetry. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 953-962. doi: 10.11862/CJIC.20230370
11. [11]
  Siyi ZHONG , Xiaowen LIN , Jiaxin LIU , Ruyi WANG , Tao LIANG , Zhengfeng DENG , Ao ZHONG , Cuiping HAN . Targeting imaging and detection of ovarian cancer cells based on fluorescent magnetic carbon dots. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1483-1490. doi: 10.11862/CJIC.20240093
12. [12]
  Li'na ZHONG , Jingling CHEN , Qinghua ZHAO . Synthesis of multi-responsive carbon quantum dots from green carbon sources for detection of iron ions and L-ascorbic acid. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 709-718. doi: 10.11862/CJIC.20240280
13. [13]
  Xiaowei TANG , Shiquan XIAO , Jingwen SUN , Yu ZHU , Xiaoting CHEN , Haiyan ZHANG . A zinc complex for the detection of anthrax biomarker. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1850-1860. doi: 10.11862/CJIC.20240173
14. [14]
  Yang YANG , Pengcheng LI , Zhan SHU , Nengrong TU , Zonghua WANG . Plasmon-enhanced upconversion luminescence and application of molecular detection. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 877-884. doi: 10.11862/CJIC.20230440
15. [15]
  Qin Hou , Jiayi Hou , Aiju Shi , Xingliang Xu , Yuanhong Zhang , Yijing Li , Juying Hou , Yanfang Wang . Preparation of Cuprous Iodide Coordination Polymer and Fluorescent Detection of Nitrite: A Comprehensive Chemical Design Experiment. University Chemistry, 2024, 39(8): 221-229. doi: 10.3866/PKU.DXHX202312056
16. [16]
  Jiatong Hu , Qiyi Wang , Ruiwen Tang , Jiajing Feng . Photocatalytic Journey of Perylene Diimides in a Competitive Arena. University Chemistry, 2025, 40(5): 328-333. doi: 10.12461/PKU.DXHX202407015
17. [17]
  Junjie Zhang , Yue Wang , Qiuhan Wu , Ruquan Shen , Han Liu , Xinhua Duan . Preparation and Selective Separation of Lightweight Magnetic Molecularly Imprinted Polymers for Trace Tetracycline Detection in Milk. University Chemistry, 2024, 39(5): 251-257. doi: 10.3866/PKU.DXHX202311084
18. [18]
  Di Yang , Jiayi Wei , Hong Zhai , Xin Wang , Taiming Sun , Haole Song , Haiyan Wang . Rapid Detection of SARS-CoV-2 Using an Innovative “Magic Strip”. University Chemistry, 2024, 39(4): 373-381. doi: 10.3866/PKU.DXHX202312023
19. [19]
  Yongzhi LI , Han ZHANG , Gangding WANG , Yanwei SUI , Lei HOU , Yaoyu WANG . A two-dimensional metal-organic framework for the determination of nitrofurantoin and nitrofurazone in aqueous solution. Chinese Journal of Inorganic Chemistry, 2025, 41(2): 245-253. doi: 10.11862/CJIC.20240307
20. [20]
  Qilong Fang , Yiqi Li , Jiangyihui Sheng , Quan Yuan , Jie Tan . Magical Pesticide Residue Detection Test Strips: Aptamer-based Lateral Flow Test Strips for Organophosphorus Pesticide Detection. University Chemistry, 2024, 39(5): 80-89. doi: 10.3866/PKU.DXHX202310004

Get Citation

PDF

XML

Metrics

PDF Downloads(105)
Abstract views(5012)
HTML views(2019)

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