Citation: Xie Zhenda, Fu Manlin, Yin Biao, Zhu Qing. Research Progress in 1, 8-Naphthalimide-Based Fluorescent Probes for Two-Photon Imaging[J]. Chinese Journal of Organic Chemistry, ;2018, 38(6): 1364-1376. doi: 10.6023/cjoc201712031 shu

Research Progress in 1, 8-Naphthalimide-Based Fluorescent Probes for Two-Photon Imaging

Key Laboratory of Bioorganic Synthesis of Zhejiang Province, College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310014

Corresponding author: Zhu Qing, zhuq@zjut.edu.cn
Received Date: 23 December 2017
Revised Date: 18 January 2018
Available Online: 6 June 2018
Fund Project: the National Natural Science Foundation of China 21272212the National Natural Science Foundation of China 21472172Project supported by the National Natural Science Foundation of China (Nos. 21472172, 21272212)

Figures(12)

Fluorescent imaging technology has received great attention owing to their advantageous features in high sensitivity, relatively simple operations and real-time living cells, tissue and in vivo imaging. Compared with one-photon confocal imaging, two-photon confocal imaging offers considerable advantages such as high resolution, deep-tissue depth, lower tissue auto-fluorescence and so on. As typical D-π-A two-photon dyes, 1, 8-naphthalimide dyes have wide application in two-photon imaging for enzyme, reactive carbon species, reactive oxygen species, reactive nitrogen species, biothiols and ions due to their advantages such as high photostability, large Stokes/anti-Stokes shifts. According to the mechanisms of intramolecular charge transfer, photoinduced electron transfer and fluorescence resonance energy transfer, etc., the application in two-photon imaging of 1, 8-naphthalimide dyes is summarized and emphasized.
- 1, 8-naphthalimide,
- fluorescent probe,
- D-π-A,
- fluorescent mechanism,
- two-photon imaging
1. [1]
  Li, X.; Gao, X.; Shi, W.; Ma, H. Chem. Rev. 2014, 114, 590. doi: 10.1021/cr300508p
2. [2]
  Chen, X.; Tian, X.; Shin, I.; Yoon, J. Chem. Soc. Rev. 2011, 40, 4783. doi: 10.1039/c1cs15037e
3. [3]
  Tang, Y.; Lee, D.; Wang, J.; Li, G.; Yu, J.; Lin, W.; Yoon, J. Chem. Soc. Rev. 2015, 44, 5003. doi: 10.1039/C5CS00103J
4. [4]
  Kikuchi, K. Chem. Soc. Rev. 2010, 39, 2048. doi: 10.1039/b819316a
5. [5]
  Kim, H. M.; Cho, B. R. Chem. Rev. 2015, 115, 5014. doi: 10.1021/cr5004425
6. [6]
  Kim, D.; Ryu, H. G.; Ahn, K. H. Org. Biomol. Chem. 2014, 12, 4550. doi: 10.1039/C4OB00431K
7. [7]
  Huang, C.; Chen, S. Prog. Chem. 2017, 29, 1215 (in Chinese).
8. [8]
  Loving, G.; Imperiali, B. J. Am. Chem. Soc. 2008. 130, 13630. doi: 10.1021/ja804754y
9. [9]
  Prezhdo, O. V.; Uspenskii, B. V.; Prezhdo, V. V.; Boszczyk, W.; Distanov, V. B. Dyes Pigm. 2009, 83, 324. doi: 10.1016/j.dyepig.2009.05.010
10. [10]
  Banerjee, S.; Veale, E. B.; Phelan, C. M.; Murphy, S. A.; Tocci, G. M.; Gillespie, L. J.; Frimannsson, D. O.; Kelly, J. M.; Gunnlaugsson, T. Chem. Soc. Rev. 2013, 42, 1601. doi: 10.1039/c2cs35467e
11. [11]
  Duke, R. M.; Veale, E. B.; Pfeffer, F. M.; Kruger, P. E.; Gunnlaugsson, T. Chem. Soc. Rev. 2010, 39, 3936. doi: 10.1039/b910560n
12. [12]
  Qian, X.; Xiao, Y.; Xu, Y.; Guo, X.; Qian, J.; Zhu, W. Chem. Commun. 2010, 46, 6418. doi: 10.1039/c0cc00686f
13. [13]
  Alexiou, M. S.; Tychopoulos, V.; Ghorbanian, S.; Tyman, J. H. P.; Brown, R. G.; Brittain, P. I. J. Chem. Soc., Perkin Trans. 2 1990, 837.
14. [14]
  de Silva, A. P.; Gunaratne, H. Q. N.; Gunnlaugsson, T.; Huxley, A. J. M.; McCoy, C. P.; Rademacher, J. T.; Rice, T. E. Chem. Rev. 1997, 97, 1515. doi: 10.1021/cr960386p
15. [15]
  Finkel, T.; Holbrook, N. J. Nature 2000, 408, 2392.
16. [16]
  Lippert, A. R.; Bittner, V.; Chang, C. J. Acc. Chem. Res. 2011, 44, 793. doi: 10.1021/ar200126t
17. [17]
  Srikun, D.; Miller, E. W.; Domaille, D. W.; Chang, C. J. J. Am. Chem. Soc. 2008, 130, 4596. doi: 10.1021/ja711480f
18. [18]
  Zdolsek, J.; Zhang, H.; Roberg, K.; Brunk, U. Free Radical Res. Commun. 1993, 18, 71. doi: 10.3109/10715769309147344
19. [19]
  Ren, M.; Deng, B.; Wang, J. Y.; Kong, X.; Liu, Z. R.; Zhou, K.; He, L.; Lin, W. Biosens. Bioelectron. 2016, 79, 237. doi: 10.1016/j.bios.2015.12.046
20. [20]
  Xu, Z.; Liu, T.; Spring, D. R.; Cui, J. Org. Lett. 2013, 15, 2310. doi: 10.1021/ol400973v
21. [21]
  Winterbourn, C. C.; Hampton, M. B.; Livesey, J. H.; Kettle, A. J. J. Biol. Chem. 2006, 281, 39860. doi: 10.1074/jbc.M605898200
22. [22]
  Pattison, D. I.; Davies, M. J. Biochemistry 2006, 45, 81522.
23. [23]
  Zhu, B.; Li, P.; Shu, W.; Wang, X.; Liu, C.; Wang, Y.; Wang, Z.; Wang, Y.; Tang, B. Anal. Chem. 2016, 88, 12532. doi: 10.1021/acs.analchem.6b04392
24. [24]
  Zhang, B.; Yang, X.; Zhang, R.; Liu, Y.; Ren, X.; Xian, M.; Ye Y., Zhao Y. Anal. Chem. 2017, 89, 10384. doi: 10.1021/acs.analchem.7b02361
25. [25]
  Wang, B.; Li, P.; Yu, F.; Song, P.; Sun, X.; Yang, S.; Lou, Z.; Han, K. Chem. Commun. 2013, 49, 1014. doi: 10.1039/C2CC37803E
26. [26]
  Lou, Z.; Li, P.; Han, K. Acc. Chem. Res. 2015, 48, 1358. doi: 10.1021/acs.accounts.5b00009
27. [27]
  Yu, F.; Li, P.; Wang, B.; Han, K. J. Am. Chem. Soc. 2013, 135, 7674. doi: 10.1021/ja401360a
28. [28]
  Yu, F.; Li, P.; Li, G.; Zhao, G.; Chu, T.; Han, K. J. Am. Chem. Soc. 2011, 133, 11030. doi: 10.1021/ja202582x
29. [29]
  Lou, Z.; Li, P.; Pan, Q.; Han, K. Chem. Commun. 2013, 49, 2445. doi: 10.1039/c3cc39269d
30. [30]
  Weidinger, A.; Kozlov, A. V. Biomolecules 2015, 5, 472. doi: 10.3390/biom5020472
31. [31]
  Radi, R. J. Biol. Chem. 2013, 288, 26464. doi: 10.1074/jbc.R113.472936
32. [32]
  Li, Y.; Xie, X.; Yang, X.; Li, M.; Jiao, X.; Sun, Y.; Wang, X.; Tang, B. Chem. Sci. 2017, 8, 4006. doi: 10.1039/C7SC00303J
33. [33]
  Brewer, T. F.; Chang, C. J. J. Am. Chem. Soc. 2015, 137, 10886. doi: 10.1021/jacs.5b05340
34. [34]
  Roth, A.; Li, H.; Anorma, C.; Chan, J. J. Am. Chem. Soc. 2015, 137, 10890. doi: 10.1021/jacs.5b05339
35. [35]
  Xie, Z.; Ge, J.; Zhang, H.; Bai, T.; He, S.; Ling, J.; Sun, H.; Zhu, Q. Sens. Actuators, B 2017, 241, 1050.
36. [36]
  Lin, J.-Y.; Zhang, M.-W.; Wang, J.-G.; Li, H.; Wei, H.-Y.; Liu, R.; Dai, G.; Liao, X. -X. Exp. Ther. Med. 2016, 11, 577. doi: 10.3892/etm.2015.2950
37. [37]
  Lin, V. S.; Chen, W.; Xian, M.; Chang, C. J. Chem. Soc. Rev. 2015, 44, 4596. doi: 10.1039/C4CS00298A
38. [38]
  Liu, X. L.; Du, X. J.; Dai, C. G.; Song, Q. H. J. Org. Chem. 2014, 79, 9481. doi: 10.1021/jo5014838
39. [39]
  Kimura, H.; Shibuya, N.; Kimura, Y. Antioxid. Redox Signaling 2012, 17, 45.
40. [40]
  Fu, Y. J.; Yao, H. W.; Zhu, X. Y.; Guo, X. F.; Wang, H. Anal. Chim. Acta 2017, 994, 1. doi: 10.1016/j.aca.2017.09.030
41. [41]
  Zhou, Y.; Zhang, J.; Yoon, J. Chem. Rev. 2014, 114, 5511. doi: 10.1021/cr400352m
42. [42]
  Zhang, H.; Wu, Y.; You, J.; Cao, L.; Ding, S.; Jiang, K.; Wang, Z. Chin. J. Org. Chem. 2016, 36, 2559 (in Chinese).
43. [43]
  Zhang, J. F.; Lim, C. S.; Bhuniya, S.; Cho, B. R.; Kim, J. S. Org. Lett. 2011, 13, 1190. doi: 10.1021/ol200072e
44. [44]
  Zhou, L.; Hu, S.; Wang, H.; Sun, H.; Zhang, X. Spectrochim. Acta, Part A 2016, 166, 25. doi: 10.1016/j.saa.2016.05.013
45. [45]
  Qian, L.; Li, L.; Yao, S. Q. Acc. Chem. Res. 2016, 49, 626. doi: 10.1021/acs.accounts.5b00512
46. [46]
  Dai, Z. R.; Ge, G. B.; Feng, L.; Ning, J.; Hu, L. H.; Jin, Q.; Wang, D. D.; Lv, X.; Dou, T. Y.; Cui, J. N.; Yang, L. J. Am. Chem. Soc. 2015. 137, 14488.
47. [47]
  Dai, Z. R.; Feng, L.; Jin, Q.; Cheng, H.; Li, Y.; Ning, J.; Yu, Y.; Ge, G. B.; Cui, J. N.; Yang, L. Chem. Sci. 2017, 8, 2795. doi: 10.1039/C6SC03970G
48. [48]
  Kaminsky, L. S.; Spivack, S. D. Mol. Aspects Med. 1999, 20, 70.
49. [49]
  Wei, C.; Caccavale, R. J.; Weyand, E. H.; Chen, S.; Iba, M. M. Cancer Lett. 2002, 178, 25. doi: 10.1016/S0304-3835(01)00809-6
50. [50]
  Satoh, T.; Hosokawa, M. J. Pestic. Sci. 2010, 35, 218. doi: 10.1584/jpestics.R10-02
51. [51]
  Pratt, S. E.; Durland-Busbice, S.; Shepard, R. L.; Donoho, G. P.; Starling, J. J.; Wickremsinhe, E. R.; Perkins, E. J.; Dantzig, A. H. Mol. Cancer Ther. 2013, 12, 481. doi: 10.1158/1535-7163.MCT-12-0654
52. [52]
  Jin, Q.; Feng, L.; Wang, D. D.; Dai, Z. R.; Wang, P.; Zou, L. W.; Liu, Z. H.; Wang, J. Y.; Yu, Y.; Ge, G. B.; Cui, J. N.; Yang, L. ACS Appl. Mater. Interfaces 2015, 7, 28474. doi: 10.1021/acsami.5b09573
53. [53]
  Hildebrandt, M.; Reutter, W.; Arck, P.; Rose, M.; Klapp, B. F. Clin. Sci. 2000, 99, 932.
54. [54]
  Zou, L. W.; Wang, P.; Qian, X. K.; Feng, L.; Yu, Y.; Wang, D. D.; Jin, Q.; Hou, J.; Liu, Z. H.; Ge, G. B.; Yang, L. Biosens. Bioelectron. 2017, 90, 283. doi: 10.1016/j.bios.2016.11.068
55. [55]
  Spergel, D. J.; Krȕth, U.; Shimshek, D. R.; Sprengel, R.; Seeburg, P. H. Prog. Neurobiol. 2001, 63, 673. doi: 10.1016/S0301-0082(00)00038-1
56. [56]
  Kamiya, M.; Asanuma, D.; Kuranaga, E.; Takeishi, A.; Sakabe, M.; Miura, M.; Nagano, T.; Urano, Y. J. Am. Chem. Soc. 2011, 133, 12960. doi: 10.1021/ja204781t
57. [57]
  Asanuma, D.; Sakabe, M.; Kamiya, M.; Yamamoto, K.; Hiratake, J.; Ogawa, M.; Kosaka, N.; Choyke, P. L.; Nagano, T.; Kobayashi, H.; Urano, Y. Nat. Commun. 2015, 6, 6463. doi: 10.1038/ncomms7463
58. [58]
  Zhang, X.; Wu, H.; Li, P.; Qu, Z.; Tan. M.; Han. K. Chem. Commun. 2016, 52, 8283. doi: 10.1039/C6CC04373A
59. [59]
  Hattori, A.; Matsumoto, H.; Mizutani, S.; Tsujimoto, M. J. Biochem. 1999, 125, 931. doi: 10.1093/oxfordjournals.jbchem.a022371
60. [60]
  Shastri, N.; Schwab, S.; Serwold, T. Annu. Rev. Immunol. 2002, 20, 463. doi: 10.1146/annurev.immunol.20.100301.064819
61. [61]
  Xu, S.; Liu, H. W.; Hu, X. X.; Huan, S. Y.; Zhang, J.; Liu, Y. C.; Yuan, L.; Qu, F. L.; Zhang, X. B.; Tan, W. Anal. Chem. 2017, 89, 7641. doi: 10.1021/acs.analchem.7b01561
62. [62]
  Ueno, T.; Urano, Y.; Kojima, H.; Nagano, T. J. Am. Chem. Soc. 2006, 128, 10640. doi: 10.1021/ja061972v
63. [63]
  Ueno, T.; Urano, Y.; Setsukinai, K.; Takakusa, H.; Kojima, H.; Kikuchi, K.; Ohkubo, K.; Fukuzumi, S.; Nagano, T. J. Am. Chem. Soc. 2004, 126, 14079. doi: 10.1021/ja048241k
64. [64]
  Zhang, P.; Wang, H.; Zhang, D.; Zeng, X.; Zeng, R.; Xiao, L.; Tao, H.; Long, Y.; Yi, P.; Chen, J. Sens. Actuators, B 2018, 255, 2223.
65. [65]
  Cnop, M.; Foufelle, F.; Velloso, L. A. Trends Mol. Med. 2012, 18, 59. doi: 10.1016/j.molmed.2011.07.010
66. [66]
  Harding, H. P.; Ron, D. Diabetes 2002, 51, S455. doi: 10.2337/diabetes.51.2007.S455
67. [67]
  Xiao, H.; Liu, X.; Wu, C.; Wu, Y.; Li, P.; Guo, X.; Tang, B. Biosens. Bioelectron. 2017, 91, 449. doi: 10.1016/j.bios.2016.12.068
68. [68]
  Weishaupt, K. R.; Gomer, C. J.; Dougherty, T. J. Cancer Res. 1976, 36, 2326.
69. [69]
  Castano, A. P.; Mroz, P.; Hamblin, M. R. Nat. Rev. Cancer 2006, 6, 535. doi: 10.1038/nrc1894
70. [70]
  Liu, H. W.; Xu, S.; Wang, P.; Hu, X. X.; Zhang, J.; Yuan, L.; Zhang, X. B.; Tan, W. Chem. Commun. 2016, 52, 12330. doi: 10.1039/C6CC05880A
71. [71]
  da Silva, T. R. M.; de Freitas, J. R.; Silva, Q. C.; Figueira, C. P.; Roxo, E.; Leao, S. C.; de Freitas, L. A. R.; Veras, P. S. T. Infect. Immun. 2002, 70, 5628. doi: 10.1128/IAI.70.10.5628-5634.2002
72. [72]
  Yu, H.; Xiao, Y.; Jin, L. J. Am. Chem. Soc. 2012, 134, 17486. doi: 10.1021/ja308967u
73. [73]
  Tang, Y.; Kong, X.; Xu, A.; Dong, B.; Lin, W. Angew. Chem., Int. Ed. 2016, 55, 3356. doi: 10.1002/anie.201510373
74. [74]
  Lee, Y. H.; Tang, Y.; Verwilst, P.; Lin, W.; Kim, J. S. Chem. Commun. 2016, 52, 112472.
75. [75]
  Ren, W. X.; Han, J. Y.; Uhm, S.; Jang, Y. J.; Kang, C.; Kim, J. H.; Kim, J. S. Chem. Commun. 2015, 51, 10403. doi: 10.1039/C5CC03075G
76. [76]
  Matafome, P.; Sena, C.; Seica, R. Endocrine 2013, 43, 472. doi: 10.1007/s12020-012-9795-8
77. [77]
  Singh, R.; Barden, A.; Mori, T.; Beilin, L. Diabetologia 2001, 44, 129. doi: 10.1007/s001250051591
78. [78]
  Tang, T.; Zhou, Y.; Chen, Y.; Li, M.; Feng, Y.; Wang, C.; Wang, S.; Zhou, X. Anal. Methods 2015, 7, 2386. 2
79. [79]
  Bulaj, G.; Kortemme, T.; Goldenberg, D. P. Biochemistry 1998, 37, 8965. doi: 10.1021/bi973101r
80. [80]
  Weerapana, E.; Wang, C.; Simon, G. M.; Richter, F.; Khare, S.; Dillon, M. B. D.; Bachovchin, D. A.; Mowen, K.; Baker, D.; Cravatt, B. F. Nature 2010, 468, 790. doi: 10.1038/nature09472
81. [81]
  Zhu, X.; Li, Y.; Zan, W.; Zhang, J.; Chen, Z.; Liu, X.; Qi, F.; Yao, X.; Zhang, X.; Zhang, H. Photochem. Photobiol. Sci. 2016, 15, 412. doi: 10.1039/C5PP00468C
82. [82]
  Chen, X. Q.; Zhou, Y.; Peng, X. J.; Yoon, J. Y. Chem. Soc. Rev. 2010, 39, 2120. doi: 10.1039/b925092a
83. [83]
  Wang, G. L.; Jiao, H. J.; Zhu, X. Y.; Dong, Y. M.; Li, Z. J. Analyst 2013, 138, 2000. doi: 10.1039/c3an36878e
84. [84]
  Liu, Y.; Liu, Y.; Liu, W.; Liang, S. Spectrochim. Acta, Part A 2015, 137, 509. doi: 10.1016/j.saa.2014.08.072
85. [85]
  Yuan, L.; Lin, W.; Zheng, K.; Zhu, S. Acc. Chem. Res. 2013, 46, 1462. doi: 10.1021/ar300273v
86. [86]
  Yao, S.; Qian, Y. Sens. Actuators, B 2017, 252, 877.
87. [87]
  Xie, X.; Tang, F.; Shangguan, X.; Che, S.; Niu J.; Xiao, Y.; Wang, X.; Tang, B. Chem. Commun. 2017, 53, 6520. doi: 10.1039/C7CC03050A
88. [88]
  Lee, D. E.; Koo, H.; Sun, I. C.; Ryu, J. H.; Kim, K.; Kwon, I. C. Chem. Soc. Rev. 2012, 41, 2656. doi: 10.1039/C2CS15261D
89. [89]
  Yuan, Y.; Zhang, R.; Cheng, X.; Xu, S.; Liu, B. Chem. Sci. 2016, 7, 4245. doi: 10.1039/C6SC00055J
90. [90]
  Shen, W.; Ge, J.; He, S.; Zhang, R.; Zhao, C.; Fan, Y.; Yu, S.; Liu, B.; Zhu, Q. Chem. -Asian J. 2017, 12, 1532. doi: 10.1002/asia.v12.13
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]
  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
3. [3]
  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
4. [4]
  Yonghui ZHOU , Rujun HUANG , Dongchao YAO , Aiwei ZHANG , Yuhang SUN , Zhujun CHEN , Baisong ZHU , Youxuan ZHENG . Synthesis and photoelectric properties of fluorescence materials with electron donor-acceptor structures based on quinoxaline and pyridinopyrazine, carbazole, and diphenylamine derivatives. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 701-712. doi: 10.11862/CJIC.20230373
5. [5]
  Lin Song , Dourong Wang , Biao Zhang . Innovative Experimental Design and Research on Preparing Flexible Perovskite Fluorescent Gels Using 3D Printing. University Chemistry, 2024, 39(7): 337-344. doi: 10.3866/PKU.DXHX202310107
6. [6]
  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
7. [7]
  Xuewei BA , Cheng CHENG , Huaikang ZHANG , Deqing ZHANG , Shuhua LI . Preparation and luminescent performance of Sr_1-xZrSi₂O₇∶xDy³⁺ phosphor with high thermal stability. Chinese Journal of Inorganic Chemistry, 2025, 41(2): 357-364. doi: 10.11862/CJIC.20240096
8. [8]
  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
9. [9]
  Zishuo Yi , Peng Liu , Yan Xu . Fluorescent “Chameleon”: A Popular Science Experiment Based on Dynamic Luminescence. University Chemistry, 2024, 39(9): 304-310. doi: 10.12461/PKU.DXHX202311079
10. [10]
  Han ZHANG , Jianfeng SUN , Jinsheng LIANG . Hydrothermal synthesis and luminescent properties of broadband near-infrared Na₃CrF₆ phosphor. Chinese Journal of Inorganic Chemistry, 2025, 41(2): 349-356. doi: 10.11862/CJIC.20240098
11. [11]
  Meirong HAN , Xiaoyang WEI , Sisi FENG , Yuting BAI . A zinc-based metal-organic framework for fluorescence detection of trace Cu²⁺. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1603-1614. doi: 10.11862/CJIC.20240150
12. [12]
  Yuan ZHU , Xiaoda ZHANG , Shasha WANG , Peng WEI , Tao YI . Conditionally restricted fluorescent probe for Fe³⁺ and Cu²⁺ based on the naphthalimide structure. Chinese Journal of Inorganic Chemistry, 2025, 41(1): 183-192. doi: 10.11862/CJIC.20240232
13. [13]
  Shuwen SUN , Gaofeng WANG . Design and synthesis of a Zn(Ⅱ)-based coordination polymer as a fluorescent probe for trace monitoring 2, 4, 6-trinitrophenol. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 753-760. doi: 10.11862/CJIC.20240399
14. [14]
  Yan ZHAO , Jiaxu WANG , Zhonghu LI , Changli LIU , Xingsheng ZHAO , Hengwei ZHOU , Xiaokang JIANG . Gd³⁺-doped Sc₂W3O₁₂: Eu³⁺ red phosphor: Preparation and luminescence performance. Chinese Journal of Inorganic Chemistry, 2025, 41(3): 461-468. doi: 10.11862/CJIC.20240316
15. [15]
  Yan ZHAO , Xiaokang JIANG , Zhonghui LI , Jiaxu WANG , Hengwei ZHOU , Hai GUO . Preparation and fluorescence properties of Eu³⁺-doped CaLaGaO₄ red-emitting phosphors. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1861-1868. doi: 10.11862/CJIC.20240242
16. [16]
  Xinyu Liu , Weiran Hu , Zhengkai Li , Wei Ji , Xiao Ni . Algin Lab: Surging Luminescent Sea. University Chemistry, 2024, 39(5): 396-404. doi: 10.3866/PKU.DXHX202312021
17. [17]
  Donghui PAN , Yuping XU , Xinyu WANG , Lizhen WANG , Junjie YAN , Dongjian SHI , Min YANG , Mingqing CHEN . Preparation and in vivo tracing of ⁶⁸Ga-labeled PM_2.5 mimetic particles for positron emission tomography imaging. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 669-676. doi: 10.11862/CJIC.20230468
18. [18]
  Liyang ZHANG , Dongdong YANG , Ning LI , Yuanyu YANG , Qi MA . Crystal structures, luminescent properties and Hirshfeld surface analyses of three cadmium(Ⅱ) complexes based on 2-(3-(pyridin-2-yl)-1H-pyrazol-1-yl)benzoate. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1943-1952. doi: 10.11862/CJIC.20240079
19. [19]
  Jingzhao Cheng , Shiyu Gao , Bei Cheng , Kai Yang , Wang Wang , Shaowen Cao . 4-氨基-1H-咪唑-5-甲腈修饰供体-受体型氮化碳光催化剂的构建及其高效光催化产氢研究. Acta Physico-Chimica Sinica, 2024, 40(11): 2406026-. doi: 10.3866/PKU.WHXB202406026
20. [20]
  Chun-Lin Sun , Yaole Jiang , Yu Chen , Rongjing Guo , Yongwen Shen , Xinping Hui , Baoxin Zhang , Xiaobo Pan . Construction, Performance Testing, and Practical Applications of a Home-Made Open Fluorescence Spectrometer. University Chemistry, 2024, 39(5): 287-295. doi: 10.3866/PKU.DXHX202311096

Get Citation

PDF

XML

Metrics

PDF Downloads(165)
Abstract views(5971)
HTML views(2419)

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