Citation: Li Meng, Lin Wei-Bin, Fang Lei, Chen Chuan-Feng. Recent Progress on Circularly Polarized Luminescence of Chiral Organic Small Molecules[J]. Acta Chimica Sinica, ;2017, 75(12): 1150-1163. doi: 10.6023/A17090440 shu

Recent Progress on Circularly Polarized Luminescence of Chiral Organic Small Molecules

Li Meng ^a ,
Lin Wei-Bin ^a,b ,
Fang Lei ^a,b ,
Chen Chuan-Feng ^a,b,,

a.
CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
b.
University of Chinese Academy of Sciences, Beijing 100049, China

Corresponding author: Chen Chuan-Feng, cchen@iccas.ac.cn
Received Date: 28 September 2017
Available Online: 1 December 2017
Fund Project: the National Natural Science Foundation of China 21602224the Strategic Priority Research Program of Chinese Academy of Sciences XDB12010400the National Natural Science Foundation of China 21572233the National Natural Science Foundation of China 51373180Project supported by the National Natural Science Foundation of China (Nos. 21602224, 51373180, 21572233), and the Strategic Priority Research Program of Chinese Academy of Sciences (No. XDB12010400)

Figures(28)

Circularly polarized luminescence (CPL) not only can reflect the excited state structure information of chiral system, but also has wide potential applications in 3D display, communication of spin information, information storage and processing, CPL laser and biological probe. Consequently, more and more attention and interests have been attracted into this field, which turns to be one of the most hot topics in organic luminescence materials in recent years. In this review, recent progress on the chiral organic small molecules with CPL properties is summarized. First, CPL concept and earlier studies of CPL and organic small molecules with CPL properties are briefly introduced. Then, chiral organic small molecules with CPL properties are classified into four types of central chirality, axial chirality, planar chirality, and helical chirality, and their progresses in recent years are systematically described, respectively. Among the small molecular systems with different types of chirality, those ones based on the biaryl skeleton and helicene derivatives show excellent CPL properties, and they could also be controlled or switched by anions, protons and others. Moreover, it should be paid attention to the applications of aggregation induced effect (AIE) and supramolecular chemistry for the chiral organic small molecules to obtain better CPL property. Finally, a conclusion and perspective on CPL materials based on chiral small molecules is provided.
- circularly polarized luminescence,
- chirality,
- helicene,
- organic small molecule
1. [1]
  (a) Brittain, H. G. Chirality 1996, 8, 357;(b) Riehl, J. P.; Richardson, F. S. Chem. Rev. 1986, 86, 1.
2. [2]
  Muller, G. Luminescence of Lanthanide Ions in Coordination Compounds and Nanomaterials, Ed.: de Bettencourt-Dias, A., Wiley, Hoboken, 2014, pp. 77~124.
3. [3]
  Yang, Y.; da Costa, R. C.; Smilgies, D.-M.; Campbell, A. J.; Fuchter, M. J. Adv. Mater. 2013, 25, 2624. doi: 10.1002/adma.201204961
4. [4]
  Farshchi, R.; Ramsteiner, M.; Herfort, J.; Tahraoui, A.; Grahn, H. T. Appl. Phys. Lett. 2011, 98, 162508. doi: 10.1063/1.3582917
5. [5]
  Yang, Y.; da Costa, R. C.; Fuchter, M. J.; Campbell, A. J. Nat. Photon. 2013, 7, 634. doi: 10.1038/nphoton.2013.176
6. [6]
  Jiménez, J.; Cerdán, L.; Moreno, F.; Maroto, B. L.; García-Moreno, I.; Lunkley, J. L.; Muller, G.; de la Moya, S. J. Phys. Chem. C 2017, 121, 5287. doi: 10.1021/acs.jpcc.7b00654
7. [7]
  (a) Muller, G. Dalton Trans. 2009, 9692;(b) Hassey, R.; Swain, E. J.; Hammer, N. I.; Venkataraman, D.; Barnes, M. D. Science 2006, 314, 1437.
8. [8]
  Sanchez-Carnerero, E. M.; Agarrabeitia, A. R.; Moreno, F.; Maroto, B. L.; Muller, G.; Ortiz, M. J.; de la Moya, S. Chem. Eur. J. 2015, 21, 13488. doi: 10.1002/chem.v21.39
9. [9]
  Lunkley, J. L.; Shirotani, D.; Yamanari, K.; Kaizaki, S.; Muller, G. J. Am. Chem. Soc. 2008, 130, 13814. doi: 10.1021/ja805681w
10. [10]
  (a) Carr, R.; Evans, N. H.; Parker, D. Chem. Soc. Rev. 2012, 41, 7673;(b) Aspinall, H. C. Chem. Rev. 2002, 102, 1807;(c) Bunzli, J. C. G.; Piguet, C. Chem. Rev. 2002, 102, 1897;(d) Heffern, M. C.; Matosziuk, L. M.; Meade, T. J. Chem. Rev. 2014, 114, 4496.
11. [11]
  (a) Yashima, E.; Ousaka, N.; Taura, D.; Shimomura, K.; Ikai, T.; Maeda, K. Chem. Rev. 2016, 116, 13752;(b) Watanabe, K.; Akagi, K. Sci. Technol. Adv. Mater. 2014, 15, 044203.
12. [12]
  Emeis, C. A.; Oosterhoff, L. J. Chem. Phys. Lett. 1967, 1, 129. doi: 10.1016/0009-2614(67)85007-3
13. [13]
  Barnett, C. J.; Drake, A. F.; Mason, S. F. Bull. Soc. Chim. Belg. 1979, 88, 853.
14. [14]
  Kawai, T.; Kawamura, K.; Tsumatori, H.; Ishikawa, M.; Naito, M.; Fujiki, M.; Nakashima, T. ChemPhysChem 2007, 8, 1465. doi: 10.1002/(ISSN)1439-7641
15. [15]
  Kumar, J.; Nakashima, T.; Kawai, T. J. Phys. Chem. Lett. 2015, 6, 3445. doi: 10.1021/acs.jpclett.5b01452
16. [16]
  Gossauer, A.; Fehr, F.; Nydegger, F.; Stöckli-Evans, H. J. Am. Chem. Soc. 1997, 119, 1599. doi: 10.1021/ja961883q
17. [17]
  Amako, T.; Nakabayashi, K.; Mori, T.; Inoue, Y.; Fujiki, M.; Imai, Y. Chem. Commun. 2014, 50, 12836. doi: 10.1039/C4CC04228J
18. [18]
  Ito, S.; Ikeda, K.; Nakanishi, S.; Imai, Y.; Asami, M. Chem. Commun. 2017, 53, 6323. doi: 10.1039/C7CC01351E
19. [19]
  Gobo, Y.; Yamamura, M.; Nakamura, T.; Nabeshima, T. Org. Lett. 2016, 18, 2719. doi: 10.1021/acs.orglett.6b01237
20. [20]
  (a) Kumar, J.; Nakashima, T.; Tsumatori, H.; Mori, M.; Naito, M.; Kawai, T. Chem. Eur. J. 2013, 19, 14090;(b) Kumar, J.; Nakashima, T.; Kawai, T. Langmuir 2014, 30, 6030.
21. [21]
  Sheng, Y.; Ma, J.; Liu, S.; Wang, Y.; Zhu, C.; Cheng, Y. Chem. Eur. J. 2016, 22, 9519. doi: 10.1002/chem.201600891
22. [22]
  (a) Liu, M.; Zhang, L.; Wang, T. Chem. Rev. 2015, 115, 7304;(b) Zhang, L.; Wang, T.; Shen, Z.; Liu, M. Adv. Mater. 2016, 28, 1044.
23. [23]
  Ikeda, T.; Masuda, T.; Hirao, T.; Yuasa, J.; Tsumatori, H.; Kawai, T.; Haino, T. Chem. Commun. 2012, 48, 6025. doi: 10.1039/c2cc31512b
24. [24]
  Liu, J.; Su, H.; Meng, L.; Zhao, Y.; Deng, C.; Ng, J. C. Y.; Lu, P.; Faisal, M.; Lam, J. W. Y.; Huang, X.; Wu, H.; Wong, K. S.; Tang, B. Z. Chem. Sci. 2012, 3, 2737. doi: 10.1039/c2sc20382k
25. [25]
  Li, H.; Cheng, J.; Deng, H.; Zhao, E.; Shen, B.; Lam, J. W. Y.; Wong, K. S.; Wu, H.; Li, B. S.; Tang, B. Z. J. Mater. Chem. C 2015, 3, 2399.
26. [26]
  Ye, Q.; Zhu, D.; Zhang, H.; Lu, X.; Lu, Q. J. Mater. Chem. C 2015, 3, 6997. doi: 10.1039/C5TC00987A
27. [27]
  Liu, S.; Li, F.; Wang, Y.; Li, X.; Zhu, C.; Cheng, Y. J. Mater. Chem. C 2017, 5, 6030. doi: 10.1039/C7TC01371J
28. [28]
  Yang, D.; Duan, P.; Zhang, L.; Liu, M. Nat. Commun. 2017, 8, 15727. doi: 10.1038/ncomms15727
29. [29]
  Kimoto, T.; Tajima, N.; Fujiki, M.; Imai, Y. Chem. Asian J. 2012, 7, 2836. doi: 10.1002/asia.201200725
30. [30]
  (a) Kitayama, Y.; Nakabayashi, K.; Wakabayashi, T.; Tajima, N.; Fujiki, M.; Imai, Y. RSC Adv. 2015, 5, 410;(b) Kitayama, Y.; Amako, T.; Suzuki, N.; Fujiki, M.; Imai, Y. Org. Biomol. Chem. 2014, 12, 4342.
31. [31]
  Kono, Y.; Nakabayashi, K.; Kitamura, S.; Kuroda, R.; Fujiki, M.; Imai, Y. Tetrahedron 2015, 71, 3985. doi: 10.1016/j.tet.2015.04.048
32. [32]
  Sanchez-Carnerero, E. M.; Moreno, F.; Maroto, B. L.; Agarrabeitia, A. R.; Ortiz, M. J.; Vo, B. G.; Muller, G.; de la Moya, S. J. Am. Chem. Soc. 2014, 136, 3346. doi: 10.1021/ja412294s
33. [33]
  Zhang, S.; Wang, Y.; Meng, F.; Dai, C.; Cheng, Y.; Zhu, C. Chem. Commun. 2015, 51, 9014. doi: 10.1039/C5CC01994J
34. [34]
  Sheng, Y.; Shen, D.; Zhang, W.; Zhang, H.; Zhu, C.; Cheng, Y. Chem. Eur. J. 2015, 21, 13196. doi: 10.1002/chem.201502193
35. [35]
  Wang, Y.; Li, X.; Li, F.; Sun, W.-Y.; Zhu, C.; Cheng, Y. Chem. Commun. 2017, 53, 7505. doi: 10.1039/C7CC04363E
36. [36]
  Maeda, H.; Bando, Y.; Shimomura, K.; Yamada, I.; Naito, M.; Nobusawa, K.; Tsumatori, H.; Kawai, T. J. Am. Chem. Soc. 2011, 133, 9266. doi: 10.1021/ja203206g
37. [37]
  (a) Tsumatori, H.; Nakashima, T.; Kawai, T. Org. Lett. 2010, 12, 2362;(b) Kumar, J.; Tsumatori, H.; Yuasa, J.; Kawai, T.; Nakashima, T. Angew. Chem. Int. Ed. 2015, 54, 5943.
38. [38]
  Langhals, H.; Hofer, A.; Bernhard, S.; Siegel, J. S.; Mayer, P. J. Org. Chem. 2011, 76, 990. doi: 10.1021/jo102254a
39. [39]
  Kogel, J. F.; Kusaka, S.; Sakamoto, R.; Iwashima, T.; Tsuchiya, M.; Toyoda, R.; Matsuoka, R.; Tsukamoto, T.; Yuasa, J.; Kitagawa, Y.; Kawai, T.; Nishihara, H. Angew. Chem. Int. Ed. 2016, 55, 1377. doi: 10.1002/anie.201509411
40. [40]
  (a) Morisaki, Y.; Gon, M.; Sasamori, T.; Tokitoh, N.; Chujo, Y. J. Am. Chem. Soc. 2014, 136, 3350;(b) Gon, M.; Morisaki, Y.; Chujo, Y. J. Mater. Chem. C 2015, 3, 521.
41. [41]
  Morisaki, Y.; Inoshita, K.; Chujo, Y. Chem. Eur. J. 2014, 20, 8386. doi: 10.1002/chem.201402930
42. [42]
  Gon, M.; Morisaki, Y.; Chujo, Y. Chem. Commun. 2017, 53, 8304. doi: 10.1039/C7CC03615A
43. [43]
  Shen, Y.; Chen, C.-F. Chem. Rev. 2012, 112, 1463. doi: 10.1021/cr200087r
44. [44]
  Field, J. E.; Muller, G.; Riehl, J. P.; Venkataraman, D. J. Am. Chem. Soc. 2003, 125, 11808. doi: 10.1021/ja035626e
45. [45]
  Sawada, Y.; Furumi, S.; Takai, A.; Takeuchi, M.; Noguchi, K.; Tanaka, K. J. Am. Chem. Soc. 2012, 134, 4080. doi: 10.1021/ja300278e
46. [46]
  Nakamura, K.; Furumi, S.; Takeuchi, M.; Shibuya, T.; Tanaka, K. J. Am. Chem. Soc. 2014, 136, 5555. doi: 10.1021/ja500841f
47. [47]
  Oyama, H.; Nakano, K.; Harada, T.; Kuroda, R.; Naito, M.; Nobusawa, K.; Nozaki, K. Org. Lett. 2013, 15, 2104. doi: 10.1021/ol4005036
48. [48]
  Goto, K.; Yamaguchi, R.; Hiroto, S.; Ueno, H.; Kawai, T.; Shinokubo, H. Angew. Chem. Int. Ed. 2012, 51, 10333 doi: 10.1002/anie.201204863
49. [49]
  Katayama, T.; Nakatsuka, S.; Hirai, H.; Yasuda, N.; Kumar, J.; Kawai, T.; Hatakeyama, T. J. Am. Chem. Soc. 2016, 138, 5210. doi: 10.1021/jacs.6b01674
50. [50]
  Sakai, H.; Kubota, T.; Yuasa, J.; Araki, Y.; Sakanoue, T.; Takenobu, T.; Wada, T.; Kawai, T.; Hasobe, T. J. Phys. Chem. C 2016, 120, 7860. doi: 10.1021/acs.jpcc.6b01344
51. [51]
  Shen, C.; Srebro-Hooper, M.; Jean, M.; Vanthuyne, N.; Toupet, L.; Williams, J. A. G.; Torres, A. R.; Riives, A. J.; Muller, G.; Autschbach, J.; Crassous, J. Chem. Eur. J. 2017, 23, 407. doi: 10.1002/chem.v23.2
52. [52]
  Sakai, H.; Shinto, S.; Kumar, J.; Araki, Y.; Sakanoue, T.; Takenobu, T.; Wada, T.; Kawai, T.; Hasobe, T. J. Phys. Chem. C 2015, 119, 13937. doi: 10.1021/acs.jpcc.5b03386
53. [53]
  Yamamoto, Y.; Sakai, H.; Yuasa, J.; Araki, Y.; Wada, T.; Sakanoue, T.; Takenobu, T.; Kawai, T.; Hasobe, T. J. Phys. Chem. C 2016, 120, 7421. doi: 10.1021/acs.jpcc.6b01123
54. [54]
  Sakai, H.; Kubota, T.; Yuasa, J.; Araki, Y.; Sakanoue, T.; Takenobu, T.; Wada, T.; Kawai, T.; Hasobe, T. Org. Biomol. Chem. 2016, 14, 6738. doi: 10.1039/C6OB00937A
55. [55]
  Otani, T.; Tsuyuki, A.; Iwachi, T.; Someya, S.; Tateno, K.; Kawai, H.; Saito, T.; Kanyiva, K. S.; Shibata, T. Angew. Chem. Int. Ed. 2017, 56, 3906 doi: 10.1002/anie.201700507
56. [56]
  Kaseyama, T.; Furumi, S.; Zhang, X.; Tanaka, K.; Takeuchi, M. Angew. Chem. Int. Ed. 2011, 50, 3684. doi: 10.1002/anie.v50.16
57. [57]
  (a) Shen, C.; Anger, E.; Srebro, M.; Vanthuyne, N.; Deol, K. K.; Jefferson, T. D., Jr.; Muller, G.; Williams, J. A. G.; Toupet, L.; Roussel, C.; Autschbach, J.; Reau, R.; Crassous, J. Chem. Sci. 2014, 5, 1915;(b) Saleh, N.; Srebro, M.; Reynaldo, T.; Vanthuyne, N.; Toupet, L.; Chang, V. Y.; Muller, G.; Williams, J. A. G.; Roussel, C.; Autschbach, J.; Crassous, J. Chem.Commun. 2015, 51, 3754.
58. [58]
  Hellou, N.; Srebro-Hooper, M.; Favereau, L.; Zinna, F.; Caytan, E.; Toupet, L.; Dorcet, V.; Jean, M.; Vanthuyne, N.; Williams, J. A. G.; Di Bari, L.; Autschbach, J.; Crassous, J. Angew. Chem. Int. Ed. 2017, 56, 8236. doi: 10.1002/anie.v56.28
59. [59]
  Shen, Y.; Lu, H.-Y.; Chen, C.-F. Angew. Chem. Int. Ed. 2014, 53, 4648. doi: 10.1002/anie.201400486
60. [60]
  Li, M.; Lu, H.-Y.; Zhang, C.; Shi, L.; Tang, Z.; Chen, C.-F. Chem. Commun. 2016, 52, 9921. doi: 10.1039/C6CC04674F
61. [61]
  He, D.-Q.; Lu, H.-Y.; Li, M.; Chen, C.-F. Chem. Commun. 2017, 53, 6093. doi: 10.1039/C7CC01882G
62. [62]
  Fang, L.; Li, M.; Lin, W.-B.; Shen, Y.; Chen, C.-F. J. Org. Chem. 2017, 82, 7402. doi: 10.1021/acs.joc.7b01087
63. [63]
  Lin, W.-B.; Li, M.; Fang, L.; Shen, Y.; Chen, C.-F. Chem. Asian J. 2017, 12, 86. doi: 10.1002/asia.v12.1
1. [1]
  Peiran ZHAO , Yuqian LIU , Cheng HE , Chunying DUAN . A functionalized Eu³⁺ metal-organic framework for selective fluorescent detection of pyrene. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 713-724. doi: 10.11862/CJIC.20230355
2. [2]
  Wenxiu Yang , Jinfeng Zhang , Quanlong Xu , Yun Yang , Lijie Zhang . Bimetallic AuCu Alloy Decorated Covalent Organic Frameworks for Efficient Photocatalytic Hydrogen Production. Acta Physico-Chimica Sinica, 2024, 40(10): 2312014-. doi: 10.3866/PKU.WHXB202312014
3. [3]
  Tiantian MA , Sumei LI , Chengyu ZHANG , Lu XU , Yiyan BAI , Yunlong FU , Wenjuan JI , Haiying YANG . Methyl-functionalized Cd-based metal-organic framework for highly sensitive electrochemical sensing of dopamine. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 725-735. doi: 10.11862/CJIC.20230351
4. [4]
  Jingjing QING , Fan HE , Zhihui LIU , Shuaipeng HOU , Ya LIU , Yifan JIANG , Mengting TAN , Lifang HE , Fuxing ZHANG , Xiaoming ZHU . Synthesis, structure, and anticancer activity of two complexes of dimethylglyoxime organotin. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1301-1308. doi: 10.11862/CJIC.20240003
5. [5]
  Wendian XIE , Yuehua LONG , Jianyang XIE , Liqun XING , Shixiong SHE , Yan YANG , Zhihao HUANG . Preparation and ion separation performance of oligoether chains enriched covalent organic framework membrane. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1528-1536. doi: 10.11862/CJIC.20240050
6. [6]
  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
7. [7]
  Lu XU , Chengyu ZHANG , Wenjuan JI , Haiying YANG , Yunlong FU . Zinc metal-organic framework with high-density free carboxyl oxygen functionalized pore walls for targeted electrochemical sensing of paracetamol. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 907-918. doi: 10.11862/CJIC.20230431
8. [8]
  Xiaoling LUO , Pintian ZOU , Xiaoyan WANG , Zheng LIU , Xiangfei KONG , Qun TANG , Sheng WANG . Synthesis, crystal structures, and properties of lanthanide metal-organic frameworks based on 2, 5-dibromoterephthalic acid ligand. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1143-1150. doi: 10.11862/CJIC.20230271
9. [9]
  Qiuyang LUO , Xiaoning TANG , Shu XIA , Junnan LIU , Xingfu YANG , Jie LEI . Application of a densely hydrophobic copper metal layer in-situ prepared with organic solvents for protecting zinc anodes. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1243-1253. doi: 10.11862/CJIC.20240110
10. [10]
  Jing SU , Bingrong LI , Yiyan BAI , Wenjuan JI , Haiying YANG , Zhefeng Fan . Highly sensitive electrochemical dopamine sensor based on a highly stable In-based metal-organic framework with amino-enriched pores. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1337-1346. doi: 10.11862/CJIC.20230414
11. [11]
  Youlin SI , Shuquan SUN , Junsong YANG , Zijun BIE , Yan CHEN , Li LUO . Synthesis and adsorption properties of Zn(Ⅱ) metal-organic framework based on 3, 3', 5, 5'-tetraimidazolyl biphenyl ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1755-1762. doi: 10.11862/CJIC.20240061
12. [12]
  Yuanpei ZHANG , Jiahong WANG , Jinming HUANG , Zhi HU . Preparation of magnetic mesoporous carbon loaded nano zero-valent iron for removal of Cr(Ⅲ) organic complexes from high-salt wastewater. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1731-1742. doi: 10.11862/CJIC.20240077
13. [13]
  Zhihuan XU , Qing KANG , Yuzhen LONG , Qian YUAN , Cidong LIU , Xin LI , Genghuai TANG , Yuqing LIAO . Effect of graphene oxide concentration on the electrochemical properties of reduced graphene oxide/ZnS. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1329-1336. doi: 10.11862/CJIC.20230447
14. [14]
  Zhuo WANG , Junshan ZHANG , Shaoyan YANG , Lingyan ZHOU , Yedi LI , Yuanpei LAN . Preparation and photocatalytic performance of CeO₂-reduced graphene oxide by thermal decomposition. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1708-1718. doi: 10.11862/CJIC.20240067
15. [15]
  Zeyu XU , Anlei DANG , Bihua DENG , Xiaoxin ZUO , Yu LU , Ping YANG , Wenzhu YIN . Evaluation of the efficacy of graphene oxide quantum dots as an ovalbumin delivery platform and adjuvant for immune enhancement. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1065-1078. doi: 10.11862/CJIC.20240099
16. [16]
  Hao BAI , Weizhi JI , Jinyan CHEN , Hongji LI , Mingji LI . Preparation of Cu₂O/Cu-vertical graphene microelectrode and detection of uric acid/electroencephalogram. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1309-1319. doi: 10.11862/CJIC.20240001
17. [17]
  Yan LIU , Jiaxin GUO , Song YANG , Shixian XU , Yanyan YANG , Zhongliang YU , Xiaogang HAO . Exclusionary recovery of phosphate anions with low concentration from wastewater using a CoNi-layered double hydroxide/graphene electronically controlled separation film. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1775-1783. doi: 10.11862/CJIC.20240043
18. [18]
  Xin XIONG , Qian CHEN , Quan XIE . First principles study of the photoelectric properties and magnetism of La and Yb doped AlN. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1519-1527. doi: 10.11862/CJIC.20240064
19. [19]
  Fan JIA , Wenbao XU , Fangbin LIU , Haihua ZHANG , Hongbing FU . Synthesis and electroluminescence properties of Mn²⁺ doped quasi-two-dimensional perovskites (PEA)₂Pb_yMn_1-yBr₄. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1114-1122. doi: 10.11862/CJIC.20230473
20. [20]
  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

Get Citation

PDF

XML

Metrics

PDF Downloads(719)
Abstract views(13660)
HTML views(5287)

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