Recent Progress of Dual Chemosensor with Copper Ion as A Host or Guest

doi:10.6023/cjoc201707027

Chin. J. Org. Chem. ›› 2017, Vol. 37 ›› Issue (12): 3076-3084.DOI: 10.6023/cjoc201707027 Previous Articles Next Articles

Reviews

铜离子作为主客体的双通道化学传感器的研究进展

党曼, 张耀辉, 吴娇, 廖承莉, 李星, 胡芳

宁波大学材料科学与化学工程学院宁波 315211

收稿日期:2017-07-23 修回日期:2017-08-13 发布日期:2017-08-18
通讯作者: 胡芳 E-mail:hufang@nbu.edu.cn
基金资助:
国家自然科学基金（No.21602122）、宁波市自然科学基金（No.2016A610051）、宁波大学人才项目（No.ZX2015000586）以及宁波大学王宽诚幸福基金资助项目.

Recent Progress of Dual Chemosensor with Copper Ion as A Host or Guest

Dang Man, Zhang Yaohui, Wu Jiao, Liao Chengli, Li Xing, Hu Fang

Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211

Received:2017-07-23 Revised:2017-08-13 Published:2017-08-18
Contact: 10.6023/cjoc201707027 E-mail:hufang@nbu.edu.cn
Supported by:
Project supported by the National Natural Science Foundation of China (No. 21602122), the Natural Science Foundation of Ningbo City (No. 2016A610051), the Research Funds of Ningbo University (No. ZX2015000586) and the K. C. Wong Magna Fund in Ningbo University.

Copper ion plays an important role in various physiological processes. The imbalance of copper ion concentration in the organism can cause some corresponding diseases, so it is very important to study copper ion. The dual chemosensor refers to a class of chemosensor that can identify selectively two kinds of different ions or molecules. Compared with single-channel chemosensor, dual chemosensor have the advantage of functional diversity. In recent years, some dual chemosensors with copper ion as host and guest has been reported widely. Based on this, the progress of dual chemosensors with copper ion as a host and guest in recent years is reviewed.

Key words: copper ion, host and guest, dual chemosensor

Cite this article

Dang Man, Zhang Yaohui, Wu Jiao, Liao Chengli, Li Xing, Hu Fang. Recent Progress of Dual Chemosensor with Copper Ion as A Host or Guest[J]. Chin. J. Org. Chem., 2017, 37(12): 3076-3084.

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References

[1] For selected review, see:Liu, S.; Wang, Y.; Han, J. J. Photochem. Photobiol. C:Photochem. Rev. 2017, 32, 78.
[2] Vellaichamy, B.; Periakaruppan, P. New J. Chem. 2017, 41, 4006.
[3] Zhou, M.; Wang, X.; Huang, K.; Huang, Y.; Hu, S.; Zeng, W. Tetrahedron Lett. 2017, 58, 991.
[4] Li, Y.; Li, J.; Xu, Y.; Jin, K.; Cao, X. Chin. J. Org. Chem. 2017, 37, 896(in Chinese). (李英俊, 李继阳, 许永廷, 靳焜, 曹欣, 有机化学, 2017, 37, 896.)
[5] For selected review, see:Sfrazzetto, G.; Satriano, C.; Tomaselli, G.; Rizzarelli, E. Coord. Chem. Rev. 2016, 311, 125.
[6] Ibrahim, I.; Lim, H.; Abou-Zied, O.; Huang, N.; Estrela, P.; Pandikumar, A. J. Phy. Chem. C 2016, 120, 22202.
[7] Yang, Y.; Ibrahim, A.; Hashemi, P.; Stockdill, J. Anal. Chem. 2016, 88, 6962.
[8] Cao, M.; Jiang, L.; Hu, F.; Zhang, Y.; Yang, W. C.; Liu, S. H.; Yin, J. RSC Adv. 2015, 5, 23666.
[9] For selected review, see:Lin, Y.; Huang, C.; Chang, H. Analyst 2011, 136, 863.
[10] Yi, W.; Zhang, R.; Gu, Z.; Li, J.; Deng, Q.; Xiang, J. Acta Chem. Sinica 2011, 69, 1024(in Chinese). (易卫国, 张荣, 顾峥, 李珺姊, 邓琴, 向建南, 化学学报, 2011, 69, 1024.)
[11] Emandi, G.; Browne, M.; Lyons, M.; Prior, C.; Senge, M. Tetrahedron 2017, 73, 2956.
[12] Li, C.; Liu, Z.; Miao, Y.; Zhou, X.; Xu, X. Dyes Pigm. 2016, 125, 292.
[13] Huang, M.; Lou, Z.; Peng, X.; He, H.; Zhang, X.; Wang, S. Chin. J. Org. Chem. 2015, 35, 1966(in Chinese). (黄敏, 娄兆文, 彭小倩, 何汉平, 张修华, 王升富, 有机化学, 2015, 35, 1966.)
[14] Zhu,Y.; Li, H.; Yan, G.; Shi, B.; Zhang, Y.; Lin, Q.; Yao, H.; Wei, T. RSC Adv. 2015, 5, 49953.
[15] Bai, X.; Li, Y.; Gu, H.; Hua, Z. RSC Adv. 2015, 5, 77217.
[16] Huang, H.; Chen, R.; Ma, J.; Yan, L.; Zhao, Y.; Wang, Y.; Zhang, W.; Fan, J.; Chen, X. Chem. Commun. 2014, 50, 15415.
[17] Muthuraj, B.; Deshmukh, R.; Trivedi, V.; Iyer, P. ACS Appl. Mater. Interfaces 2014, 6, 6562.
[18] Wang, W.; Wen, Q.; Zhang, Y.; Fei, X.; Li, Y.; Yang, Q.; Xu, X. Dalton. Trans. 2013, 42, 1827.
[19] Biswas, A.; Pandey, R.; Kushwaha, D.; Shahid, M.; Tiwari, V.; Misra, A.; Pandy, D. Tetrahedron Lett. 2013, 54, 4193.
[20] Zhou, X.; Lü, S.; Liu, Q.; Shen, Z. Chin. J. Inorg. Chem. 2012, 28, 1483(in Chinese). (周晓彦, 吕树升, 刘泉, 沈珍, 无机化学学报, 2012, 28, 1483.)
[21] Guo, Y.; Yang, L.; Li, W.; Wang, X.; Shang, Y.; Li, B. Microchimica Acta 2016, 183, 1416.
[22] Zhao, X.; Huang, C. Biosens. Bioelectron. 2011, 30, 282.
[23] Liu, H.; Zhang, B.; Tan, C.; Liu, F.; Cao, J.; Tan, Y.; Jiang, Y. Talanta 2016, 161, 309.
[24] García-Gutiérrez, Y.; Huerta-Aguilar, C.; Thangarasu, P.; Vázquez-Ramos, J. Sens. Actuators B:Chem. 2017, 248, 447.
[25] Hou, L.; Feng, J.; Wang, Y.; Dong, C.; Shuang, S.; Wang, Y. Sens. Actuators, B:Chem. 2017, 247, 451.
[26] Sinha, S.; Kumar, S.; Koner, R.; Mathew, J.; Nandi, C.; Ghosh, S. RSC Adv. 2013, 3, 6271.
[27] Yang L.; Zhu, W.; Fang, M.; Zhang, Q.; Li, C. Spectrochim. Acta, Part A 2013, 109, 186.
[28] Anbu, S.; Ravishankaran, R.; Guedes da Silva, M.; Karande, A.; Pombeiro, A. Inorg. Chem. 2014, 53, 6655.
[29] Fegade, U.; Sahoo, S.; Singh, A.; Singh, N.; Attarde, S.; Kuwar, A. Anal. Chim. Acta 2015, 872, 63.
[30] Singh, A.; Ramanathan, G. J. Lumin. 2017, 182, 220.
[31] Kaur, N.; Kumar, S. Chem. Commun. 2007, 3069.
[32] Hu, F.; Li, R.; Wang, J.; He, L.; Li, X.; Yin, J.; Liu, S. H. Chin. J. Chem. 2016, 34, 931.
[33] Lian, C.; Guo, X.; Long, Y.; Yang, L. Russ. J. Coord. Chem.2017, 43, 338.
[34] Yang, X.; Zeng, W.; Wang, L.; Lu, X.; Yan, Y.; Qu, J.; Liu, R. RSC Adv. 2014, 4, 22613.
[35] Lee, S.; Bok, K.; Kim, J.; Kim, S.; Kim, C. Tetrahedron 2016, 72, 5563.
[36] Wang, W.; Wen, Q.; Zhang, Y.; Fei, X.; Li, Y.; Yang, Q.; Xu, X. Dalton Trans. 2013, 42, 1827.
[37] Tarai, A.; Baruah, J. J. Mol. Struct. 2015, 1091, 147.
[38] Sutariya, P.; Pandya, A.; Lodha, A.; Menon, S. Analyst 2013, 138, 2531.
[39] Liu, Y.; Sun, Y.; Du, J.; Lv, X.; Zhao, Y.; Chen, M.; Wang, P.; Guo, W. Org. Biomol. Chem. 2011, 9, 432.
[40] Wang, H.; Liu, P.; Chen, H.; Xu, N.; Zhou, Z.; Zhou, S. RSC Adv. 2015, 5, 65110.
[41] Wu, Y.; Yang, G.; Zhao, Y.; Wu, W.; Liu, B.; Wang, Y. Dalton Trans. 2015, 44, 3271.
[42] Xia, S.; Liu, G.; Pu, S. Z. J. Mater. Chem. C 2015, 3, 4023.
[43] Jia, H.; Pu, S.; Fan, C.; Liu, G.; Zheng, C. Dyes Pigm. 2015, 121, 211.
[44] For selected review, see:Mei, J.; Leung, N.; Kwok, R.; Lam, J.; Tang, B. Z. Chem. Rev. 2015, 115, 11718.
[45] Yang, Y.; Gao, C.; Zhang, N.; Dong, D. Sens. Actuators,B:Chem. 2016, 222, 741.
[46] Samanta, S.; Manna, U.; Ray, T.; Das, G. Dalton Trans. 2015, 44, 18902.

铜离子作为主客体的双通道化学传感器的研究进展

Recent Progress of Dual Chemosensor with Copper Ion as A Host or Guest

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