Chinese Journal of Organic Chemistry >
Synthesis of Novel Rhodamine B Fluorescent Probe and Recognition Study to Fe3+
Received date: 2013-07-24
Revised date: 2013-08-29
Online published: 2013-10-10
Supported by
Project supported by the National Natural Science Foundation of China (No. 21172178).
A novel rhodamine B derivative L1 was synthesized facilely by the condensation reaction of rhodamine B hydrazide and 3-aminopyridine, and its structure was characterized by 1H NMR, IR, HRMS-ESI and X-ray techniques. The recognition properties of the target compound L1 with metal ions had been investigated in water solution by the fluorescence spectrophotometry. The results showed that the probe L1 exhibited the selective colorimetric recognition to Fe3+than other metal ions. When the concentration of Fe3+ was in the range of 1×10-6~9×10-6 mol/L, there was a good linearity between the fluorescence intensity of the probe L1 and the concentration of Fe3+.
Key words: fluorescent probe; rhodamine; iron ion; recognition; fluorescence response
Meng Wenfei , Yang Meipan , Cheng Zhao , Li Shaoni , Yang Bingqin . Synthesis of Novel Rhodamine B Fluorescent Probe and Recognition Study to Fe3+[J]. Chinese Journal of Organic Chemistry, 2014 , 34(2) : 398 -402 . DOI: 10.6023/cjoc201307039
[1] James, P.; Raoul, K. Analyst 2005, 130, 528.
[2] Weizman, H.; Ardon, O.; Mester, B.; Libman, J.; Dwir, O.; Hadar, Y.; Chen, Y.; Shanzer, A. J. Am. Chem. Soc. 1996, 118, 12368.
[3] Hu, X.-H. J. Pract. Radiol. 2011, 27, 791 (in Chinese).
(胡晓华, 实用放射学杂志, 2011, 27, 791.)
[4] Aquino, D.; Bizzi, A.; Grisoli, M. Radiology 2009, 252, 165.
[5] Mao, J.; He, Q.; Liu, W.-S. Talanta 2010, 80, 2093.
[6] Ma, Y.-M.; Hider, R. C. Bioorg. Med. Chem. 2009, 17, 8093.
[7] Dornelles, A. S.; Garcia, V. A.; Vedana, G.; Alcalde, L. A.; Bogo, M. C.; Schroder, N. Neurochem. Res. 2010, 35, 564.
[8] Crichton, R. R.; Dexter, D. T.; Ward, R. J. Coord. Chem. Rev. 2008, 252, 1189.
[9] Esposito, B. P.; Epsztejn, S.; Breue, W.; Cabantchik, Z. I. Anal. Biochem. 2002, 304, 18.
[10] Lunvongsa, S.; Oshima, M.; Motomizu, S. Talanta 2006, 68, 969.
[11] Tesfaldet, Z. O.; Van Staden, J. F.; Stefan, R. I. Talanta 2004, 64, 1189.
[12] Ohashi, A.; Ito, H.; Kanai, C.; Imura, H.; Ohashi, K. Talanta 2005, 65, 525.
[13] Bobrowski, A.; Nowak, K.; Zarebski, J. Anal. Bioanal. Chem. 2005, 382, 1691.
[14] Donga, L.; Wua, C.; Zenga, X.; Mua, L.; Xuea, S. F.; Taoa, Z. Sens. Actuators, B 2010, 145, 433.
[15] Xiang, Y.; Tong, A.-J. Org. Lett. 2006, 8, 1549.
[16] Mansell, D.; Rattray, N.; Etchells, L. L.; Schwalbe, C. H.; Blake, A. J.; Bichenkova, E. V. Chem. Commun. 2008, 5161.
[17] Lin, W.-Y.; Yuan, L.; Feng, J.-B.; Cao, X.-W. Eur. J. Org. Chem. 2008, 2689.
[18] Yuan, Y.-H.; Tian, M.-Z.; Feng, F.; Meng, S.-M.; Bai, Y.-F. Prog. Chem. 2010, 22, 1093 (in Chinese).
(袁跃华, 田茂忠, 冯锋, 孟双明, 白云峰, 化学进展, 2010, 22, 1093.)
[19] Sun, W.; Hu, D.-Y.; Wu, Z.-B.; Song, B.-A.; Yang, S. Chin. J. Org. Chem. 2011, 31, 997 (in Chinese).
(孙伟, 胡德禹, 吴志兵, 宋宝安, 杨松, 有机化学, 2011, 31, 997.)
[20] Li, N.; Liu, M.-L.; Yin, W.-T.; Yang, Z.; Li, J.-L.; Shi, Z. Chin. J. Org. Chem. 2011, 31, 39 (in Chinese).
(李娜, 刘美玲, 尹文婷, 杨 征, 李剑利, 史真, 有机化学, 2011, 31, 39.)
[21] Kaewtong, C.; Wanno, B.; Uppa, Y.; Morakot, N.; Pulpokac, B.; Tuntulanic, T. Dalton Trans. 2011, 40, 12578.
[22] Luo, J.; Jiang, S.-S.; Qin, S.-H.; Wu, H.-Q.; Wang, Y.; Jiang, J.-Q.; Liu, X.-Y. Sens. Actuators, B 2011, 160, 1191.
[23] Chereddy, N. R.; Suman, K.; Korrapati, P. S.; Thennarasu, S.; Mandal, A. B. Dyes Pigm. 2012, 95, 606.
[24] Li, J.-B.; Hu, Q.-H.; Zeng, Y.; Yu, X.-L.; Pan, Z.-Q. Prog. Chem. 2012, 24, 823 (in Chinese).
(黎俊波, 胡启辉, 曾阳, 余响林, 潘志权, 化学进展, 2012, 24, 823.)
[25] Zhang, W.-J.; Wang, Z.-M.; Qu, F.-L. Chem. Sensors 2010, 30, 36 (in Chinese).
(张卫军, 王作茂, 渠凤丽, 化学传感器, 2010, 30, 36.)
[26] Yang, Z.; She, M.-Y.; Yin, B.; Cui, J.-H.; Zhang. Y.-Z.; Sun, W.; Li, J.-L.; Shi, Z. J. Org. Chem. 2012, 77, 1143.
/
〈 |
|
〉 |