Browse > Article
http://dx.doi.org/10.5012/bkcs.2014.35.11.3326

A Quinoline-thiooxorhodamine Conjugate for Fluorescent Hg2+ Recognition in Aqueous Media and Living Cells  

Tang, Lijun (Department of Chemistry, Liaoning Provincial Key Laboratory for the Synthesis and Application of Functional Compounds, Bohai University)
Wen, Xin (Department of Chemistry, Liaoning Provincial Key Laboratory for the Synthesis and Application of Functional Compounds, Bohai University)
Dai, Xin (Department of Chemistry, Liaoning Provincial Key Laboratory for the Synthesis and Application of Functional Compounds, Bohai University)
Wu, Di (Department of Chemistry, Liaoning Provincial Key Laboratory for the Synthesis and Application of Functional Compounds, Bohai University)
Huang, Zhenlong (Department of Chemistry, Liaoning Provincial Key Laboratory for the Synthesis and Application of Functional Compounds, Bohai University)
Publication Information
Abstract
A quinoline-thiooxorhodamine conjugate fluorescent sensor (1) has been synthesized. Sensor 1 exhibits high selectivity and sensitivity to $Hg^{2+}$ in $H_2O$/DMSO (95/5, v/v, HEPES 20 mM, pH = 7.4) solution with fluorescence detection. Other tested metal ions do not induce any significant fluorescence intensity changes. Sensor 1 interacts with $Hg^{2+}$ through a 1:1 binding stoichiometry with a good anti-inference ability. In addition, fluorescent imaging of $Hg^{2+}$ in Hela cells is also successfully demonstrated.
Keywords
Fluorescence; Hg(II) recognition; Rhodamine; Cell imaging;
Citations & Related Records
연도 인용수 순위
  • Reference
1 (b) Valeur, B.; Leray, I. Coord. Chem. Rev. 2000, 205, 3-40.   DOI   ScienceOn
2 (a) 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, 1515-1566.   DOI   ScienceOn
3 (c) Du, J.; Hu, M.; Fan, J.; Peng, X. Chem. Soc. Rev. 2012, 41, 4511-4535.   DOI   ScienceOn
4 (d) Formica, M.; Fusi, V.; Giorgi, L.; Micheloni, M. Coord. Chem. Rev. 2012, 256, 170-192.   DOI   ScienceOn
5 Tchounwou, P. B.; Ayensu, W. K.; Ninashvili, N.; Sutton, D. Environ. Toxicol. 2003, 18, 149-175.   DOI   ScienceOn
6 Zalups, R. K. Pharmacol. Rev. 2000, 52, 113-144.
7 Strong, L. E. J. Chem. Edu. 1972, 49, 28-29.   DOI
8 (b) Eun Jun, M.; Roy, B.; Han Ahn, K. Chem. Commun. 2011, 7583-7601.
9 (c) Quang, D. T.; Kim, J. S. Chem. Rev. 2010, 110, 6280-6301.   DOI   ScienceOn
10 (d) Wang, M.; Yan, F.-Y.; Zou, Y.; Yang, N.; Chen, L.; Chen, L.-G. Spectrochimi. Acta, Part A 2014, 123, 216-223.   DOI   ScienceOn
11 (e) Li, M.; Jiang, Y.; Zhang, D.; Ding, P.; Wang, Z.; Ye, Y.; Zhao, Y. J. Lumin. 2014, 148, 219-224.   DOI   ScienceOn
12 (f) Park, S.; Kim, W.; Swamy, K. M. K.; Lee, H. Y.; Jung, J. Y.; Kim, G.; Kim, Y.; Kim, S.-J.; Yoon, J. Dyes Pigm. 2013, 99, 323-328.   DOI   ScienceOn
13 (g) Zhong, K.; Zhou, X.; Hou, R.; Zhou, P.; Hou, S.; Bian, Y.; Zhang, G.; Tang, L.; Shang, X. RSC Adv. 2014, 4, 16612-16617.   DOI   ScienceOn
14 Wysocki, L. M.; Lavis, L. D. Curr. Opin. Chem. Biol. 2011, 15, 752-759.   DOI   ScienceOn
15 Ramette, R. W.; Sandell, E. B. J. Am. Chem. Soc. 1956, 78, 4872-4878.   DOI
16 (a) Chen, X.; Pradhan, T.; Wang, F.; Kim, J. S.; Yoon, J. Chem. Rev. 2012, 112, 1910-1956.   DOI   ScienceOn
17 (b) Kim, H. N.; Lee, M. H.; Kim, H. J.; Kim, J. S.; Yoon, J. Chem. Soc. Rev. 2008, 37, 1465-1472.   DOI   ScienceOn
18 (c) Beija, M.; Afonso, C. A. M.; Martinho, J. M. G. Chem. Soc. Rev. 2009, 38, 2410.   DOI   ScienceOn
19 (g) Wang, F.; Nam, S.-W.; Guo, Z.; Park, S.; Yoon, J. Sens. Actuators, B 2012, 161, 948-953.   DOI   ScienceOn
20 (d) Zhang, J.; Zhou, Y.; Hu, W.; Zhang, L.; Huang, Q.; Ma, T. Sens. Actuators, B 2013, 183, 290-296.   DOI   ScienceOn
21 (e) Zhang, D.; Li, M.; Wang, M.; Wang, J.; Yang, X.; Ye, Y.; Zhao, Y. Sens. Actuators, B 2012, 177, 997-1002.
22 Chandrasekhar, V.; Hossain, S.; Das, S.; Biswas, S.; Sutter, J.-P. Inorg. Chem. 2013, 52, 6346-6353.   DOI   ScienceOn
23 (f) Mahato, P.; Saha, S.; Suresh, E.; Di Liddo, R.; Parnigotto, P. P.; Conconi, M. T.; Kesharwani, M. K.; Ganguly, B.; Das, A. Inorg. Chem. 2012, 51, 1769-1777.   DOI   ScienceOn
24 (h) Park, S.; Kim, W.; Swamy, K. M. K.; Lee, H. Y.; Jung, J. Y.; Kim, G.; Kim, Y.; Kim, S.-J.; Yoon, J. Dyes Pigm. 2013, 99, 323-328.   DOI   ScienceOn
25 Zhou, Y.; You, X.-Y.; Fang, Y.; Li, J.-Y.; Liu, K.; Yao, C. Org. Biomol. Chem. 2010, 8, 4819-4822.   DOI   ScienceOn
26 Jin, Z.; Xie, D.-X.; Zhang, X.-B.; Gong, Y.-J.; Tan, W. Anal. Chem. 2012, 84, 4253-4257.   DOI   ScienceOn
27 Conner, K. A. Binding Constants-the Measurement of Molecular Complex Stability; John Wiley & Sons: New York, USA, 1987.
28 Lin, W.; Yuan, L.; Cao, Z.; Feng, Y.; Long, L. Chem.-Eur. J. 2009, 15, 5096-5103.   DOI   ScienceOn
29 Tian, M.; Peng, X.; Fan, J.; Wang, J.; Sun, S. Dyes Pigm. 2012, 95, 112-115.   DOI   ScienceOn
30 (a) Culzoni, M. J.; Munoz de la Pena, A.; Machuca, A.; Goicoechea, H. C.; Babiano, R. Anal. Methods 2013, 5, 30-49.   DOI