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SYNTHESIS AND CHARACTERIZATION OF A NOVEL LIGAND AND SPECTROSCOPIC STUDY OF THE FORMATION OF ITS COMPLEXES WITH DIFFERENT CATIONS AND THEIR SENSORY CHARACTERISTICS

Abstract

A new ligand (L), N,N′-bis(2-hydroxybenzyl)-1,2-diaminoethane, was synthesized and characterized. The sensing behavior of L toward various metal ions was investigated by spectrofluorometric and UV-Vis spectrophotometric methods. The sensor displayed selective and sensitive recognition toward Fe3+ and Fe2+ in acetonitrile. The fluorescence of L was quenched mainly by Fe3+ , and a considerable enhancement of fluorescence was observed in the presence of Zn2+ . Using multivariate hard modeling and stoichiometry, the concentration, spectral profiles, and formation constants of the studied complexes were calculated.

About the Authors

M. . Shariati-Rad
Razi University
Russian Federation


M. . Karimi
Razi University
Russian Federation


M. . Rezaeivala
Hamedan University of Technology
Russian Federation


References

1. A. P. D. Silva, H. Q. N. Gunaratne, T. Gunnlaugsson, A. J. M. Huxley, C. P. McCoy, J. T. Rademacher, Chem. Rev., 97, 1515 (1997).

2. W. T. Mason, Fluorescent and Luminescent Probes for Biological Activity, Academic Press, San Diego (1999).

3. S. R. Liu, S. P. Wu, Sens. Actuators B, 171, 1110 (2012).

4. Z. J. Jiang, H. S. Lv, J. Zhu, B. X. Zhao, Synth. Met., 162, 2112 (2012).

5. R. Azadbakht, H. Keypour, H. Amiri Rudbari, A. H. Mohammad Zaheri, S. Menati, J. Lumin., 132, 1860 (2012).

6. X. Wang, W. Zheng, H. Lin, G. Liu, Y. Chen, Y. Fang, J. Tetrahedron Lett., 50, 1536 (2009).

7. P. S. Hariharan, N. Hari, S. P. Anthony, Inorg. Chem. Commun., 48, 1 (2014).

8. Y. Liu, E.-B. Yang, R. Han, D. Zhang, Y. Ye, Y.-F. Zhao, Chin. Chem. Lett., 25, 1065 (2014).

9. R. Azadbakht, T. Almasi, H. Keypour, M. Rezaeivala, Inorg. Chem. Commun., 33, 63 (2013).

10. C. Y. Li, Y. Zhoua, Y. F. Li, X. F. Kong, C. X. Zou, C. Weng, Anal. Chim. Acta, 774, 79 (2013).

11. R. Martínez-Máñez, F. Sancenón, Coord. Chem. Rev., 250, 3081 (2006).

12. M. Vazquez, L. Fabbrizzi, A. Taglietti, R. M. Pedrido, A. M. Gonzalez-Noya, M. R. Bermejo, Angew. Chem. Int. Ed., 44, 1962 (2004).

13. J. V. Ros-Lis, R. Martínez-Máñez, Soto, J. Org. Lett., 7, 2337 (2005).

14. T. Gunnlaugsson, M. Glynn, G. M. Tocci, P. E. Kruger, F. M. Pfeffer, Coord. Chem. Rev., 250, 3094 (2006).

15. G. Sivaraman, V. Sathiyaraja, D. Chellappa, J. Lumin., 145, 480 (2014).

16. M. W. Henze, M. U. Muckenthaler, B. Galy, C. Camaschella, Cell, 142, 24 (2010). 1014-9

17. X. F. Liu, E. C. Theil, Acc. Chem. Res., 38, 167 (2005).

18. C. A. Perez, Y. Tong, M. Guo, Cur. Bioact. Compd., 4, 150 (2008).

19. M. José Casanueva Marenco, C. Fowley, B. W. Hyland, G. R.C. Hamilton, D. Galindo-Riaño, J. F. Callan, Tetrahedron Lett., 53, 670 (2012).

20. A. F. Oliverra, J. A. Nobrega, O. Fatibello-Filho, Talanta, 49, 505 (1995).

21. W. Qin, Z. J. Zhang, F. C. Wang, Fresenius J. Anal. Chem., 360, 130 (1998).

22. J. M. T.Carneiro, A. C. B. Dias, E. A. G. Zagatto, R.S. Honorato, Anal. Chim. Acta, 455, 327 (2002).

23. A. Safavi, H. Abdollahi, M. R. Hormozi-Nezhad, Talanta, 56, 699 (2002).

24. B. M. Nagabhushana, G. T. Chandrappa, B. Nagappa, N. H. Nagaraj, Anal. Bioanal. Chem., 373, 299 (2002).

25. J. Zolgharnein, H. Abdollahi, D. Jaefarifar, G. H. Azimi, Talanta, 57, 1067 (2002).

26. L. Donga, C. Wu, X. Zeng, L. Mu, S. F. Xue, Z. Tao, J. X. Zhang, Sens. Actuators B, 145, 433 (2010).

27. E. M. Nolan, S. J. Lippard, Acc. Chem. Res., 42, 193 (2009).

28. S. J. Lippard, J. M. Berg, Principles of Bioinorganic Chemistry, University Science Book, Mill Valley, CA, 10, 14, 78-183 (1994).

29. B. L. Vallee, K. H. Falchuk, Physiol. Rev., 73, 79 (1993).

30. J. J. R. F. de Silva, R. J. P. Williams, The Biological Chemistry of Elements: the Inorganic Chemistry of Life, 2nd ed., Oxford University Press, New York (2001).

31. A. I. Bush, W. H. Pettingell, G. Multhaup, M. Paradis, J. P. Vonsattel, J. F. Gusella, K. Beyreuther, C. L. Masters, R.E. Tanzi, Science, 265, 1464 (1994).

32. J. Y. Koh, S. W. Suh, B. J. Gwag, Y. Y. He, C. Y. Hsu, D.W. Choi, Science, 272, 1013 (1996).

33. C. F. Walker, R. E. Black, Annu. Rev. Nutr., 24, 255 (2004).

34. E. M. Nolan, S. J. Lippard, Inorg. Chem., 43, 8310 (2004).

35. E. M. Nolan, S. C. Burdette, J. H. Hervey, S. A. Hilderbrand, S. J. Lippard, Inorg. Chem., 43, 2624 (2004).

36. S. Aoki, D. Kagata, M. Shiro, K. Takeda, E. Kimura, J. Am. Chem. Soc., 126, 13377 (2004).

37. R. Parkesh, T. C. Lee, T. Gunnlaugsson, Org. Biomol. Chem., 5, 310 (2007).

38. M. Maeder, Y.-M. Neuhold, Practical Data Analysis in Chemistry, Elsevier, Amsterdam (2007).

39. M. Maeder, H. Abdollahi, J. Iran. Chem. Soc., 5, 522 (2008).

40. H. S. Jung, P. S. Kwon, J. W. Lee, J. I. Kim, C. S. Hong, J. W. Kim, S. Yan, J. Y. Lee, J. H. Lee, T. Joo, J. S. Kim, Chem. Soc., 131, 2008 (2009).

41. G. E. Malashkevich, M. V. Korzhik, M. G. Livshits, V. B. Pavlenko, A. L. Blinov, M. A. Borik, The Sov. J. Glass Phys. Chem., 15, 397 (1990).

42. J. P. Sumner, R. Kopelman, Analyst, 130, 528 (2005).

43. Y. Ma, W. Luo, P. J. Quinn, Z. Liu, R. C. Hider, J. Med. Chem., 47, 6349 (2004).

44. J. M. Liu, Q. Y. Zheng, J. L. Yang, C. F. Chen, Z. T. Huang, Tetrahedron Lett., 43, 9209 (2002).

45. G. Puxty, M. Maeder, K. Hungerbühler, Chemom. Intell. Lab. Syst., 81, 149 (2006).

46. N. McCann, M. Maeder, Anal. Chim. Acta, 647, 31 (2009).

47. M. Shariati-Rad, M. Hasani, Anal. Chim. Acta, 648, 60 (2009).

48. Y. W. Choi, G. J. Park, Y. J. Na, H. Y. Jo, S. A. Lee, G. R. You, C. Kim, Sens. Actuators B, 194, 343 (2014).

49. W. Zhu, L. Yang, M. Fang, Z. Wu, Q. Zhang, F. Yin, Q. Huang, C. Li, J. Lumin., 158, 38 (2015).

50. S. Devaraj, Y. K. Tsui, C. Y. Chiang, Y. P. Yen, Spectrochim. Acta A, 96, 594 (2012).

51. L. Wang, H. Li, D. Cao, Sens. Actuators B, 181, 749 (2013).


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For citations:


Shariati-Rad M., Karimi M., Rezaeivala M. SYNTHESIS AND CHARACTERIZATION OF A NOVEL LIGAND AND SPECTROSCOPIC STUDY OF THE FORMATION OF ITS COMPLEXES WITH DIFFERENT CATIONS AND THEIR SENSORY CHARACTERISTICS. Zhurnal Prikladnoii Spektroskopii. 2017;84(6):1014(1)-1014(9). (In Russ.)

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