European Journal of Chemistry

A selective fluorescent sensor for Cu(II) ion in ethanol and acetone based on BODIPY

Crossmark


Main Article Content

Fengchao Dong
Zhenyu Zhang
Yongwu He
Zhu Ming
Pengfei Li
Li Bian

Abstract

A selective fluorescent sensor for Cu(II) ion in ethanol and acetone based on boradiazaindacene (BODIPY) has been studied. The selectivity towards Cu(II) ion is good over Ag(I), Cd(II), Fe(III), Hg(II), Ni(II), Pb(II), and Zn(II) ions, only Fe(III), Hg(II) and Ni(II) ions showed a slight interference. The solution showed strong fluorescence intensity after addition of triethanolamine, indicating that the Sensor 1-Cu(II) complex could be reversed by triethanolamine.


icon graph This Abstract was viewed 3765 times | icon graph Article PDF downloaded 695 times

How to Cite
(1)
Dong, F.; Zhang, Z.; He, Y.; Ming, Z.; Li, P.; Bian, L. A Selective Fluorescent Sensor for Cu(II) Ion in Ethanol and Acetone Based on BODIPY. Eur. J. Chem. 2018, 9, 63-66.

Article Details

Share
Crossref - Scopus - Google - European PMC
References

[1]. Bissel, R. A.; De Silva, A. P.; Gunaratne, H. Q. N.; Lynch, P. L. M.; Maguire, G. E. M.; Sandanayake, K. R. A. S. Chem. Soc. Rev. 1992, 21, 187-195.
https://doi.org/10.1039/CS9922100187

[2]. 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.
https://doi.org/10.1021/cr960386p

[3]. Prodi, L.; Bolletta, F.; Montalti, M.; Zaccheroni, N. Coord. Chem. Rev. 2000, 205, 59-83.
https://doi.org/10.1016/S0010-8545(00)00242-3

[4]. Valeur, B.; Leray, I. Coord. Chem. Rev. 2000, 205, 3-40.
https://doi.org/10.1016/S0010-8545(00)00246-0

[5]. De Silva, A. P.; Fox, D. B.; Huxley A. J. M.; Moody, T. S. Coord. Chem. Rev. 2000, 205, 41-57.
https://doi.org/10.1016/S0010-8545(00)00238-1

[6]. Li, X. L.; He, Y. W.; Yang, S. I. B. Kor. Chem. Soc. 2011, 32, 338-340.
https://doi.org/10.5012/bkcs.2011.32.1.338

[7]. Uauy, R.; Olivares, M.; Gonzalez, M. Am. J. Clin. Nutr. 1998, 67, 952-959.
https://doi.org/10.1093/ajcn/67.5.952S

[8]. Yu, M. X.; Shi, M.; Chen, Z. G.; Li, F. Y.; Li, X. X.; Gao, Y. H.; Xu, J.; Yang, H.; Zhou, Z. G.; Yi, T.; Huang, C. H. Chem. Eur. J. 2008, 14, 6892-6900.
https://doi.org/10.1002/chem.200800005

[9]. Linder, M. C.; Hazegh-Azam, M. Am. J. Clin. Nutr. 1996, 63, 797-811.

[10]. Mei Y. J.; Bentley P. A.; Wang W. Tetrahedron Lett. 2006, 47, 2447-2449.
https://doi.org/10.1016/j.tetlet.2006.01.091

[11]. Georgopoulos, P. G.; Roy, A.; Yonone-Lioy, M. J.; Opiekun, R. E.; Lioy, P. J. J. Toxicol. Env. Heal. B 2001, 4, 341-394.
https://doi.org/10.1080/109374001753146207

[12]. Harris, Z. L.; Gitlin, J. D. Am. J. Clin. Nutr. 1996, 63, 836-841.
https://doi.org/10.1093/ajcn/63.5.836

[13]. Scheinberg, I. H.; Sternlieb, I. Am. J. Clin. Nutr. 1996, 63, 842-845.
https://doi.org/10.1093/ajcn/63.5.842

[14]. Gaggelli, E.; Kozlowski, H.; Valensin, G. Chem. Rev. 2006, 106, 1995-2044.
https://doi.org/10.1021/cr040410w

[15]. Torrado, A.; Walkup, G. K.; Imperiali, B. J. Am. Chem. Soc. 1998, 120, 609-610.
https://doi.org/10.1021/ja973357k

[16]. Kramer, R. Angew. Chem. Int. Ed. 1998, 37, 772-773.
https://doi.org/10.1002/(SICI)1521-3773(19980403)37:6<772::AID-ANIE772>3.0.CO;2-Z

[17]. Grandini, P.; Mancin, F.; Tecilla, P.; Scrimin, P.; Tonellato, U. Angew. Chem. Int. Ed. 1999, 38, 3061-3064.
https://doi.org/10.1002/(SICI)1521-3773(19991018)38:20<3061::AID-ANIE3061>3.0.CO;2-A

[18]. Zheng, Y.; Huo, Q.; Kele, P.; Andreopoulos, F. M.; Pham, S. M.; Leblanc, R. M. Org. Lett. 2001, 3, 3277-3280.
https://doi.org/10.1021/ol0101638

[19]. Martinez R.; Zapata F.; Caballero A.; Espinosa A.; Tarraga A.; Molina P. Org. Lett. 2006, 8, 3235-3238.
https://doi.org/10.1021/ol0610791

[20]. Yu M. X.; Shi M.; Chen Z. G.; Li F. Y.; Li X. X.; Gao Y. H.; Xu J.; Yang H.; Zhou Z. G.; Yi T.; Huang C. H. Chem. Eur. J. 2008, 14, 6892-6900.
https://doi.org/10.1002/chem.200800005

[21]. Kim H. J.; Hong J.; Hong A.; Ham S.; Lee J. H.; Kim J. S. Org. Lett. 2008, 10, 1963-1966.
https://doi.org/10.1021/ol800475d

[22]. Chang F.; Park, S. H.; Kim, H. B. Kor. Chem. Soc. 2008, 29, 1327-1331.
https://doi.org/10.5012/bkcs.2008.29.7.1327

[23]. De Silva, A. P.; Nimal Gunaratne, H. O.; Gunnlaugusson, T.; Huxley, A. J. M.; McCoy, C. P.; Rademacher, J. T.; Rice, T. E. Chem. Rev. 1997, 97, 1515-1566.
https://doi.org/10.1021/cr960386p

[24]. Bargossi, C.; Fiorini, M. C.; Montalti, M.; Prodi, L.; Zaccheroni, N. Coordin. Chem. Rev. 2000, 208, 17-32.
https://doi.org/10.1016/S0010-8545(00)00252-6

[25]. Pina, F.; Bernardo, M. A.; Garcia-Espana, E. Eur. J. Inorg. Chem. 2000, 2000(10), 2143-2157.
https://doi.org/10.1002/1099-0682(200010)2000:10<2143::AID-EJIC2143>3.0.CO;2-3

[26]. Fabbrizzi, L.; Licchelli, M.; Pallavicini, P.; Parodi, L.; Taglietti, A. In Transition Metals in Supramolecular Chemistry, PerspectiVe in Supramolecular Chemistry, Sauvage, J. P. , Ed. , John Wiley & Sons, 1999.

[27]. Chemosensors of Ion and Molecule Recognition, Desvergne, J. P. , Czarnik, A. W. , Eds. , NATO ASI Series, Kluwer Academic Publishers, 1997.

[28]. Fabbrizzi, L.; Licchelli, M.; Pallavicini, P.; Perotti, A.; Taglietti, A.; Sacchi, D. Chem. Eur. J. 1996, 2, 75-82.
https://doi.org/10.1002/chem.19960020114

[29]. Klein, G.; Kaufmann, D.; Schurch S.; Reymond, J. L. Chem. Commun. 2001, 0, 561-562.
https://doi.org/10.1039/b100535i

[30]. Zheng, Y.; Gattas-Asfura, K. M.; Konka V.; Leblanc, R. M. Chem. Commun. 2002, 0, 2350-2351.
https://doi.org/10.1039/B208012E

[31]. Zheng, Y.; Orbulescu, J.; Ji, X.; Andreopoulos, F. M.; Pham S. M.; Leblanc, R. M. J. Am. Chem. Soc. 2003, 125, 2680-2686.
https://doi.org/10.1021/ja0293610

[32]. Boiocchi, M.; Fabbrizzi, L.; Licchelli, M.; Sacchi, D.; Vazquez, M.; Zampa, C. Chem. Commun. 2003, 0, 1812-1813.
https://doi.org/10.1039/B305456J

[33]. Roy, B. C.; Chandra, B.; Hromas, D.; Mallik, S. Org. Lett. 2003, 5, 11-14.
https://doi.org/10.1021/ol026891s

[34]. Kaur, S.; Kumar, S. Tetrahedron Lett. 2004, 45, 5081-5085.
https://doi.org/10.1016/j.tetlet.2004.04.185

[35]. Mei, Y.; Bentley, P. A.; Wang, W. Tetrahedron Lett. 2006, 47, 2447-2449.
https://doi.org/10.1016/j.tetlet.2006.01.091

[36]. Varnes, A. V.; Dodson R. B.; Whery, E. L. J. Am. Chem. Soc. 1972, 94, 946-950
https://doi.org/10.1021/ja00758a037

[37]. Kemlo J. A.; Shepherd, T. M. Chem. Phys. Lett. 1977, 47, 158-162.
https://doi.org/10.1016/0009-2614(77)85329-3

[38]. Rurack, K.; Resch, U.; Senoner M.; Daehne, S. J. Fluoresc. 1993, 3, 141-143.
https://doi.org/10.1007/BF00862731

[39]. Haugland, R. P. Handbook of Fluorescent Probes and Research Products, 9th ed.; Molecular Probes: Eugene, 2002.

[40]. Vos de Wael, E.; Pardoen, J. A.; van Koeveringe, J. A.; Lugtenburg, J. Rec. Trav. Chim. Pays. Bas. 1977, 96, 306-309.

[41]. Johnson, I. D.; Kang, H. C.; Haugland, R. P. Anal. Biochem. 1991, 198, 228-237.
https://doi.org/10.1016/0003-2697(91)90418-S

[42]. Karolin, J.; Johansson, L. B. A.; Strandberg, L.; Ny, T. J. Am. Chem. Soc. 1994, 116, 7801-7806.
https://doi.org/10.1021/ja00096a042

Most read articles by the same author(s)
TrendMD

Dimensions - Altmetric - scite_ - PlumX

Downloads and views

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...
License Terms

License Terms

by-nc

Copyright © 2024 by Authors. This work is published and licensed by Atlanta Publishing House LLC, Atlanta, GA, USA. The full terms of this license are available at https://www.eurjchem.com/index.php/eurjchem/terms and incorporate the Creative Commons Attribution-Non Commercial (CC BY NC) (International, v4.0) License (http://creativecommons.org/licenses/by-nc/4.0). By accessing the work, you hereby accept the Terms. This is an open access article distributed under the terms and conditions of the CC BY NC License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited without any further permission from Atlanta Publishing House LLC (European Journal of Chemistry). No use, distribution, or reproduction is permitted which does not comply with these terms. Permissions for commercial use of this work beyond the scope of the License (https://www.eurjchem.com/index.php/eurjchem/terms) are administered by Atlanta Publishing House LLC (European Journal of Chemistry).