A selective fluorescent sensor for Cu(II) ion in ethanol and acetone based on BODIPY | European Journal of Chemistry

Default Image

PDF

Published: Mar 31, 2018

DOI: https://doi.org/10.5155/eurjchem.9.1.63-66.1686

Keywords:

Sensor, BODIPY, Metal ions, Copper ion, Fluorescence, Fluorescent sensor

Section

Research Article

Issue

Vol. 9 No. 1 (2018): March 2018

Dates

Received 2018-02-11
Accepted 2018-03-05
Published 2018-03-31

Crossmark

Fengchao Dong

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

http://orcid.org/0000-0003-4336-3541

Zhenyu Zhang

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

https://orcid.org/0000-0002-8227-4640

Yongwu He

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

https://orcid.org/0000-0003-0424-0282

Zhu Ming

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

https://orcid.org/0000-0002-5035-497X

Pengfei Li

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

https://orcid.org/0000-0002-7696-0468

Li Bian

eMail

College of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, P. R. China

https://orcid.org/0000-0002-0945-4290

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.

This Abstract was viewed 4008 times |

Article PDF downloaded 894 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.

Share

Links for Article

Crossref - Scopus - Google - European PMC

Crossref

Scopus

Google Scholar

Europe 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

Supporting Agencies

Scientific and Technological Research Development Project of Handan City (Project No. 1622201049-2), Handan, China

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 © 2025 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).