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

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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

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Fengchao Dong

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

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

Zhenyu Zhang

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

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

Yongwu He

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

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

Zhu Ming

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

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

Pengfei Li

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

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

Li Bian

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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.

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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.

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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

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