Abstract
In this study, two new complexes of Cd(II) 4-fluorobenzoate (4-FB)/3-fluorobenzoate (3-FB) with 3-hydroxypyridine (3-HPY) have been synthesized and structural characterizations have been performed by using elemental analysis, FT-IR spectroscopy, and single-crystal X-ray diffraction methods. In both complexes, the metal atom is chelated by two carboxylate groups from two 4- or 3-fluorobenzoate anions and coordinated by two 3-hydroxypyridine (HPY) molecules. In both complexes, an oxygen atom of carboxylate from the adjacent anion bridges to the Cd atom, completing the distorted seven-coordination geometry. The only difference between complexes is the positions of fluorine atoms in fluorobenzoic acids (4-fluorobenzoic acid (complex 1) and 3-fluorobenzoic acid (complex 2)). Antibacterial resistance of two new complexes to some bacteria has been investigated.
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REFERENCES
S. Noro, H. Miyasaka, S. Kitagawa, et al. Inorg. Chem. 44, 133 (2005). https://doi.org/10.1021/ic049550e
P. Teo and T. S. A. Hor, Coord. Chem. Rev. 255, 273 (2011). https://doi.org/10.1016/j.ccr.2010.08.014
T. Güdüz, Koordinasyon Kimyası (Gazi Kitabevi, Ankara, 2005).
K. Yamada, S. Yagishita, H. Tanaka, et al., Chem. Weinh. Bergstr. Ger. 10, 2647 (2004). https://doi.org/10.1002/chem.200305640
M. Salehi, M. Galini, M. Kubicki, and A. Khaleghian, Russ. J. Inorg. Chem. 64, 18 (2019). https://doi.org/10.1134/S0036023619010170
X. W. Zhu, Russ. J. Coord. Chem. 45, 608 (2019). https://doi.org/10.1134/S1070328419080104
M. Rezaeiyala, R. Golbedaghi, M. Khalili, et al., Russ. J. Coord. Chem. 45, 142 (2019). https://doi.org/10.1134/S1070328419020064
V. Uivarosi, Molecules 18, 11153 (2013). https://doi.org/10.3390/molecules180911153
M. Rizzotto, Search Antibact. Agents (2012). https://doi.org/10.5772/45651
N. Abdolhi, M. Aghaei, A. Soltani, et al., J. Struct. Chem. 60, 845 (2019). https://doi.org/10.1134/S0022476619050196
C. Kantar, B. Kaya, M. Turk, and S. Sasmaz, J. Struct. Chem. 59, 1241 (2018). https://doi.org/10.1134/S0022476618050335
B. Jabali and H. Abu Ali, Polyhedron 117, 249 (2016). https://doi.org/10.1016/j.poly.2016.06.003
R. Spector and C. E. Johanson, J. Neurochem. 103, 425 (2007). https://doi.org/10.1111/j.1471-4159.2007.04773.x
J. Zempleni, J. W. Suttie, J. F. G. Iii, et al., Handbook of Vitamins (CRC Press, 2013). https://doi.org/10.1201/b15413
T. Dang, I. S. Nizamov, R. Z. Salikhov, et al., Bioorg. Med. Chem. 27, 100 (2019). https://doi.org/10.1016/j.bmc.2018.11.017
S. A. Waksman, Mycologia 39, 565 (1947).
S. B. Singh, K. Young, and L. L. Silver, Biochem. Pharmacol. 133, 63 (2017). https://doi.org/10.1016/j.bcp.2017.01.003
J.-M. Rolain, C. Abat, M.-T. Jimeno, et al., Clin. Microbiol. Infect. 22, 408 (2016). https://doi.org/10.1016/j.cmi.2016.03.012
R. Kumar, P. Kumar, M. Kumar, and B. Narasimhan, Med. Chem. Res. 21, 4301 (2012). https://doi.org/10.1007/s00044-011-9954-0
K. Gould, J. Antimicrob. Chemother. 71, 572 (2016). https://doi.org/10.1093/jac/dkv484
F. Tabak, in I.Ü. CerrahpasaTıp Fakültesi Sürekli Tıp Egitimi Etkinlikleri (İstanbul, 2002), p. 101.
E. Tacconelli, E. Carrara, A. Savoldi, et al., Lancet Infect. Dis. 18, 318 (2018). https://doi.org/10.1016/S1473-3099(17)30753-3
L. B. Rice, Biochem. Pharmacol. 71, 991 (2006). https://doi.org/10.1016/j.bcp.2005.09.018
I. A. Holder and S. T. Boyce, Burns 20, 426 (1994). https://doi.org/10.1016/0305-4179(94)90035-3
C. Pérez, M. Pauli, P. Bazerque, C. Perez-Eid, and W.M. Pauli, P. Bazerque (Publication date). Journal: Acta Biologiaeet Medecine Experimentaalis 15, 113 (1990).
A. Lapasam, V. Banothu, U. Addepally, and M. R. Kollipara, J. Mol. Struct. 1191, 314 (2019). https://doi.org/10.1016/j.molstruc.2019.04.116
C. E. Satheesh, P. R. Kumar, N. Shivakumar, et al., Inorg. Chim. Acta 495, UNSP 118929 (2019). https://doi.org/10.1016/j.ica.2019.05.028
M. Sertçelik, F. E. Özbek, S. Sugeçti̇, and H. Necefoğlu, Iğdır Üniv. Fen Bilim. Enstitüsü Derg. 8, 189 (2018). https://doi.org/10.21597/jist.408109
D. L. Pavia, G. M. Lampman, G. S. Kriz, and J. A. Vyvyan, Introduction to Spectroscopy (Cengage Learning, 2008).
F. E. Ozbek, M. Sertcelik, M. Yuksek, et al., J. Coord. Chem. 72, 786 (2019). https://doi.org/10.1080/00958972.2019.1590560
B. Dojer, A. Pevec, Z. Jagličić, and M. Kristl, J. Mol. Struct. 1128, 724 (2017). https://doi.org/10.1016/j.molstruc.2016.09.023
T. Hökelek, E. G. Sağlam, B. Tercan, et al., Acta Crystallogr. Sect. E Struct. Rep. Online 66, m1559 (2010). https://doi.org/10.1107/S1600536810046258
T. Hökelek, Y. Süzen, B. Tercan, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 66, m782 (2010). https://doi.org/10.1107/S160053681002163X
T. Hökelek, F. Yılmaz, B. Tercan, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 65, m1416 (2009). https://doi.org/10.1107/S1600536809042640
T. Hökelek, H. Dal, B. Tercan, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 65, m627 (2009). https://doi.org/10.1107/S1600536809016602
T. Hökelek, H. Dal, B. Tercan, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 65, m1037 (2009). https://doi.org/10.1107/S1600536809027093
T. Hökelek, H. Dal, B. Tercan, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 65, m1365 (2009). https://doi.org/10.1107/S1600536809041208
T. Hökelek and H. Necefouglu, Acta Crystallogr., Sect. C 52, 1128 (1996). https://doi.org/10.1107/S0108270195015976
F. T. Greenaway, A. Pezeshk, A. W. Cordes, et al., Inorg. Chim. Acta 93, 67 (1984). https://doi.org/10.1016/S0020-1693(00)87890-1
J. Bernstein, R. E. Davis, L. Shimoni, and N.-L. Chang, Angew. Chem. Int. Ed. Engl. 34, 1555 (1995). https://doi.org/10.1002/anie.199515551
D. C. Onwudiwe, Y. B. Nthwane, A. C. Ekennia, and E. Hosten, Inorg. Chim. Acta 447, 134 (2016). https://doi.org/10.1016/j.ica.2016.03.033
S. M. H. Al-Majidi, J. Saudi Chem. Soc. 18, 893 (2014). https://doi.org/10.1016/j.jscs.2011.11.008
APEX2, SAINT and SADABS (Bruker, Madison, 2009).
G. M. Sheldrick, Acta Crystallogr., Sect. A 64, 112 (2008). https://doi.org/10.1107/S0108767307043930
L. J. Farrugia, J. Appl. Crystallogr. 45, 849 (2012). https://doi.org/10.1107/S0021889812029111
A. L. Spek, Acta Crystallogr., Sect. D: Biol. Crystallogr. 65, 148 (2009). https://doi.org/10.1107/S090744490804362X
ACKNOWLEDGMENTS
We would like to thank Tuncer HÖKELEK, Hacali NECEFOĞLU and F.Elif ÖZTÜRKKAN for the X-ray analysis and helpful discussions. This article was obtained from the master thesis of Murat Durman.
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Mustafa Sertçelik, Murat Durman Synthesis, Characterization, and Antibacterial Activity of Cd(II) Complexes with 3-/4-Fluorobenzoates and 3-Hydroxypiridine as Co-Ligands. Russ. J. Inorg. Chem. 65, 1351–1359 (2020). https://doi.org/10.1134/S0036023620090168
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DOI: https://doi.org/10.1134/S0036023620090168