European Journal of Chemistry

Synthesis, characterization and biological activity of some nickel(II) mixed ligands complexes of dithiocarbamate and 1,10-phenanthroline



Main Article Content

Salih Hamza Abbas

Abstract

Two ligands; pyrrolidine-1-carbodithioate sodium (L1) and piperidine-1-carbodithioate sodium salt(L2) and their nickel(II) mixed ligands complexes with 1,10-phenanthroline (L3) have been synthesized and characterized by FT-IR, UV-visible,1H NMR spectra. The biological activities of these complexes were also evaluated. The spectral data indicated that the 1,10-phenanthrolineand dithiocarbamate ligands are considered as a bidentate nitrogen and sulfur ligands, respectively. The study suggested that the above ligands formed complexes of general formula [Ni(Lx)2(L3)1] and [Ni(Lx)1(L3)2]Cl (x=1 or 2) mononuclear (monomer) complexes. The complexes show moderate and selective activity against tested microorganisms.


icon graph This Abstract was viewed 1500 times | icon graph Article PDF downloaded 754 times

How to Cite
(1)
Abbas, S. H. Synthesis, Characterization and Biological Activity of Some nickel(II) Mixed Ligands Complexes of Dithiocarbamate and 1,10-Phenanthroline. Eur. J. Chem. 2017, 8, 367-370.

Article Details

Share
Crossref - Scopus - Google - European PMC
References

[1]. Menezes, D. C.; Viera, F. T.; DeLima, G. M. A.; Porto, A. O.; Cortes, M. E.; Ardisson, J.; Albrecht-Schmitt, T. E. Eur. J. Med. Chem. 2005, 40, 1277-1282.
https://doi.org/10.1016/j.ejmech.2005.07.008

[2]. Halls, D. J. Microchim. Acta 1969, 57(1), 62-77.
https://doi.org/10.1007/BF01216666

[3]. Djordjevic, C.; Lee, M.; Sinn, E. Synth. Inorg. Chem. 1989, 28(4), 719-723.
https://doi.org/10.1021/ic00303a022

[4]. Kana, A. T.; Hibbert, T. G.; Mahon, M. F.; Molloy, K. C.; Parkin, I. P.; Price, L. S. Polyhedron 2001, 20(24), 2989-2995.
https://doi.org/10.1016/S0277-5387(01)00908-1

[5]. Law, N. A.; Dietzsch, W.; Duffy, N. V. Polyhedron 2003, 22(27), 3423-3432.
https://doi.org/10.1016/j.poly.2003.08.010

[6]. Chaturvedi, D.; Ray, S. Monatsh. Chem. / Chem. Mon. 2006, 137(3), 311-317.
https://doi.org/10.1007/s00706-006-0438-8

[7]. Devdutt, C.; Nisha, M.; Virendra, M. Synthesis (Stuttg). 2008, 3, 355-357.

[8]. Chaturvedi, D. J. Sulfur Chem. 2005, 26(4-5), 365-371.
https://doi.org/10.1080/17415990500404848

[9]. Rudorf, W. D. J. Sulfur Chem. 2007, 28(3), 295-339.
https://doi.org/10.1080/17415990701245107

[10]. Alizadeh, A.; Rostamnia, S.; Zohreh, N.; Hosseinpour, R. Tetrahedron Lett. 2009, 50, 1533-1535.
https://doi.org/10.1016/j.tetlet.2008.12.107

[11]. Cui, J. L.; Ge, Z. M.; Cheng, T. M.; Li, R. Synth. Commun. 2003, 33(12), 1969-1976.
https://doi.org/10.1081/SCC-120021023

[12]. Azizi, N.; Pourhasan, B.; Aryanasab, F.; Saidi, M. R. Synlett. 2007, 8, 1239-1242.

[13]. Azizi, N.; Aryanasab, F.; Torkiyan, L.; Ziyaei, A.; Saidi, M. R. J. Org. Chem. 2006, 71(9), 3634-3635.
https://doi.org/10.1021/jo060048g

[14]. Siddiqi, K. S.; Nami, S. A. A.; Lutfulla; Chebude, Y. Synth. React. Inorg. Met. Nano-Metal Chem. 2005, 35(6), 445-451.
https://doi.org/10.1081/SIM-200066980

[15]. Cervantes, G.; Moreno, V.; Molins, E.; Miravitlles, C. Met. Based. Drugs 1997, 4(6), 317-325.
https://doi.org/10.1155/MBD.1997.317

[16]. Mohammad, A.; Varshney, C.; Nami, S. A. A. Spectrochim. Acta A 2009, 73(1), 20-24.
https://doi.org/10.1016/j.saa.2009.01.005

[17]. Kaul, B. B.; Pandeya, K. B. Transit. Met. Chem. 1979, 4(2), 112-114.
https://doi.org/10.1007/BF00618836

[18]. Manav, N.; Mishra, A. K.; Kaushik, N. K. Spectrochim. Acta A 2006, 65(1), 32-35.
https://doi.org/10.1016/j.saa.2005.09.023

[19]. Azizi, N.; Ebrahimi, F.; Aakbari, E.; Aryanasab, F.; Saidi, M. R. Synlett. 2007, 18, 2797-2800.
https://doi.org/10.1055/s-2007-991085

[20]. Uddin, M. N.; Chowdhury, D. A; Islam, M. T.; Hoque, F. Orbital 2012, 4(4), 273-287.

[21]. Smania Jr, A.; Monache, F. D.; Smania, E. D. F. A.; Cuneo, R. S. Int. J. Med. 1999, 1(4), 325-330.

[22]. Odola, A. J.; Woods, J. A. O. Arch. Appl. Sci. Res. 2011, 3(4), 463-470.

[23]. Prakasam, B. A.; Ramalingam, K.; Baskaran, R.; Bocelli, G.; Cantoni, A. Polyhedron 2007, 26(5), 1133-1138.
https://doi.org/10.1016/j.poly.2006.10.006

[24]. Fahdawi, A. S.; Al-Kafajy, H. A. Iraqi Natl. J. Chem. 2013, 52, 414-429.

[25]. Al-Jeboori, M. J.; Al-Jebouri, F. A.; Al-Azzawi, M. A. R. Inorg. Chim. Acta 2011, 379(1), 163-170.
https://doi.org/10.1016/j.ica.2011.10.013

[26]. Ekennia, A. C.; Onwudiwe, D. C.; Ume, C.; Ebenso, E. E. Bioinorg. Chem. Appl. 2015, 2015(2), 1-10.

[27]. Li, M. Y.; Hu, P. Z.; Zhu, J. C.; Liu, Y.; Xu, K. X. Chinese J. Chem. 2004, 22(2), 162-166.
https://doi.org/10.1002/cjoc.20040220211

[28]. Hasan, A. H.; Yousif, E. I.; Al-Jeboori, M. J. Glob. J. Inorg. Chem. 2012, 1(2), 132-138.

[29]. Srinivasan, N.; Thirumaran, S.; Ciattini, S. J. Mol. Struct. 2009, 921(1-3), 63-67.
https://doi.org/10.1016/j.molstruc.2008.12.041

[30]. Hassan, A. F. J. Chem. Mater. Res. 2015, 7(4), 9-16.

[31]. Yilmaz, T. K.; Yazicilar, H.; Cesur, R.; Ozkanca; Maros, F. Z. Synth. React. Inorg. Met-Org. Chem. 2003, 33(4), 589-600.
https://doi.org/10.1081/SIM-120020326

[32]. Ronconi, L.; Giovagnini, L.; Marzano, C.; Bettio, F.; Graziani, R.; Pilloni, G.; Fregona, D. Inorg. Chem. 2005, 44(6), 1867-1881.
https://doi.org/10.1021/ic048260v

[33]. Christian, G. D. Analytical Chemistry, 6th Ed.; John Wiley and Sons Inc., Washington, 2004.

Supporting Agencies

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).