Synthesis, Characterization and Thermogravimetric Study of Some Metal Complexes of Selenazone Ligand Nanoparticles Analogue of Dithizone

https://doi.org/10.22146/ijc.65763

Zuhair Ali Abdulnabi(1*), Faris Abdulridhah Jassim Al-doghachi(2), Hassan Thamir Abdulsahib(3)

(1) Department of Marine Chemistry, Marine Science Center, University of Basrah, 61004, Basrah, Iraq
(2) Department of Chemistry, Faculty of Science, University of Basrah, 61004, Basrah, Iraq
(3) Department of Chemistry, Faculty of Science, University of Basrah, 61004, Basrah, Iraq
(*) Corresponding Author

Abstract


A new method for preparing 1,5-diphenylselenocarbazone (selenazone) nanoparticles and their complexes with Pb2+, Cd2+, Co2+, and Ni2+ has been performed using hot methanol solvent. The ligand and its complexes were characterized using FT-IR, UV-Vis, 1H-NMR, 13C-NMR, X-ray powder diffraction (XRD), EI-mass spectrometry, scanning electron microscopy (SEM), HG and flame-atomic absorption spectrophotometer, thermal analysis (TG/DTA), and molar conductance measurements. The molar conductance measurements in all complexes were recorded low values in DMSO, indicating that all the metal complexes were non-electrolytes except the nickel complex that possessed an electrolytic nature. Kinetic and thermodynamic parameters of complexes (A, E, ∆H, ∆S, and ∆G) have been computed using three kinetic models of Coast-Redfern, Broido, and Horowitz-Metzger, that illustrated the decomposition reactions in all steps were nonspontaneous. Thermogravimetric analyses (TG/DTA) were consistent with the atomic spectroscopy data proving that the geometry shape of all the complexes was octahedral.

Keywords


selenazone nanoparticle; thermal analyses; kinetic models

Full Text:

Full Text PDF


References

[1] Perrone, D., Monteiro, M., and Nunes, J.C., 2015, “Chapter 1 The Chemistry of Selenium” in Selenium: Chemistry, Analysis, Function and Effects, 1st Ed., Eds. Preedy, V., The Royal Society of Chemistry, London, UK.

[2] Li, Q., Zhang, Y., Chen, Z., Pan, X., Zhang, Z., Zhu, J., and Zhu, X., 2020, Organoselenium chemistry-based polymer synthesis, Org. Chem. Front., 7 (18), 2815–2841.

[3] Wirth, T., 2012, Organoselenium Chemistry: Synthesis and Reactions, 1stEd., Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim, Germany.

[4] Ward, V.R., 2012, Aspects of organoselenium chemistry, Dissertation, School of Chemistry and Physics, University of Adelaide.

[5] Achibat, H., AlOmari, N.A., Messina, F., Sancineto, L., Khouili, M., and Santi, C., 2015, Organoselenium compounds as phytochemicals from the Natural Kingdom, Nat. Prod. Commun., 10 (11), 1885–1892.

[6] Shini, S., Sultan, A., and Bryden, W.L., 2015, Selenium biochemistry and bioavailability: Implications for animal agriculture, Agriculture, 5 (4), 1277–1288.

[7] Coleman, R.A., Kazan, J., and Vega, M.L., 1968, Synthesis of Chromotropic Colorants, Project Reference: 1KO-24401-A113, U.S. Army Materiel Command, U.S. Army Natick Laboratories, Massachusetts.

[8] Ramakrishna, R.S., and Irving, H.M.N.H., 1969, Selenazone: The analogue of dithizone, Anal. Chim. Acta, 48 (2), 251–266.

[9] Shen, H., Zhu, H., Song, M., Tian, Y., Huang, Y., Zheng, H., Cao, R., Lin, J., Bi, Z. and Zhong, W., 2014, A selenosemicarbazone complex with copper efficiently down-regulates the 90-kDa heat shock protein HSP90AA1 and its client proteins in cancer cells, BMC Cancer, 14 (1), 629.

[10] Ebrahimi, H.P., Hadi, J.S., Abdulnabi, Z.A., and Bolandnazar, Z., 2014, Spectroscopic, thermal analysis and DFT computational studies of salen-type Schiff base complexes, Spectrochim. Acta, Part A, 117, 485–492.

[11] Abdulsahib, H.T., 2015, Synthesis and characterization of some polymers for the removal of some heavy metal ions and bentonite in wastewaters, Dissertation, University of Basrah, Iraq.

[12] Fresneda, M.A.R., Martín, J.D., Bolívar, J.G., Cantos, M.V.F., Bosch-Estévez, G., Moreno, M.F.M., and Merroun, M.L., 2018, Green synthesis and biotransformation of amorphous Se nanospheres to trigonal 1D Se nanostructures: Impact on Se mobility within the concept of radioactive waste disposal, Environ. Sci.: Nano, 5 (9), 2103–2116.

[13] Shah, C.P., Singh, K.K., Kumar, M., and Bajaj, P.N., 2010, Vinyl monomers-induced synthesis of polyvinyl alcohol-stabilized selenium nanoparticles, Mater. Res. Bull., 45 (1), 56–62.

[14] Brgaal, K.S., 2020, Adsorption and biochemical study for the removal of dyes from water using modified organic compounds obtained from scrap ground tire rubber, Dissertation, University of Basrah, Iraq.

[15] Juhász, L., Moldován, K., Gurikov, P., Liebner, F., Fábián, I., Kalmár, J., and Cserháti, C., 2021, False morphology of aerogels caused by gold coating for SEM imaging, Polymers, 13 (4), 588.

[16] Bhatia, P., Pandey, S., Prakash, R., and Nagaraja, T.P., 2014, Enhanced anti-oxidant activity as a function of Selenium hyperaccumulation in Agaricus bisporus cultivated on Se-rich Agri-residues, J. Biol. Act. Prod. Nat., 4 (5-6), 354–364.

[17] Karcz, D., Matwijczuk, A., Kamiński, D., Creaven, B., Ciszkowicz, E., Lecka-Szlachta, K., and Starzak, K., 2020, Structural features of 1,3,4-thiadiazole-derived ligands and their Zn(II) and Cu(II) complexes which demonstrate synergistic antibacterial effects with Kanamycin, Int. J. Mol. Sci., 21, 5735.

[18] Aly, S.A., and Fathalla, S.K., 2020, Preparation, characterization of some transition metal complexes of hydrazone derivatives and their antibacterial and antioxidant activities, Arabian J. Chem., 13 (2), 3735–3750.

[19] Dianu, M.L., Kriza, A.A, Stanica, N., and Musuc, A.M., 2010, Transition metal M(II) complexes with isonicotinic acid 2-(9-anthrylmethylene)-hydrazide, J. Serb. Chem. Soc., 75 (11), 1515–1531.

[20] Ntoi, L.L.A., 2016, Multiple chromisms associated with dithizone, Dissertation, University of the Free State, Bloemfontein, South Africa.

[21] Ahmadi, R.A., Hasanvand, F., Bruno, G., Rudbari, H.A., and Amani, S., 2013, Synthesis, spectroscopy, and magnetic characterization of copper(II) and cobalt(II) complexes with 2-amino-5-bromopyridine as ligand, Int. Scholarly Res. Not., 2013, 426712.

[22] Perera, T., Marzilli, P.A., Fronczek, F.R., and Marzilli, L.G., 2010, NH NMR shifts of new, structurally characterized fac-[Re(CO)3(polyamine)]n+ complexes probed via outer-sphere H-bonding interactions to anions, including the paramagnetic [ReIVBr6]2− anion, Inorg. Chem., 49 (12), 5560–5572.

[23] Palu, D.S., Paoli, M., Casabianca, H., Casanova, J., and Bighelli, A., 2020, New compounds from the roots of corsican Calicotome villosa (Poir.) Link.: Two pterocarpans and a dihydrobenzofuran, Molecules, 25 (15), 3467.

[24] Hadi, J.S., Abdulnabi, Z.A., and Dhumad, A.M., 2017, Synthesis, spectral characterization, thermal analysis and DFT computational studies of 2-(1H-indole-3-yl)-5-methyl-1H-benzimidazole and their Cu(II), Zn(II) and Cd(II) complexes, Eur. J. Chem., 8 (3), 252–257.

[25] Haines, P.J., 1995, Thermal Methods of Analysis, Springer Science, Netherlands.

[26] Hadi, J.S., and Abdul Kareem, A.A., 2020, Thermogravimetric study of some Schiff base metal complexes, Int. J. Appl. Chem., 7 (1), 34–44.

[27] Abdulnabi, Z.A., 2013, Preparation, spectroscopic characterization, thermal study and biological activity of some complexes derived from Schiff base and benzimidazole derived from 4-methylphenelendiamine, Thesis, University of Basrah, Iraq.

[28] Gopalakrishnan, S., and Sujatha, R., 2011, Comparative thermoanalytical studies of polyurethanes using Coats-Redfern, Broido and Horowitz-Metzger methods, Chem. Sin., 2 (5), 103–117.

[29] Ofem, M.I., Muhammed, M., and Umar, M., 2015, Thermal properties of chitin whiskers reinforced poly(acrylic acid), Int. J. Sci. Technol. Res., 4 (9), 281–288.

[30] Gul, H., Shah, A.H., Gul, S., Arjomandi, J., and Bilal, S., 2018, Study on the thermal decomposition kinetics and calculation of activation energy of degradation of poly(o-toluidine) using thermogravimetric analysis, Iran. J. Chem. Chem. Eng., 37 (1), 193–204.



DOI: https://doi.org/10.22146/ijc.65763

Article Metrics

Abstract views : 2396 | views : 2078


Copyright (c) 2021 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.