Synthesis, characterization and crystal structure of cadmium(II) nano coordination compound: A precursor to produce nano-sized cadmium oxide and cadmium iodide | ||
| شیمى کاربردى روز | ||
| Article 13, Volume 13, Issue 49, December 2018, Pages 89-102 PDF (952.32 K) | ||
| Document Type: Original Article | ||
| DOI: 10.22075/chem.2019.15120.1458 | ||
| Authors | ||
| Maryam Ranjbar* 1; Mostafa Yousefi1; Robabeh Nozari2; Shabnam Sheshmani2 | ||
| 1Department of Chemical Technologies, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran | ||
| 2Department of Chemistry, Faculty of Sciences, Islamic Azad University, Shahr-e-Rey Branch, Tehran, Iran | ||
| Receive Date: 02 October 2018, Revise Date: 02 January 2019, Accept Date: 26 February 2019 | ||
| Abstract | ||
| In this research, a cadmium(II) nano coordination compound, [Cd(dmph)I2] (1), {dmph= 2,9-dimethyl-1,10-phenanthroline (neocuproine)}, was synthesized by sonochemical method from cadmium(II) acetate, KI and the neocuproine ligand. The nano-structure (1) was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), elemental analyses and IR spectroscopy. The compound 1 was structurally characterized by single crystal X-ray diffraction and showed that Cd(II) ion is four-coordinated in a distorted tetrahedral configuration with two N atoms from a neocuproine ligand and two terminal iodine atoms. The thermal stability of compound 1 both in its bulk form and nano-size form had been studied by thermal gravimetric (TG) and differential thermal analyses (DTA) for comparsion with each other. Pure phase CdO and CdI2 nanoparticles were prepared by calcination of compound 1 at 700 °C under air atmosphere and hydrothermal processing from the same compound at 150 °C for 48 h, respectively. The morphology and phase of the prepared samples were further studied using SEM and XRD. The sonochemical method resulted in a significant reduction of reaction time, reaction temperature and particle sizes of the products. Keywords: Coordination compound; Nano CdO; Nano CdI2; Neocuproine; Sonochemical method. | ||
| Keywords | ||
| Coordination compound; Nano CdO; Nano CdI2; Neocuproine; Sonochemical method | ||
| References | ||
|
[1] H.H. Nalwa, Boston: Academic Press, (2000).
[2] M. Ranjbar, M. Yousefi, R. Nozari, S. Sheshmani, Int. J. Nanosci. Nanotechnol., 9 (2013) 203.
[3] M. Ranjbar, M. Yousefi, M. Lahooti, A. Malekzadeh, Int. J. Nanosci. Nanotechnol., 8 (2012) 191.
[4] K.-T. Wong, J.-M. Lehn, S.-M. Peng, G.-H. Lee, Chem. Commun., (2000) 2259.
[5] A.G. Bunn, P.J. Carroll, B.B. Wayland, Inorg. Chem., 31 (1992) 1297.[6] M.A.M. Abu-Youssef, A. Escuer, D. Gatteschi, M.A.S. Goher, F.A. Mautner, R. Vicente, Inorg. Chem., 38 (1999) 5716.[7] A. Tanatani, M.J. Moi, J.S. Moore, J. Am. Chem. Soc., 123 (2001) 1792.[8] M. Fujita, Y.J. Kwon, S. Washizu, K.J. Ogura, J. Am. Chem. Soc., 116 (1994) 1151.[9] B. Notash, N. Safari, A. Abedi, V. Amani, H.R. Khavasi, J. Coord. Chem., 62 (2009) 1638.
[10] Z. Rashidi Ranjbar, A. Morsali, Polyhedron, 30 (2011) 929.
[11] G.H. Shahverdizadeh, A. Morsali, J. Inorg. Organomet. Polym., 21 (2011) 694.
[12] M. Payehghadr, V. Safarifard, M. Ramazani, A. Morsali, J. Inorg. Organomet. Polym., 22 (2012) 543.
[13] D.M. Ciurtin, Y.-B. Dong, M.D. Smith, T. Barclay, H.-C. Loye, Inorg. Chem., 40 (2001) 2825.
[14] M.-H. Kim, Y.-U. Kwon, J. Phys. Chem. C, 113 (2009) 17176.
[15] M. Burbano, D.O. Scanlon, G.W. Watson, J. Am. Chem. Soc., 133 (2011) 15065.
[16] D.M. Yufanyi, J.F. Tendo, A.M. Ondoh, J.K. Mbadcam, J. Mat. Sci. Res., 3 (2014) 1.
[17] A.S. Aldwayyan, F.M. Al-Jekhedab, M. Al-Noaimi, B. Hammouti, T.B. Hadda, M. Suleiman, I. Warad, Int. J. Electrochem. Sci., 8 (2013) 10506.
[18] V. Safarifard, A. Morsali, Ultrason. Sonochem., 19 (2012) 1227.
[19] M. Ghosh, C.N.R. Rao, Chem. Phys. Lett., 393 (2004) 493.
[20] W. Dong, C. Zhu, Opt. Mater., 22 (2003) 227.
[21] M. Ranjbar, E. Malakooti, S. Sheshmani, J. Chem., (2013) doi: 10.1155/2013/560983.
[22] N. Akbarzadeh Torbati, A.R. Rezvani, N. Safari, V. Amani, H.R. Khavasi, Acta Cryst. E, 66 (2010) m1236.
[24] B. S. Wang, H. Zhong, Acta Cryst. E, 65 (2009) m1156.
[25] J.H. Bang, K.S. Suslick, Adv. Mater., 22 (2010) 1039.
[26] W.-J. Son, J. Kim, J. Kim, W.-S. Ahn, Chem. Commun., (2008) 6336.
[27] L.-G. Qiu, Z.-Q. Li, Y. Wu, W. Wang, T. Xu, X. Jiang, Chem. Commun., (2008) 3642.
[28] M. Yousefi, M. Ranjbar, J. Inorg. Organomet. Polym., 27 (2017) 633.
[29] M. Ranjbar, M. Yousefi, J. Inorg. Organomet. Polym., 24 (2014) 652.
[30] M. Ranjbar, M. Lahooti, M. Yousefi,A. Malekzadeh, J. Iran. Chem. Soc., 11 (2014) 1257.
[31] M. Ranjbar, M. Nabitabar, Ö. Çelik, M. Yousefi, J. Iran. Chem. Soc., 12 (2015) 551.
[32] M. Ranjbar, M. Yousefi, Iran. J. Sci. Technol. Trans. Sci., (2016) doi: 10.1007/s40995-016-0069-9.
[33] M. Ranjbar, M. Yousefi, Int. J. Nanosci. Nanotechnol., 12 (2016) 109.
[34] M. Rafigh Esmaeel Zaee, H. Saravani, M. Shahraki, Journal of Applied Chemistry, 13 (2018) 83.
[35] Mercury 1.4.1, Copyright Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK, 2001–2005.
[36] Bruker, SADABS. Bruker AXS Inc., Madison, Wisconsin, USA, (2007).
[37] G.M. Sheldrick, Acta Cryst. A, 64 (2008) 112.
[38] A. Morsali, M.Y. Masoomi, Coord. Chem. Rev., 253 (2009) 1882.
[39] V. Viossat, P. Lemoine, E. Dayan, N.-H. Dung, B. Viossat, J. Mol. Struc., 741 (2005) 45.
[40] H. P. Klug, L. E. Alexander, New York: Wiley, (1974). | ||
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