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Electrochemical Synthesis of Organoantimony Compounds and their Coordination Compounds
Corresponding Author(s) : Sarbjit Rala
Asian Journal of Chemistry,
Vol. 31 No. 3 (2019): Vol 31 Issue 3
Abstract
Electrochemical reactions of bromoethane, 1-bromopropane, 1-chlorobutane and chlorobenzene have been carried out in acetonitrile at sacrificial antimony anode using tetrabutylammonium chloride as supporting electrolyte. The products isolated from the anode compartment have been characterized by elemental analysis and infrared spectral studies and are identified as organoantimony compounds. Coordination compounds of same have been synthesized with ligand (1,10-phenanthroline and 2,2'-bipyridyl). All these reactions proceed with high current efficiencies.
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- J.R. Ugal, F. Mohammad and Z.K. Ali, Int. J. ChemTech Res., 10, 805 (2017).
- I.I. Ozturk, J. Turk. Chem. Soc., 4, 81 (2017).
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- P.K. Sharma, H. Rehwani, A.K. Rai, R.S. Gupta and Y.P. Singh, Bioinorg. Chem. Appl., 2006, Article ID 16895 (2006); https://doi.org/10.1155/BCA/2006/16895.
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- M.A. Matthews, Pure Appl. Chem., 73, 1305 (2001); https://doi.org/10.1351/pac200173081305.
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- M.K. Khosa, M. Mazhar, S. Ali, K. Shaid and F. Malik, Turk. J. Chem., 30, 345 (2006).
- M.K. Khosa, M. Mazhar, S. Ali, K.C. Molloy, S. Dastgir and F. Shaheen, Turk. J. Chem., 30, 731 (2006).
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References
J.R. Ugal, F. Mohammad and Z.K. Ali, Int. J. ChemTech Res., 10, 805 (2017).
I.I. Ozturk, J. Turk. Chem. Soc., 4, 81 (2017).
P. Sharma, D. Perez, A. Cabrera, N. Rosas and J.L. Arias, Acta Pharmacol. Sin., 29, 881 (2008); https://doi.org/10.1111/j.1745-7254.2008.00818.x.
V. Sheikhmoradi, S. Saberi, L. Saghaei, N. Pestehchian and A. Fassihi, Res. Pharm. Sci., 13, 111 (2018); https://doi.org/10.4103/1735-5362.223793.
I.I. Ozturk, N. Kourkoumelis, S.K. Hadjikakou, M.J. Manos, A.J. Tasiopoulos, I.S. Butler, J. Balzarini and N. Hadjiliadis, J. Coord. Chem., 64, 3859 (2011); https://doi.org/10.1080/00958972.2011.633603.
P.K. Sharma, H. Rehwani, A.K. Rai, R.S. Gupta and Y.P. Singh, Bioinorg. Chem. Appl., 2006, Article ID 16895 (2006); https://doi.org/10.1155/BCA/2006/16895.
L.G. Wade Jr., Organic Chemistry, Jo Blackburn Richland College, Dallas, TX Dallas County Community College District , Prentice Hall, edn 5 (2003).
M.A. Matthews, Pure Appl. Chem., 73, 1305 (2001); https://doi.org/10.1351/pac200173081305.
E. Steckhan, T. Ams, W.R. Heineman, G. Hitt, D. Hoorman, J. Jorissen, L. Kröner, B. Lewall and H. Pütter, Chemosphere, 63, 43 (2001); https://doi.org/10.1016/S0045-6535(00)00325-8.
M.K. Khosa, M. Mazhar, S. Ali, K. Shaid and F. Malik, Turk. J. Chem., 30, 345 (2006).
M.K. Khosa, M. Mazhar, S. Ali, K.C. Molloy, S. Dastgir and F. Shaheen, Turk. J. Chem., 30, 731 (2006).
O.S. Urgut, I.I. Ozturk, C.N. Banti, N. Kourkoumelis, M. Manoli, A.J. Tasiopoulos and S.K. Hadjikakou, Mater. Sci. Eng., 58, 396 (2016); https://doi.org/10.1016/j.msec.2015.08.030.
N.A. Jamaluddin, I. Baba and N. Ibrahim, Malays. J. Anal. Sci., 18, 251 (2014).