Abstract
Herein, we report the coordination behavior of 2-Acetyl thiophene thiosemicarbazone with copper chloride at various pH. Three copper complexes, [Cu(C7H9N3S2)2Cl2]Cl2, [Cu(C7H9N3S2)2(H2O)2]Cl2, [Cu(C7H9N3S2)2]Cl2 were synthesized at pH 4, 7, 10 and their structure was characterized. The electrical conductance value of the complexes (176.0 × 103, 184.0, 191.0 (173 Ohm−1 cm2 mole−1) showed that the Schiff base derivative is attached to the metal in 2:1 ratio. The board electronic spectral values (15,400 to 15,950 cm−1) data showed that the complexes were found in the distorted octahedral structure. The value of magnetic moment ranged from 1.90 to 1.95 showing that the complexes were paramagnetic in nature. An IR study showed that all three complexes bind in different coordination modes with the copper such as nitrogen atoms of C=N–, and sulfur atoms of C=S–, Cl−, and sulfur atom of five-membered rings of thiophene.
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References
R.S. Varma, W.L. Nobles, J. Med. Chem. 10(5), 972–974 (1967)
K. Bajaj, R.M. Buchanan, C.A. Grapperhaus, J. Inorg. Biochem. 225, 111620 (2021). https://doi.org/10.1016/j.jinorgbio.2021.111620
C. Mohan, K. Sharma, S. Chandra, Jordan J. Chem. 12(1), 39–50 (2017)
V. Singh, S. Singh, A. Verma, R.R. Choudhary, S. Gupta, Mater. Today 51, 496–501 (2022). https://doi.org/10.1016/j.matpr.2021.05.591
V. Singh, S. Singh, A. Verma, R.R. Choudhary, S. Gupta, Solid State Technol. 63(6), 20406–20416 (2020)
S. Banerjee, S. Ganguly, K.K. Sen, B.W. Bardhamann, J. Adv. Pharm. Edu. Res. 3(3), 102–116 (2013)
S.D. Khanye, W. Baojie, S.G. Franzblau, J. Gut, P.J. Rosenthal, G.S. Smith, K. Chibale, J. Organomet. Chem. 696(21), 3392–3396 (2011). https://doi.org/10.1016/j.jorganchem.2011.07.026
A. Rodrigo, C. Quintana, C. Biot, M.E. Medina, S.C. Kremer, L. Kremer, A.H. Klahn, Inorg. Chem. Commun. 55, 139–142 (2015). https://doi.org/10.1016/j.inoche.2015.03.036
C. Mohan, K. Sharma, S. Chandra, Anal. Bioanal. Electrochem. 9(1), 35–46 (2017). https://doi.org/10.1149/07516.0319ecst
A. Chalana, R.K. Rai, R. Karri, K.K. Jha, B. Kumar, G. Roy, Polyhedron 215, 115647 (2022). https://doi.org/10.1016/j.poly.2021.115647
M.S. Refat, A.F.A. Saif, Russ J Gen Chem. 84, 143–156 (2014). https://doi.org/10.1134/S1070363214010228
A.S. Ramasubramanian, B.R. Bhat, R. Dileep, S. Rani, J. Serb. Chem. Soc. 76, 75–83 (2011)
N.S. Raman, S. Ravichandran, C. Thangaraja, J. Chem. Sci. 116, 215–219 (2004). https://doi.org/10.1016/j.jscs.2012.08.001
S. Chandra, J. Deepali, A.K. Sharma, P. Sharma, Molecules 14, 174–190 (2009). https://doi.org/10.3390/molecules14010174
F.A. Cotton, D.M.L. Goodgame, U.M. Goodgame, J. Am. Chem. Soc. 83, 4690–4699 (1961). https://doi.org/10.1021/ja01484a002
R.L. Belford, M. Calvin, G. Belford, Bonding in Copper (II) chelates: solvent effects in their visible absorption spectra. J. Chem. Phys. 26(5), 1165–1174 (1957). https://doi.org/10.1063/1.1743485
X. Xuan, Y. Wang, N. Wang, Spectrochim. Acta A 81(1), 236–241 (2011). https://doi.org/10.1016/j.saa.2011.05.110
F.A. Cotton, O.D. Faut, J.T. Mague, Inorg. Chem. 3(1), 17–21 (1964)
A. Chalana, R. Karri, R. Das, B. Kumar, R.K. Rai, H. Saxena, A. Gupta, M. Banerjee, K.K. Jha, G. Roy, ACS Appl. Mater. Interfaces 11, 4766–4776 (2019). https://doi.org/10.1021/acsami.8b16786
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Kumar, M., Mohan, C., Kumar, S. et al. Coordination behavior of Schiff base copper complexes and structural characterization. MRS Advances 7, 939–943 (2022). https://doi.org/10.1557/s43580-022-00348-6
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DOI: https://doi.org/10.1557/s43580-022-00348-6