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This work is licensed under a Creative Commons Attribution 4.0 International License.
High Diffusivity Coefficient of Cyclic Voltammetric Behaviour of Semicarbazones and Thiosemicarbazones and their Antimicrobial Studies
Corresponding Author(s) : J.B. Veeramalini
Asian Journal of Chemistry,
Vol. 32 No. 12 (2020): Vol 32 Issue 12, 2020
Abstract
In this work, a series of N-hydroxy-2,6-diaryl-3-alkylpiperidin-4-one semicarbazones and thiosemicarbazones have been synthesized and also subjected towards cyclic voltammetric studies. The structure of reduced products was confirmed by FTIR, 1H & 13C NMR spectral analysis. Further products were also screened for antimicrobial activities and it shows high significant effect towards Aspergillus niger among the eight tested fungal species. The propency towards order of reduced products is observed sharply and it was established that irreversible reduction of two electron transfers has taken for all four synthesized compounds and highly pH dependent. Among the synthesized compound, thiosemicarbzones showed versatile features with high diffusion coefficient value in minimum power consumption of current function.
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- A.M. Asiri and S.A. Khan, Molecule, 15, 4784 (2010); https://doi.org/10.3390/molecules15074784
- S. Källström and R. Leino, Bioorg. Med. Chem., 16, 601 (2007); https://doi.org/10.1016/j.bmc.2007.10.018
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- R.N. Goyal and A. Minocha, J. Indian Chem. Soc., 62, 202 (1985).
- P.M. Guto, J.M. Kiratu, L.S. Daniel, E.M.R. Kiremir and G.N. Kamau, Int. J. BioChemiPhysics, 19, 47 (2015).
- T. Hemalatha, P.K. Imran, A. Gnanamani and S. Nagarajan, Biol. Chem., 19, 303 (2008).
- M. Jayalakshmi and K. Balasubramanian, Int. J. Electrochem. Sci., 3, 1277 (2008).
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- S.A.M. Refaey, A.A. Hassan and H.S. Shehata, Int. J. Electrochem. Sci., 3, 325 (2008).
- R. Sangtyani, V. Kumar, R.C. Meena and A.K. Varshney, Int. J. ChemTech Res., 4, 180 (2012).
- G. Yammouri, H. Mohammadi and A. Amine, Chemistry Africa, 2, 291 (2019); https://doi.org/10.1007/s42250-019-00058-x
- S. Sangtyani, S. Soni, A.K. Varshney and S. Varshney, Chem. Sci. Rev. Lett., 3, 224 (2014).
- K. Sapna, N.K. Sharma and S. Kohli, Orient. J. Chem., 28, 969 (2012); https://doi.org/10.13005/ojc/280244
- S. Mubarak, P. Sirajudheen, K.S.M. Shebin, M. Muhasina and T. Rishana, Org. Chem. Curr. Res., 4, 141 (2015); https://doi.org/10.4172/2161-0401.1000141
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A.M. Asiri and S.A. Khan, Molecule, 15, 4784 (2010); https://doi.org/10.3390/molecules15074784
S. Källström and R. Leino, Bioorg. Med. Chem., 16, 601 (2007); https://doi.org/10.1016/j.bmc.2007.10.018
N. Rameshkumar, A. Veena, R. Ilavarasan, P. Shanmugapandiyan, M. Adiraj and S.K. Sridhar, Biol. Pharm. Bull., 26, 188 (2003); https://doi.org/10.1248/bpb.26.188
S. Balasubramanian, G. Aridoss, P. Parthiban, C. Ramalingan and S. Kabilan, Biol. Pharm. Bull., 29, 125 (2006); https://doi.org/10.1248/bpb.29.125
G. Baskar, M. Gopalakrishnan and J. Winfred, Indian J. Chem., 48B, 580 (2009).
A. Wcislo, I. Dabkowska, J. Czupryniak, T. Ossowski and D. Zarzeczanska, J. Mol. Liq., 279, 154 (2019); https://doi.org/10.1016/j.molliq.2019.01.115
B. Kumar and A. Kumar, Int. J. Scientif. Eng. Appl. Sci., 1, 405 (2015).
D. Cheng, S. Valente, S. Castellano, G. Sbardella, R. Di Santo, R. Costi, M.T. Bedford and A. Mai, J. Med. Chem., 54, 4928 (2011); https://doi.org/10.1021/jm200453n
K. Deka and D.K. Das, Indian J. Chem. Technol., 24, 102 (2017).
R.N. Goyal and A. Minocha, J. Indian Chem. Soc., 62, 202 (1985).
P.M. Guto, J.M. Kiratu, L.S. Daniel, E.M.R. Kiremir and G.N. Kamau, Int. J. BioChemiPhysics, 19, 47 (2015).
T. Hemalatha, P.K. Imran, A. Gnanamani and S. Nagarajan, Biol. Chem., 19, 303 (2008).
M. Jayalakshmi and K. Balasubramanian, Int. J. Electrochem. Sci., 3, 1277 (2008).
W.J.C. Ouedraogo, I. Tapsoba, B. Guel, F.S. Sib and Y.L. Bonzi-Coulibaly, Bull. Chem. Soc. Ethiop., 27, 117 (2013).
J.-S. Yun, S. Kim, B.-W. Cho, K.-Y. Lee, K.Y. Chung and W. Chang, Bull. Korean Chem. Soc., 34, 433 (2013); https://doi.org/10.5012/bkcs.2013.34.2.433
J.B. Veeramalini and G. Baskar, J. Adv. Chem., 13, 6088 (2017).
K.G. Krishnan, R. Sivakumar and V. Thanikachalam, Can. Chem. Trans., 2, 353 (2014).
G.P. Mamatha, B.S. Sherigera and K.M. Mahadevan, Indian J. Chem. Technol., 14, 566 (2007).
J. Narendranath, R. Muruganantham, N. Balasubramanian and J. Manokaran, Indian J. Chem., 56A, 63 (2017).
R.J. Mascarenhas, Y. Shivaraj, B.S. Sherigara, K.M. Mahadevan and B. Kalluraya, Russ. J. Electrochem., 42, 776 (2006); https://doi.org/10.1134/S1023193506070111
N. Soltani, H. Salavati, N. Rasouli and M. Paziresh, Iran. J. Anal. Chem., 2, 22 (2015).
C.R. Noller and V. Baliah, J. Am. Chem. Soc., 70, 3853 (1948); https://doi.org/10.1021/ja01191a092
S.A.M. Refaey, A.A. Hassan and H.S. Shehata, Int. J. Electrochem. Sci., 3, 325 (2008).
R. Sangtyani, V. Kumar, R.C. Meena and A.K. Varshney, Int. J. ChemTech Res., 4, 180 (2012).
G. Yammouri, H. Mohammadi and A. Amine, Chemistry Africa, 2, 291 (2019); https://doi.org/10.1007/s42250-019-00058-x
S. Sangtyani, S. Soni, A.K. Varshney and S. Varshney, Chem. Sci. Rev. Lett., 3, 224 (2014).
K. Sapna, N.K. Sharma and S. Kohli, Orient. J. Chem., 28, 969 (2012); https://doi.org/10.13005/ojc/280244
S. Mubarak, P. Sirajudheen, K.S.M. Shebin, M. Muhasina and T. Rishana, Org. Chem. Curr. Res., 4, 141 (2015); https://doi.org/10.4172/2161-0401.1000141
S.N. Pandeya, Acta Pharm., 62, 263 (2012); https://doi.org/10.2478/v10007-012-0030-1
R.J. Waltman, J. Bargon and A.F. Diaz, J. Phys. Chem., 87, 1459 (2012); https://doi.org/10.1021/j100231a035