Synthesis, spectroscopic characterization and antimicrobial evaluation of some (E)-N-(4-substitutedbenzylidene)-4-fluorobenzenesulfonamides

• Authors: P. Jayanthi , G. Jesu Retna Raj , M. Sekar , V. Thanikachalam
• Languages of publication: EN

Abstracts

EN

In the present study, six numbers of Schiff bases (1-6) have been synthesized by the condensation of 4-fluorobenzenesulfonamide and substituted aromatic aldehyde. The purities of these Schiff bases have been checked by their physical constants, IR, 1H NMR and 13CNMR spectral data. The antimicrobial activities of these Schiff bases have been evaluated using Bauer-Kirby method.

Keywords

EN

4-fluorobenzenesulfonamide; Bauer-Kirby; IR spectra; NMR spectra; antimicrobial activities

Discipline

• CHEMISTRY: CHEMISTRY

• Publisher: Scientific Publishing House „DARWIN”
• Journal: World News of Natural Sciences
• Year: 2017
• Volume: 13
• Pages: 101-112

Contributors

author

P. Jayanthi

• PG & Research Department of Chemistry, Government Arts College, C. Mutlur, Chidambaram - 608102, India

author

G. Jesu Retna Raj

• PG & Research Department of Chemistry, Government Arts College, C. Mutlur, Chidambaram - 608102, India

author

M. Sekar

• PG & Research Department of Chemistry, Government Arts College, C. Mutlur, Chidambaram - 608102, India

author

V. Thanikachalam

• Department of Chemistry, Annamalai University, Annamalainagar - 608002, Tamil Nadu, India

References

• [1] M. Behpour, S.M. Ghoreishi, A. Gandomi-Niasar, N. Soltani and M. Salavati-Niasari (2009). J. Mater. Sci. 44, 2444.
• [2] A. Asan, S. Soylu, T. Kıyak and F. Yıldırım (2006). Corros. Sci. 48, 3933.
• [3] M. Behpour, S.M. Ghoreishi, N. Soltani, M. Salavati-Niasari, M. Hamadanian and A. Gandomi (2008). Corros. Sci. 50(8), 2172.
• [4] A.M. Abdel-Gaber, M.S. Masoud, E.A. Khalil and E.E. Shehata (2009). Corros. Sci. 51, 3021.
• [5] S. Chitra, K. Parameswari and A. Selvaraj (2010). Int. J. Electrochem. Sci. 5, 1675.
• [6] R. Solmaz (2010). Corros. Sci. 52, 3321.
• [7] R. Solmaz, Ece Altunbaşb and G. Kardas (2011). Mater. Chem. Phys. 125, 796.
• [8] M.G. Hosseini, M. Ehteshamzadeh and T. Shahrabi (2007). Electrochim. Acta 52, 3680.
• [9] R. Álvarez-Bustamante, G. Negrón-Silva, M. Abreu-Quijano, H. Herrera-Hernández, M. Romero-Romo, A. Cuán and M. Palomar-Pardavé (2009). Electrochim. Acta 54, 5393.
• [10] N.A. Negm and M.F. Zaki (2008). Colloid Surf. 322(A), 97.
• [11] M. Ehteshamzadeh, A.H. Jafari, N. Esmaeel and M.G. Hosseini (2009). Mater. Chem. Phys. 113, 986.
• [12] H. Shokry, M. Yuasa, I. Sekine, R.M. Issa, H.Y. El-Baradie and G.K. Gomma (1998). Corros. Sci., 40, 2173.
• [13] S. Patai Ed., The Chemistry of the Carbon-Nitrogen Double Bond, J. Wiley & Sons, 1970, London.
• [14] E. Jungreis and S. Thabet. Marcell Dekker, 1969, New York.
• [15] V. V. Kuznetsov, A. R. Palma, A. E. Aliev, A. V. Varlamov and N. S. Prostakov, Zh. Org. Khim. (1991), l27, 1579.
• [16] A. Taggi, A. M. EHafez, H. Wack, B. Young, D. Ferrari and T. Lectka. J. Am. Chem. Soc. (2002), 124, 6626.
• [17] O. Tsuge and R. Kanemasa, Adv. Heterocycl. Chem. (1989) 45231.
• [18] N. L. Owen and M. V. S. Sultanbawa. J. Chem. Soc. (1949) 3098.
• [19] M. J. Gemi, C. Biles, B. J. Keiser, S. M. Poppe, S. M. Swaney, W. G. Tarapley, D. L. Romeso and Y. Yage. J. Med. Chem. (2000), 43(5), 1034.
• [20] W. A. Al‐Masoudi, H. Tooama, J. Hammed, Basrah J. Vet. Res. (2014) 7, 33,
• [21] W. O. Foye, Principles of Medicinal Chemistry, 3rd edition, Varghese Publishing House, Bombay, (1989) 728.
• [22] Z. Y. Guo, R. Xing, S. Liu, Z. Zhong, X. Ji, L. Wang andP. C. Li. Carbohydrate Res. (2007), 342(10), 1329.
• [23] S. J. Wadher, M. P. Puranik, N. A. Karande andP. G. Yeole. Int. J. Pharm. Tech. Res. (2009), 1(1), 22.
• [24] C. Spinu, M. Pleniceanu and C. Tigae, Turk. J. Chem. (2008) 32, 487.
• [25] H. Temel and H. Hosgoren. Trans. Met. Chem. (2002) 27(6), 609.
• [26] A. Yildiz, B. Kiraz and Dülger. J. Serb. Chem. Soc. (2007) 72, 215.
• [27] R. Gudipati, R. N. R. Anreddy and S. Manda. Saudi Pharm. J. (2011). 19, 153.
• [28] M. Verma, S. N. Pandeya, K. N. Singh and J. P. Stables. Acta Pharm. (2004), 54, 49.
• [29] S. Ghosh, S. Malik, B. Jain and S. A. Iqbal. J. Saudi Chem. Soc. (2012), 16, 137.
• [30] W. Meiyi, L. Zhengming and L. Yonghong. Chin. J. Org. Chem. (2010), 30, 877.
• [31] A. Pandey, R. Rajavel, S. Chandraker and D. Dash. E-J. Chem. (2012), 9, 2524
• [32] F. Shabani, L. A. Saghatforoush and S. Ghammamy. Bull. Chem. Soc. Ethiop. (2010), 24, 193.
• [33] A. W. Bauer, W. M. M. Kirby, J. C. Sherris and M. Truck. Am. J. Clin. Pathol. (1996), 45, 493.

• Document Type: article