PL EN


Preferences help
enabled [disable] Abstract
Number of results
2017 | 66 | 20-42
Article title

Spectral studies and antimicrobial activities of some (E)-N-(substituted benzylidene)-2,6-diisopropylanilines

Content
Title variants
Languages of publication
EN
Abstracts
EN
A series of Schiff’s base compounds were synthesized from 2,6-di(propan-2-yl) aniline with substituted aromatic aldehydes. The structures of all the synthesized compounds were characterized by physical constants, IR and NMR spectroscopic techniques. All the observed IR frequencies νC=N (cm-1), NMR δ(ppm) of C-H & C=N chemical shifts have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analyses in order to study the effect of substituents on these spectral data has been studied. All the synthesized Schiff’s base compounds were screened for their antimicrobial activity by disc diffusion method.
Year
Volume
66
Pages
20-42
Physical description
Contributors
author
  • PG and Research Department of Chemistry, Government Arts College, C-Mutlur - 608 102, India
  • PG and Research Department of Chemistry, Government Arts College, C-Mutlur - 608 102, India
author
  • PG and Research Department of Chemistry, Government Arts College, C-Mutlur - 608 102, India
author
  • Department of Chemistry, University College of Engineering, Panruti - 607 106, India
References
  • [1] K. Y. Lau, A. Mayr, K. K. Cheung, Inorg. Chim. Acta 285 (1999) 223.
  • [2] A. S. Shawali, N. M. S. Harb, K. O. Badahdah, J. Heterocycl. Chem. 22 (1985) 1397.
  • [3] M. Mustapha, B. R. Thorat, R. G. Sudhir Sawant, R. Atram, J. Yamgar, Chem. Pharm. Res. 3 (4) (2011) 5.
  • [4] F. D. Popp, J. Org. Chem. 26 (1961) 1566.
  • [5] D. Kong, X. Zhang, Q. Zhu, J. Xie, X. Zhou, Zhongguo Yaown Huaxue Zazhi, 8(4) (1998) 245.
  • [6] D. J. Hadjipavlou-litina, A. A. Geronikaki, Drug Des. Discov., 15 (1996) 199.
  • [7] S. S. Murthy, A. Kaur, B. Sreenivasalu, R. N. Sarma, Indian J. Exp. Biol. 36 (1998) 724.
  • [8] K. N. Venugopala, V.A. Jayashree, Indian J. Pharm. Sci. 70 (2008) 88.
  • [9] N. Solak, S. Rollas, Arkivoc. Xii ( 2006) 173.
  • [10] S. J. Wadher, M.P. Puranik, N. A. Karande, P. G. Yeole, Int. J. Pharm. Tech. Res., 1 (2009) 22.
  • [11] A. L. Cates, S. M. Rasheed, Pharm. Res. 6 (1984) 271.
  • [12] V. V. Kuznetsov, A. R. Palma, A. E. Aliev, A. V. Varlamov, N. S. Prostakov, Zh. Org. Khim., l27 (1991) 1579.
  • [13] A. E. Taggi, A. M. Hafez, H. Wack, B. Young, D. Ferraris, T. Lectka, J. Am. Chem. Soc., 124 (2002) 6626.
  • [14] (a) O. Tsuge, R. Kanemasa, Adv. Heterocycl. Chem. 45 (1989) 231.
  • (b) M. F. Aly, M. I. Younes, S. A. M. Metwally, Tetrahedron. 50 (1994) 3159.
  • [15] M. Mustapha, B. R. Thorat, SudhirSawant, R. G. Atram, R. Yamgar, J. Chem. Pharm. Res. 3(4) (2011) 5.
  • [16] R. Yamgar, P. Kamat, D. Khandekar, S. Sawant, J. Chem. Pharm. Res. 3 (2011)188.
  • [17] K. C. Gupta and A. K. Sutar. Coord. Chem. Rev. 252 (2008) 1420.
  • [18] M. Yuan, F. Zhao, W. Zhang, Z. M. Wang and S. Gao, Inorg. Chem. 46 (2007)11235.
  • [19] H. Fukuda, K. Amimoto, H. Koyama and T. Kawato, Tetrahedron Lett. 50 (2009) 5376.
  • [20] Y.C. Liu and C.Y. Yang, Inorg. Chem. Commun. 12 (2009) 704.
  • [21] A. Bongini, M. Panunzio, G. Piersanti, E. Bandini, G. Martelli, G. Spunta and A. Venturini, Euro. J. Org. Chem., 13 (2000) 2379.
  • [22] V. V. Mulwad and J. M. Shirodkar, Indian J. Het. Chem., 11(2002)199.
  • [23] C. Ainsworth, J. American Chem. Soc., 77 (1995)1148.
  • [24] G. Weber and J. Messerschmidt, Ana. Chimi. Acta., 545 (2005) 166.
  • [25] R. Singh and N. K. Kaushik, Main. Gro. Met. Chemi., 30 (2007)333
  • [26] S. Zhu, Z. Zhou and B. Zhao Huaxue, Yu Shengwu Gong Cheng., 25 (2008) 34.
  • [27] C. F. Zhu, G. Z. Yuan, E. H. Sheng and Y. Cui, Jiegou Huaxue., 28 (2009) 1304.
  • [28] J. Wang, Y. Song and X. Gao, Hecheng Huaxue., 16 (2008) 225.
  • [29] Q. F. Cheng, X. Y. Xu, Q. F. Wang, B. H. Qian, W. J. Liu and X. J. Yang, Jie. Hua., 28 (2009) 1281.
  • [30] J. H. Xie, S. F. Zhu, Q. L. Zhou, Chem. Rev., 111 (2011) 1713.
  • [31] J. E. Robertson, H. J. Biel and T. F. Mitchell, J. Med. Chem., 6 (1963) 805.
  • [32] H. J. Biel, W. K .Hoya and H. A. Leiser, J. Am. Chem. Soc., 81 (1959) 2527.
  • [33] K. Neuvonen, F. Fulop, H. Neuvonen, A. Koch, E. Kleinpeter and K. Pihlaja, J. Org. Chem., 68 (2002) 2151.
  • [34] R. Senbagam, G. Vanangamudi and G. Thirunarayanan, Annales Umcs Chemia., 70(2) (2015) 169.
  • [35] R. Suresh, D. Kamalakkannan, V. Mala, K. Sathiyamoorthiy, R. Sndararajan, S. P. Sakthinathan, R. Arulkumaran, G. Vanangamudi, G. Thirunarayanan, Adv. Appl. Res., 7(1) (2015) 27.
  • [36] R. Senbagam, R. Vijayakumar, M. Rajarajan, S. Balaji, V. Manikandan, G. Vanangamudi and G. Thirunarayanan, Kar. Int. Jour. Mod. Sci., 2 (2016) 56.
  • [37] C. G. Swain and E. C. Lupton, J. Am. Chem. Soc. 90 (1968) 4328.
  • [38] A. W. Bauer, W. M. M. Kirby, J. C. Sherris and M. Truck, Am. J. Clin. Pathol., 45 (1966) 493
Document Type
article
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.psjd-09f912c6-21f5-4c5c-9965-0e520ce16dca
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.