PL EN


Preferences help
enabled [disable] Abstract
Number of results
2016 | 52 | 228-246
Article title

Study of IR and NMR spectral correlations and biological evaluation of 4-(6-ethyl-2-(substituted phenyl)-6H-pyrido[3,2-b]carbazol-4-yl) aniline derivatives

Content
Title variants
Languages of publication
EN
Abstracts
EN
A series of seven titled compounds have been prepared and their purities were examined by literature method. The characteristic infrared stretching frequencies (, cm-1) and the NMR chemical shifts (, ppm) of these anilines were assigned. These assigned spectral data were correlated with Hammett substituent constants, F and R parameters using single and multi-regression analysis. From the statistical results the effect of substituents on the spectral data have been discussed. The antimicrobial activities of these aniline derivatives have been evaluated by Bauer-Kirby disc-diffusion method.
Year
Volume
52
Pages
228-246
Physical description
References
  • [1] G. Thirunarayanan, Indian Journal of Chemistry Sec., B. 46(9) (2007) 1511-1517.
  • [2] P. Janaki, K. G. Sekar, G. Thirunarayanan, Journal of Saudi Chemical Society, 20 (2016) 58-68.
  • [3] R. Arulkumaran, R. Sundararajan, S. Vijayakumar, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, K. Ranganathan, G. Vanangamudi and G. Thirunarayanan, Journal of Saudi Chemical Society., (2012). Accepted and in press Doi: 10.1016/j.jscs. 2012.09.006.
  • [4] G. Thirunarayanan and G. Vanangamudi, Arabian Journal of Chemistry,7 (2014) 1055-1064.
  • [5] G. Thirunarayanan, Q-Science Connect., 2014; DOI: http://dx.doi.org/10.5339/ connect. 2014.18.
  • [6] T. Ohmura, S. Yorozuya, T. Yamamoto, N. Miyaura, Organometallics, 9(4) (2000) 365-367.
  • [7] A. Perjessy, M. Laucova, Collection of Czechoslovak Chemical Communications, 36 (1971) 2944-2950.
  • [8] S. Sun, N. del Rosario, Journal of the Organic Chemistry, 35(12) (1970) 4025-4027
  • [9] G. Perin, R. G. Jacob, F. Azambuja, G. V. Botteselle, G. M. Siqueira, R. A. Freitag, E. J. Lenardao, Tetrahedron Letters, 46(10) (2005) 1975-1979.
  • [10] G. Thirunarayanan, World Scientific News, 33 (2016) 79-95.
  • [11] G. Thirunarayanan, J. Saudi Chem. Soc., 18 (2014) 854-863.
  • [12] G. Thirunarayanan and M. Suresh, Int. Lett. Chem. Phys. Astro. 23 (2014) 1-11.
  • [13] M. Rajarajan, R. Senbagam, R. Vijayakumar, V. Manikandan, S. Balaji, G. Vanangamudi, G. Thirunarayanan, World Scientific News, 3 (2015) 155-171.
  • [14] G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 14 (2013) 152-161.
  • [15] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran and K. Ravi, Indian Journal of Chemistry, 50B(4) (2011) 593-604.
  • [16] G.K. Dass, Indian Journal of Chemistry, 40(A) (2001) 223-226.
  • [17] C.M. Deiva, N.B. Pappano, N. B. Debattista, Reviews in Microbiology, 29 (1998) 307-310.
  • [18] A. Sharma, V.P. Gupta, A. Virdi; Indian Journal Pure and Applied Physics, 40(4) (2002) 246-249.
  • [19] V. Krishnakumar, R. Ramasamy, Indian Journal of Pure and Applied Physics, 40(4) (2002) 252-255.
  • [20] V. Horv´ath, Z. Varga, A. Kov´acs, Journal of Molecular Structure: THEOCHEM, 755(1-3) (2005) 247-251.
  • [21] Y.H. Wang, J.W. Zou, B. Zhang, Y.X. Lu, H.X. Jin, Q.S. Yu, Journal of Molecular Structure: THEOCHEM., 755(1-2) (2005) 31-37
  • [22] J.C. Chen, L. Qian, W.J. Wu, L.M. Chen, K.C. Zheng, J. Molecular Structure: THEOCHEM., 732(1-3) (2005) 7-20.
  • [23] K. Senthilkumar, M. Sethu Raman, P. Kolandaivel, J.C. Chen, L. Qian, W.J. Wu, L.M. Chen, K.C. Zheng, Journal of Molecular Structure: THEOCHEM., 758(2-3) (2006) 107-112.
  • [24] E. Dumont, P. Chaquin, Journal of Molecular Structure: THEOCHEM, 758 (2006) 161-167.
  • [25] D. Kaur, P. Sharma, P.V. Bharatam, N. Dogra, Journal of Molecular Structure: THEOCHEM., 759 (2006) 41-49.
  • [26] M. Izadar, M.R. Gholami, Journal of Molecular Structure: THEOCHEM, 759 (2006) 11-15.
  • [27] D. Moraleda, D.E. Abed, H. Pellissier, M. Santelli, Journal of Molecular Structure: THEOCHEM., 760 (2006) 113-119.
  • [28] O. Y. Rodionova, A. L. Pomerantsev, Russian Chemical Reviews 75(4) (2006) 271-287.
  • [29] (Q) SAR and other (non) testing data in Integrated Testing Strategies using standardised Weight of Evidence criteria/Etje Hulzebos, 2012 xx pagina’s, Proefschrift Universiteit van Amsterdam – Met samenvatting in het Nederlands.
  • [30] J. A. C. Garita, C. Abadd, J. E. R. Borgesb, Y. M. Poncec, F. Torrensc, Current Topics in Medicinal Chemistry 12 (2012) 852-865.
  • [31] S. Manikandan, G. Thirunarayanan, World Scientific News 3 (2015) 132-154.
  • [32] S. Manikandan, G. Thirunarayanan, World Scientific News 5 (2015) 1-7.
  • [33] R. Senbagam, R. Vijayakumar, M. Rajarajan, S. Balaji, V. Manikandan, G. Vanangamudi and G. Thirunarayanan, Karbala International Journal of Modern Science 2 (2016) 56-62.
  • [34] R. Senbagam, M. Rajarajan, R. Vijayakumar, V. Manikandan, S. Balaji, G. Vanangamudi and G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 53 (2015) 154-164.
  • [35] R. Senbagam, M. Rajarajan, R. Vijayakumar, V. Manikandan, S. Balaji, G. Vanangamudi, G. Thirunarayanan, World Scientific News 2 (2015) 211-226.
  • [36] G. Thirunarayanan, Physical Chemistry: An Indian Journal 11(1) (2016) 23-44.
  • [37] A.W. Bauer, W.M.M. Kirby, J. C. Sherris and M.Truck, Americal Journal of Clinical Pathology 45 (1966) 493-496.
  • [38] G. Thirunarayanan, Ovidius Univesity of Annals of Chemistry, 27(1) PP XXX, (2016) DOI: 10.1515/auoc-2016-0003.
  • [39] K. Thirumurthy and G. Thirunarayanan, Arabian Journal of Chemistry, Accepted and in press, 2015. DOI: http://dx.doi.org/10.1016/j.arabjc.2015.04.015.
  • [40] C.G. Swain, E.C. Lupton Jr., Journal of the American Chemical Society, 90 (1968) 4328-4337.
Document Type
article
Publication order reference
YADDA identifier
bwmeta1.element.psjd-fcd2f05e-65ed-4592-ad97-52e2cba9a46e
Identifiers
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.