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Tytuł artykułu

Effect of Substituents on Phenazine Derivatives by Spectral Studies

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of eleven substituted dipyrido[3,2-a; 2′,3′-c]phenazine derivatives have been synthesized and examined their purities by literature method. The infrared and 13C NMR spectral data of prepared phenazines were correlated with Hammett substituent constants, F and R parameters using single and multi-regression analysis. From the results of statistical analysis, the effect of substituents on the infrared frequencies (ν, cm-1) and 13C nmr chemical shifts(δ, ppm) has been studied.
Rocznik
Tom
Strony
114--122
Opis fizyczny
Bibliogr. 36 poz., tab., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar-608 002, India
autor
  • Department of Chemistry, Annamalai University, Annamalainagar-608 002, India
  • Department of Chemistry, Sourashtra College, Madurai-625 004, India
Bibliografia
  • [1] B. Elias, C. Creely, G. W. Doorely, M. M. Feeney, C. Moucheron, A. K. DeMesmaeker, J. Dyer, D. C. Grills, M. W. George, P. Matousek, A. W. Parker, M, Towrie and J. M. Kelly, Chem. Eur. J., 14 (2008) 369-375
  • [2] W. Michal, A. J. Smith, S. Vasudevan, S. J. Quinn and J. M. Kelly, Phtochem. Photobiol Sci., 9 (2010)1196-1202
  • [3] S. Vidhisha, K. L. Reddy, Y. Praveen Kumar, M. Srijana and Satyanarayana, Int. J. Pharm. Sci. Rev. Res., 25 (2014) 197-205
  • [4] P. Naishadham and S. Satyanarayana, Int. J. Pharm. Sci. Rev., 4 (2013) 2265-2273
  • [5] J. G. Liu, B. H. Ye, H. Li, L. N. Ji, R. H. Li and J. Y. Zhou, J. Bioorg. Chem., 73(1999) 117-122
  • [6] S. Vasudevan, J. A. Smith, M. Wojdyla, R. McCabe, N. C. Fletcher, S. J. Quinn and J. M. Kelly, Dalton Trans, 39(2010) 3990-3998
  • [7] T. M. Santos, J. Madureira, B. J. Goodfellow, M. G. B. Drew, J. P. Dejesus and V. Felix, Metal based Drugs., 8 (2001) 125-136.
  • [8] M.S. A. begum, S. Saha, A. Hussain and A. R. Chakravarthy, Indian J. Chem., 48A (2009) 9-14
  • [9] S. Saha, D. Mallick, R. Majumdar, M. Roy, R. R. Dighe, E. D. Jemmis and A. R. Chakravarthy, Inorg. Chem., 50 (2011) 2975-2987
  • [10] M. slim, N. Duristic, P.Grutter and H. F. Sleiman, ChemBioChem., 8(2007) 804-812.
  • [11] M. I. J. Palson, S. L. Howell, A. H. Flood, A. K. Burrell, A. G. Blackman and K. C. Gordon, Polyhedron., 23(2004)1427-1439
  • [12] M. Towric and A. W. Parker, S. P. Foxon and J. A. Thomas, Lasers for Science Facility Programme; Central Laser Facility Annual Report, (2005-2006)162-164.
  • [13] K. Maruyama, Y. Mishima, Y. Nakabayashi and J. Motonaka, Nucleic Acids Symposium Series, Oxford University Press, No. 44 (2000) 59-60
  • [14] H. J. Zhong, H. Yang, D. S. H. Chan, C. H. Leung, H. M. Wang, D. L. Ma, Plos One, 7(2012) e49574. doi:10.1371/journal.pone.0049574.
  • [15] F. R. Svensson, M. Matson, M. Li and P. Lincoln, Biophy. Chem., Accepted article, (2010); doi: 10.1016/j.bpc.2010.04.006
  • [16] D. Villagra, R. Lopez, S. A. Moya, C. Claver and A. Bastero, Organometallics., 27(2008) 1019-1021
  • [17] R. B. Nair, B. M. Kullum and C. J. Murphy, Inorg Chem., 36(1997) 962-965
  • [18] K. Sathiyamoorthy, V. Mala, S.P. Sakthinathan, D. Kamalakkannan, R. Suresh, G. Vanangamudi and G. Thirunarayanan, Spectrochim. Acta, 112A(2013) 245-256
  • [19] S. Sasikala, K. Thirumurthy, P. Mayavel and G. Thirunarayanan, Org. Med. Chem. Lett. (2012.) doi:10.1186/2191-2858-2-20.
  • [20] R. Suresh, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S.P. Sakthinathan, S. Vijayakumar, K. Sathiyamoorthy, V. Mala, G. Vanangamudi, K. Thirumurthy, P. Mayavel and G. Thirunarayanan, Spectrochim. Acta. 101A (2013) 239-248
  • [21] G. Thirunarayanan and K, G. Sekar, Int. Lett. Chem. Phys. Astro. 6 (2014) 39-47
  • [22] R. Arulkumaran, R. Sundararajan, V. Manikandan, V. Sathiyendiran, S. Pazhamalai, G. Thirunarayanan, Int. Lett. Chem. Phys. Astro, 19(1) (2014) 25-15
  • [23] K. G. Sekar and G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 8(2) (2013) 160-174
  • [24] G. Thirunarayanan, Int. J. Sci. Res. Know. 1(12) (2013) 480-596
  • [25] G. Thirunarayanan and G. Vanangamudi, Spectrochim Acta, 81A (2011) 390-396
  • [26] K. G Sekar and G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 8(3) (2013) 249-258
  • [27] G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 9(2) (2013) 152-161
  • [28] G. Thirunarayanan and M. Suresh, Int. Lett. Chem. Phys. Astro. 4 (1) (2014) 1-11
  • [29] G. Thirunarayanan, Bull. Chem. Soc. Ethiop. 28(1) (2014)73-79
  • [30] G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 5 (2014) 89-98
  • [31] G. Thirunarayanan and K. G. Sekar, J. Taibah Univ. Sci. 8 (2014)124-136
  • [32] G. Thirunarayanan, K.G. Sekar and R. Lakshmi Narayanan, Int. Lett. Chem. Phys. Astro. 13(1) (2014) 88-94
  • [33] P. Mayavel, K. Thirumurthy, S. Dineshkumar, G. Thirunarayanan, Q-Science Connect. (2014) DOI: http://dx.doi.org/10.5339/connect.2014.10
  • [34] V. Sathiyendiran, K. G. Sekar, G. Thirunarayanan, R. Arulkumaran, R. Sundararajan, D. Kamalakkannan, R. Suresh, V. Manikanadan, R. Vijayakumar, G. Vanangamudi, Int. Lett. Chem. Phys. Astro. 11(1) (2014) 33-43
  • [35] G. Thirunarayanan, I. Muthuvel and V. Sathiyendiran, Int. Lett. Chem. Phys. Astro. 19(2) (2014) 198-207
  • [36] C. G. Swain and E. C. Lupton, Jr, J. Am. Chem. Sco. 90 (1968) 4328-4337
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-54ffa192-8851-4f49-8e05-dde5c24b8a7f
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