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Vol. 30 No. 7 (2018): Vol 30 Issue 7

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Template Engineered Tetraazamacrocyclic Complexes and their Antibacterial Studies

https://doi.org/10.14233/ajchem.2018.20984
Monika Kamboj
Department of Chemistry, Amity School of Applied Sciences, Amity University Uttar Pradesh, Lucknow Campus, Lucknow-226 028, India
Kiran Jain
Department of Chemistry, M.L.N. College, Yamunanagar-135 001, India
D.P. Singh
Department of Chemistry, National Institute of Technology, Kurukshetra-136 119, India

Corresponding Author(s) : Monika Kamboj

monikakamboj@yahoo.com

Asian Journal of Chemistry, Vol. 30 No. 7 (2018): Vol 30 Issue 7

Abstract

Template condensation reaction of ethylenediamine and acetonylacetone in the presence of metal ions(III) was implemented to synthesize 16 membered macrocyclic complexes as [M(C16H28N4)X]X2]. The characterization of synthesized complexes was done by means of various physio-chemical techniques. Template synthesis, characterization, molecular modeling and in vitro antibacterial activities have been discussed.

Keywords

Antibacterial Macrocyclic complexes Template Molecular modeling
Kamboj, M., Jain, K., & Singh, D. (2018). Template Engineered Tetraazamacrocyclic Complexes and their Antibacterial Studies. Asian Journal of Chemistry, 30(7), 1431–1434. https://doi.org/10.14233/ajchem.2018.20984
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References
  1. B. Hariprasath, Deepthi, I.S. Babu, P. Venkatesh, S. Sharfudeen and V. Soumya, J. Chem. Pharm. Res., 2, 496 (2010).
  2. S. Chandra and M. Pundir, Spectrochim. Acta A, 69, 1 (2008); https://doi.org/10.1016/j.saa.2007.02.019.
  3. S. Chandra, R. Gupta, N. Gupta and S.S. Bawa, Transition Met. Chem., 31, 147 (2006); https://doi.org/10.1007/s11243-005-6194-5.
  4. K. Kumar and M.F. Tweedle, Pure Appl. Chem., 65, 515 (1993); https://doi.org/10.1351/pac199365030515. S.C. Jackels, B.R. Kroos, W.H. Hinson, N. Karstaedt and P.R. Moran, Radiology, 159, 525 (1986); https://doi.org/10.1148/radiology.159.2.3961187.
  5. A.D. Watson, S.M. Rockladge and C.B. Higgins, Magnetic Resonance Imaging of the Body, Raven Press, New York (1992).
  6. J.R. Morrow and É. Toth, Inorg. Chem., 56, 6029 (2017); https://doi.org/10.1021/acs.inorgchem.7b01277.
  7. D.P. Singh, R. Kumar, M. Kamboj and K. Jain, Acta Chim. Slov., 56, 780 (2009).
  8. A.I. Vogel, A Text Book of Quantitative Chemical Analysis, Longman, London (1989).
  9. I. Ahmad and A.Z. Beg, J. Ethnopharmacol., 74, 113 (2001); https://doi.org/10.1016/S0378-8741(00)00335-4.
  10. P. Rathi, K. Sharma and D.P. Singh, Spectrochim. Acta A, Mol. Biomol. Spectrosc., 130, 72 (2014); https://doi.org/10.1016/j.saa.2014.03.046.
  11. R. Kumar and R. Singh, Turk. J. Chem., 30, 77 (2006).
  12. Q. Zeng, J. Sun, S. Gou, K. Zhou, J. Fang and H. Chen, Transition Met. Chem., 23, 371 (1998); https://doi.org/10.1023/A:1006994300484.
  13. A.K. Singh, R. Singh and P. Saxena, Transition Met. Chem., 29, 867 (2004); https://doi.org/10.1007/s11243-004-1732-0.
  14. L.K. Gupta and S. Chandra, Transition Met. Chem., 31, 368 (2006); https://doi.org/10.1007/s11243-005-0002-0.
  15. A.K. Mohamed, K.S. Islam, S.S. Hasan and M. Shakir, Transition Met. Chem., 24, 198 (1999); https://doi.org/10.1023/A:1006903000739.
  16. C. Lodeiro, R. Basitida, E. Bertolo, A. Macias and R. Rodriguez, Transition Met. Chem., 28, 388 (2003); https://doi.org/10.1023/A:1023672629805.
  17. F.M.A.M. Aqra, Transition Met. Chem., 24, 337 (1999); https://doi.org/10.1023/A:1006962812246.
  18. S. Chandra and R. Kumar, Transition Met. Chem., 29, 269 (2004); https://doi.org/10.1023/B:TMCH.0000020359.84853.72.
  19. V.B. Rana, D.P. Singh, P. Singh and M.P. Teotia, Transition Met. Chem., 7, 174 (1982); https://doi.org/10.1007/BF01035836.
  20. V.P. Krzyminiewska, H. Litkowska and W.R. Paryzek, Monatsh. Chem., 130, 243 (1999);https://doi.org/10.1007/PL00010204.
  21. D.P. Singh, V. Malik, K. Kumar, C. Sharma and K.R. Aneja, Spectrochim. Acta A, 76, 45 (2010); https://doi.org/10.1016/j.saa.2010.02.044.
  22. Z.A. Siddiqi, S. Kumar, M. Khalid and M. Shahid, Spectrochim. Acta A, 72, 970 (2009); https://doi.org/10.1016/j.saa.2008.12.019.
  23. D.P. Singh, R. Kumar and J. Singh, Eur. J. Med. Chem., 44, 1731 (2009); https://doi.org/10.1016/j.ejmech.2008.03.007.
  24. D.P. Singh, R. Kumar and J. Singh, J. Enzyme Inhib. Med. Chem., 24, 883 (2009); https://doi.org/10.1080/14756360802456397.
  25. J.S. Wood, Prog. Inorg. Chem., 16, 227 (1972).
  26. D.P. Singh, V. Malik, R. Kumar and J. Singh, J. Enzyme Inhib. Med. Chem., 24, 1201 (2009); https://doi.org/10.1080/14756360902779383.
  27. D.P. Singh, M. Kamboj, K. Kumar, K. Jain and C. Sharma, J. Coord. Chem., 64, 502 (2011); https://doi.org/10.1080/00958972.2010.545398.
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