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Microwave-assisted synthesis, structural elucidation, antimicrobial and pesticidal activity of heterobimetallic complexes of Copper(II)

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Abstract

The present study was aimed to synthesize and characterize monometallic complex of Cu(II) using different diamines, i.e., 4-chloro-1,2-phenylenediamine and 4-fluoro-1,2-phenylenediamine, in the presence of CuCl2 to form complexes of the type [Cu(C12H14N4Cl2)]Cl2 and [Cu(C12H14N4FCl)]Cl2. These synthesized complexes were further treated with organotin dichlorides (R2SnCl2), where R = CH3 and C6H5 for the synthesis of heterobimetallic complexes. The complexes have been synthesized using both conventional and microwave heating techniques. The complexes synthesized have been further characterized by elemental analysis, infrared spectra, electronic spectra, ESR, conductance measurement, mass spectra and X-ray powder diffraction studies. On the basis of these studies, distorted octahedral geometry has been proposed for the heterobimetallic complexes synthesized by utilizing monometallic complexes. The newly synthesized complexes have been screened for their antimicrobial activity. The results obtained were compared with the standards used during antifungal and antibacterial activity (i.e., Bavistin and Streptomycin). The pesticidal activity of these complexes was also evaluated against nymph and adult species of Chrotogonus trachypterus by taking into consideration their mortality rate.

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Environmentally benign synthesis of biologically potent heterobimetallic complexes of copper.

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References

  1. M.B. Gawande, S.N. Shelke, R. Zboril, R.S. Varma, Acc. Chem. Res. 47, 1338 (2014)

    Article  CAS  Google Scholar 

  2. M. Gaba, N. Dhingra, Int. J. Pharm. Educ. Res. 45, 175 (2011)

    Google Scholar 

  3. M. Usharani, E. Akila, P. Jayaseelan, R. Rajavel, IJSER 4, 1055 (2013)

    Google Scholar 

  4. C.A. Puckett, J.K. Barton, Biochemistry 47, 11711 (2008)

    Article  CAS  Google Scholar 

  5. J.R. Anacona, K. Mago, J. Camus, Appl. Organomet. Chem. 32, 1 (2018)

    Google Scholar 

  6. Z.C. Liu, B.D. Wang, B. Li, Q. Wang, Z.Y. Yang, T.R. Li, Y. Li, Eur. J. Med. Chem. 45, 5353 (2010)

    Article  CAS  Google Scholar 

  7. I. Iakovidis, I. Delimaris, S.M. Piperakis, Mol. Biol. Int. 2011, 1 (2011)

    Article  CAS  Google Scholar 

  8. H. Iqbal, S. Ali, S. Shahzadi, S.K. Sharma, K. Qanungo, M. Shahid, J. Coord. Chem. 68, 2434 (2015)

    Article  CAS  Google Scholar 

  9. J.O. Adeyemi, D.C. Onwudiwe, Molecules 23, 1 (2018)

    Article  CAS  Google Scholar 

  10. R. Vinayak, D. Dey, D. Ghosh, D. Chattopadhyay, A. Ghosh, H.P. Nayek, Appl. Organomet. Chem. 32, 1 (2018)

    Article  CAS  Google Scholar 

  11. A. Chaudhary, A.K. Singh, R.V. Singh, J. Inorg. Biochem. 100, 1632 (2006)

    Article  CAS  Google Scholar 

  12. F.P. Carvalho, Food Energy Secur. 6, 48 (2017)

    Article  Google Scholar 

  13. A. Singh, A. Chaudhary, Silicon (2018). https://doi.org/10.1007/s12633-018-9971-4

    Article  Google Scholar 

  14. A.I. Vogel, A Textbook of Organic Quantitative Analysis, 5th edn. (Wiley, New York, 2004)

    Google Scholar 

  15. A. Singh, A. Chaudhary, Bioinorg. Chem. Appl. 2018, 1 (2018)

    Article  CAS  Google Scholar 

  16. A.I. Vogel, A Textbook of Quantitative Chemical Analysis, 6th edn. (Pearson Education, London, 2006)

    Google Scholar 

  17. A.I. Vogel, A Text Book of Inorganic Analysis (Longmans Green and Co, London, 1968)

    Google Scholar 

  18. N. Fahmi, I. Masih, K. Soni, J. Macromol. Sci. A 52, 548 (2015)

    Article  CAS  Google Scholar 

  19. V. Pushpanathan, D.S. Kumar, Int. J. Inorg. Bioinorg. Chem. 3, 35 (2013)

    Google Scholar 

  20. D.J. Finney, Probit Analysis, 3rd edn. (University Press, Cambridge, 1971)

    Google Scholar 

  21. N. Fahmi, S. Shrivastava, R. Meena, S.C. Joshi, R.V. Singh, New J. Chem. 37, 1445 (2013)

    Article  CAS  Google Scholar 

  22. S. Yadav, A. Moheman, K.S. Siddiqi, Arab. J. Chem. 9, 1747 (2016)

    Article  CAS  Google Scholar 

  23. S. Chandra, M. Tyagi, J. Serb. Chem. Soc. 73, 727 (2008)

    Article  CAS  Google Scholar 

  24. J.H. Deshmukh, M.N. Deshpande, ijCEPr 2, 20 (2011)

    CAS  Google Scholar 

  25. S. Gunasekaran, S. Seshadri, S. Muthu, Ind. J. Pure Appl. Phys. 44, 581 (2006)

    CAS  Google Scholar 

  26. S. Chandra, M. Tyagi, K. Sharma, J. Iran. Chem. Soc. 6, 310 (2009)

    Article  CAS  Google Scholar 

  27. K.S. Siddiqi, H. Afaq, S.A.A. Nami, A. Umar, Synth. React. Inorg. Met. Org. Chem. 33, 1459 (2003)

    Article  CAS  Google Scholar 

  28. D.P. Singh, K. Kumar, S.S. Dhiman, J. Sharma, J. Enzyme Inhib. Med. Chem. 24, 795 (2009)

    Article  CAS  Google Scholar 

  29. R.P.A. Bhoopathy, M. Malathy, R. Jyalakshmi, R. Rajavel, Int. J. Pharm. Biol. Chem. Sci. 5, 11 (2016)

    Google Scholar 

  30. K.S. Siddiqui, F.M.A.M. Aqra, S.A.A. Zaidi, Trans. Met. Chem. 18, 420 (1993)

    Google Scholar 

  31. K. Sharma, N. Fahmi, R.V. Singh, Appl. Organomet. Chem. 15, 221 (2001)

    Article  CAS  Google Scholar 

  32. S. Tabassum, M. Zaki, F. Arjmand, I. Ahmad, J. Photochem. Photobiol. B 114, 108 (2012)

    Article  CAS  Google Scholar 

  33. S. Chandra, S. Kumar, Spectrochim. Acta A 135, 356 (2015)

    Article  CAS  Google Scholar 

  34. A.N.M.A. Alaghaz, Y.A. Ammara, H.A. Bayoumi, S.A. Aldhlmanid, J. Mol. Struct. (2014). https://doi.org/10.1016/j.molstruc.2014.05.078

    Article  Google Scholar 

  35. A.P. Mishra, R.K. Jain, J. Saudi Chem. Soc. 18, 814 (2014)

    Article  Google Scholar 

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Acknowledgements

The authors are grateful to the Council of Scientific and Industrial Research (CSIR), New Delhi, India, for financial assistance in the form of SRF vide letter No. 09/105(0221)/2015-EMR-I.

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Correspondence to Ashu Chaudhary.

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Singh, A., Chaudhary, A. Microwave-assisted synthesis, structural elucidation, antimicrobial and pesticidal activity of heterobimetallic complexes of Copper(II). J IRAN CHEM SOC 17, 973–983 (2020). https://doi.org/10.1007/s13738-019-01829-6

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  • DOI: https://doi.org/10.1007/s13738-019-01829-6

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