Journals / Turkish Journal of Chemistry / 2005 / Cilt: 29 - Sayı: 3

New Complexes of Organotin(IV) 2-(N-Maleoylamino)-2-methylpropanoate: Synthesis, Spectroscopic Characterization and Biological Activity

Pages
299–308
Publication Date
2005-03-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These results show that triorganotin(IV) carboxylates are more active against the animal and plant pathogens tested as compared to diorganotin dicarboxylates.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Organotin(IV) complexes of 2-(N-maleoylamino)-2-methylpropanoate were prepared by treating the ligand acid with diorganotin dichloride and triorganotin chloride in 1:2 and 1:1 molar ratios, respectively.
📊
Key Findings & Data:These reactions proceeded smoothly to completion and the complexes formed were characterized by elemental analysis, infrared, multinuclear NMR (1H, 13C, 119Sn) and mass spectrometry.
💡
Conclusion & Impact:These results show that triorganotin(IV) carboxylates are more active against the animal and plant pathogens tested as compared to diorganotin dicarboxylates.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Organotin(IV) carboxylates · spectroscopic studies · biological activity.

Abstract

Organotin(IV) complexes of 2-(N-maleoylamino)-2-methylpropanoate were prepared by treating the ligand acid with diorganotin dichloride and triorganotin chloride in 1:2 and 1:1 molar ratios, respectively. These reactions proceeded smoothly to completion and the complexes formed were characterized by elemental analysis, infrared, multinuclear NMR (1H, 13C, 119Sn) and mass spectrometry. The biological activities of the tin complexes were studied by screening the compounds against various animal and plant pathogens. These results show that triorganotin(IV) carboxylates are more active against the animal and plant pathogens tested as compared to diorganotin dicarboxylates.

Özet

Organotin(IV) complexes of 2-(N-maleoylamino)-2-methylpropanoate were prepared by treating the ligand acid with diorganotin dichloride and triorganotin chloride in 1:2 and 1:1 molar ratios, respectively. These reactions proceeded smoothly to completion and the complexes formed were characterized by elemental analysis, infrared, multinuclear NMR (1H, 13C, 119Sn) and mass spectrometry. The biological activities of the tin complexes were studied by screening the compounds against various animal and plant pathogens. These results show that triorganotin(IV) carboxylates are more active against the animal and plant pathogens tested as compared to diorganotin dicarboxylates.

🔖

Cite This Article

AHMAD, S., ALI, S., SHAHZADI, S., AHMED, F., KHAN, K. M. (2005). New Complexes of Organotin(IV) 2-(N-Maleoylamino)-2-methylpropanoate: Synthesis, Spectroscopic Characterization and Biological Activity. Turkish Journal of Chemistry, Cilt: 29 - Sayı: 3, 299–308. https://ajindex.com/articles/185429

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (27)

  1. L. Pellerito and L. Nagy, Coord. Chem. Rev., 224, 111 (2002).
  2. S.J. Blunden, P.A. Cussack and R. Hill, The Industrial Uses of Tin Compounds., Royal Society of Chemistry, London, (1985).
  3. Y. Arakawa, Main Group Met. Chem., 17, 225 (1994).
  4. M. Gielen, M. Boualam, B. Bahieu and E.R.T. Tiekink, Appl. Organomet. Chem., 8, 19 (1994).
  5. A. Kumari, I. Singh and J.P. Tandon, Appl. Organomet. Chem., 9, 127 (1995).
  6. H. Masood, S. Ali, M. Mazhar, S. Shahzadi and K. Shahid, Turk. J. Chem., 28, 75 (2004).
  7. K. Shahid, S. Ali, S. Shahzadi and Z. Akhtar, Turk. J. Chem., 27, 209 (2003).
  8. S. Ahmad, S. Ali, F. Ahmed, M.H. Bhatti, A. Badshah, M. Mazhar and K.M. Khan, Synth. React. Inorg. Met.-Org. Chem., 32, 1521 (2002).
  9. S. Ali, M. Danish and M. Mazhar, Heteroatom. Chem., 8, 273 (1997).
  10. S. Shahzadi, M.H. Bhatti, K. Shahid, S. Ali, S.R. Tariq, M. Mazhar and K.M. Khan, Monatsh. Chem., 133, 1089 (2002).
  11. A. Badshah, S. Anwer, S. Ali, M. Danish, M. Mazhar and M.I. Chaudhary, Pak. J. Pharmacol., 13, 49 (1996).
  12. A. Kalsoom, M. Mazhar, S. Ali, M.F. Mahon, K.C. Molloy and M.I. Chaudhary, Appl. Organomet. Chem., 11, 47 (1997).
  13. W.F.F. Armarego and C.L.L. Cahi, Purification of Laboratory Chemicals., 5thEd., Butterworth: Oxford, (2003).
  14. H.K. Sharma, S. Lata, K.K. Sharma, K.C. Molloy and P.C. Waterfield, J. Organomet. Chem., 9, 353 (1988).
  15. C. Vasta, V.K. Jain, T. Kesavadas and E.R.T. Tiekink, J. Organomet. Chem., 135, 410 (1991).
  16. G.K. Sandhu and N.S. Boparoy, J. Organomet. Chem., 423,183 (1992).
  17. T. P. Lockhart, W.F. Manders and E.M. Holt, J. Am. Chem. Soc., 108, 6611 (1986).
  18. M. Danish, S. Ali, A. Badshah, M. Mazhar, H. Masood, A. Malik and G. Kehr, Synth. React. Inorg. Met.-Org. Chem., 27, 863 (1997).
  19. A.K. Gupta, S. Sharma, H.P.S. Chauhan and R.J. Rao, Synth. React. Inorg. Met.-Org. Chem., 21, 497 (1991).
  20. R. Willem, H. Dialil, P. Brockaert, M. Biesemans, L. Ghys, K. Nooter, D. de Vos, F. Ribot and M. Gielen, Main Group Met. Chem., 20, 535 (1997).
  21. M. Gielen, A. El-Khloufi, M. Biesemans and R. Willem, Appl. Organomet. Chem., 7, 119 (1993).
  22. M. Gielen, J.M. Piret, M. Biesemans, R. Willem and A. El-Khloufi, Appl. Organomet. Chem., 6, 59 (1992).
  23. M. Dansih, S. Ali, M. Mazhar, A. Badshah, M.I. Choudhary, A.G. Helmut and G. Kehr, Polyhedron., 14, 3115 (1995).
  24. M.H. Bhatti, S. Ali, H. Masood, M. Mazhar and S.I. Qureshi, Synth. React. Inorg. Met.-Org. Chem., 30, 1715 (1997).
  25. H. Blank and G. Rewbell, Arch. Derm., 92, 319 (1965).
  26. S.S. Shaukat, N.A. Khan and F. Ahmed, Pak. J. Bot., 12, 97 (1980).
  27. Atta-ur-Rahman, M