Journals / Turkish Journal of Chemistry / 2013 / Cilt: 37 - Sayı: 1

Synthesis and characterization of Ni(II) and Cu(II) complexes derived from novel phenolic Mannich bases

Pages
101–110
Publication Date
2013-01-01
DOI
—
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AI Summary & Key Takeaways

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

Electronic spectra and magnetic susceptibility measurements suggested tetrahedral geometry for Ni(II) (3), square planar geometry for Cu(II) (4) complexes of 1, and octahedral geometries for both Ni(II) (5) and Cu(II) (6) complexes of 2.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The novel phenolic Mannich bases 2,2'-(2-hydroxy-4,5- dimethylbenzylazanediyl)diethanol (1) and 2-((2-(4-(2-hydroxy-4,5- dimethylbenzyl)piperazin-1-yl)ethylamino)methyl)-4,5-dimethylphenol (2) have been synthesized in good yield by using a microwave-induced technique from 3,4-dimethylphenol and corresponding amines in the presence of formaldehyde.
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Key Findings & Data:Metal complexes of 1 and 2 for Ni(II) (3 and 5) and for Cu(II) (4 and 6) have also been prepared and all compounds have been characterized by elemental and spectral analyses.
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Conclusion & Impact:Electronic spectra and magnetic susceptibility measurements suggested tetrahedral geometry for Ni(II) (3), square planar geometry for Cu(II) (4) complexes of 1, and octahedral geometries for both Ni(II) (5) and Cu(II) (6) complexes of 2.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Mannich base · 4-dimethylphenol · piperazine

Abstract

The novel phenolic Mannich bases 2,2'-(2-hydroxy-4,5- dimethylbenzylazanediyl)diethanol (1) and 2-((2-(4-(2-hydroxy-4,5- dimethylbenzyl)piperazin-1-yl)ethylamino)methyl)-4,5-dimethylphenol (2) have been synthesized in good yield by using a microwave-induced technique from 3,4-dimethylphenol and corresponding amines in the presence of formaldehyde. Metal complexes of 1 and 2 for Ni(II) (3 and 5) and for Cu(II) (4 and 6) have also been prepared and all compounds have been characterized by elemental and spectral analyses. Thermal, magnetic, and electronic studies have also been reported for metal complexes. Electronic spectra and magnetic susceptibility measurements suggested tetrahedral geometry for Ni(II) (3), square planar geometry for Cu(II) (4) complexes of 1, and octahedral geometries for both Ni(II) (5) and Cu(II) (6) complexes of 2.

Özet

The novel phenolic Mannich bases 2,2'-(2-hydroxy-4,5- dimethylbenzylazanediyl)diethanol (1) and 2-((2-(4-(2-hydroxy-4,5- dimethylbenzyl)piperazin-1-yl)ethylamino)methyl)-4,5-dimethylphenol (2) have been synthesized in good yield by using a microwave-induced technique from 3,4-dimethylphenol and corresponding amines in the presence of formaldehyde. Metal complexes of 1 and 2 for Ni(II) (3 and 5) and for Cu(II) (4 and 6) have also been prepared and all compounds have been characterized by elemental and spectral analyses. Thermal, magnetic, and electronic studies have also been reported for metal complexes. Electronic spectra and magnetic susceptibility measurements suggested tetrahedral geometry for Ni(II) (3), square planar geometry for Cu(II) (4) complexes of 1, and octahedral geometries for both Ni(II) (5) and Cu(II) (6) complexes of 2.

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Cite This Article

BÜYÜKKIDAN, N., ÖZER, S. (2013). Synthesis and characterization of Ni(II) and Cu(II) complexes derived from novel phenolic Mannich bases. Turkish Journal of Chemistry, Cilt: 37 - Sayı: 1, 101–110. https://ajindex.com/articles/184817

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References (28)

  1. Haidue, L.; Coord. Chem. Rev. 1990, 99, 253–256.
  2. Singh, B.; Singh, R. N.; Aggarwal, R. C. Polyhedron 1985, 4, 401–407.
  3. Mishra, A. P.; Srivastavan, S. K. J. Indian Council Chem. 1994, 10, 2–7.
  4. Sujatha, S.; Rajendiran, T. M.; Kannappan, R.; Venkatesan, R.; Sambasiva Rao, P. Proc. Indian Acad. Sci. (Chem. Sci.) 2000, 112, 559–572.
  5. Bertoncello, K.; Fallon, G. D.; Hodgkin, J. H.; Murray, K. S. Inorg. Chem. 1988, 27, 4750–4758.
  6. Diril, H.; Chang, H. R.; Zhang, X.; Potenza, S. K.; Piperpont, C. G.; Schugar, H. J.; Isied, S. S. D.; Hendrickson, N. J. Am. Chem. Soc. 1987, 109, 6207–6208.
  7. Buchanan, R. M.; Oberhausen, K. J.; Richardson, J. F. Inorg. Chem. 1987, 26, 971–973.
  8. Dimmock, J. R.; Kumar, P. Curr. Med. Chem. 1997, 4, 1–22.
  9. Dimmock, J. R.; Vashishtha, S. C.; Quail, J. W.; Pugazhenthi, U.; Zimpel, Z.; Sudom, A. M.; Allen, T. M.; Kao, G. Y.; Balzarini, J.; De Clercq, E. J. Med. Chem. 1998, 41, 4012–4020.
  10. Rao, H. S. P.; Poonguzhali, E.; Senthilkumar, S. P. Synt. Commun. 2008, 38, 937–942.
  11. Palaniappan, S.; John, A.; Amarnath, C. A.; Rao, V. J. J. Mol. Catal. A: Chemical 2004, 218, 47–53.
  12. Loh, T. P.; Chen, S. L. Org. Lett. 2002, 4, 3647–3650.
  13. Ollevier, T.; Nadeau, E. J. Org. Chem. 2004, 69, 9292–9295.
  14. Wang, L. M.; Han, J. W.; Sheng, J.; Tian, H.; Fan, Z. Y. Catal. Commun. 2005, 6, 201–204.
  15. Rondot, C. J. Zhu, Org. Lett. 2005, 7, 1641–1644.
  16. Pandey, G.; Singh, R. P.; Garg, A.; Singh, V. K. Tetrahedron Lett. 2005, 46, 2137–2140.
  17. Manabe, K.; Mori, Y.; Kobayashi, S. Tetrahedron 2001, 57, 2537–2544.
  18. Azizi, N.; Torkiyan, L.; Saidi, M. R. Org. Lett. 2006, 8, 2079–2082.
  19. Hayashi, Y.; Urushima, T.; Shin, M.; Shoji, M. Tetrahedron Lett. 2005, 61, 11393–11404.
  20. Ibrahem, I.; Zou, W. B.; Engqvist, M.; Xu, Y. M.; Cordova, A. Chem. Eur. J. 2005, 11, 7024–7029.
  21. Hayashi, Y.; Tsuboi, W.; Ashimine, I.; Urushima, T.; Shoji, M.; Sakai, K. Angew. Chem. Int. Ed. 2003, 42, 3677–3680.
  22. Raman, N.; Esthar, S.; Thangaraja, C. J. Chem. Sci. 2004, 116, 209–213.
  23. Omar, M. M.; Mohamed, G. G. Spectrochim. Acta A 2005, 61, 929–936.
  24. Supriya, S.; Raghavan, A.; Vijayaraghavan, V. R.; Chinnakali, K.; Fun, H. K.; Subramanian, J. Polyhedron 2007, 26, 3217–3226.
  25. Chkaku, N.; Nakamoto, K. Inorg. Chem. 1971, 10, 768–772.
  26. Kapahi, A.; Pandeya, K. P.; Singh, R. P. J. Inorg. Nucl. Chem. 1987, 40, 355–361.
  27. El-Shazly, R. M.; Al-Hazmi, G. A. A.; Ghazy, S. E.; El-Shahawi, M. S.; El-Asmy, A. A. Spectr. Chim. Acta 2005, 61A, 243–248.
  28. Yenikaya, C.; Poyraz, M.; Sarı, M.; Demirci, F.; ˙Ilkimen, H.; B¨ uy¨ ukg¨ ung¨ or, O. Polyh