Journals / Turkish Journal of Chemistry / 2006 / Cilt: 30 - Sayı: 1

Synthesis and Characterization of Metal Complexes of Cu(II), Ni(II), Zn(II), Co(II), Mn(II) and Cd(II) with Tetradentate Schiff Bases

Pages
41–48
Publication Date
2006-01-01
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)

The results suggest that the metal is bonded to the ligand through the phenolic oxygen and the imino nitrogen.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:4-(Benzeneazo)salicylaldehyde was synthesized with aniline, sodium nitrite and salicylaldehyde.
📊
Key Findings & Data:Two tetradentate ligands, N,N'-bis[4-(benzeneazo) salicylaldehyde]-o-phenylenediamine (H2L) and N,N'-bis[4-(benzeneazo) salicylaldehyde]ethylenediamine (H2L') were formed by the 2:1 molar condensation of 4-(benzeneazo) salicylaldehyde with o-phenylenediamine or ethylenediamine.
💡
Conclusion & Impact:The results suggest that the metal is bonded to the ligand through the phenolic oxygen and the imino nitrogen.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Synthesis · Tetradentate Schiff Base · Metal Complex

Abstract

4-(Benzeneazo)salicylaldehyde was synthesized with aniline, sodium nitrite and salicylaldehyde. Two tetradentate ligands, N,N'-bis[4-(benzeneazo) salicylaldehyde]-o-phenylenediamine (H2L) and N,N'-bis[4-(benzeneazo) salicylaldehyde]ethylenediamine (H2L') were formed by the 2:1 molar condensation of 4-(benzeneazo) salicylaldehyde with o-phenylenediamine or ethylenediamine. Their Cu(II), Ni(II), Zn(II), Co(II), Mn(II) and Cd(II) complexes were synthesized and characterized by elemental analysis, molar conductivity measurements, and infrared and electronic spectral data. Two ligands and their Ni(II) and Zn(II) complexes were further identified using 1H NMR spectra. The results suggest that the metal is bonded to the ligand through the phenolic oxygen and the imino nitrogen.

Özet

4-(Benzeneazo)salicylaldehyde was synthesized with aniline, sodium nitrite and salicylaldehyde. Two tetradentate ligands, N,N'-bis[4-(benzeneazo) salicylaldehyde]-o-phenylenediamine (H2L) and N,N'-bis[4-(benzeneazo) salicylaldehyde]ethylenediamine (H2L') were formed by the 2:1 molar condensation of 4-(benzeneazo) salicylaldehyde with o-phenylenediamine or ethylenediamine. Their Cu(II), Ni(II), Zn(II), Co(II), Mn(II) and Cd(II) complexes were synthesized and characterized by elemental analysis, molar conductivity measurements, and infrared and electronic spectral data. Two ligands and their Ni(II) and Zn(II) complexes were further identified using 1H NMR spectra. The results suggest that the metal is bonded to the ligand through the phenolic oxygen and the imino nitrogen.

🔖

Cite This Article

LIU, J., WU, B., ZHANG, B., LIU, Y. (2006). Synthesis and Characterization of Metal Complexes of Cu(II), Ni(II), Zn(II), Co(II), Mn(II) and Cd(II) with Tetradentate Schiff Bases. Turkish Journal of Chemistry, Cilt: 30 - Sayı: 1, 41–48. https://ajindex.com/articles/220585

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (16)

  1. M. Mokhles and Abd-Elzaher. J. Chin. Chem. Soc-Taip. 48, 153-158 (2001).
  2. R. Ramesh, P.K. Suganthy and K. Natarajan, Synth. Inorg. Met. –Org. Chem. 26, 47-60 (1996).
  3. Zhu Xinde, Wang Chenggang, Lu Zhiping, Le Zhifeng and Wu Zhshen. Synth. Inorg. Met. –Org. Chem., 955-966 (1996).
  4. R.A. Siddiqui, P. Raj and A.K. Saxena. Synth. Inorg. Met. –Org. Chem. 26, 1189-1203 (1996). B.N. Ghose and K.M. Lasisi. Synth. Inorg. Met. –Org. Chem. 16, 1121 (1986).
  5. R. Yuan, Y. Chai, D. Liu, D. Gao, J. Li and R.Yu. Anal. Chem. 65, 2572-2575 (1993). N.K. Jha and D.M. Joshi. Synth. Inorg. Met. –Org. Chem. 14, 455-465 (1984). Y. Ohashi. Bull. Chem. Soc. Jpn. 70, 1319-1324 (1997).
  6. Yee-Lok Wong, Jian-Fang Ma, Wing-Fong Law, Yan Yan, Wing-Tak Wong, Ze-Ying Zhang, C. W. Mak Thomas and K.P. Ng Dennis. Eur. J. Inorg. Chem. 313-321 (1999).
  7. Huseyin Koksal, Mustafa Dolaz, Mehmet Tumer and Selahattin Serin Synth. Inorg. Met. –Org. Chem., 1141-1162 (2001). L.J. Boucher and C.G. Coe. Inorg. Chem. 15, 1334-1340 (1976).
  8. Roslyn Atkins, Gren Bewer, Ernest Kokot, Garry M. Mockler and Ekk Sinn Inorg. Chem. 24,127-134 (1985).
  9. B. S.Tovrog, D. J.Kitko and R. S.Drago J. Am. Chem. Soc. 98, 5144-5153 (1976). P.S. Dixit and K. Srinivason. Inorg. Chem. 27, 4507-4509 (1988).
  10. Akira Nishinaga, Tetsuo Tojo and Teruo Matsuura. J.C.S. Chem. Comm. 896-897 (1974).
  11. S.L. Kessel, R.M. Emberson, P.G. Debunner and D.N. Hendrickson. Inorg. Chem. 19, 1170-1178 (1980).
  12. N.A. Bailey, B.M. Higson, and E.D. Mekenzie. J. Chem. Soc. Dalton Trans 503-508 (1972).
  13. D. Cummins, E.D. Mckenzie and H. Milburb. J. Chem. Soc. Dalton Trans. 130-135 (1976).
  14. F. Kratz, B. Nuber, J. Weib and B.K. Keppler. Synth. Inorg. Met. –Org. Chem. 21, 1601-1613 (1991). P. Toyssie and J. J. Charette. Spectrochim. Acta. 19, 1407-1423 (1963). Keihei Uneo and Arthur E. Martell. J. Phys. Chem. 60,1270-1275 (1956). N.S. Biradar and V.H. Kulkami. J. Inorg. Nucl. Chem. 33, 3781-3786 (1971). J.N.R. Ruddick and J.R. Sams. J. Organomet. Chem. 60, 233-246 (1973).
  15. S. Sarawat, G.S. Srivastava and R.C. Mehrotra. J. Organomet. Chem. 129, 155-161 (1977). G. Wang and J.C. Chang. Synth. Inorg. Met. –Org. Chem. 24, 1091-1097 (1994).
  16. S.J. Gruber, C.M. Harris and E. Sinn. Inorg. Nucl. Chem. 30, 1805-1830 (1968).