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Synthesis, characterization and extraction studies of N,N″-bis[1-biphenyl-2-hydroxyimino-2-(4-acetylanilino)-1-ethylidene]-diamines and their homo-and heteronuclear copper(II) complexes

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Abstract

A new series of homo- and heteropolynuclear copper(II) complexes of N,N″-bis[1-biphenyl-2-hydroxyimino-2-(4-acetylanilino)-1-ethylidene]-diamines have been prepared and characterized by different physical techniques. The starting point of the research was the reaction of chloroacetyl chloride with biphenyl in the presence of aluminum chloride. 4-Biphenylhydroximoyl chloride was obtained by reacting synthesized 4-(chloroacetyl)biphenyl with alkyl nitrite. Substituted 4-(alkylaminoisonitrosoacetyl) biphenyl (ketooxime) was prepared by reacting 4-biphenylhydroximoyl chloride with 4-aminoacetophenone in EtOH. Homodi-, homotrinuclear and heterodinuclear copper(II) perchlorate complexes of tetradentate Schiff bases which possess N4 donor sets derived from the condensation of 4-(arylaminoisonitrosoacetyl)biphenyl and diamine derivatives were synthesized and characterized. Elemental analysis, FT-IR, ESR, molar conductivity, magnetic moment measurements and thermal analyses studies were utilized for the investigation of the complexes. The free ligands were also characterized by 1H- and 13C-NMR spectra. Elemental analyses, stoichiometric and spectroscopic data of the metal complexes indicated that the metal:ligand ratio of dinuclear copper(II) complexes were found to be 2: 1 while this ratio was 3: 2 in trinuclear copper(II) complexes and the metal complexes indicated that the metal ions are coordinated to the oxime and imine nitrogen atoms. The extraction abilities of the novel ligands were also evaluated in chloroform by using several transition metal picrates such as Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Pb2+, Cd2+, Hg2+. It has been observed that both ligands show a high affinity to Cu2+ ions.

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References

  1. Casellato U and Vigato P A 1977 Coord. Chem. Rev. 23 31

    Article  CAS  Google Scholar 

  2. Ramade I, Khan O, Jeannin Y and Robert F 1977 Inorg. Chem. 36 930

    Article  Google Scholar 

  3. Rodriquez de Barbarin C O, Bailey N A, Fenton D E and He Q-Y 1997 J. Chem. Soc. Dalton Trans. 161

  4. Miyasaka H, Ieda H, Matsumoto N, Crescenzi R and Floriani C 1998 Inorg. Chem. 37 255

    Article  CAS  Google Scholar 

  5. Khan M M T, Shukla S and Shark J 1990 J. Mol. Catal. 57 301

    Article  CAS  Google Scholar 

  6. Georgieva I, Tredafilova N and Bauer G 2006 Spectrochim. Acta A63 403

    Google Scholar 

  7. Poddar S N 1957 Analyt. Bioanalyt. Chem. 154 254

    Article  CAS  Google Scholar 

  8. Akagi F, Michihiro Y, Nakao Y, Matsumoto K, Sato T and Mori W 2004 Inorg. Chim. Acta 357 684

    Article  CAS  Google Scholar 

  9. Dhar S, Nethaji M and Chakravarty A R 2005 Inorg. Chim. Acta. 358 2437

    Article  CAS  Google Scholar 

  10. Reddy K H, Reddy P S and Babu P R 2000 Transition Met. Chem. 25 505

    Article  CAS  Google Scholar 

  11. Sağlam N, Çolak A, Serbest K, Dülger S, Güner S, Karaböcek S and Beldüz A O 2002 BioMetals 15 357

    Article  Google Scholar 

  12. Li L Z, Zhao C, Xu T, Ji H W, Yu Y H, Guo G Q and Chao H 2005 J. Inorg. Biochem. 99 1076

    Article  CAS  Google Scholar 

  13. Babu M S S, Reddy K H and Krishna P G 2007 Polyhedron 26 572

    Article  CAS  Google Scholar 

  14. Pope L E and Sigman D S 1984 Proc. Natl. Acad. Sci. USA 81 3

    Article  CAS  Google Scholar 

  15. Güp R and Giziroğlu E 2006 Spectrochim. Acta A65 719

    Google Scholar 

  16. Karipcin F and Arabalı F 2006 Russ. J. Inorg. Chem. 51 1467

    Article  Google Scholar 

  17. Serbest K, Karaböcek S, Değirmencioğlu İ, Güner S and Kormali F 2001 Transition Met. Chem. 26 375

    Article  CAS  Google Scholar 

  18. Pedersen C J 1968 Fed. Am. Soc. Exp. Biol. 27 1305

    CAS  Google Scholar 

  19. Levin N and Hartung W H 1942 J. Org. Chem. 7 408

    Article  CAS  Google Scholar 

  20. Uçan S Y and Mercimek B 2005 Synth. React. Inorg. Met.-Org. Chem. 35 197

    Article  CAS  Google Scholar 

  21. Gaber M, Ayad M M and El-Sayed Y S Y 2005 Spectrochim. Acta A62 694

    Google Scholar 

  22. Shauib N M, Elassar A A and El-Dissouky A 2006 Spectrochim. Acta A63 714

    Google Scholar 

  23. Nakamoto K 1978 Infrared and Raman spectra of inorganic and coordination compounds (New York: Wiley)

    Google Scholar 

  24. Silverstein R M, Bassler O G and Morrill T C 1974 Spectrophotometic identification of organic compounds (New York: Wiley)

    Google Scholar 

  25. Ferraro J R 1971 Low frequency vibrations of inorganic and coordination compounds (New York: Plenum Press)

    Google Scholar 

  26. Hathaway B J and Underhill A E 1961 J. Chem. Soc. 3091

  27. Nakamoto K 1986 Infrared and Raman spectra of inorganic and coordination compounds (New York: Wiley) 4th edn

    Google Scholar 

  28. Rosenthall M R 1973 T. Chem. Edu. 50 331

    Article  Google Scholar 

  29. Geary W J 1971 Coord. Chem. Rev. 7 81

    Article  CAS  Google Scholar 

  30. Kulkarrni N D and Bhattcharya P K 1989 Transition Met. Chem. 14 303

    Article  Google Scholar 

  31. Ruiz R, Lloret F, Julve M, Faus J, Munoz M C and Solans X 1993 Inorg. Chim. Acta 213 261

    Article  CAS  Google Scholar 

  32. Luneau D, Oshio H, Okawa H, Koikawa M and Kida S 1990 Bull. Chem. Soc. Jpn. 63 2212

    Article  CAS  Google Scholar 

  33. Djebbar-Sid S, Benali-Baitich O and Deloume J P 1998 Transition Met. Chem. 23 443

    Article  CAS  Google Scholar 

  34. Li Y T, Yan C W and Guan H S 2003 Polyhedron 22 3223

    Article  CAS  Google Scholar 

  35. Youngme S, Phuengphai P, Chaichit N, Pakawatchai C, van Albada G A, Roubeau O and Reedijk J 2004 Inorg. Chim. Acta 357 3603

    Article  CAS  Google Scholar 

  36. Belaid S, Landreau A, Djebbar S, Benali-Baitich O, Bouet G and Bouchara J P 2008 J. Inorg. Biochem. 102 63

    Article  CAS  Google Scholar 

  37. Deepalatha S, Sambasiva Rao P and Venkatesan R 2006 Spectrochim. Acta A64 178

    Google Scholar 

  38. Hathaway B J and Billing O E 1970 Coord. Chem. Rev. 5 143

    Article  CAS  Google Scholar 

  39. Maajan M, Saxena K N and Saxena C P 1981 J. Inorg. Nucl. Chem. 43 2148

    Article  Google Scholar 

  40. Einstein J C 1958 J. Chem. Phys. 28 323

    Article  Google Scholar 

  41. Sharma K K and Chandra S 1984 Transition Met. Chem. 9 401

    Article  CAS  Google Scholar 

  42. Villa J F and Hatfield W E 1972 Inorg. Chem. 11 1331

    Article  CAS  Google Scholar 

  43. Güp R, Alpoğuz H K and Bedük A D 2002 Collect. Czech. Chem. Commun. 67 209

    Article  CAS  Google Scholar 

  44. Dalman Ö, Tüfekçi M, Nohut S, Güner S and Karaböcek S 2002 J. Pharm. Biomed. Anal. 27 183

    Article  CAS  Google Scholar 

  45. Karaböcek S, Nohut S, Dalman Ö, and Güner S 2000 Anal. Chim. Acta. 408 163

    Article  Google Scholar 

  46. Alguacil F J, Coba A and Alonso M 2002 J. Chem. Eng. 85 259

    Article  CAS  Google Scholar 

  47. Srinivasa Rao K, Devi N N and Reddy B R 2000 Hydrometallurgy 57 269

    Article  Google Scholar 

  48. Deligöz H and Yılmaz M 1995 Solvent Extr. Ion Exch. 13 19

    Article  Google Scholar 

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Correspondence to Bülent Dede.

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Dede, B., Karipcin, F. & Cengiz, M. Synthesis, characterization and extraction studies of N,N″-bis[1-biphenyl-2-hydroxyimino-2-(4-acetylanilino)-1-ethylidene]-diamines and their homo-and heteronuclear copper(II) complexes. J Chem Sci 121, 163–171 (2009). https://doi.org/10.1007/s12039-009-0018-7

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  • DOI: https://doi.org/10.1007/s12039-009-0018-7

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