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dc.contributor.authorHowlader, M B H-
dc.contributor.authorHossain, M B-
dc.contributor.authorAkhter, N-
dc.date.accessioned2008-03-31T10:08:56Z-
dc.date.available2008-03-31T10:08:56Z-
dc.date.issued2008-02-
dc.identifier.issn0376-4710-
dc.identifier.urihttp://hdl.handle.net/123456789/591-
dc.description214-219en_US
dc.description.abstractReceived 22 August 2007; revised 8 January 2008 Reaction of 2-aminophenol with Cu(II), Co(II), Fe(III), Mn(II), Zn(II) and Cd(II) ions in presence of 4-benzyloxybenzaldehyde and 2-butenal yields the complexes [Cu(L)₂] 1, [Co(L)₂(H₂O)₂] 2, [Fe(L)₂(H₂O)Cl] 3, [Mn(L)₂ (H₂O)₂] 4, [Zn(L)₂] 5, [Cd(L)₂] 6, [Cu(L')₂] 7, [Co(L')₂ (H₂O)₂] 8, [Fe(L')₂ (H₂O)Cl] 9, [Mn(L')₂ (H₂O)₂] 10, [Zn(L')₂] 11 and [Cd(L')₂] 12 (where L = C₆H5CH₂OC₆H₄CH=NC₆H₄O and L' = CH₃CHCHCH=NC₆H₄O). The complexes have been formed by template method, not via ligand formation. Complexes 1 and 7 are square planar, 2-4 and 8-10 are octahedral and 5-6 and 11-12 are tetrahedral in nature. Nickel(II) does not form complexes under the experimental condition. All the complexes are biologically active against six pathogenic bacteria (S. dysenteria, E. coli, P. aeruginosa, B. subtilis, S. lutea and S. aureus). Complexes 1, 2, 6, 9, 10, 11 and 12 show good activity as compared to the ligand precursor, 2-aminophenol, with complex 10 showing the best activity (MIC of complex 10 = 16 μg/mL for S. dysenteria and B. subtilies).en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl. ⁸ C07F1/08; C07F3/06; C07F3/08; C07F15/02; C07F15/06; C07F13/00en_US
dc.sourceIJCA Vol.47A(1) [February 2008]en_US
dc.titleTemplate synthesis of Cu(II), Co(II), Fe(III), Mn(II), Zn(II) and Cd(II) complexes of 2-aminophenol in presence of 4-benzyloxybenzaldehyde and 2-butenalen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.47A(02) [February 2008]

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