Template synthesis and structure of Co(II), Ni(II), and Cu(II) complexes with pyridoxilydenetaurinate Schiff base ligand

[Display omitted] •Stoichiometry of all three complexes is identical: [ML2(H2O)2].•The Schiff base ligand is bonded by N and O atoms, forming a chelate ring.•The equivalent donor atoms (N, O, Owater) are in trans arrangement.•IR spectra of the ligand K+ salt and of the complexes were compared.•In cr...

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Published in:Inorganica Chimica Acta Vol. 477; pp. 248 - 256
Main Authors: Guricová, Miroslava, Pižl, Martin, Smékal, Zdeněk, Nádherný, Ladislav, Čejka, Jan, Eigner, Václav, Hoskovcová, Irena
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 24.05.2018
Elsevier Science Ltd
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ISSN:0020-1693, 1873-3255
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Summary:[Display omitted] •Stoichiometry of all three complexes is identical: [ML2(H2O)2].•The Schiff base ligand is bonded by N and O atoms, forming a chelate ring.•The equivalent donor atoms (N, O, Owater) are in trans arrangement.•IR spectra of the ligand K+ salt and of the complexes were compared.•In crystal, ligands of the [CoL2(H2O)2] are puckered: pyridine and chelate rings and not co-planar. Co(II), Ni(II), and Cu(II) complexes with a Schiff base ligand pyridoxylidenetaurinate (L−) were prepared by a template reaction of pyridoxal (3-hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carbaldehyde), taurine (2-aminoethane-1-sulfonic acid), and the corresponding metal acetate in water–ethanol solution. Composition of the product was [ML2(H2O)2] for all three central metals. Coordination geometry varied from weakly distorted octahedral (Co, Ni) to strongly distorted octahedral (Cu) with trans arrangement of both water molecules and imine N atoms. Each bidentate ligand formed one chelate ring via iminic N and phenolic O donor atoms. The complexes were characterised by elemental analysis, FTIR spectroscopy, and XRD crystal and powder analyses. All complexes crystallize in monoclinic system with space group P21/c. IR spectra of the complexes showed changes typical for Schiff base coordination, comparing with IR spectrum of the ligand.
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ISSN:0020-1693
1873-3255
DOI:10.1016/j.ica.2018.03.031