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Complexes of divalent transition metal chlorides with the tetradentate Schiff base ligand 1,2-bis(2′-pyridylmethyleneimino)-benzene

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dc.contributor.author Kasselouri, S en
dc.contributor.author Garoufis, A en
dc.contributor.author Kalkanis, G en
dc.contributor.author Perlepes, SP en
dc.contributor.author Hadjiliadis, N en
dc.date.accessioned 2014-03-01T01:41:48Z
dc.date.available 2014-03-01T01:41:48Z
dc.date.issued 1993 en
dc.identifier.issn 03404285 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/23645
dc.title Complexes of divalent transition metal chlorides with the tetradentate Schiff base ligand 1,2-bis(2′-pyridylmethyleneimino)-benzene en
heal.type journalArticle en
heal.identifier.primary 10.1007/BF00136621 en
heal.identifier.secondary http://dx.doi.org/10.1007/BF00136621 en
heal.publicationDate 1993 en
heal.abstract Transition metal(II) chloro complexes of the new Schiff base ligand 1,2-bis(2′-pyridylmethyleneimino)benzene (L), derived from 2-pyridinecarboxaldehyde and 1,2-phenylenediamine, were prepared. Compounds of [MnLCl2]-H2O, [CoLCl2]·2H2O, [NiLCl2] and [Zn3L2Cl4]Cl2 were prepared. Details are given of the formation of the complex [Cu(L·EtOH)Cl2], in which one molecule of EtOH adds across only one of the Schiff base {ie531-01} groups to give the coordinated ligand L·EtOH. The rationalization of this type of reaction by considering the steric requirements of the ligand is given. The complexes were characterized by elemental analyses, conductivity measurements, thermal techniques, mass spectra, magnetic susceptibilities and spectroscopic (i.r., ligand field, e.s.r.,1H n.m.r.) studies. The nitrogen donor atoms of the tetradentate ligands L and L·EtOH are assumed to adopt an essentially planar arrangement about manganese(II), cobalt(II), nickel(II) and copper(II), with the remaining axial coordination sites occupied by chloro ligands to yield high-spin octahedral molecules. A trinuclear structure, based on tetrahedrally coordinated metal ions, is proposed for the zinc(II) complex. © 1993 Chapman & Hall. en
heal.publisher Kluwer Academic Publishers en
heal.journalName Transition Metal Chemistry en
dc.identifier.doi 10.1007/BF00136621 en
dc.identifier.volume 18 en
dc.identifier.issue 5 en
dc.identifier.spage 531 en
dc.identifier.epage 536 en


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