Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/159720
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dc.contributor.authorMaity, Manoranjan-
dc.contributor.authorMajee, Mithun Chandra-
dc.contributor.authorKundu, Sanchita-
dc.contributor.authorSamanta, Swarna Kamal-
dc.contributor.authorSañudo Zotes, Eva Carolina-
dc.contributor.authorGhosh, Sanjib-
dc.contributor.authorChaudhury, Muktimoy-
dc.date.accessioned2020-05-12T08:35:42Z-
dc.date.available2020-05-12T08:35:42Z-
dc.date.issued2015-10-19-
dc.identifier.issn0020-1669-
dc.identifier.urihttp://hdl.handle.net/2445/159720-
dc.description.abstractA new family of pentanuclear 3d-4f heterometal complexes of general composition [LnIII2(MIIL)3(μ3-O)3H](ClO4)·xH2O (1-5) [Ln = Nd, M = Zn, 1; Nd, Ni, 2; Nd, Cu, 3; Gd, Cu, 4; Tb, Cu, 5] have been synthesized in moderate yields (50-60%) following a self-assembly reaction involving the hexadentate phenol-based ligand, viz., N,N-bis(2-hydroxy-3-methoxy-5-methylbenzyl)-N′,N′-diethylethylenediamine (H2L). Single-crystal X-ray diffraction analyses have been used to characterize these complexes. The compounds are all isostructural, having a 3-fold axis of symmetry that passes through the 4f metal centers. The [MIIL] units in these complexes are acting as bis-bidentate metalloligands and, together with μ3-oxido bridging ligands, complete the slightly distorted monocapped square antiprismatic nine-coordination environment around the 4f metal centers. The cationic complexes also contain a H+ ion that occupies the central position at the 3-fold axis. Magnetic properties of the copper(II) complexes (3-5) show a changeover from antiferromagnetic in 3 to ferromagnetic 3d-4f interactions in 4 and 5. For the isotropic CuII-GdIII compound 4, the simulation of magnetic data provides very weak Cu-Gd (J1 = 0.57 cm-1) and Gd-Gd exchange constants (J2 = 0.14 cm-1). Compound 4 is the only member of this triad, showing a tail of an out-of-phase signal in the ac susceptibility measurement. A large-spin ground state (S = 17/2) and a negative value of D (-0.12 cm-1) result in a very small barrier (8 cm-1) for this compound. Among the three NdIII2MII3 (M = ZnII, NiII, and CuII) complexes, only the ZnII analogue (1) displays an NIR luminescence due to the 4F3/2 → 4I11/2 transition in NdIII when excited at 290 nm. The rest of the compounds do not show such NdIII/TbIII-based emission. The paramagnetic CuII and NiII ions quench the fluorescence in 2-5 and thereby lower the population of the triplet state-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/acs.inorgchem.5b01142-
dc.relation.ispartofInorganic Chemistry, 2015, vol. 54, num. 20, p. 9715-9726-
dc.relation.urihttps://doi.org/10.1021/acs.inorgchem.5b01142-
dc.rights(c) American Chemical Society , 2015-
dc.subject.classificationMetalls de terres rares-
dc.subject.classificationPropietats magnètiques-
dc.subject.classificationLuminescència-
dc.subject.classificationLligands-
dc.subject.otherRare earth metals-
dc.subject.otherMagnetic properties-
dc.subject.otherLuminescence-
dc.subject.otherLigands-
dc.titlePentanuclear 3d-4f heterometal complexes of MII3LnIII2 (M = Ni, Cu, Zn and Ln = Nd, Gd and Tb) combinations: syntheses, structures, magnetism and photoluminescence properties-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec655078-
dc.date.updated2020-05-12T08:35:43Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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