New hexanuclear Fe-III clusters with the gem-diol hydrated form of di(2-pyridyl)ketone and carboxylato ligands: Crystal structures and magnetic properties
Abstract
The hexanuclear compounds [Fe6O2Cl2{(py)(2)CO2}(2)(pyOH)(2)(pyCOO)(2)((BuCOO)-C-t)(6)] (1) and [Fe6O2{(py)(2)CO2}(2)(pyCOO)(4)((BuCOO)-C-t)(6)] (2) were obtained by condensation of the trinuclear mu(3)-oxo-centered iron(III) pivalate [Fe3O((BuCOO)-C-t)(6)(H2O)(3)](+) in the presence of di(2-pyridyl)ketone [(py)(2)CO] in MeCN at ambient temperature. Both complexes contain an analogous core which can be described as two {Fe3O}(7+) units joined by gem-diolato (py)(2)CO22- bridges. Variable-temperature magnetic susceptibility measurements in polycrystalline samples of 1 and 2 reveal strong antiferromagnetic couplings between the iron(III) ions leading to S = 0 ground states. (C) 2019 Elsevier Ltd. All rights reserved.
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Título según WOS: | New hexanuclear Fe-III clusters with the gem-diol hydrated form of di(2-pyridyl)ketone and carboxylato ligands: Crystal structures and magnetic properties |
Título según SCOPUS: | New hexanuclear FeIII clusters with the gem-diol hydrated form of di(2-pyridyl)ketone and carboxylato ligands: Crystal structures and magnetic properties |
Título de la Revista: | POLYHEDRON |
Volumen: | 174 |
Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
Fecha de publicación: | 2019 |
Idioma: | English |
DOI: |
10.1016/j.poly.2019.114165 |
Notas: | ISI, SCOPUS |