dc.creator | Baggio, Ricardo | |
dc.creator | Calvo, Rafael | |
dc.creator | Garland, María Teresa | |
dc.creator | Peña, Octavio | |
dc.creator | Perec, Mireille | |
dc.creator | Slep, Leonardo D. | |
dc.date.accessioned | 2018-12-20T15:10:00Z | |
dc.date.available | 2018-12-20T15:10:00Z | |
dc.date.created | 2018-12-20T15:10:00Z | |
dc.date.issued | 2007 | |
dc.identifier | Inorganic Chemistry Communications, Volumen 10, Issue 11, 2018, Pages 1249-1252 | |
dc.identifier | 13877003 | |
dc.identifier | 10.1016/j.inoche.2007.07.028 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/158097 | |
dc.description.abstract | The oxydiacetate-bridged copper(II) complex [Cu(oda)(1,10-phen)] · 3H2O (oda = oxydiacetate dianion, 1,10-phen = 1,10-phenanthroline) has been characterized. The complex is dinuclear and centrosymmetric with each copper atom residing in a CuN2O4 octahedral environment. The Cu(II) ions are bridged by two carboxylate-oxygen atoms in a strictly planar Cu2O2 core with a Cu-Cu distance of 3.417(2) Å. The magnetic susceptibility measurements (2-300 K) show weak ferromagnetic coupling between the copper ions with J = 3.3 cm-1. The results are compared with those of the homologous [Cu(tda)(1,10-phen)]2tda (tda = thiodiacetate dianion). A model proposed for the electronic structures of the complexes based on the density functional theory (DFT) satisfactorily accounts for the magnetic results. © 2007 Elsevier B.V. All rights reserved. | |
dc.language | en | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Inorganic Chemistry Communications | |
dc.subject | Copper(II) | |
dc.subject | Crystal structure | |
dc.subject | Magnetism | |
dc.subject | Oxydiacetate | |
dc.title | A new copper(II) di-μ2-carboxylato bridged dinuclear complex: [Cu(oda)phen]2 · 6H2O (oda = oxydiacetate, phen = phenanthroline) | |
dc.type | Artículo de revista | |