Magneto-structural correlations of cyclo-tetravanadates functionalized with mixed-ligand copper(ii) complexes. (3rd March 2021)

• Record Type: Journal Article
• Authors: Sánchez-Lara, Eduardo; García-García, Amalia; González-Vergara, Enrique; Cepeda, Javier; Rodríguez-Diéguez, Antonio
• Is Part Of: New journal of chemistry. Volume 45:Number 11(2021)
• Page Start: 5081
• Page End: 5092
• Publication Date: 2021-03-03
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d0nj06004f
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : Bimetallic materials based on tetravanadate anions and mixed ligand copper(ii ) complexes were readily synthesized under non-hydrothermal conditions. The compounds show interesting structural and magnetic diversity mediated by copper symmetry. Abstract : Tetravanadate [V4 O12 ] 4− anion, one of the cyclic polyoxovanadates formed by the condensation of VO4 units, was used as the bidentate bridging ligand to design bimetallic materials from its functionalization with copper(ii ) complexes based on α-amino acids and typical aromatic ligands. The complexes {[Cu(Orn)(phen)]2 [μ2 -V4 O12 ]}·6H2 O (1 ), {[Cu(Lys)(bipy)]4 [μ2 -V4 O12 ]·14H2 O} n (2 ) and {[Cu(Gly)(phen)]2 [μ2 -V4 O12 ]} [Cu(Gly)(phen)(H2 O)]2 ·10H2 O (3 ) (Orn = ornithine, phen = 1, 10-phenanthroline, Lys = lysine, bipy = 2, 2′-bipyridine, Gly = glycine) were prepared under non-hydrothermal conditions. These compounds were obtained at basic pH values (close to 9), which facilitated the formation of tetravanadate anion (from the precursor NH4 VO3 ) and its stabilization with the metal complexes. All compounds crystallized in the triclinic system and showed an interesting structural and magnetic diversity, despite the fact that the components that form them are very similar. Although in compounds 1 and 3 the copper atoms are separated by the inorganic [V4 O12 ] 4− anion by about 10 Å, the magnetic properties suggest antiferromagnetic interactions, which are explained through the intermolecular Cu⋯Cu interactions and the magnetic exchange pathways between the COO − groups and the magnetic centres. The most striking feature of compound 2 was the formation of a 1D polymeric chain constructed with [V4 O12 ] 4− units separated by [Cu(Lys)(bipy]2 4+ dinuclear bridges. The intramolecular Cu⋯Cu separation in this compound was 5.2 Å, and the magnetic properties suggest a canted antiferromagnetic ordering at low applied magnetic fields.