Ferromagnetic coupling in a dicopper(ii) oxamate complex bridged by carboxylate groups

Autor: Cynthia L. M. Pereira, Fabio Furlan Ferreira, Cleverton O. C. da Silveira, Willian X. C. Oliveira, Emerson F. Pedroso, Eufrânio N. da Silva Júnior, Tamyris T. da Cunha, Vitor M. M. Barbosa
Rok vydání: 2021
Předmět:
Zdroj: CrystEngComm. 23:1885-1897
ISSN: 1466-8033
DOI: 10.1039/d0ce01742f
Popis: Three new air-stable coordination compounds [Cu(HL)2(H2O)2]2·2H2O (1), [Cu(HL)2]n (1a), and [Zn(HL)2(H2O)2] (2), where HL = N-(4-hydroxyphenyl)oxamate, were successfully synthesized and characterized. Single-crystal X-ray analysis reveals 1 as a dinuclear copper(II) complex, in which the metal ions are connected through the carboxylate moieties of the oxamate ligands. The crystal structure of 1a is solved using powder X-ray diffraction data and stands for an anhydrous mononuclear copper(II) oxamate complex. 2 corresponds to the first example of a mononuclear Zn2+ oxamate complex containing both ligands and water solvent molecules in the cis arrangement. The presence of a phenol group in the oxamate ligand leads to different hydrogen bond patterns in the crystal packing in 1, 1a, and 2, resulting in supramolecular 3D architectures. Magnetic measurements of 1 reveal a ferromagnetic coupling between the copper(II) ions through the carboxylate–oxamate bridge [J = +0.829 cm−1, g = 2.101, zJ = +0.154 cm−1; H = −JSCu1·SCu2, where SCu1 = SCu2 = 1/2]. DFT calculations based on the broken symmetry formalism (DFT-BS) were performed to provide insight into the magnetic behavior.
Databáze: OpenAIRE