6533b7d8fe1ef96bd1269865

RESEARCH PRODUCT

A triple-bridged azido-Cu(II) chain compound fine-tuned by mixed carboxylate/ethanol linkers displays slow-relaxation and ferromagnetic order: synthesis, crystal structure, magnetic properties and DFT calculations.

Sanping ChenBing YinEmilio PardoHongshan KeShengli GaoQing WeiXiangyu LiuXiangyu LiuGang XieThais Grancha

subject

Inorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismStereochemistryHydrogen bondOctahedral molecular geometryRelaxation (NMR)MoleculeCarboxylateCrystal structureIon

description

A new azido-Cu(II) compound, [Cu(4-fba)(N3)(C2H5OH)] (4-fba = 4-fluorobenzoic acid) (1), has been synthesized and characterized. The X-ray crystal structure analysis demonstrates that only one crystallographically independent Cu(II) ion in the asymmetric unit of 1 exhibits a stretched octahedral geometry in which two azido N atoms and two carboxylic O atoms locate in the equatorial square, while two ethanol O atoms occupy the apical positions, forming a 1D Cu(II) chain with an alternating triple-bridge of EO-azido, syn,syn-carboxylate, and μ2-ethanol. The title compound consists of ferromagnetically interacting ferromagnetic chains, which exhibit ferromagnetic order (Tc = 7.0 K). The strong ferromagnetic coupling between adjacent Cu(II) ions within each chain is due to the countercomplementarity of the super-exchange pathways, whereas the ferromagnetic interchain interactions – responsible for the long-range magnetic ordering – are most likely due to the presence of coordinated ethanol molecules establishing hydrogen bonds with neighboring chains. DFT calculations have been performed on compound 1 to offer a qualitative theoretical explanation of the magnetic behavior.

10.1039/c4dt02195ahttps://pubmed.ncbi.nlm.nih.gov/25188558