Synthesis, crystal structure, magnetic and redox properties of Cu(II)–Cu(II) binuclear complexes of bis(phenol) amine ligands

Copper(II) complexes of a series of tripodal ligands containing two phenolate moieties and NO2X (X = S or O donor ligands) coordination sphere were synthesized: N,N-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-2-(aminomethyl) furan, N,N-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-2-(methoxyethylamine) and newly synthesized N,N-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-2-(aminomethyl) thiophene H2L have been used. The ligands H2L yielded three binuclear [L2Cu2II] complexes, which have been characterized by X-ray crystallography, UV–Vis and magnetic susceptibility measurements. The phenolate moieties of the copper complexes were electrochemically oxidized to phenoxyl radicals. The ferro- and antiferromagnetic exchange coupling of two copper centers of these complexes have been investigated by magnetic susceptibility (2–290 K) measurements. A weaker antiferromagnetic coupling is found in copper complex with methoxy arm, and a weaker ferromagnetic coupling has been observed in two other complexes with furan and thiophene arms, compared to other phenoxo-bridged dicopper(II) complexes. The weak exchange coupling constants (J) of these complexes, when compared to the literature values, is most likely attributed to the smaller Cu⋯Cu distance and Cu–O(Ph)–Cu angle.

Three novel phenoxo-bridged dicopper(III) complexes of bis(phenol) amine ligands with methoxy, furan and thiophene arms have been synthesized and characterized by X-ray crystallography, IR, UV–Vis, cyclic voltammetry and magnetic susceptibility measurements.Figure optionsDownload as PowerPoint slide