Synthesis, structure, and characterisation of a ferromagnetically coupled dinuclear complex containing Co(ii) ions in a high spin configuration and thiodiacetate and phenanthroline as ligands and of a series of isomorphous heterodinuclear complexes containing different Co: Zn ratios

Abstract

We report the synthesis, crystal structure, and characterisation of a dinuclear Co(ii) compound with thiodiacetate (tda) and phenanthroline (phen) as ligands (1), and of a series of metal complexes isomorphous to 1 with different Co : Zn ratios (2, 4 : 1; 3, 1 : 1; 4, 1 : 4; 5, 1 : 10). General characterisation methodologies and X-ray data showed that all the synthesised complexes are isomorphous to Zn(ii) and Cu(ii) analogues (CSD codes: DUHXEL and BEBQII). 1 consists of centrosymmetric Co(ii) ion dimers in which the ions are 3.214 Å apart, linked by two μ-O bridges. Each cobalt atom is in a distorted octahedral environment of the N2O3S type. UV-vis spectra of 1 and 5 are in line with high spin (S = 3/2) Co(ii) ions in octahedral coordination and indicate that the electronic structure of both Co(ii) ions in the dinuclear unit does not significantly change relative to that of the magnetically isolated Co(ii) ion. EPR spectra of powder samples of 5 (Co : Zn ratio of 1 : 10) together with spectral simulation indicated high spin Co(ii) ions with high rhombic distortion of the zfs [E/D = 0.31(1), D > 0]. DC magnetic susceptibility experiments on 1 and analysis of the data constraining the E/D value obtained by EPR yielded g = 2.595(7), |D| = 61(1) cm−1, and an intradimer ferromagnetic exchange coupling of J = 1.39(4) cm−1. EPR spectra as a function of Co : Zn ratio for both powder and single crystal samples confirmed that they result from two effective S′ = 1/2 spins that interact through dipolar and isotropic exchange interactions to yield magnetically isolated S′ = 1 centres and that interdimeric exchange interactions, putatively mediated by hydrophobic interactions between phen moieties, are negligible. The latter observation contrasts with that observed in the Cu(ii) analogue, where a transition from S = 1 to S′ = 1/2 was observed. Computational calculations indicated that the absence of the interdimeric exchange interaction in 1 is due to a lower Co(ii) ion spin density delocalisation towards the metal ligands.