Four novel Co(II) coordination compounds 1-4 of the general formula [Co(L)][Co(NCY)]·CHCN (where L are tridentate ligands L1 = 2,6-bis(1-hexyl-1-benzimidazol-2-yl)pyridine for 1 and 2; L2 = 2,6-bis(1-octyl-1-benzimidazol-2-yl)pyridine for 3; L3 = 2,6-bis(1-dodecyl-1-benzimidazol-2-yl)pyridine for 4, Y = O for 1, 3, and 4 and Y = S for 2; = 0 for 1 and 3, = 0.5 for 2 and = 2 for 4) were prepared and characterised. The molecular structures of all four compounds consist of the hexacoordinate complex cation [Co(L)] and tetracoordinate complex anion [Co(NCY)], with distorted octahedral and tetrahedral symmetry of coordination polyhedra, respectively. The electronic structures of all compounds feature an orbitally non-degenerate ground state well-separated from the lowest excited state, which allows the analysis of the magnetic anisotropy by the spin Hamiltonian model. ZFS parameters, derived from both CASSCF-NEVPT2 calculations and magnetic data analysis, indicate that tetrahedral anions [Co(NCY)] exhibit small axial parameters || spanning the range of 2.2 to 7.7 cm, while octahedral cations [Co(L)] display significantly larger || parameters in the range of 37 to 95 cm. For 1-3, the Fourier-transform infrared magnetic spectroscopy (FIRMS) revealed a reasonable transmission with a magnetic absorption around the expected value for the ZFS accompanied by features allowing to identify phonon frequencies and simulate spin-phonon couplings. Dynamic magnetic investigations unveiled the field-induced slow relaxation of magnetisation, with maximal relaxation times () of 92(2) μs for 2 at 2 K and = 0.3 T. The temperature evolution of was analysed using a combination of Orbach, direct and Raman relaxations ( = 8(1) K (5.6 cm)) or Orbach, direct and spin-phonon induced relaxations ( = 10.3(9) K (7.2 cm)). The rest of the complexes, namely 1, 3, and 4 show field-induced slow relaxation of magnetisation with smaller than 16 μs.
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http://dx.doi.org/10.1039/d4dt01509f | DOI Listing |
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