Multi-Technique Experimental Benchmarking of the Local Magnetic Anisotropy of a Cobalt(II) Single-Ion Magnet.

A comprehensive understanding of the ligand field and its influence on the degeneracy and population of -orbitals in a specific coordination environment are crucial for the rational design and enhancement of magnetic anisotropy of single-ion magnets (SIMs). Herein, we report the synthesis and comprehensive magnetic characterization of a highly anisotropic Co SIM, [LCo](TBA) (L is an ,'-chelating oxanilido ligand), that is stable under ambient conditions. Dynamic magnetization measurements show that this SIM exhibits a large energy barrier to spin reversal > 300 K and magnetic blocking up to 3.

Magneto-structural Correlations in Ni-Halide···Halide-Ni Chains.

We present the magnetic properties of a new family of = 1 molecule-based magnets, NiF(3,5-lut)·2HO and NiX(3,5-lut), where X = HF, Cl, Br, or I (lut = lutidine CHN). Upon creation of isolated Ni-X···X-Ni and Ni-F-H-F···F-H-F-Ni chains separated by bulky and nonbridging lutidine ligands, the effect that halogen substitution has on the magnetic properties of transition-metal-ion complexes can be investigated directly and in isolation from competing processes such as Jahn-Teller distortions. We find that substitution of the larger halide ions turns on increasingly strong antiferromagnetic interactions between adjacent Ni ions via a novel through-space two-halide exchange.

Quantifying magnetic anisotropy using X-ray and neutron diffraction.

In this work, the magnetic anisotropy in two iso-structural distorted tetrahedral Co(II) complexes, Co tmtu [ = Cl() and Br(), tmtu = tetra-methyl-thio-urea] is investigated, using a combination of polarized neutron diffraction (PND), very low-temperature high-resolution synchrotron X-ray diffraction and CASSCF/NEVPT2 calculations. Here, it was found consistently among all methods that the compounds have an easy axis of magnetization pointing nearly along the bis-ector of the compression angle, with minute deviations between PND and theory. Importantly, this work represents the first derivation of the atomic susceptibility tensor based on powder PND for a single-molecule magnet and the comparison thereof with calculations and high-resolution X-ray diffraction.

Magnetic anisotropies of Ho(III) and Dy(III) single-molecule magnets experimentally determined polarized neutron diffraction.

We present the magnetic anisotropy of two isostructural pentagonal-bipyramidal complexes, [Ln(HO)(HMPA)]I·2HMPA (HMPA = hexamethylphosphoramide, Ln = Dy, Ho). Using ac magnetic susceptibility measurements, we find magnetic relaxation barriers of 600 K and 270 K for the Dy- and Ho-compounds, respectively. This difference is supported by polarized neutron diffraction (PND) measured at 5 K and 1 T which provides the first experimental evidence that the transverse elements in the magnetic anisotropy of the Ho-analogue are significant, whereas the Dy-analogue has a near-axial magnetic anisotropy with vanishing transverse contributions.

Spin-resolved atomic orbital model refinement for combined charge and spin density analysis: application to the YTiO perovskite.

A new crystallographic method is proposed in order to refine a spin-resolved atomic orbital model against X-ray and polarized neutron diffraction data. This atomic orbital model is applied to the YTiO perovskite crystal, where orbital ordering has previously been observed by several techniques: X-ray diffraction, polarized neutron diffraction and nuclear magnetic resonance. This method gives the radial extension, orientation and population of outer atomic orbitals for each atom.

Spin resolved electron density study of YTiO in its ferromagnetic phase: signature of orbital ordering.

The present work reports on the charge and spin density modelling of YTiO in its ferromagnetic state ( = 27 K). Accurate polarized neutron diffraction and high-resolution X-ray diffraction (XRD) experiments were carried out on a single crystal at the ORPHÉE reactor (LLB) and SPRING8 synchrotron source. The experimental data are modelled by the spin resolved pseudo-atomic multipolar model (Deutsch , 2012 ▸).

Joint refinement model for the spin resolved one-electron reduced density matrix of YTiO using magnetic structure factors and magnetic Compton profiles data.

In this paper, we propose a simple cluster model with limited basis sets to reproduce the unpaired electron distributions in a YTiO ferromagnetic crystal. The spin-resolved one-electron-reduced density matrix is reconstructed simultaneously from theoretical magnetic structure factors and directional magnetic Compton profiles using our joint refinement algorithm. This algorithm is guided by the rescaling of basis functions and the adjustment of the spin population matrix.