Abstract
A comprehensive understanding of the ligand field and its influence on the degeneracy and population of d-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(II) SIM, [L(2)Co](TBA)(2) (L is an N,N'-chelating oxanilido ligand), that is stable under ambient conditions. Dynamic magnetization measurements show that this SIM exhibits a large energy barrier to spin reversal U (eff) > 300 K and magnetic blocking up to 3.5 K, and the property is retained in a frozen solution. Low-temperature single-crystal synchrotron X-ray diffraction used to determine the experimental electron density gave access to Co d-orbital populations and a derived U (eff), 261 cm(-1), when the coupling between the d (x (2) - y (2)) and d(xy) orbitals is taken into account, in very good agreement with ab initio calculations and superconducting quantum interference device results. Powder and single-crystal polarized neutron diffraction (PNPD, PND) have been used to quantify the magnetic anisotropy via the atomic susceptibility tensor, revealing that the easy axis of magnetization is pointing along the N-Co-N' bisectors of the N,N'-chelating ligands (3.4° offset), close to the molecular axis, in good agreement with complete active space self-consistent field/N-electron valence perturbation theory to second order ab initio calculations. This study provides benchmarking for two methods, PNPD and single-crystal PND, on the same 3d SIM, and key benchmarking for current theoretical methods to determine local magnetic anisotropy parameters.