Orbital angular momentum is a prerequisite for magnetic anisotropy, although in transition metal complexes it is typically quenched by the ligand field. By reducing the basicity of the carbon donor atoms in a pair of alkyl ligands, we synthesized a cobalt(II) dialkyl complex, Co(C(SiMe2ONaph)3)2 (where Me is methyl and Naph is a naphthyl group), wherein the ligand field is sufficiently weak that interelectron repulsion and spin-orbit coupling play a dominant role in determining the electronic ground state. Assignment of a non-Aufbau (dx2–y2, dxy)3(dxz, dyz)3(dz2)1 electron configuration is supported by dc magnetic susceptibility data, experimental charge density maps, and ab initio calculations. Variable-field far-infrared spectroscopy and ac magnetic susceptibility measurements further reveal slow magnetic relaxation via a 450–wave number magnetic excited state.

Anionic two-coordinate complexes of first-row transition-metal(I) centres are rare molecules that are expected to reveal new magnetic properties and reactivity. Recently, we demonstrated that a N(SiMe3)2(-) ligand set, which is unable to prevent dimerisation or extraneous ligand coordination at the +2 oxidation state of iron, was nonetheless able to stabilise anionic two-coordinate Fe(I) complexes even in the presence of a Lewis base. We now report analogous Cr(I) and Co(I) complexes with exclusively this amido ligand and the isolation of a [Mn(I){N(SiMe3)2}2]2(2-) dimer that features a Mn-Mn bond. Additionally, by increasing the steric hindrance of the ligand set, the two-coordinate complex [Mn(I){N(Dipp)(SiMe3)}2](-) was isolated (Dipp=2,6-iPr2-C6H3). Characterisation of these compounds by using X-ray crystallography, NMR spectroscopy, and magnetic susceptibility measurements is provided along with ligand-field analysis based on CASSCF/NEVPT2 ab initio calculations.

First-row two-coordinate complexes are attracting much interest. Herein, we report the high-yield isolation of the linear two-coordinate iron(I) complex salt [K(L)][Fe{N(SiMe3 )2 }2 ] (L=18-crown-6 or crypt-222) through the reduction of either [Fe{N(SiMe3 )2 }2 ] or its three-coordinate phosphine adduct [Fe{N(SiMe3 )2 }2 (PCy3 )]. Detailed characterization is gained through X-ray diffraction, variable-temperature NMR spectroscopy, and magnetic susceptibility studies. One- and two-electron oxidation through reaction with I2 is further found to afford the corresponding iodo iron(II) and diiodo iron(III) complexes.

The tetranuclear cobalt cluster compound [Co(μ-NPBu)][B(CF)] (Bu = tert-butyl) was synthesized by chemical oxidation of Co(NPBu) with [FeCp][B(CF)] and magnetically characterized to study the effect of electronic communication between low-coordinate metal centers on slow magnetic relaxation in a transition metal cluster. The dc magnetic susceptibility data reveal that the complex exhibits a well-isolated S = / ground state, which persists even to 300 K and is attributed to the existence of direct metal-metal orbital overlap. The ac magnetic susceptibility data further reveals that the complex exhibits slow magnetic relaxation in the absence of an applied field, and that the relaxation dynamics can be fit with a combination of Orbach, quantum tunneling, and Raman relaxation processes. The effective spin reversal barrier for this molecule is 87 cm, the largest reported to date for a transition metal cluster, and arises due to the presence of a large easy-axis magnetic anisotropy. The complex additionally exhibits waist-restricted magnetic hysteresis and magnetic blocking below 3.6 K. Taken together, these results indicate that coupling of low-coordinate metal centers is a promising strategy to enhance magnetic anisotropy and slow magnetic relaxation in transition metal cluster compounds.

We propose a new application of single molecule magnet crystals: their use as "magnetic bubble chambers" for the direct detection of sub-GeV dark matter. The spins in these macroscopic crystals effectively act as independent nano-scale magnets. When anti-aligned with an external magnetic field they form meta-stable states with a relaxation time that can be very long at sufficiently low temperatures. The Zeeman energy stored in this system can be released through localized heating, caused for example by the scattering or absorption of dark matter, resulting in a spin avalanche (or "magnetic deflagration") that amplifies the effects of the initial heat deposit, enabling detection.Much like the temperature and pressure in a conventional bubble chamber, the temperature and external magnetic field set the detection threshold for a single molecule magnet crystal. We discuss this detector concept for dark matter detection and propose ways to ameliorate backgrounds. If successfully developed, this detector concept can search for hidden photon dark matter in the meV -eV mass range with sensitivities exceeding current bounds by several orders of magnitude.