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Here we report the synthesis, structure and detailed characterisation of three n-membered oxovanadium rings, Na$_n$[(V=O)$_n$Na$_n$(H$_2$O)$_n$($\alpha$, $\beta$, or $\gamma$-CD)$_2$]$m$H$_2$O (n = 6, 7, or 8), prepared by the reactions of (V=O)SO$_4$$\cdot$$x$H$_2$O with $\alpha$, $\beta$, or $\gamma$-cyclodextrins (CDs) and NaOH in water. Their alternating heterometallic vanadium/sodium cyclic core structures were sandwiched between two CD moieties such that O-Na-O groups separated neighbouring vanadyl ions. Antiferromagnetic interactions between the $S$ = 1/2 vanadyl ions led to $S$ = 0 ground states for the even-membered rings, but to two quasi-degenerate $S$ = 1/2 states for the spin-frustrated heptanuclear cluster., Comment: 8 pages, 8 figures, accepted for publication in Chemistry - A European Journal

The X-ray absorption near-edge structure (XANES) of Mn in a spin-crossover compound, [Mn$^{\textrm{III}}$(taa)], was studied in pulsed high magnetic fields up to 37T. By applying magnetic fields to the low-temperature low-spin (LS) state, significant changes in the spectra were observed, suggesting a magnetic-field-induced spin-crossover to the high-spin (HS) state. At low temperatures, the magnetic field dependence of the changes in the spectra exhibited hysteresis. Furthermore, when the magnetic field was set to zero, a considerable remanent component was observed. The energy barrier of the HS $\to$ LS transition was evaluated from the temperature dependence of the decay time of the remanent signal. The energy barrier of the transition was found to be 134K, which is notably lower than that for other spin-crossover compounds reported previously. Since the fraction of the field-induced HS state was at most 30% and the thermodynamic macroscopic field-induced phase transition was expected to occur in fields higher than 55T, the observed field-induced transition at low temperatures down to 17K could be understood as a localized microscopic transition at the single-molecular level., Comment: 14 pages, 7 figures

The preparation and physical characterization are reported for several single-molecule magnet salts to investigate the effects of paramagnetic cations on the magnetization relaxation behavior of [Mn12]- anionic single-molecule magnets., Comment: 30 pages, 5 tables, 15 figures

The preparations, X-ray structures, and detailed physical characterizations are presented for two new mixed-valence tetranuclear manganese complexes that function as single-molecule magnets (SMM's): [Mn4(hmp)6Br2(H2O)2]Br2.4H2O and [Mn4(6-me-hmp)6Cl4].4H2O, where hmp- is the anion of 2-hydroxymethylpyridine and 6-me-hmp- is the anion of 6-methyl-2-hydroxymethylpyridine., Comment: 33 pages, 5 tables, 23 figures

The first cobalt molecule to function as a single-molecule magnet, [Co4(hmp)4(MeOH)4Cl4], where hmp- is the anion of hydroxymethylpyridine, is reported. The core of the molecule consists of four Co(II) cations and four hmp- oxygen atoms ions at the corners of a cube. Variable-field and variable-temperature magnetization data have been analyzed to establish that the molecule has a S=6 ground state with considerable negative magnetoanisotropy. Single-ion zero-field interactions (DSz2) at each cobalt ion are the origin of the negative magnetoanisotropy. A single-crystal of the compound was studied by means of a micro-SQUID magnetometer in the range of 0.040-1.0K. Hysteresis was found in the magnetization versus magnetic field response of this single crystal. It is concluded that this is the first cobalt molecule to function as a single-molecule magnet., Comment: 10 pages, 4 figure, 2001 MMM conference