32 research outputs found

    Influencing the properties of dysprosium single-molecule magnets with phosphine, phosphide and phosphinidene ligands

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    Single-molecule magnets are a type of coordination compound that can retain magnetic information at low temperatures. Single-molecule magnets based on lanthanides have accounted for many important advances, including systems with very large energy barriers to reversal of the magnetization, and a di-terbium complex that displays magnetic hysteresis up to 14 K and shows strong coercivity. Ligand design is crucial for the development of new single-molecule magnets: organometallic chemistry presents possibilities for using unconventional ligands, particularly those with soft donor groups. Here we report dysprosium single-molecule magnets with neutral and anionic phosphorus donor ligands, and show that their properties change dramatically when varying the ligand from phosphine to phosphide to phosphinidene. A phosphide-ligated, trimetallic dysprosium single-molecule magnet relaxes via the second-excited Kramers’ doublet, and, when doped into a diamagnetic matrix at the single-ion level, produces a large energy barrier of 256 cm1 and magnetic hysteresis up to 4.4 K

    Organometallic neptunium(III) complexes

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    Studies of transuranic organometallic complexes provide a particularly valuable insight into covalent contributions to the metal–ligand bonding, in which the subtle differences between the transuranium actinide ions and their lighter lanthanide counterparts are of fundamental importance for the effective remediation of nuclear waste. Unlike the organometallic chemistry of uranium, which has focused strongly on UIII and has seen some spectacular advances, that of the transuranics is significantly technically more challenging and has remained dormant. In the case of neptunium, it is limited mainly to NpIV. Here we report the synthesis of three new NpIII organometallic compounds and the characterization of their molecular and electronic structures. These studies suggest that NpIII complexes could act as single-molecule magnets, and that the lower oxidation state of NpII is chemically accessible. In comparison with lanthanide analogues, significant d- and f-electron contributions to key NpIII orbitals are observed, which shows that fundamental neptunium organometallic chemistry can provide new insights into the behaviour of f-elements

    In search for molecules displaying ferromagnetic exchange: multiple-decker Ni12 and Ni16 complexes from the use of pyridine-2-amidoxime

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    The use of pyridine-2-amidoxime (pyaoxH2) in Ni chemistry has provided access to a dodecanuclear complex and a hexadecanuclear Ni cluster, namely [Ni12(pyaox)6(pyaoxH)6(MeOH)2Cl2]Cl4·5MeOH (1·5MeOH) and [Ni16(pyaox)8(pyaoxH)8(MeOH)4](SO4)4·10H2O·26MeOH (2·10H2O·26MeOH). Complex 1·5MeOH was isolated by the reaction of NiCl2·6H2O, pyaoxH2 and NaOMe in a 1 : 1 : 2 molar ratio in MeOH in 60% yield. Treatment of NiSO4·6H2O with pyaoxH2 and NEt3 in a 1 : 1 : 2 molar ratio in MeOH afforded 2·10H2O·26MeOH in good yield (65%). The two compounds display a multi-decker configuration based on stacked Ni4 layers, {Ni4(pyaox)2(pyaoxH)2}2+x (x = 3, 1·5MeOH; x = 4, 2·10H2O·26MeOH); each deck consists of two square planar and two octahedral NiII centres. The number of decks observed in 1·5MeOH and 2·10H2O·26MeOH depends on the nature of the inorganic anion that is present in the reaction system, which provides elements of synthetic control towards new high nuclearity NiII species. 2·10H2O·26MeOH is the first structurally characterized complex of any metal displaying a quadruple-decker configuration, being also the highest nuclearity metal cluster bearing pyaoxH2 and the highest nuclearity NiII cluster with any type of 2-pyridyl oxime. Each cluster cation displays ferromagnetic exchange between the octahedral NiII ions resulting in a spin ground state of S = 6 for 1 and S = 8 for 2. Magnetothermal studies have been performed and discussed for both clusters.CP and CE thank the School of Chemistry, NUI Galway, for the financial support. RI thanks the Royal Society of Edinburgh and ME thanks Spanish MINECO (MAT2015-68204-R) for funding. LCS acknowledges the financial support by FEDER (Fundo Europeu de Desenvolvimento Regional) through PT2020, by FCT (Fundação para a Ciência e a Tecnologia) for the research centre REQUIMTE/LAQV (UID/QUI/50006/2013) and for the grant SFRH/BPD/111899/2015.Peer Reviewe

    Molecular and electronic structure of terminal and alkali metal-capped uranium(V) nitride complexes

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    Determining the electronic structure of actinide complexes is intrinsically challenging because inter-electronic repulsion, crystal field, and spin–orbit coupling effects can be of similar magnitude. Moreover, such efforts have been hampered by the lack of structurally analogous families of complexes to study. Here we report an improved method to U≡N triple bonds, and assemble a family of uranium(V) nitrides. Along with an isoelectronic oxo, we quantify the electronic structure of this 5f1 family by magnetometry, optical and electron paramagnetic resonance (EPR) spectroscopies and modelling. Thus, we define the relative importance of the spin–orbit and crystal field interactions, and explain the experimentally observed different ground states. We find optical absorption linewidths give a potential tool to identify spin–orbit coupled states, and show measurement of UV···UV super-exchange coupling in dimers by EPR. We show that observed slow magnetic relaxation occurs via two-phonon processes, with no obvious correlation to the crystal field

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    Influence of Pyrazolate vs <i>N</i>‑Heterocyclic Carbene Ligands on the Slow Magnetic Relaxation of Homoleptic Trischelate Lanthanide(III) and Uranium(III) Complexes

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    Two isostructural series of trigonal prismatic complexes, M­(Bp<sup>Me</sup>)<sub>3</sub> and M­(Bc<sup>Me</sup>)<sub>3</sub> (M = Y, Tb, Dy, Ho, Er, U; [Bp<sup>Me</sup>]<sup>−</sup> = dihydrobis­(methypyrazolyl)­borate; [Bc<sup>Me</sup>]<sup>−</sup> = dihydrobis­(methylimidazolyl)­borate) are synthesized and fully characterized to examine the influence of ligand donor strength on slow magnetic relaxation. Investigation of the dynamic magnetic properties reveals that the oblate electron density distributions of the Tb<sup>3+</sup>, Dy<sup>3+</sup>, and U<sup>3+</sup> metal ions within the axial ligand field lead to slow relaxation upon application of a small dc magnetic field. Significantly, the magnetization relaxation is orders of magnitude slower for the <i>N</i>-heterocyclic carbene complexes, M­(Bc<sup>Me</sup>)<sub>3</sub>, than for the isomeric pyrazolate complexes, M­(Bp<sup>Me</sup>)<sub>3</sub>. Further, investigation of magnetically dilute samples containing 11–14 mol % of Tb<sup>3+</sup>, Dy<sup>3+</sup>, or U<sup>3+</sup> within the corresponding Y<sup>3+</sup> complex matrix reveals thermally activated relaxation is favored for the M­(Bc<sup>Me</sup>)<sub>3</sub> complexes, even when dipolar interactions are largely absent. Notably, the dilute species U­(Bc<sup>Me</sup>)<sub>3</sub> exhibits <i>U</i><sub>eff</sub> ≈ 33 cm<sup>–1</sup>, representing the highest barrier yet observed for a U<sup>3+</sup> molecule demonstrating slow relaxation. Additional analysis through lanthanide XANES, X-band EPR, and <sup>1</sup>H NMR spectroscopies provides evidence that the origin of the slower relaxation derives from the greater magnetic anisotropy enforced within the strongly donating <i>N-</i>heterocyclic carbene coordination sphere. These results show that, like molecular symmetry, ligand-donating ability is a variable that can be controlled to the advantage of the synthetic chemist in the design of single-molecule magnets with enhanced relaxation barriers
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