Magnetism of Dendrimer-Coated Gold Nanoparticles: A Size and Functionalization Study.

Highly sensitive magnetometry reveals paramagnetism in dendrimer-coated gold nanoparticles. Different types of such nanoparticles, as a result of (i) functionalizing with two distinct Percec-type dendrons, linked to gold via dodecanethiol groups, and (ii) postsynthesis annealing in a solvent-free environment that further promotes their growth have been prepared. Ultimately, for each of the two functionalization configurations, we obtain highly monodisperse and stable nanoparticles of two different sizes, with spherical shape.

Broad-band spectroscopy of a vanadyl porphyrin: a model electronuclear spin qudit.

We explore how to encode more than a qubit in vanadyl porphyrin molecules hosting a = 1/2 electronic spin coupled to a = 7/2 nuclear spin. The spin Hamiltonian and its parameters, as well as the spin dynamics, have been determined a combination of electron paramagnetic resonance, heat capacity, magnetization and on-chip magnetic spectroscopy experiments performed on single crystals. We find low temperature spin coherence times of micro-seconds and spin relaxation times longer than a second.

Charge Delocalization, Oxidation States, and Silver Mobility in the Mixed Silver-Copper Oxide AgCuO ¤.

The electronic structure of AgCuO, and more specifically the possible charge delocalization and its implications for the transport properties, has been the object of debate. Here the problem is faced by means of first-principles density functional theory calculations of the electron and phonon band structures as well as molecular dynamics simulations for different temperatures. It is found that both Cu and Ag exhibit noninteger oxidation states, in agreement with previous spectroscopic studies.

Quantum Monte Carlo simulations of a giant {NiGd} cage with a S = 91 spin ground state.

The detailed analysis of magnetic interactions in a giant molecule is difficult both because the synthesis of such compounds is challenging and the number of energy levels increases exponentially with the magnitude and number of spins. Here, we isolated a {NiGd} nanocage with a large number of energy levels (≈5 × 10) and used quantum Monte Carlo (QMC) simulations to perform a detailed analysis of magnetic interactions. Based on magnetization measurements above 2 K, the QMC simulations predicted very weak ferromagnetic interactions that would give a record S = 91 spin ground state.

Rational electrostatic design of easy-axis magnetic anisotropy in a Zn(II) -Dy(III) -Zn(II) single-molecule magnet with a high energy barrier.

Two novel trinuclear complexes [ZnCl(μ-L)Ln(μ-L)ClZn][ZnCl3 (CH3 OH)]⋅3 CH3 OH (Ln(III) =Dy (1) and Er (2)) have been prepared from the compartmental ligand N,N'-dimethyl-N,N'-bis(2-hydroxy-3-formyl-5-bromo-benzyl)ethylenediamine (H2 L). X-ray studies reveal that Ln(III) ions are coordinated by two [ZnCl(L)](-) units through the phenoxo and aldehyde groups, giving rise to a LnO8 coordination sphere with square-antiprism geometry and strong easy-axis anisotropy of the ground state. Ab initio CASSCF+RASSI calculations carried out on 1 confirm that the ground state is an almost pure MJ =±15/2 Kramers doublet with a marked axial anisotropy, the magnetic moment is roughly collinear with the shortest DyO distances.

Origin of slow magnetic relaxation in Kramers ions with non-uniaxial anisotropy.

Transition metal ions with long-lived spin states represent minimum size magnetic bits. Magnetic memory has often been associated with the combination of high spin and strong uniaxial magnetic anisotropy. Yet, slow magnetic relaxation has also been observed in some Kramers ions with dominant easy-plane magnetic anisotropy, albeit only under an external magnetic field.

Two C3 -symmetric Dy3III complexes with triple di-μ-methoxo-μ-phenoxo bridges, magnetic ground state, and single-molecule magnetic behavior.

Two series of isostructural C(3)-symmetric Ln(3) complexes Ln(3)⋅[BPh(4)] and Ln(3)⋅0.33[Ln(NO(3))(6)] (in which Ln(III) =Gd and Dy) have been prepared from an amino-bis(phenol) ligand. X-ray studies reveal that Ln(III) ions are connected by one μ(2)-phenoxo and two μ(3)-methoxo bridges, thus leading to a hexagonal bipyramidal Ln(3)O(5) bridging core in which Ln(III) ions exhibit a biaugmented trigonal-prismatic geometry.

Insertion of a single-molecule magnet inside a ferromagnetic lattice based on a 3D bimetallic oxalate network: towards molecular analogues of permanent magnets.

The insertion of the single-molecule magnet (SMM) [Mn(III)(salen)(H2O)]2(2+) (salen(2-) = N,N'-ethylenebis-(salicylideneiminate)) into a ferromagnetic bimetallic oxalate network affords the hybrid compound [Mn(III)(salen)(H2O)]2[Mn(II)Cr(III)(ox)3]2â‹…(CH3OH)â‹…(CH3CN)2 (1). This cationic Mn2 cluster templates the growth of crystals formed by an unusual achiral 3D oxalate network. The magnetic properties of this hybrid magnet are compared with those of the analogous compounds [Mn(III)(salen)(H2O)]2[Zn(II)Cr(III)(ox)3]2â‹…(CH3OH)â‹…(CH3CN)2 (2) and [In(III)(sal2-trien)][Mn(II)Cr(III)(ox)3]â‹…(H2O)0.

A molecular [Mn14] coordination cluster featuring two slowly relaxing nanomagnets.

An extended polypyrazolyl ligand has been used to assemble Mn ions into high spin entities, in the form of one stable molecule composed of two well defined clusters. The slow relaxation of the magnetisation observed is demonstrated to arise from each "half-SMM" composing this molecular cluster pair.

Single-molecule magnetic behavior in a neutral terbium(III) complex of a picolinate-based nitronyl nitroxide free radical.

The terdentate anionic picolinate-based nitronyl nitroxide (picNN) free radical forms neutral and robust homoleptic complexes with rare earth-metal ions. The nonacoordinated Tb(3+) complex Tb(picNN)(3)·6H(2)O is a single-molecule magnet with an activation energy barrier Δ = 22.8 ± 0.