296 research outputs found
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange
Successive chemical reductions of the heteroleptic complex [(tpy)Cr III(tphz)] 3+(tpy = terpyridine; tphz = tetrapyridophenazine) give rise to the mono- and di-radical redox isomers, [(tpy)Cr III(tphz? -)] 2+and [(tpy? -)Cr III(tphz? -)] +, respectively. As designed, the optimized overlap of the involved magnetic orbitals leads to extremely strong magnetic interactions between theS= 3/2 metal ion andS= 1/2 radical spins, affording well isolatedS T= 1 andS T= 1/2 ground states at room temperature. </p
Glauber dynamics in a single-chain magnet: From theory to real systems
The Glauber dynamics is studied in a single-chain magnet. As predicted, a
single relaxation mode of the magnetization is found. Above 2.7 K, the
thermally activated relaxation time is mainly governed by the effect of
magnetic correlations and the energy barrier experienced by each magnetic unit.
This result is in perfect agreement with independent thermodynamical
measurements. Below 2.7 K, a crossover towards a relaxation regime is observed
that is interpreted as the manifestation of finite-size effects. The
temperature dependences of the relaxation time and of the magnetic
susceptibility reveal the importance of the boundary conditions.Comment: Submitted to PRL 10 May 2003. Submitted to PRB 12 December 2003;
published 15 April 200
Reactive Solubilization of Heterometallic Clusters by Treatment of (TrBi) Anions (Tr = Ga, In, Tl) with [Mn{N(SiMe)}]
Using Redox-Active πbridging Ligand as a Control Switch of Intramolecular Magnetic Interactions
Intramolecular
magnetic interactions in the dinuclear complexes
[(tpy)Ni(tphz)Ni(tpy)]<sup><i>n</i>+</sup> (<i>n</i> = 4, 3, and 2; tpy, terpyridine; tphz, tetrapyridophenazine) were
tailored by changing the oxidation state of the pyrazine-based bridging
ligand. While its neutral form mediates a weak antiferromagnetic (AF)
coupling between the two <i>S</i> = 1 Ni(II), its reduced form, tphz<sup>•–</sup>, promotes
a remarkably large ferromagnetic exchange of +214(5) K with Ni(II)
spins. Reducing twice the bridging ligand affords weak Ni–Ni
interactions, in marked contrast to the Co(II) analogue. Those experimental
results, supported by a careful examination of the involved orbitals,
provide a clear understanding of the factors which govern strength
and sign of the magnetic exchange through an aromatic bridging ligand,
a prerequisite for the rational design of strongly coupled molecular
systems and high <i>T</i><sub>C</sub> molecule-based magnets
A remarkably unsymmetric hexairon core embraced by two high-symmetry tripodal oligo-α-pyridylamido ligands
Oligo-α-pyridylamides offer an appealing route to polyiron complexes with short Fe-Fe separations and large room temperature magnetic moments. A derivative of tris(2‐aminoethyl)amine (H6tren) containing three oligo-α-pyridylamine branches and thirteen nitrogen donors (H6L) reacts with [Fe2(Mes)4] to yield an organic nanocage built up by two tripodal ligands with interdigitated branches (HMes = mesitylene). The nanocage has crystallographic D3 symmetry but hosts a remarkably unsymmetric hexairon-oxo core, with a central Fe5(μ5-O) square pyramid, two oxygen donors bridging basal sites, and an additional Fe center residing in one of the two tren-like pockets. Bond Valence Sum (BVS) analysis, Density Functional Theory (DFT) calculations, and electrochemical data were then used to establish the protonation state of oxygen atoms and the formal oxidation states of the metals. To this purpose, a specialized set of BVS parameters was devised for Fe2+-N3- bonds with nitrogen donors of oligo-α-pyridylamides. This allowed us to formulate the compound as [Fe6O2(OH)(H3L)L], with nominally four FeII and two FeIII ions. Mössbauer spectra indicate that the compound contains two unique FeII sites, identified as a pair of closely spaced hydroxo-bridged metal ions in the central Fe5(μ5-O) pyramid, and a substantially valence-delocalized FeII2FeIII2 unit. Broken-symmetry DFT calculations predict strong ferromagnetic coupling between the two iron(II) ions, leading to a local S = 4 state that persists to room temperature and explaining the large magnetic moment measured at 300 K. The compound behaves as a single-molecule magnet, with magnetization dynamics detectable in zero static field and dominated by an Orbach-like mechanism with Ueff/kB = 49(2) K and τ0 = 4(2)·10−10 s
Synthesis, Crystal Structure, Magnetic, and Electron Paramagnetic Resonance Properties of a Spiroconjugated Biradical. Evidence for Spiroconjugation Exchange Pathway
A spiroconjugated nitronyl nitroxide biradical, 6,6‘-(4,4,5,5-tetramethylimidazolidine-3-oxide-1-oxyl)-3,3,3‘,3‘-tetramethyl-1,1‘-spirobisindane (1), has been prepared by functionalization of a 3,3,3‘,3‘-tetramethyl-1,1‘-spirobisindane framework followed by Ullman condensation and subsequent oxidation. The biradical crystallizes in the monoclinic space group C2/c with four molecules in the unit cell of dimensions a = 24.861(10) Å, b = 12.129(3) Å, and c = 12.258(6) Å. X-ray analysis of a blue-plate single crystal has revealed dihedral angles of 28° between the nitronyl nitroxide moiety and aromatic ring with intramolecular through space radical−radical distances of 8.25 and 10.11 Å. In the solid state, the temperature dependence of the molar magnetic susceptibility reveals antiferromagnetic interactions. These interactions are best fit using a pair model, affording the value J = −4.0 cm^(-1) where J is the interaction parameter appearing in the spin Hamiltonian H = −JS_1·S_2. The field dependence of the magnetization measured at 2 K is consistent with a pair model. Frozen matrix EPR spectra of biradical 1 in CH_2Cl_2 at 100 K shows a half field transition at 1700 G. Temperature dependence of the half field transition intensity has been found to be consistent with a ground singlet state and thermally accessible triplet state. The magnetic interaction observed in the solid state is also observed in solution. Thus, room-temperature solution spectra display a nine-line pattern, with hyperfine coupling to four “equivalent” nitrogen atoms and a hyperfine coupling constant a_N = 3.8 G. Temperature dependence of the solution EPR spectra of biradical 1 displays alternating line width effects caused by conformational dynamics in solution. This behavior has been attributed to modulation of exchange and hyperfine interactions most likely caused by rotational motion about the nitronyl nitroxide−phenyl bond. Biradical 1 therefore exists as a ground-state singlet with a thermally accessible triplet at ca. 4 cm^(-1) higher in energy with a conformational dependence of intramolecular exchange in solution. This coupling may present evidence for spiroconjugation as an exchange pathway. Density functional calculations (B3/6-311G(D)) have been performed to investigate this possibility
Synthesis, Crystal Structure, Magnetic, and Electron Paramagnetic Resonance Properties of a Spiroconjugated Biradical. Evidence for Spiroconjugation Exchange Pathway
Structural variation in cation-assisted assembly of high-nuclearity Mn arsonate and phosphonate wheels
Cyanomethylene-bis(phosphonate)-Based Lanthanide Complexes: Structural, Photophysical, and Magnetic Investigations
10 pagesInternational audienceThe syntheses, structural investigations, magnetic and photophysical properties of a series of 10 lanthanide mononuclear complexes, containing the heteroditopic ligand cyanomethylene-bis(5,5-dimethyl-2-oxo-1,3,2λ5-dioxa-phosphorinane) (L), are described. The crystallographic analyses indicate two structural types: in the first one, [LnIII(L)3(H2O)2]*H2O (Ln = La, Pr, Nd), the metal ions are eight-coordinated within a square antiprism geometry, while the second one, [LnIII(L)3(H2O)]*8H2O (Ln = Sm, Eu, Gd, Tb, Dy, Ho, Er), contains seven-coordinated LnIII ions within distorted monocapped trigonal prisms...
- …