RESUMO
The thermally induced Spin-CrossOver (SCO) undergone by the mononuclear iron(ii) complex [Fe(PM-AzA)2(NCS)2] (PM = N-2'-pyridylmethylene, AzA = 4-(phenylazo)aniline) is fully pictured by a quasi-continuous structural determination all along the spin-state modification within the sample. This large scale multi-temperature Single-Crystal X-Ray Diffraction (SCXRD) investigation leads to making structural movies. The latter reveal or confirm some features of the SCO that are subsequently validated by the same systematic investigation performed on a zinc isostructural analogue complex. Notably, the continuous views of the temperature dependencies of the unit-cell parameters, the dilatation tensors, the metal coordination sphere geometry and the intermolecular distances confirm a few of the structure-property relationships already known for SCO materials. In parallel, the examination of the temperature dependencies of the atomic coordinates and the atomic displacement parameters reveals unexpected behaviours in this gradual SCO material such as antagonistic atomic movements due to the single SCO and the pure thermal effects.
RESUMO
While uranium hydridoborate complexes containing the [BH4](-) moiety have been well-known in the literature for many years, species with functionalized borate centers remained considerably rare. We were now able to prepare several uranium hydridoborates (1-4) with amino-substituted borate moieties with high selectivity by smooth reaction of [Cp*2UMe2] (Cp* = C5Me5) and [Cp'2UMe2] (Cp' = 1,2,4-tBu3C5H2) with the aminoborane H2BN(SiMe3)2. A combination of nuclear magnetic resonance spectroscopy, deuteration experiments, magnetic SQUID measurements, and X-ray/neutron diffraction studies was used to verify the anticipated molecular structures and oxidation states of 1-4 and helped to establish a linear tridentate coordination mode of the borate anions.
Assuntos
Boratos/química , Fenômenos Magnéticos , Difração de Nêutrons , Compostos Organometálicos/química , Compostos Organometálicos/síntese química , Urânio/química , Difração de Raios X , Técnicas de Química Sintética , Modelos Moleculares , Conformação MolecularRESUMO
Aperiodic composite crystals present long-range order without translational symmetry. These materials may be described as the intersection in three dimensions of a crystal which is periodic in a higher-dimensional space. In such materials, symmetry breaking must be described as structural changes within these crystallographic superspaces. The increase in the number of superspace groups with the increase in the dimension of the superspace allows many more structural solutions. This is illustrated in n-nonadecane-urea, revealing a fifth higher-dimensional phase at low temperature.
RESUMO
We report on the neutral-to-ionic (N-I) phase transition in the one-dimensional organic complex (BEDT-TTF)-(ClMeTCNQ). The X-ray studies at room temperature show that the neutral phase of (BEDT-TTF)-(ClMeTCNQ) is already characterized by a polar long-range ordering, at variance with other charge-transfer compounds comprising noncentrosymmetric molecules. From a detailed neutron diffraction study of this complex under high pressure, we present the phase diagram of the N-I transition down to the quantum limit. We discuss the symmetry breaking associated with the transition and the evolution of its first-order character under pressure.
Assuntos
Nitrilas/química , Transição de Fase , Compostos de Sulfidrila/química , Íons , Conformação Molecular , Difração de Nêutrons , Pressão , Difração de Raios XRESUMO
We report on the direct observation by x-ray diffuse scattering measurements of thermally induced one-dimensional nanoscale ordered fluctuations in the mixed-stack charge-transfer molecular system tetrathiafulvalene-p chloranil (TTF-CA), the prototype for the neutral-ionic phase transition. The unusual physical properties of this compound are considered to be driven by such one-dimensional excitations. The results are discussed in relation to previous experimental and theoretical experiments both at thermal equilibrium and under light irradiation.