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1.
Allison M. Mills Daniel Brunling Michael Ruck 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(8):i70-i72
A redetermination of the structure of `La32.66Fe11S60' in the trigonal space group Rm led to the new formula La52Fe12S90 and to a redefinition of the structure type. In the structure, the Fe2+ cations occur in Fe2S9 dimers of face‐sharing octahedra (with 3m symmetry). The dimers are linked by face‐ and vertex‐sharing bi‐ and tricapped LaS6 trigonal prisms (with m symmetry) to form a three‐dimensional network containing two types of cuboctahedral cavities. The larger cavities remain empty, while the smaller ones accommodate alternative sites for disordered La3+ cations. 相似文献
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Th. Doert A. Schneidewind M. Hölzel O. StockertD. Rutzinger M. Ruck 《Journal of magnetism and magnetic materials》2012,324(6):1157-1164
CeAgAs2, an HfCuSi2 like layered pnictide, orders antiferromagnetically at TN=6.2(1) K. The ordering process was monitored in neutron diffraction experiments in the temperature range 10 K≥T≥3.5 K. At T=4 K the lattice parameters are a=5.7438(1) Å, b=5.7696(1) Å and c=21.0067(2) Å. The diffraction pattern of the antiferromagnetic phase with a propagation vector k=[0,0,0] point towards ferromagnetically ordered moments in Ce layers stacked along [001], the individual layers are coupled antiferromagnetically with a +− −+type sequence. The alignment of moments within the Ce layers cannot be determined reliably from the experimental data so that two different structure models are discussed. The proposed metamagnetic transition was confirmed by diffraction experiments applying an external magnetic field at T<TN. In the interval 4 K≤T≤6 K, a relatively small field of μ0H≈0.3 T suffices to fully suppress the antiferromagnetic ordering. The effect is completely reversible yet subject to hysteresis: After switching off the external field at any T<TN the magnetic reflections gain their original intensity within several 10 min indicating the restoring of the antiferromagnetic phase. 相似文献
7.
The application of ionic liquids for the dissolution of metal oxides is a promising field for the development of more energy- and resource-efficient metallurgical processes. Using such solutions for the production of valuable chemicals or electrochemical metal deposition requires a detailed understanding of the chemical system and the factors influencing it. In the present work, several compounds are reported that crystallize after the dissolution of copper(II) oxide in the ionic liquid [Hbet][NTf2]. Dependent on the initial amount of chloride, the reaction temperature and the purity of the reagent, copper crystallizes in complexes with varying coordination geometries and ligands. Subsequently, the influence of these different complex species on electrochemical properties is shown. For the first time, copper is deposited from the ionic liquid [Hbet][NTf2], giving promising opportunities for more resource-efficient copper plating. The copper coatings were analyzed by SEM and EDX measurements. Furthermore, a mechanism for the decomposition of [Hbet][NTf2] in the presence of chloride is suggested and supported by experimental evidence. 相似文献
8.
Michael Ruck 《无机化学与普通化学杂志》2002,628(2):453-457
Ruby‐red crystals of Ag2Bi2S3Cl2 were synthesized from AgCl and Bi2S3 by cooling a melt from 770 K to room temperature. X‐ray diffraction on powders and single‐crystals revealed a triclinic crystal structure with special lattice constants (P &1macr; (No. 2), a = 1085.0(2), b = 717.2(1), c = 1137.6(1) pm, α = 89.80(1)?, β = 74.80(1)?, γ = 87.81(1)?). In the structure [BiIIIS3Cl4] polyhedra form 2[BiS3/2Cl4/4]‐ double‐layers by sharing common faces and edges. The silver(I) cations between the layers are coordinated either octahedrally by sulfide ions or tetrahedrally by sulfide and chloride ions. The deviations from the monoclinic space group P 1 21/c 1 are small and induce twinning along [010]. Further pseudosymmetry is based on the stacking of layer packages with the symmetry of the layer group P (2/c) 21/c 2/b. 相似文献
9.
Bi2S3 was dissolved in the presence of NaCl in the ionic liquid [BMIm]Cl ⋅ 4AlCl3 (BMIm=1-n-butyl-3-methylimidazolium) through annealing the mixture at 180 °C. Upon cooling to room temperature, orange, air-sensitive crystals of Na(Bi7S8)[S(AlCl3)3]2[AlCl4]2 ( 1 ) precipitated. X-ray diffraction on single-crystals of 1 revealed a triclinic crystal structure that contains (Bi7S8)5+ spiro-dicubanes, [S(AlCl3)3]2− tetrahedra triples, isolated [AlCl4]− tetrahedra, and sodium cations. 相似文献
10.
Maximilian Knies Dr. Matthias F. Groh Tobias Pietsch Mai Lê Anh Prof. Dr. Michael Ruck 《ChemistryOpen》2021,10(2):110-116
Bi2S3 was dissolved in the presence of either AuCl/PtCl2 or AgCl in the ionic liquids [BMIm]Cl ⋅ xAlCl3 (BMIm=1-n-butyl-3-methylimidazolium; x=4–4.3) through annealing the mixtures at 180 or 200 °C. Upon cooling to room temperature, orange, air-sensitive crystals of [BMIm](Bi4S4)[AlCl4]5 ( 1 ) or Ag(Bi7S8)[S(AlCl3)3]2[AlCl4]2 ( 2 ) precipitated, respectively. 1 did not form in the absence of AuCl/PtCl2, suggesting an essential role of the metal cations. X-ray diffraction on single-crystals of 1 revealed a monoclinic crystal structure that contains (Bi4S4)4+ heterocubanes and [AlCl4]− tetrahedra as well as [BMIm]+ cations. The intercalation of the ionic liquid was confirmed via solid state NMR spectroscopy, revealing unusual coupling behavior. The crystal structure of 2 consists of (Bi7S8)5+ spiro-dicubanes, [S(AlCl3)3]2− tetrahedra triples, isolated [AlCl4]− tetrahedra, and heavily disordered silver(I) cations. No cation ordering took place in 2 upon slow cooling to 100 K. 相似文献