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21.
Zusammenfassung Das -Isomer des Antimontribenzoats kristallisiert rhomboedrisch (hexagonale Aufstellung) in der Raumgruppe R3 mita=1944.0 pm,c=422.3 pm undZ=3. Die Moleküle sind parallel zu 001 gestapelt. Sb hat gegenüber O die Koordinationszahl 3+3 (Sb-O: 208 bzw. 256 pm).
Antimonytribenzoate
Summary The isomer of (C6H5CO2)3Sb crystallizes rhombohedrally (hexagonal axes) in the space group R3 witha=1944.0 pm,c=422.3 pm, andZ=3. The molecules are stacked parallel to 001; Sb has a coordination number of 3+3 (Sb-O: 208 and 256 pm, resp.).相似文献
22.
《Surface and interface analysis : SIA》2004,36(7):654-657
The mineral chemistry of enargite surfaces and near‐surfaces prepared by fracture within an ultrahigh vacuum are investigated using XPS and synchrotron radiation XPS (SRXPS). The purpose of the study is to identify surface core‐level line positions in high‐resolution photoelectron spectra. The XPS spectra obtained using monochromatic Al Kα radiation show that there are near‐identical monosulphide line positions in S 2p spectra for the As–S and Cu–S bonds in enargite. The SRXPS spectra for sulphur are remarkably similar to the XPS spectra for sulphur, showing that there is minimal difference in the chemical environment between sulphur atoms at the surface and in the mineral matrix. The Cu 2p XPS data have only cuprous contributions and a minor surface contribution. The surface Cu contribution is observed as a high‐binding‐energy tail in the Cu 2p3/2 spectrum. The As 3d data for both XPS and SRXPS show contributions from arsenic atoms at the surface and in the bulk mineral matrix. The surface contribution is distinct and is found 1 eV below the bulk contribution. The results of the study suggest that, following fracture, the enargite surface is reorganized in such a manner that the surface is characterized by protrusions of individual arsenic atoms. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
23.
24.
Heterometallic Complexes with E6 Ligands (E = P, As) The reaction of [Cp*Co(μ-CO)]2 1 with the sandwich complexes [Cp*Fe(η5-E5)] 2 a: E = P, 2 b: E = As in decalin at 190°C affords besides [CpCo2E4] 4: E = P, 7: E = As and [CpFe2P4] 5 the trinuclear complexes [(Cp*Fe)2(Cp*Co)(μ-η2-P2)(μ3-η1:2:1-P2)2] 3 as well as [(Cp*Fe)2(Cp*Co)(μ3-η2:2:2-As3)2] 6 . With [Mo(CO)5(thf)] 3 and 6 form in a build-up reaction the tetranuclear clusters [(Cp*Fe)2(Cp*Co)E6{Mo(CO)3}] 10: E = P, 11: E = As. 3, 6 and 11 have been further characterized by an X-ray crystal structure determination. 相似文献
25.
S. Cattarin M.M. Musiani U. Casellato P. Guerriero R. Bertoncello 《Journal of Electroanalytical Chemistry》1995,380(1-2)
In+As+Sb alloys have been deposited onto Ni and Ti cathodes from tartaric acid solutions at pH 2. Homogeneous deposits of composition suitable for achieving InAsxSb1−x can be obtained from this medium. The As-to-Sb ratio can be controlled by properly selecting solution composition and deposition potential.X-ray photoelectron spectroscopy and X-ray diffraction analyses show that formation of III–V compounds occurs at room temperature. In reacts preferentially with As rather than with Sb, but crystalline phases formed at room temperature are Sb-rich. After annealing the In+As+Sb alloys at 250°C, the composition calculated from cell parameters appears similar to that measured by energy-dispersive X-ray analysis, suggesting that the entire deposit has been converted into the InAsxSb1−x crystalline phase. 相似文献
26.
Ralf Garbe Jürgen Pebler Kurt Dehnicke Dieter Fenske Helmut Goesmann Gerhard Baum 《无机化学与普通化学杂志》1994,620(4):592-598
Phosphorane Iminato Complexes of Antimony. The Crystal Structures of [Sb2Cl5(NPMe3)2][SbCl6] · CH3CN and [SbCl(NPPh3)]2[SbCl6]2 · 6 CH3CN The title compounds are formed by reaction of antimony pentachloride in acetonitrile solution with the phosphorane iminato complexes SbCl2(NPMe3) and SbCl2(NPPh3), respectively, which themselves are synthesized by reaction of antimony trichloride with Me3SiNPR3 (R = Me, Ph). The complexionic compounds are characterized by 121Sb Mössbauer spectroscopy and by crystal structure determinations. [Sb2Cl5(NPMe3)2][SbCl6] · CH3CN: Space group P41, Z = 4, 3 698 observed unique reflections, R = 0.022. Lattice dimensions at ?60°C: a = b = 1 056.0(1), c = 2 709.6(2) pm. The structure consists of SbCl6? ions and cations [Sb2Cl5(NPMe3)2(CH3CN)]+, in which one SbIII atom and one SbV atom are bridged by the N atoms of the phosphorane iminato ligands. [SbCl(NPPh3)]2[SbCl6]2 · 6 CH3CN: Space group P1 , Z = 2, 5 958 observed unique reflections, R = 0.033. Lattice dimensions at ?60°C: a = 989.4(11), b = 1 273(1), c = 1 396(1) pm, α = 78.33(7), β = 77.27(8)°, γ = 86.62(8)°. The structure consists of SbCl6? ions and centrosymmetric cations [SbCl(NPPh3)(CH3CN)2]22+, in which the antimony atoms are bridged by the N atoms of the phosphorane iminato ligands. 相似文献
27.
A novel and simple flow-based method was developed for the simultaneous determination of As(III) and As(V) in freshwater samples. Two miniature columns with a solid phase anion exchange resin, placed on two 6-way valves were utilized for the solid-phase collection/concentration of arsenic(III) and arsenic(V), respectively. As(III) could be retained on the column after its oxidation to As(V) species with an oxidizing agent. The collected analytes were then sequentially eluted by 2 M nitric acid and introduced into ICP-AES. Potassium permanganate was examined as potential oxidizing agent for conversion of As(III) to As(V). The standard deviation of the analytical signals (peak height) for the replicate analysis (n = 5) of 0.5 μg l−1 solution were 3 and 5% for As(III) and As(V), respectively. The limit of detection (3σ) for both As(III) and As(V) were 0.1 μg l−1. The proposed system produced satisfactory results on the application to the direct analysis of inorganic arsenic species in freshwater samples. 相似文献
28.
29.
The mutual influence of the atoms on the composition of solid fluorine-containing antimony(iii) complexes formed in aqueous solutions in the (MF)
x
−(M′F)
n−x
−SbF3 (M, M′=Na, K, Rb, Cs, and NH4;n=1, 2;x=0 to 2), (KNO2)
n
−(KY)
n
−SbF3 (Y=F, Cl, SO4;n=0.5, 1), and K2SbF5−K2SbCl5 systems was investigated by elemental, X-ray, and thermogravimetric analyses and by IR and121,123Sb NQR spectroscopy. The isomorphism conditions for fluorine-containing antimony(iii) compounds resulting in the formation of complexes NaM′SbF5·1.5H2O (M′=K and Rb), K2SbF5·1.5H2O, NaCs3Sb4F16·H2O, KsbF3Cl, K2SbF2Cl3 with constant compositions, continuous M
x
M′2−x
SbF5 (0<x<2) and limited M
x
M′1−x
SbF4 (0.25<x<0.75; M, M′=K, Rb, Cs, and NH4) solid solutions or LiF+MSbF4 (M=Na, K, Rb, and Cs), M2SbF5+Cs2SbF5 (M=Na and K) and MSbF4+NaSbF4 (M=Rb and NH4) mechanical mixtures were determined.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 103–108, January, 1999. 相似文献
30.
Isabel Pizarro Ma Milagros Gomez Carmen Cámara Ma Antonia Palacios 《International journal of environmental analytical chemistry》2013,93(10):879-890
Gradient ion chromatographic separation coupled with ICP-MS was used to resolve and determine the most common arsenic species in environmental and biological samples of carrots, trout, soil, sediment and river water from Region II of Chile. The carrot and trout samples showed a concentration of 49 and 168 µg g?1, respectively, of total As. Both concentrations are high considering the basal level. In the carrots, percentage of 45 and 31% of total As were found for As(III) and As(V) species, respectively. In the trout, the higher concentration related to AsB at 39% of the total As. As(III) and DMA were also present in relatively high concentrations. The River Loa and the soil in which the carrots are growing also present very high As(V) concentrations of 100 and 17 µg g?1, respectively. The ratio between the concentration for the same As species found in the living organisms (carrots and trout) and the environment in which they grow (soil and water) can provide important information about the possible absorption or biotransformation of As species in living beings. As(III) and DMA are the species in which the greatest accumulation occurs with respect to the medium in which they are present, and biotransformation also appears to take place. 相似文献