By replacing Mn in YCa3(MnO)3(BO3)4 with trivalent Al and Ga, two new borates with the compositions of YCa3(MO)3(BO3)4 (M=Al, Ga) were prepared by solid-state reaction. Structure refinements from X-ray powder diffraction data revealed that both of them are isostructural to gaudefroyite with a hexagonal space group P63/m. Cell parameters of a=10.38775(13)Å, c=5.69198(10)Å for the Al-containing compound and a=10.5167(3)Å, c=5.8146(2)Å for the Ga analog were obtained from the refinements. The structure is constituted of AlO6 or GaO6 octahedral chains interconnected by BO3 groups in the ab plane to form a Kagomé-type lattice, leaving trigonal and apatite-like tunnels. It is found that most rare-earth and Cr, Mn ions can be substituted into the Y3+ and M3+ sites, respectively, and the preference of rare-earth ions to locate in the trigonal tunnel is correlated to the sizes of the M3+ ions. 相似文献
A new ruthenium-rhodium mixed-metal cluster HRuRh3(CO)12 and its derivatives HRuRh3(CO)10(PPh3)2 and HRuCo3(CO)10(PPh3)2 have been synthesized and characterized. The following crystal and molecular structures are reported: HRuRh3(CO)12: monoclinic, space group P21/c, a 9.230(4), b 11.790(5), c 17.124(9) Å, β 91.29(4)°, Z = 4; HRuRh3(CO)10(PPh3)2·C6H14: triclinic, space group P, a 11.777(2), b 14.079(2), c 17.010(2) Å, α 86.99(1), β 76.91(1), γ 72.49(1)°, Z = 2; HRuCo3(CO)10(PPh3)2·CH2Cl2: triclinic, space group P, a 11.577(7), b 13.729(7), c 16.777(10) Å, α 81.39(4), β 77.84(5), γ 65.56°, Z = 2. The reaction between Rh(CO)4? and (Ru(CO)3Cl2)2 tetrahydrofuran followed by acid treatment yields HRuRh3(CO)12 in high yield. Its structural analysis was complicated by a 80–20% packing disorder. More detailed structural data were obtained from the fully ordered structure of HRuRh3(CO)10(PPh3)2, which is closely related to HRuCo3(CO)10(PPh3)2 and HFeCo3(CO)10(PPh3)2. The phosphines are axially coordinated. 相似文献
Two new compounds Pd2Os3(CO)12
, 13 and Pd3Os3(CO)12
, 14 have been obtained from the reaction of
with Os3(CO)12 at room temperature. The products were formed by the addition of two and three
groups to the Os–Os bonds of Os3(CO)12. Compounds 13 and 14 interconvert between themselves by intermolecular exchange of the
groups in solution. Compounds 13 and 14 have been characterized by single crystal X-ray diffraction analyses.Dedicated to Professor Brian F. G. Johnson on the occasion of his retirement – 2005. 相似文献
The thermal decomposition reactions were determined for [Co(en)3](N03)3 and [Co(en)3(HSO4)3 in a dynamic nitrogen gas atmosphere and vacuo, where en represents ethylenediamine. Data were obtained using thermogravimetry, DTA, thermomagnetic analysis, and mass spectrometry. The dissociation reactions in nitrogen were found to be as follows: and In vacuo, the dissociation process for [Co(en)3](N03)3 is the same as in nitrogen. Also, the decomposition of [Co(en)3](HSO4)3 is the same except for the first step which is: 相似文献
The magnetic properties of Cu(NH3)4(NO3)2 have been measured at low temperatures. Broad maxima in both the susceptibility and specific heat are observed and are consistent with linear chain behavior of a Heisenberg antiferromagnet, with J/k = 3.9 ± 0.1 K. Long-range order sets in at Tc = 0.15 ± 0.01 K, and the ratio kTc/|J| = 0.038 is the lowest observed as yet for a one-dimensional, S = 1/2 antiferromagnet. 相似文献
The nitrosation of Na[W(CO)5CN] using amyl nitrite and sulphuric acid in a two phase water— diethyl ether system gives the trinuclear compound W3(μCN)3(NO)3(CO)9. A single crystal X-ray diffraction study showed that the compound contains a nine-membered ring of three tungsten atoms and three bridging cyanide groups. The terminal carbonyl and nitrosyl ligands were not distinguishable. 相似文献
The thermolysis of complexes [Co(NH3)6][Fe(CN)6] and [Co(NH36]4[Fe(CN)6]3 under an air or hydrogen atmosphere at 200, 350, and 500°C is studied. The composition and properties of thermolysis products
are determined. The oxidative thermolysis yields mixtures of oxides of the central metals; the reductive thermolysis yields
intermetallic compounds CoFe. The density of the complexes and the specific surface area of the intermetallic compounds are
measured. Average particle sizes are calculated. The morphology and dispersion of the powders are dictated by the shape and
density of the crystals of the precursor double salts and the thermolysis temperature. The thermolysis chemism in the oxidative
and reductive atmospheres is discussed in the context of the nature of the complex anion.
Original Russian Text ? S.I. Pechenyuk, D.P. Domonov, D.L. Rogachev, A.T. Belyavskii, 2007, published in Zhurnal Neorganicheskoi
Khimii, 2007, Vol. 52, No. 7, pp. 1110–1115. 相似文献
Electrical conductivities were measured for the ternary systems Y(NO3)3+La(NO3)3+H2O, La(NO3)3+Ce(NO3)3+H2O, La(NO3)3+Nd(NO3)3+H2O, and their binary subsystems Y(NO3)3+H2O, La(NO3)3+H2O, Ce(NO3)3+H2O, and Nd(NO3)3+H2O at (293.15, 298.15 and 308.15) K. The measured conductivities were used to test the generalized Young’s rule and the semi-ideal
solution theory. The comparison results show that the generalized Young’s rule and the semi-ideal solution theory can yield
good predictions for the conductivities of the ternary electrolyte solutions, implying that the conductivities of aqueous
solutions of (1:3 + 1:3) electrolyte mixtures can be well predicted from those of their constituent binary solutions by the
simple equations. 相似文献
X-ray crystallographic analyses of H2Os3(CO)10, H(SC2H5)Os3(CO)10 and (OCH3)2Os3(CO)10 are reported. Although hydrogen atom positions have not been located, the essential isostructural nature of the three commplexes establishes the hydride ligands as bridging two metal atoms, separated by 2.670 Å, with a formal bond order of two; the bridging hydrido- and thiolato-ligands span an osmium---osmium bond of length 2.863 Å and formal bond order one; the two μ-methoxy ligands bridge two metal atoms separated by 3.078 Å which, by simple 18 electron rule counting, has a metal---metal bond order of zero. Some general comments are made on the structures of polynuclear transition metal carbonyls. 相似文献
Phase equilibria in the Ba3(VO4)2-K2Ba(MoO4)2 and Pb3(VO4)2-K2Pb(MoO4)2 systems have been investigated. In the first system, a continuous series of substitutional solid solutions with the palmierite
structure is formed, and in the second one, the polymorphic transition in lead orthovanadate at 100°C restricts the extent
of the palmierite-type solid solution to 10–100 mol % K2Pb(MoO4)2.
Original Russian Text ? V.D. Zhuravlev, Yu.A. Velikodnyi, A.S. Vinogradova-Zhabrova, A.P. Tyutyunnik, V.G. Zubkov, 2008, published
in Zhurnal Neorganicheskoi Khimii, 2008, Vol. 53, No. 10, pp. 1746–1748. 相似文献
