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1.
Reaction of Rhenium(VII) Oxide with 1,4-Dioxane. Re2O62-OH)2 · 3 C4H8O2— a Novel Oxide Hydroxide with Metal-(1,4-Dioxane) Bonds The reaction of Re2O7 with 1,4-dioxane in the presence of small amounts of H2O yields the compound Re2O6(OH)2 · 3(1,4-dioxane). It crystallizes in the triclinic space group P¯1 with a = 10.907(3), b = 12.875(4), c = 7.943(2) Å; α = 108.64(2), β = 103.00(2), γ = 102.29(2)°; Z = 2. The complete X-ray structure analysis (R = 2.9? ) shows the crystals to contain dimeric centrosymmetric Re2O6(OH)2-units with two bridging μ2-OH groups. The ligand spheres around Re are completed towards distorted octahedra by coordinated 1,4-dioxane molecules (one O donor per Re), the latter linking the dimeric units to endless chains. The rest of the 1,4-dioxane molecules are bonded to the OH-groups through hydrogen bridges and have no contact to Re. Mean bond distances are: Re? O(bridge) 2.065 (2.059…2.070(4)) Å, Re? O(1,4-dioxane) 2.478 (2.469 and 2.486(5)) Å, Re? O (terminal) 1.707 (1.694…1.720(5)) Å.  相似文献   

2.
Salts of Halogenophosphoric Acids. XIX. Preparation of Copper(II) Monofluorophosphate Solvates and the Crystal Structure of Aquamonofluorophosphatocopper(II)-1,4-Dioxane 2/1, 2[Cu(H2O)PO3F] · C4H8O2 The mixed solvate Aquamonofluorophosphatocopper(II)-1,4-Dioxane 2/1 1 was obtained by the reaction of aqueous solutions of NH4HPO3F and acidified (NH4)2PO3F, respectively, using 1,4-dioxane as precipitating agent. 1 crystallizes in the monoclinic space group C2/m with a = 2130.9(2), b = 655.45(6), c = 447.30(4) pm, b? = 96.207(7)° and Z = 2. Copper(II) monofluorophosphate-methanol 1/1, CuPO3F · CH3OH 2 was obtained by the reaction of copper(II) salts with alkaline or ammoniummonofluorophosphates in methanol. 1 and 2 react in the presence of water vapor to copper(II) monofluoro phosphate dihydrate, CuPO3F · 2H2O 3 , which reacts reversibly with dioxan or CH3OH under formation of 1 and 2 , respectively.  相似文献   

3.
Synthesis of [Cu(m-HBH)2(OH2)2](NO3)2·2H2O, where m-HBH = C7H8O2N2 (3-hydroxybenzoylhydrazine), is described. The structure of the compound was studied by X-ray phase analysis and IR spectroscopy; crystal data are a = 57.415(6) Å, b = 19.760(2) Å, c = 7.586(2) Å; Fdd 2, Z = 16, R(F) = 0.053. The compound consists of [Cu(m-HBH)2(OH2)2]2+ complex cations, NO 3 ? anions, and two water molecules. The similarity between the IR spectra of Cu(m-HBH)2(NO3)2·nH2O and Co(m-HBH)2(NO3)2·5H2O, element analysis data, and crystal data obtained at the first stage of X-ray analysis show that the structures and compositions of these compounds are identical relative to the type of surroundings of the central atom. In contrast to the cobalt compound [Co(m-HBH)2(OH2)2](NO3)2·3H2O, in which the cobalt atom has a nearly regular octahedron as a coordination polyhedron, the copper(II) compound has a square bipyramid around the copper atom; c.n. is 6 = 4 + 2 (planar distances: 2.013(2) Å, 2.021(2) Å, 2.033(3) Å, 2.087(3) Å; axial distances: 2.367(3) Å, 2.374(3) Å) and lacks one crystallization water molecule.  相似文献   

4.
Reactions of 1,10‐phenanthroline monohydrate, Na2C4H4O4 · 6 H2O and MnSO4 · H2O in CH3OH/H2O yielded a mixture of [Mn2(H2O)4(phen)2(C4H4O4)2] · 2 H2O ( 1 ) and [Mn(phen)2(H2O)2][Mn(phen)2(C4H4O4)](C4H4O4) · 7 H2O ( 2 ). The crystal structure of 1 (P1 (no. 2), a = 8.257(1) Å, b = 8.395(1) Å, c = 12.879(2) Å, α = 95.33(1)°, β = 104.56(1)°, γ = 106.76(1)°, V = 814.1(2) Å3, Z = 1) consists of the dinuclear [Mn2(H2O)4(phen)2(C4H4O4)2] molecules and hydrogen bonded H2O molecules. The centrosymmetric dinuclear molecules, in which the Mn atoms are octahedrally coordinated by two N atoms of one phen ligand and four O atoms from two H2O molecules and two bis‐monodentate succinato ligands, are assembled via π‐π stacking interactions into 2 D supramolecular layers parallel to (101) (d(Mn–O) = 2.123–2.265 Å, d(Mn–N) = 2.307 Å). The crystal structure of 2 (P1 (no. 2), a = 14.289(2) Å, b = 15.182(2) Å, c = 15.913(2) Å, α = 67.108(7)°, β = 87.27(1)°, γ = 68.216(8)°, V = 2934.2(7) Å3, Z = 2) is composed of the [Mn(phen)2(H2O)2]2+ cations, [Mn(phen)2(C4H4O4)] complex molecules, (C4H4O4)2– anions, and H2O molecules. The (C4H4O4)2– anions and H2O molecules form 3 D hydrogen bonded network and the cations and complex molecules in the tunnels along [001] and [011], respectively, are assembled via the π‐π stacking interactions into 1 D supramolecular chains. The Mn atoms are octahedrally coordinated by four N atoms of two bidentate chelating phen ligands and two water O atoms or two carboxyl O atoms (d(Mn–O) = 2.088–2.129 Å, d(Mn–N) = 2.277–2.355 Å). Interestingly, the succinato ligands in the complex molecules assume gauche conformation bidentately to chelate the Mn atoms into seven‐membered rings.  相似文献   

5.
The adducts [Cp2Y(μ-Cl)]2 · 2THF (5), {[Cp2Y(μ-Cl)]2 · 1,4-dioxane}n (6), and Cp2Y(DME)(μ-Cl)(Cl)YCp2 (7) have been synthesized and studied by X-ray crystallography. In 5, the (Cp2YCl)2 moiety is coordinated to two THF molecules (d (Y-O) = 2.478 Å); in 6 the (Cp2YCl)2 dimers are linked by 1,4-dioxane to form a polymer chain (d (Y-O) = 2.601 Å). In asymmetric adduct 7, the DME molecule is bound through both O atoms to the same Y atom (d (Y-O) = 2.382 and 2.448 Å), and one of the chlorine atoms is bridging and the other chlorine atom is terminal.  相似文献   

6.
Coordination-chemistry of cis-Trioxotungsten(VI) Complexes. Crystal Structures of LWO3 · 3 H2O, [L′WO2(OH)]Br, [LWO2Br]Br, [L2W2O5](S2O6) · 4 H2O and [LWO2(μ-O)WO(O2)2(OH2)] (L = 1,4,7-Triazacyclonane; L′ = 1,4,7-Trimethyl-1,4,7-triazacyclononane) The cyclic triamines 1,4,7-triazacyclononane (L; C6H15N3) and 1,4,7-trimethyl-1,4,7-triazacyclononane (L′; C9H21N3) react in aqueous solution with WO3 affording LWO3 · 3 H2O, 1 , and L′WO3 · 3 H2O, respectively, which yield [L′WO2(OH)]Br, 2 , and [LWO2Br]Br, 3 , in concentrated HBr solutions. In aqueous CH3SO3H solution 1 dimerizes. The iodide and dithionate 4 salts of [L2W2O5]2+ have been isolated. In 35% H2O2 complex 1 yields the neutral species [LWO2(μ-O)WO(O2)2(H2O)] 5 . The crystal structures of 1 – 5 have been determined by X-ray analysis. Crystal data: 1 : P21/c; a = 7.729(2), b = 14.887(3), c = 10.774(2) Å, β = 90.77(2)°, Z = 4; 2 : Cc; 8.910(3), b = 12.220(6), c = 13.279(6) Å, β = 101.31(3)°, Z = 4; 3 : Cmc21, a = 8.857(5), b = 12.062(7), c = 11.218(7) Å, Z = 4; 4 : Cc, a = 17.601(7), b = 12.906(7), c = 14.107(8) Å, β = 124.08(4)°, Z = 4; 5 : P212121; a = 8.452(4), b = 11.301(6), c = 13.750(6) Å, Z = 4.  相似文献   

7.
The compound (NH4)2[Re2(HPO4)4 · 2H2O] has been synthesized and characterized by electronic and vibrational spectroscopy. The molecular structure has been determined by X-ray diffraction (MoK α radiation, λ = 0.71073 Å). The (NH4)2[Re2(HPO4)4 · 2H2O] coordination units form centrosymmetrical binuclear ordering with each metal atom being coordinated in a distorted octahedron incorporating one rhenium atom, one oxygen atom of the water molecule, and four phosphate oxygen atoms in the equatorial plane. The rhenium-rhenium bond length (2.2207 Å) corresponds to a quadruple bond between the atoms. The [Re2(HPO4)4 · 2H2O]2- complex anions in the crystal are associated through strong hydrogen bonds formed by the phosphate O-H···O groups. The stability of dirhenium(III) tetra-μ-phosphates in aqueous solutions is considered.  相似文献   

8.
Reactions of a freshly prepared Zn(OH)2‐2x(CO3)x · yH2O precipitate, phenanthroline with azelaic and sebacic acid in CH3OH/H2O afforded [Zn(phen)(C9H15O4)2] ( 1 ) and [Zn2(phen)2(H2O)2(C10H16O4)2] · 3H2O ( 2 ), respectively. They were structurally characterized by X‐ray diffraction methods. Compound 1 consists of complex molecules [Zn(phen)(C9H15O4)2] in which the Zn atoms are tetrahedrally coordinated by two N atoms of one phen ligand and two O atoms of different monodentate hydrogen azelaato groups. Intermolecular C(alkyl)‐H···π interactions and the intermolecular C(aryl)‐H···O and O‐H···O hydrogen bonds are responsible for the supramolecular assembly of the [Zn(phen)(C9H15O4)2] complexes. Compound 2 is built up from crystal H2O molecules and the centrosymmetric binuclear [Zn2(phen)2(H2O)2(C10H16O4)2] complex, in which two [Zn(phen)(H2O)]2+ moieties are bridged by two sebacato ligands. Through the intermolecular C(alkyl)‐H···O hydrogen bonds and π‐π stacking interactions, the binuclear complex molecules are assembled into layers, between which the lattice H2O molecules are sandwiched. Crystal data: ( 1 ) C2/c (no. 15), a = 13.887(2), b = 9.790(2), c = 22.887(3)Å, β = 107.05(1)°, U = 2974.8(8)Å3, Z = 4; ( 2 ) P1¯ (no. 2), a = 8.414(1), b = 10.679(1), c = 14.076(2)Å, α = 106.52(1)°, β = 91.56(1)°, γ = 99.09(1)°, U = 1193.9(2)Å3, Z = 1.  相似文献   

9.
Crystal Structure of CaZn2(OH)6 · 2 H2O The electrochemical oxidation of zinc in a zinc/iron-pair leads in an aqueous NH3 solution of calciumhydroxide at room temperature to colourless crystals of CaZn2(OH)6 · 2 H2O. The X-ray structure determination was now successful including all hydrogen positions. P21/c, Z = 2, a = 6.372(1) Å, b = 10.940(2) Å, c = 5.749(2) Å, β = 101.94(2)° N(F ≥ 3σF) = 809, N(Var.) = 69, R/RW = 0.011/0.012 The compound CaZn2(OH)6 · 2H2O contains Zn2+ in tetrahedral coordination by OH? and Ca2+ in octahedral coordination by four OH? and two H2O. The tetrahedra around Zn2+ form corner sharing chains, three-dimensionally linked by isolated polyhedra around Ca2+. Weak hydrogen bridge bonds result between H2O as donor and OH?.  相似文献   

10.
The solid‐state‐melt reaction of (NH4)2[Re2F8] · 2H2O with 2‐hydroxypyridine (2‐HOpy) produced dark‐red Re2(2‐Opy)4F2 ( 1 ). This air‐stable compound was obtained in crystalline form as 1· CHCl3. It was characterized in the solid state by single‐crystal X‐ray diffraction and in solution by UV/Vis spectroscopy and cyclic voltammetry. 1· CHCl3 forms triclinic crystals with α = 8.3254(5) Å, b = 8.5563(5) Å, c = 11.6784(8) Å, α = 82.723(3)°, β = 75.769(3) °, γ = 64.407(2) °. The Re–Re and Re–F distances were 2.2091(7) and 2.115(6) Å, respectively. The molecule is isostructural with the corresponding chloro derivative.  相似文献   

11.
Single crystals of 1-cyclohexylpiperazine-1,4-diium dichromate(VI), (C10H22N2)[Cr2O7], were obtained by slow evaporation at room temperature from an aqueous solution of potassium dichromate, hydrochloric acid and 1-cyclohexylpiperazine. (C10H22N2)[Cr2O7] is triclinic (P\(\bar 1\)) with a = 10.351(2) Å, b = 12.766(3) Å, c = 6.111(1) Å, α = 91.50(2)°, β = 104.26(3)°, γ = 94.91(2)°, V = 778.8(3) Å3, and Z = 2. The structure determination performed from single crystal X-ray diffraction data leads to R1/wR2 reliability factors of 0.032/0.078. The asymmetric unit of the title salt C10H22N22+·Cr2O72?, consists of one 1-cyclohexylpiperazine-1,4-diium dication and one dichromate dianion. These entities are linked together by N–H···O hydrogen bonds to form {(C10H22N2)[Cr2O7]}n infinite chains lying parallel to the (100) plane and running along the c axis. The intermolecular N–H···O hydrogen bonds link these chains into a two-dimensional network structure consolidated through C–H···O weak interactions.  相似文献   

12.
Light‐yellow single crystals of the mixed‐valent mercury‐rich basic nitrate Hg8O4(OH)(NO3)5 were obtained as a by‐product at 85 °C from a melt consisting of stoichiometric amounts of (HgI2)(NO3)2·2H2O and HgII(OH)(NO3). The title compound, represented by the more detailed formula HgI2(NO3)2·HgII(OH)(NO3)·HgII(NO3)2·4HgIIO, exhibits a new structure type (monoclinic, C2/c, Z = 4, a = 6.7708(7), b = 11.6692(11), c = 24.492(2) Å, β = 96.851(2)°, 2920 structure factors, 178 parameters, R1[F2 > 2σ(F2)] = 0.0316) and is made up of almost linear [O‐HgII‐O] and [O‐HgI‐HgI‐O] building blocks with typical HgII‐O distances around 2.06Å and a HgI‐O distance of 2.13Å. The Hg22+ dumbbell exhibits a characteristic Hg‐Hg distance of 2.5079(7) Å. The different types of mercury‐oxygen units form a complex three‐dimensional network exhibiting large cavities which are occupied by the nitrate groups. The NO3? anions show only weak interactions between the nitrate oxygen atoms and the mercury atoms which are at distances > 2.6Å from one another. One of the three crystallographically independent nitrate groups is disordered.  相似文献   

13.
A new ammonium vanadium tellurate, (NH4)4{(VO2)2[Te2O8(OH)2]}·2H2O ( 1 ) was hydrothermally synthesized and characterized by elemental analyses, IR spectrum, TG analysis, and single crystal X–ray diffraction. Compound 1 crystallizes in the monoclinic system, space group P21/n, a = 7.3843(15) Å, b = 17.111(3) Å, c = 7.3916(15) Å, β = 118.88(3)°, V = 817.9(3) Å3, Z = 2, R1 (I>2σ(I)) = 0.0235, wR2 (all data) = 0.0462. The structure of 1 consists of infinite anionic chains, {(VO2)2[Te2O8(OH)2]}4? which contain octahedral VO6 and TeO5OH units. Each octahedral VO6 and TeO5OH unit is connected by sharing an edge to form V2O10 and Te2O8(OH)2 binuclear units. The V2O10 and Te2O8(OH)2 binuclear units are alternatively connected to one another, creating complete infinite {(VO2)2[Te2O8(OH)2]}4? chains along the c direction. The anionic chains are separated by ammonium cations and water molecules that link the chains through a network of hydrogen bonds. In addition, the structure contains an extended network of O–H·····O hydrogen bonds between the chains.  相似文献   

14.
Pale pink crystals of Nd2(SeO3)2(SeO4) · 2H2O were synthesized under hydrothermal conditions from H2SeO3 and Nd2O3 at about 200 °C. X‐ray diffraction on powder and single‐crystals revealed that the compound crystallizes with the monoclinic space group C 2/c (a = 12.276(1) Å, b = 7.0783(5) Å, c = 13.329(1) Å, β = 104.276(7)°). The crystal structure of Nd2(SeO3)2(SeO4) · 2H2O is an ordered variant of the corresponding erbium compound. Eight oxygen atoms coordinate the NdIII atom in the shape of a bi‐capped trigonal prism. The oxygen atoms are part of pyramidal (SeIVO3)2? groups, (SeVIO4)2? tetrahedra and water molecules. The [NdO8] polyhedra share edges to form chains oriented along [010]. The selenate ions link these chains into layers parallel to (001). The layers are interconnected by the selenite ions into a three‐dimensional framework. The dehydration of Nd2(SeO3)2(SeO4) · 2H2O starts at 260 °C. The thermal decomposition into Nd2SeO5, SeO2 and O2 at 680 °C is followed by further loss of SeO2 leaving cubic Nd2O3.  相似文献   

15.
Reaction of MnSO4 · H2O, 2,2′‐bipyridine (bpy), suberic acid and Na2CO3 in CH3OH/H2O yielded a mixture of [Mn2(H2O)4(bpy)2(C8H12O4)2] · 2 H2O ( 1 ) and [Mn(H2O)2‐ (bpy)(C8H12O4)2/2] · H2O ( 2 ). In both complexes, the Mn atoms are octahedrally coordinated by two N atoms of one bpy ligand and four O atoms of two trans positioned H2O molecules and two suberato ligands (d(Mn–O) = 2.107–2.328 Å; d(Mn–N) = 2.250–2.330 Å). The bis‐monodentate suberato ligands bridge Mn atoms to form dinuclear [Mn2(H2O)4(bpy)2(C8H12O4)2] complex molecules in 1 and 1D [Mn(H2O)2(bpy)(C8H12O4)2/2] chains in 2 . Via the intermolecular hydrogen bondings and π‐π stacking interactions, the dinuclear molecules in 1 are assembled into 2D networks parallel to (100), between which the crystal H2O molecules are sandwiched. The polymeric chains in 2 are linked together by interchain hydrogen bonding and π‐π stacking interactions into 3D networks with the crystal H2O molecules located in tunnels along [010]. Crystal data for 1 : P21/c (no. 14), a = 10.092(1) Å, b = 11.916(2) Å, c = 17.296(2) Å, β = 93.41(1)° and Z = 2. Crystal data for 2 : P21/c (no. 14), a = 11.176(2) Å, b = 9.688(1) Å, c = 37.842(6) Å, β = 90.06(1)° and Z = 8.  相似文献   

16.
Structure and Thermal Behaviour of Gadolinium(III)-sulfate-octahydrate Gd2(SO4)3 · 8 H2O . Gd2(SO4)3 · 8 H2O crystallizes monoclinic with space group C2/c and the lattice constants a = 13.531(7), b = 6.739(2), c = 18.294(7) Å, β = 102.20(8)°. In the structure Gd is coordinated by 4 oxygen atoms of crystal water and 4 oxygens of sulfate giving rise to a distorted square antiprism. During DTA-TG-experiments the title compound first loses crystal water in a two-step mechanism in the temperature range 130–306°C. The resulting Gd2(SO4)3 is amorphous and recrystallization occurs in the range 380–411°C. The so-obtained low-temperature modification β-Gd2(SO4)3, undergoes a monotropic phase transition at about 750°C to the high-temperature form α-Gd2(SO4)3. The powder pattern of this modification was indexed based on monoclinic symmetry with space group C2/c and lattice constants a = 9.097(3), b = 14.345(5), c = 6.234(2) Å, β = 97.75(8)°. The hightemperature modification of gadolinium-sulfate shows decomposition to Gd2O2SO4 at 900°C and, subsequently, decomposition at 1 200°C yields the formation of C-Gd2O3.  相似文献   

17.
Two novel As‐V‐O cluster supported transition metal complexes, [Zn(en)2][Zn(en)2(H2O)2][{Zn(en)(enMe)}As6V15O42(H2O)]·4H2O ( 1 ) and [Zn2(enMe)2(en)3][{Zn(enMe)2}As6V15O42(H2O)]·4H2O ( 2 ), have been hydrothermally synthesized. The single X‐ray diffraction studies reveal that both compounds consist of discrete noncentral polyoxoanions [{Zn(en)(enMe)}As6V15O42(H2O)]4? or [{Zn(enMe)2}As6V15O42(H2O)]4? cocrystallized with respective zinc coordination complexes. Interestingly, compounds 1 and 2 exhibit the first two polyoxovanadates containing As8V15O42‐(H2O)]6? cluster decorated by only one transition metal complex. Crystal data: 1 , monoclinic, P21/n, a = 14.9037(4) Å, b = 18.1243(5) Å, c = 27.6103(7) Å, β = 105.376(6)°, Z = 4; 2 monoclinic, P21/n, a = 14.9786(7) Å, b = 33.0534(16) Å, c = 14.9811(5) Å, Z = 4.  相似文献   

18.
Contributions on Crystal Chemistry and Thermal Behaviour of Anhydrous Phosphates. XXXIII [1] In2P2O7 an Indium(I)‐diphosphatoindate(III), and In4(P2O7)3 — Synthesis, Crystallization, and Crystal Structure Solid state reactions via the gas phase lead to the new mixed‐valence indium(I, III)‐diphosphate In2P2O7. Colourless single crystals of In2P2O7 have been grown by isothermal heating of stoichiometric amounts of InPO4 and InP (800 °C; 7d) using iodine as mineralizer. The structure of In2P2O7 [P21/c, a = 7.550(1) Å, b = 10.412(1) Å, c = 8.461(2) Å, b = 105.82(1)°, 2813 independent reflections, 101 parameter, R1 = 0.031, wR2 = 0.078] is the first example for an In+ cation in pure oxygen coordination. Observed distances d(InI‐O) are exceptionally long (dmin(InI‐O) = 2.82 Å) and support assumption of mainly s‐character for the lone‐pair at the In+ ion. Single crystals of In4(P2O7)3 were grown by chemical vapour transport experiments in a temperature gradient (1000 → 900 °C) using P/I mixtures as transport agent. In contrast to the isostructural diphosphates M4(P2O7)3 (M = V, Cr, Fe) monoclinic instead of orthorhombic symmetry has been found for In4(P2O7)3 [P21/a, a = 13.248(3) Å, b = 9.758(1) Å, c = 13.442(2) Å, b = 108.94(1)°, 7221 independent reflexes, 281 parameter, R1 = 0.027, wR2 = 0.067].  相似文献   

19.
Crystal Structure of Sodium Dihydrogencyamelurate Tetrahydrate Na[H2(C6N7)O3] · 4 H2O Sodium dihydrogencyamelurate‐tetrahydrate Na[H2(C6N7)O3]·4 H2O was obtained by neutralisation of an aqueous solution, previously prepared by hydrolysis of the polymer melon with sodium hydroxide. The crystal structure was solved by single‐crystal X‐ray diffraction ( a = 6.6345(13), b = 8.7107(17), c = 11.632(2) Å, α = 68.96(3), β = 87.57(3), γ = 68.24(3)°, V = 579.5(2) Å3, Z = 2, R1 = 0.0535, 2095 observed reflections, 230 parameters). Both hydrogen atoms of the dihydrogencyamelurate anion are directly bound to nitrogen atoms of the cyameluric nucleus, thus proving the preference of the keto‐tautomere in salts of cyameluric acid in the solid‐state. The compound forms a layer‐like structure with an extensive hydrogen bonding network.  相似文献   

20.
The first selenite chloride hydrates, Co(HSeO3)Cl · 3 H2O and Cu(HSeO3)Cl · 2 H2O, have been prepared from solution and characterised by single‐crystal X‐ray diffraction. The cobalt phase adopts an unusual “one‐dimensional” structure built up from vertex‐sharing pyramidal [HSeO3]2–, and octahedral [CoO2(H2O)4]2– and [CoO2(H2O)2Cl2]4– units. Inter‐chain bonding is by way of hydrogen bonds or van der Waals' interactions. The atomic arrangement of the copper phase involves [HSeO3]2– pyramids and Jahn‐Teller distorted [CuCl2(H2O)4] and [CuO4Cl2]8– octahedra, sharing vertices by way of Cu–O–Se and Cu–Cl–Cu bonds. Crystal data: Co(HSeO3)Cl · 3 H2O, Mr = 276.40, triclinic, space group P 1 (No. 2), a = 7.1657(5) Å, b = 7.3714(5) Å, c = 7.7064(5) Å, α = 64.934(1)°, β = 68.894(1)°, γ = 71.795(1)°, V = 337.78(7) Å3, Z = 2, R(F) = 0.036, wR(F) = 0.049. Cu(HSeO3)Cl · 2 H2O, Mr = 263.00, orthorhombic, space group Pnma (No. 62), a = 9.1488(3) Å, b = 17.8351(7) Å, c = 7.2293(3) Å, V = 1179.6(2) Å3, Z = 8, R(F) = 0.021, wR(F) = 0.024.  相似文献   

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