Two caesium vanadium hydrogenphosphates with tunnelled structures: Cs2V2O3(PO4)(HPO4) and Cs2[(VO)3(HPO4)4(H2O)]·H2O

Dicaesium divanadium trioxide phosphate hydrogenphosphate, Cs₂V₂O₃(PO₄)(HPO₄), (I), and dicaesium tris[oxidovanadate(IV)] hydrogenphosphate dihydrate, Cs₂[(VO)₃(HPO₄)₄(H₂O)]·H₂O, (II), crystallize in the monoclinic system with all atoms in general positions. The structures of the two compounds are built up from VO₆ octahedra and PO₄ tetrahedra. In (I), infinite chains of corner‐sharing VO₆ octahedra are connected to V₂O₁₀ dimers by phosphate and hydrogenphosphate groups, while in (II) three vanadium octahedra share vertices leading to V₃O₁₅(H₂O) trimers separated by hydrogenphosphate groups. Both structures show three‐dimensional frameworks with tunnels in which Cs⁺ cations are located.     

Na2Co(H2PO4)4·4H2O

In the title compound, disodium cobalt tetrakis­(dihydrogen­phosphate) tetrahydrate, the Co^II ion lies on an inversion centre and is octahedrally surrounded by two water molecules and four H₂PO₄ groups to give a cobalt complex anion of the form [Co(H₂PO₄)₄(OH₂)]^2?. The three‐dimensional framework results from hydrogen bonding between the anions. The relationship with the structures of Co(H₂PO₄)₂·2H₂O and K₂CoP₄O₁₂·5H₂O is discussed.     

ChemInform Abstract: Two Caesium Vanadium Hydrogenphosphates,with Tunnelled Structures: Cs2V2O3(PO4)(HPO4) and Cs2 [(VO)3(HPO4)4(H2O)] ·H2O.

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Na6(H2O)20(V10O28)·4H2O,a novel polyvanadate(V) with a three‐dimensional framework

The novel title polyvanadate(V), poly[[octa‐μ‐aqua‐dodecaaqua‐μ₄‐octacosaoxidodecavanadato‐hexasodium] tetrahydrate], [Na₆(H₂O)₂₀(V₁₀O₂₈)·4H₂O]_n, contains [V₁₀O₂₈]⁶⁻ anions which lie about inversion centres and have approximate 2/m symmetry and which are linked to [Na₃(H₂O)₁₀]³⁺ cations through two terminal and two μ₂‐bridging O atoms. The structure contains three inequivalent Na⁺ cations, two of which form [Na₂(H₂O)₈]_n chains, which are linked via NaO₆ octahedra involving the third Na⁺ ion, thus forming a three‐dimensional framework.     

A hydrated ethyl­ene­di­ammonium salt of a new polymeric polyoxoanion: (H2en)4[Co(H2O)2(OH)2(VO)6(HPO4)4(PO4)4]·3H2O

The title compound, tetrakis­(ethyl­enedi­ammonium) tetra‐μ‐hydrogenphosphato‐di‐μ‐hydro­xo‐ tetra‐μ‐phosphato‐bis­(aqua­cobalt)­hexakis­(oxovanadium) trihydrate, was synthesized hydro­thermally at moderate temperature. The structure consists of diprotonated ethyl­enedi­ammonium cations and layers of the polyanions. The polyanion contains four PO₄ tetrahedra and three VO₅ square pyramids that are linked through corner‐sharing by alternating P—O—V, which gives rise to a chain. The chains, connected by CoO₄(H₂O)₂ octahedra, form layers, resulting in a two‐dimensional layered structure. The Co—O distances are in the range 1.984 (3)–2.038 (4) Å, the P—O distances 1.508 (3)–1.575 (3) Å and the V—O distances 1.585 (3)–2.010 (3) Å.     

(C5H14N2)[Zn3(HPO4)4], a New 3D Open‐framework Zincophosphate Synthesized by Hydrothermal Reversible Transformation of (C5H14N2)[Zn2(HPO4)3]·H2O

In the system ZnO/H₃PO₄/H₂O/1,4‐diazacycloheptane (C₅H₁₂N₂), a new zincophosphate (ZnPO), (C₅H₁₄N₂)[Zn₃(HPO₄)₄] ( I ), was prepared by hydrothermal transformation (180 °C) of the known ZnPO hydrate (C₅H₁₄N₂)[Zn₂(HPO₄)₃]·H₂O ( II ). The thermally‐induced transformation is reversible; upon keeping the heterogeneous mixture of I and mother liquor at 80 °C recrystallization of II was observed. Single‐crystal X‐ray crystallography revealed that I possesses a unique three‐dimensional (3D) open‐framework structure built from corner‐linked ZnO₄ and HPO₄ tetrahedra. The (3,4)‐connected framework of I differs considerably from the 3D open‐framework ZnPO structure of II . Crystal data for I : Monoclinic system, space group Cc (No. 9) , Z = 4, a = 9.1389(6), b = 23.627(2), c = 9.3073(6) Å, β = 109.463(7)°, T = 298 K.     

Preparation and Crystal Structure of Potassium Iron Hydrogen Phosphate,KFe3(HPO4)2(H2PO4)6 · 4 H2O

Single crystals of potassium iron hydrogen phosphate, KFe₃(HPO₄)₂(H₂PO₄)₆ · 4 H₂O, were prepared hydrothermally by heating a mixture of Fe₂O₃, H₃PO₄ and K₂CO₃ with a small amount of water. It crystallizes monoclinic, space group C2/c (N° 15 Int. Tab.) with Z = 4 and a = 1701(2), b = 960.4(5), c = 1750(1) pm, β = 90.88(7)°. The crystal structure was solved by using 1716 unique reflections F₀ > 4σ(F₀) with a final wR2 value of 0.126 (SHELXL-93). The main feature of the crystal structure are layers formed by PO₄-tetrahedra around the FeO₆-octahedra parallel to (001). K⁺ and H₂O molecules connect these layers. Effective Coordination Numbers (ECoN), Mean Fictive Ionic Radii (MEFIR), Charge Distribution (CHARDI) and the Madelung Part of Lattice Energy (MAPLE) are calculated for the title compound. The existence of hydrogen bonds is confirmed by these calculations.     

CsAlZr2(PO4)4: an anhydrous aluminium zirconium phosphate with a novel three‐dimensional framework

Caesium aluminium dizirconium tetrakis[phosphate(V)], CsAlZr₂(PO₄)₄, has been synthesized by high‐temperature reaction and studied by single‐crystal X‐ray diffraction at room temperature. This represents the first detailed structural analysis of an anhydrous phosphate containing both zirconium and aluminium. The structure features a complicated three‐dimensional framework of [AlZr₂(PO₄)₄] constructed by PO₄, AlO₄ and ZrO₆ polyhedra interconnected via corner‐sharing O atoms, and one‐dimensional Cs chains which are located in the infinite tunnels within the [AlZr₂(PO₄)₄] framework, which run along the c axis. The Cs, Al, one P and two O atoms lie on a mirror plane, while a second P atom lies on a twofold axis.     

新型磷酸钒孔道结构化合物(H3NCH2CH2NH3)3- [ (VO)4(PO4)2 (HPO4)4]的水热 合成及结构表征

以有机分子乙二胺作为模板剂合成了新型磷酸钒孔道化合物(H3NCH2CH2NH3)3^-[(VO)4(PO4)2(HPO4)4,并通过X射线单晶衍射实验进行了结构表征,晶体学数据为：C2/c,a=1.8505(9)nm,b=0.7089(4)nm,c=2.3304(10)nm,β=96.43(3)°,V-3.038(3)nm^3,Z=8,R=0.067,Rw^b=0.1635,该化合物具有非常独特和规整的二维孔道骨架结构,进一步的晶体化学研究表明该化合物为一新的VPO物相。     

Synthesis and characterization of the layered vanadium borophosphate (imidazolium)3.8(H3O)1.2[(VO)4(BO)2(PO4)5].0.3H2O

The first layered vanadium borophosphate (imidazolium)3.8(H3O)1.2[(VO)4(BO)2(PO4)5].0.3H2O (1) has been synthesized hydrothermally and characterized by chemical analysis, infrared and Raman spectroscopy, and thermogravimetric and magnetic measurements. The compound crystallizes in the monoclinic space group C2/c, a = 9.4737 (5) A, b = 22.1444 (12) A, c = 17.2192 (13) A, beta = 105.936 (1) degrees, Z = 4. The structure contains a novel borophosphate secondary building unit, [B2P5O22], in which two BP2O10 trimers are linked by an additional PO4 tetrahedron. These units are connected by V(IV)2O8 dimers and V(IV)O5 square pyramids to form layers. The space between the layers is filled by disordered imidazolium and hydronium cations and water molecules that form a complex network of hydrogen bonds. A model for the interlayer disorder is proposed.     

Preparation and Crystal Structure of Sodium Iron Hydrogen Phosphate,NaFe(HPO4)(H2PO4)2 · H2O

Single crystals of sodium iron hydrogen phosphate, NaFe(HPO₄)(H₂PO₄)₂ · H₂O, were prepared hydrothermally by heating a mixture of Fe₂O₃, H₃PO₄ and Na₂CO₃ with a small amount of water. It crystallizes orthorhombic (Pbcn (N° 60), Z = 8, a = 872.91(7), b = 1249.54(8), c = 1894.4(1) pm). The crystal structure was solved by using 1121 unique reflections I > 2σ(I) and refined for a final conventional residual R = 0.039 (188 variables, 25 atoms including hydrogen in the asymmetric unit). The main feature of the crystal structure is a ReO₃-like network formed by hydrogenphosphate-, dihydrogenphosphate-groups and Fe O₆ octahedra with channels along the [201], [010] and [201] directions. Na⁺ and H₂O molecules are occupying these channels. Effective Coordination Numbers (ECoN), Mean Fictive Ionic Radii (MEFIR) and the Madelung Part of Lattice Energy (MAPLE) are calculated for the title compound.     

(NH4)3[VO2(SO4)2(H2O)2]·1.5H2O

The title compound, tri­ammonium cis‐di­aqua‐cis‐dioxo‐trans‐disulfatovanadate 1.5‐hydrate, was obtained by oxidizing V^IV to V^V in a 2 M sulfuric acid solution of vanadyl­ sulfate and adding ammonium sulfate. Here, the V atom is sandwiched by two sulfate groups by corner‐sharing to form a discrete [VO₂(SO₄)₂(OH₂)₂]^3? anion. The water mol­ecules occupy cis positions in the equatorial plane of the vanadium octahedron.     

Coordination polymer chains built from CuII and adipate ions linked by hydrogen bonds to form a three‐dimensional framework structure

In the title compound, catena‐poly[bis[(2,2′‐bipyridine‐κ²N,N′)(1,1,3,3‐tetracyano‐2‐ethoxypropenido‐κN)copper(II)]‐μ₄‐hexanedioato‐κ⁶O¹,O^1′:O¹:O⁶,O^6′:O⁶], [Cu₂(C₉H₅N₄O)₂(C₆H₈O₄)(C₁₀H₈N₂)₂]_n, the adipate (hexanedioate) dianion lies across a centre of inversion in the space group P. The Cu^II centre adopts a distorted form of axially elongated (4+2) coordination, and the Cu^II and adipate components form a one‐dimensional coordination polymer from which the 2,2′‐bipyridine and 1,1,3,3‐tetracyano‐2‐ethoxypropenide components are pendent, and where each adipate dianion is bonded to four different Cu^II centres. The coordination polymer chains are linked into a three‐dimensional framework structure by a combination of C—H...N and C—H...O hydrogen bonds, augmented by a π–π stacking interaction.     

Assembly of helical hydrogen bonds in a new layered aluminophosphate [C6N3H17][Al2(HPO4)(PO4)2

A new layered aluminophosphate, [C6N3H17][Al2(HPO4)(PO4)2] (denoted AlPO-CJ21), has been prepared in an alcoholic system by the use of N-(2-aminoethyl)-piperazine (AEPP) as the template. Its inorganic layer containing a series of bridged six-membered rings (MRs) is a new type of 4.6-net sheet built up from AlO4, PO2(OH)(=O), and PO3(=O) tetrahedra. Interestingly, inorganic helical chains of right- or left-handedness are presented in the aluminophosphate layers, and fascinating hydrogen-bonded helices are self-assembled under solvothermal conditions between organic templates and inorganic sheets via strong hydrogen bondings of O...N atoms. Crystal data: monoclinic, P2(1) (No. 4), a = 10.069(2) A, b = 8.0875(16) A, c = 10.598(2) A, beta = 94.71(3) degrees, z = 2, R(1) = 0.0325 [I > 2sigma(I)], and wR(2) = 0.0807 (all data); Flack parameter: 0.03.