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Bis(4-amino-pyridinium) μ6-oxido-dodeca-μ2-oxido-hexaoxido[rhenium(VII)tetratungsten(VI)vanadium(V)]ate hepta-hydrate.

ABSTRACT: In the title organic-inorganic hybrid compound, (C5H7N2)2[ReVW4O19]·7H2O, the Lindqvist-type polyoxido anion has crystallographically imposed mm2 symmetry and is built up by six MO6 (M = W, V, Re) edge-sharing distorted octa-hedra. The Re and V atoms share the same crystallographic site in a 0.5:0.5 ratio. The 4-amino-pyridinium cations lie on a mirror plane. Three of the four independent water O atoms in the asymmetric unit are located on a mirror plane whereas the remaining O atom has mm2 site symmetry. In the crystal, the cations, anions and water mol-ecules are linked into a three-dimensional network through O-H⋯O and N-H⋯O hydrogen-bonding inter-actions.

SUBMITTER: Maaloui A

PROVIDER: S-EPMC3884996 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Crystal structure of octa-kis-(N,N-di-methyl-formamide-κO)europium(III) tetra-cosa-μ2-oxido-dodeca-oxido-μ12-phosphato-dodeca-molybdate(VI).

Project description:In the title salt, [Eu(C3H7NO)8][PMo12O40], the asymmetric unit comprises one α-Keggin-type [PMo12O40](3-) polyoxidometalate anion and one distorted dodeca-hedral [Eu(C3H7NO)8](3+) complex cation. In the crystal, the isolated polyoxidometalate anions are packed into hexa-gonally arranged rows extending parallel to [001]. The complex cations are situated between the rows and are linked to the neighbouring anions through weak C-H⋯O hydrogen-bonding inter-actions, leading to the formation of a three-dimensional network structure.

| S-EPMC4910337 | biostudies-literature

Hexakis(2-amino-pyridinium) di-?(6)-oxido-tetra-?(3)-oxido-tetra-deca-?(2)-oxido-octa-oxidodeca-vanadium(V) dihydrate.

Project description:In the title compound, (C(5)H(7)N(2))(6)[V(10)O(28)]·2H(2)O, the [V(10)O(28)](6-) anion is generated by crystallographic inversion symmetry and each of the five vanadium centres adopts a distorted VO(6) octa-hedral geometry. In the crystal structure, a network of N-H?O, N-H?(O,O) and O-H?O hydrogen bonds helps to establish the packing.

| S-EPMC2968550 | biostudies-literature

Penta-ammonium hepta-sodium bis-[penta-kis(μ(2)-oxido)deca-oxido-bis-(μ(5)-phosphato)penta-molybdenum(VI)] henicosa-hydrate.

Project description:The title compound, (NH(4))(5)Na(7)[Mo(5)P(2)O(23)](2)·21H(2)O, was prepared under atmospheric conditions in aqueous solution at room temperature. The structure contains the [Mo(5)P(2)O(23)](6-) heteropolyoxometallate anion, which has been previously reported a number of times with a variety of differing counter-cations. Each anion is built up of five MoO(6) octa-hedra sharing an edge and forming a ring which is closed by common corners of the terminal octa-hedra. The rings are closed on both sides by two asymmetric PO(4) tetra-hedra, sharing three corners with three MoO(6) octa-hedra. The anions are chiral and the two independent anions in the asymmetric unit were arbitarily chosen with the same chirality, but the centrosymmetric crystal contains both enanti-omers. The structure can alternatively be described as a succession of layers parallel to (101), formed by the [Mo(5)P(2)O(23)](6-) anions and linked by sodium chains. Water mol-ecules and ammonium ions fill the remaining space and ensure the cohesion through extensive N-H⋯O and O-H⋯O hydrogen bonding.

| S-EPMC2983582 | biostudies-literature

Tris(morpholinium) hexa-?(3)-hydroxido-hexa-?(2)-oxido-dodeca-oxidohexa-molybdenum(VI)chromate(III) tetra-hydrate.

Project description:In the title organic-inorganic hybrid compound, (C(4)H(10)NO)(3)[H(6)CrMo(6)O(24)]·4H(2)O, the Anderson-type [H(6)CrMo(6)O(24)](3-) polyoxoanion is centrosymmetric, with the Cr(III) ion lying on an inversion center. One of the two crystallographiclly independent morpholinium cations is half-occupied. Inter-molecular N-H?O and O-H?O hydrogen bonds link the cations, polyoxoanions and uncoordinated water mol-ecules.

| S-EPMC3120305 | biostudies-literature

Tetra-imidazolium hexa-?(4)-oxido-dodeca-?(2)-oxido-dodeca-oxidohexa-arsenate(III)hexa-molybdenum(VI)cuprate(II).

Project description:The title compound, (C(3)H(5)N(2))(4)[As(6)CuMo(6)O(30)], is made up of a centrosymmetric anionic cluster and four imidazolium cations. In the cluster, the central Cu(II) atom is six-coordinated and lies on an inversion center. Adjacent clusters are linked via N-H?O hydrogen bonds between the imidazole cations and polyoxidoanions into a three-dimensional supra-molecular architecture.

| S-EPMC2983113 | biostudies-literature

Tetra-ammonium bis-(metforminium) di-μ6-oxido-tetra-μ3-oxido-tetra-deca-μ2-oxido-octa-oxidodeca-vanadium(V) hexa-hydrate.

Project description:The title compound, (NH4)4(C4H12N5)2[V10O28]·6H2O, crystallizes with the deca-vanadate anion placed on an inversion centre in space group P . This anion is surrounded by a first shell of ammonium cations and water mol-ecules, forming efficient N-H⋯O and O-H⋯O hydrogen bonds. A second shell includes metforminium monocations with a twisted geometry, also forming numerous inter-molecular hydrogen bonds. The complex three-dimensional network of non-covalent inter-actions affords a crystal structure in which the cations and anions are densely packed.

| S-EPMC9462348 | biostudies-literature

2-Amino-5-chloro-pyridinium 6-oxo-1,6-dihydro-pyridine-2-carboxyl-ate 0.85-hydrate.

Project description:In the title salt, C(5)H(6)ClN(2) (+)·C(6)H(4)NO(3) (-)·0.85H(2)O, the pyridin-ium ring is planar, with a maximum deviation of 0.010 (2) Å. In the crystal structure, the cations, anions and water mol-ecules are linked via N-H⋯O, O-H⋯O and C-H⋯O hydrogen bonds, forming a three-dimensional network.

| S-EPMC3007856 | biostudies-literature

Tetra-kis(2-amino-4-methyl-pyridinium) cyclo-tetra-?(2)-oxido-tetra-kis-[dioxido-vanadate(V)] tetra-hydrate.

Project description:The asymmetric unit of the title compound, (C(6)H(9)N(2))(4)[V(4)O(12)]·4H(2)O, contains half of a [V(4)O(12)](4-) anion, two 2-amino-4-methyl-pyridinium, (2a4mpH)(+), cations and two water mol-ecules. One water mol-ecule is disordered over two sets of sites with equal occupancies and the H atoms for this mol-ecule were not included in the refinement. The cation lies on an inversion center with four tetra-hedral VO(4) units each sharing two vertices, forming an eight-membered ring. In the crystal, the components are linked by inter-molecular N-H?O hydrogen bonds, forming a one-dimensional network along [100]. Further stabilization is provided by weak inter-molecular C-H?O hydrogen bonds. In addition, ?-? stacking inter-actions with centroid-centroid distances of 3.5420?(18), 3.7577?(18) and 3.6311?(19)?Å are observed.

| S-EPMC3212164 | biostudies-literature

Bis[tris-(ethyl-enediamine-?N,N')cobalt(III)] octa-kis-?-(3)-oxido-hexa-deca-?(2)-oxido-tetra-deca-oxido-?(12)-tetra-oxo-silicato-octa-molybdenum(VI)hexa-vanadium(IV,V) hexa-hydrate.

Project description:The title compound, [Co(C(2)H(8)N(2))(3)](2)[SiMo(8)V(4)O(40)(VO)(2)]·6H(2)O, was prepared under hydro-thermal conditions. The asymmetric unit consists of a transition metal complex [Co(en)(3)](3+) cation (en is ethyl-enediamine), one half of an [SiMo(8)V(4)O(40)(VO)(2)](6-) heteropolyanion, two solvent water mol-ecules in general positions and two half-mol-ecules of water located on a mirror plane. In the complex cation, the Co(3+) ion is in a distorted octa-hedral coordination environment formed by six N atoms of the three chelating en ligands. One of the en ligands exhibits disorder of its aliphatic chain over two sets of sites of equal occupancy. The [SiMo(8)V(4)O(40)(VO)(2)](6-) heteropolyanion is a four-electron reduced bivanadyl-capped ?-Keggin-type molybdenum-vanadium-oxide cluster. In the crystal, it is located on a mirror plane, which results in disorder of the central tetra-hedral SiO(4) group: the O atoms of this group occupy two sets of sites related by a mirror plane. Furthermore, all of the eight ?(2)-oxide groups are also disordered over two sets of sites with equal occupancy. There are extensive inter-molecular N-H?O hydrogen bonds between the complex cations and inorganic polyoxidoanions, leading to a three-dimensional supra-molecular network.

| S-EPMC3238691 | biostudies-literature

Rhenium(VII) catalysis of Prins cyclization reactions.

Project description:The rhenium(VII) complex O3ReOSiPh3 is a particularly effective catalyst for Prins cyclizations using aromatic and alpha,beta-unsaturated aldehydes. The reaction conditions are mild, and the highly substituted 4-hydroxytetrahydropyran products are formed stereoselectively. Rhenium(VII) complexes appear to spontaneously form esters with alcohols and to directly activate electron-rich alcohols for solvolysis. Re2O7 and perrhenic acid are equally effective in catalyzing these cyclizations.

| S-EPMC2665917 | biostudies-literature

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