Browse
Submit Data
Databases
API
Help

Dataset Information

20 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Synthese et structure cristalline d'un materiau noir AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5.

ABSTRACT: A new silver aluminium trimangan-ese penta-molybdate {silver(I) trimanganese(II) aluminium penta-kis-[tetra-oxidomolybdate(VI)]}, AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5, has been synthesized using solid-state methods. The structure is composed of M 2O10 dimers, M 3O14 (M = Mn, Al) trimers and MoO4 tetra-hedra sharing corners and forming three types of layers A, B and B'. The sequence of the constituting layers is A-BB'-A-BB', with B' obtained from B by inversion symmetry, forming a three-dimensional structure with large channels in which the positionally disordered and partially occupied Ag(+) ions reside. The Mn(III) and Al(III) atoms share the same site, M. AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5 is isotypic with the NaMg3 X(MoO4)5 (X = Al, In) family and with NaFe4(MoO4)5. A comparative structural description is provided between the structure of the title compound and those of related phases containing dimers, trimers and tetra-mers.

SUBMITTER: Bouzidi C

PROVIDER: S-EPMC4350738 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Synthèse et structure cristalline d'un matériau noir AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5.

Bouzidi Chahira C Frigui Wafa W Zid Mohamed Faouzi MF

Acta crystallographica. Section E, Crystallographic communications 20150221 Pt 3

A new silver aluminium trimangan-ese penta-molybdate {silver(I) trimanganese(II) aluminium penta-kis-[tetra-oxidomolybdate(VI)]}, AgMn(II) 3(Mn(III) 0,26Al0,74)(MoO4)5, has been synthesized using solid-state methods. The structure is composed of M 2O10 dimers, M 3O14 (M = Mn, Al) trimers and MoO4 tetra-hedra sharing corners and forming three types of layers A, B and B'. The sequence of the constituting layers is A-BB'-A-BB', with B' obtained from B by inversion symmetry, forming a three-dimensio ...[more]

PMID: 25844193

Similar Datasets

Synthese, etude et validation structurale d'un triple bis-molybdate en couches, Ag0.60Na0.40Fe(MoO4)2 lie a yavapaiite.

Project description:The title compound, Ag0.60Na0.40Fe(MoO4)2 {silver sodium iron(III) bis-[molyb-date(VI)]}, was synthesized by a solid-state reaction. The structure is built up from FeO6 octa-hedra and MoO4 tetra-hedra sharing corners to form a two-dimensional framework parallel to the (001) plane. The occupationally disordered (Ag/Na)(+) cations are located in the inter-layer space. These [Fe(MoO4)2 (-)] n layers are similar to those in the isotypic yavapaiite-related structure of NaFe(MoO4)2. All atoms are on general positions except for Fe (site symmetry -1) and Ag/Na (site symmetry 2). The Ag/Na occupancies of the latter site were refined to 0.597 (4):0.403 (5). The title structure is compared to similar structures.

| S-EPMC4908507 | biostudies-literature

Synthese et etude structurale de Na9Cr(MoO4)6.

Project description:The title compound, nona-sodium chromium(III) hexa-kis[molybdate(VI)], Na9Cr(MoO4)6 was prepared by solid-state reactions. The basic structure units are isolated polyhedral clusters composed of a central CrO6 octa-hedron sharing vertices with six MoO4 tetrahedra to form an open framework in which the Na(+) cations are bound to the free vertices of the MoO4 tetra-hedra. The Cr(3+) cation has site symmetry of 32 (6a), one Na atom sits on a twofold axis (18e), and all other atoms are at general positions. The bond-valance-sum model confirms the expected values of ion charges. The title compound is isotypic with Na9Sc(MoO4)6 and Na9Fe(MoO4)6. It is compared and discussed with similar structures.

| S-EPMC4420133 | biostudies-literature

Structure cristalline de type alluaudite KNa5Mn3(MoO4)6.

Project description:The new phase potassium penta-sodium trimanganese hexa-kis(molybdate), KNa5Mn3Mo6O24, has been synthesized using solid-state methods. The structure is composed of M 2O10 (M = Mn, Na) dimers and MoO4 tetra-hedra (point group symmetry 2) sharing corners and forming layers parallel to (100), which are linked via common corners of another type of MO4 tetra-hedra, forming a three-dimensional structure with two types of large channels along [001] in which two types of Na(+) cations (one with site symmetry 2, one with -1) and K(+) cations (site symmetry 2, half-occupation) are located. Mn(2+) and the third type of Na(+) cations are located at the same site M with occupancies of 0.75 and 0.25, respectively. A comparative structural description is provided between the structure of the title compound and those of the related phases Cu1.35Fe3(PO4)3 and NaAgFeMn2(PO4)3.

| S-EPMC4331917 | biostudies-literature

Structure cristalline de type alluaudite K0.4Na3.6Co(MoO4)3.

Project description:A new triple molybdate, potassium sodium cobalt tris-(molybdate), K0.4Na3.6Co(MoO4)3, was synthesized using solid-state reactions. The Co(2+) and one Na(+) cation are located at the same general site, each with occupancy 0.5. Another site (site symmetry 2) is occupied by Na(+) and K(+) cations, with occupancies of 0.597 (7) and 0.402 (6), respectively. The other two Na(+) cations and one of the two Mo atoms lie on special positions (site symmetries -1, 2 and 2, respectively). The structure is characterized by M 2O10 (M = Co/Na) dimers, which are linked by MoO4 tetra-hedra, forming infinite layers. The latter are connected firstly by insertion of one type of MoO4 tetra-hedra and secondly by sharing corners with the other type of MoO4 tetra-hedra. This results in an open three-dimensional framework with the cavities occupied by the Na(+) and K(+) cations. The structure is isotypic with Na3In2As3O12 and Na3In2P3O12. A comparison is made with structures such as K2Co2(MoO4)3 and β-NaFe2(MoO4)3 and their differences are discussed.

| S-EPMC4331865 | biostudies-literature

Synthese et etude structrale de lyonsite-type (Na0,4,Li0,6)(Fe,Li2)(MoO4)3.

Project description:The new compound (Na0.4,Li0.6)(Fe,Li2)(MoO4)3 was synthesized by cooling from the melt. Its anionic framework is built up from two distinct MO6 octa-hedra, each containing disordered Li(+) and Fe(3+) ions in 0.6:0.4 and 0.7:0.3 ratios, and two MoO4 tetra-hedra, which link by vertex-sharing of their O atoms. These tetra-meric units are further linked by sharing edges between octa-hedra and by formation of M-O-Mo (M = Fe/Li) bridges, forming ribbons propagating in the [100] direction. The ribbons are cross-linked in both the b- and c-axis directions, giving rise to a three-dimensional framework having [100] tunnels in which the monovalent Na(+)/Li(+) cations (0.4:0.6 ratio) lie. Bond-valence calculations are consistent with the disorder model for the cations. The structure of the title compound, which is isotypic with Li3Fe(MoO4)3 and Li3Ga(MoO4)3, is compared briefly with those of LiFeMo2O8 and Li1.6Mn2.2(MoO4)3.

| S-EPMC4459335 | biostudies-literature

Structure cristalline de la triple molybdate Ag0.90Al1.06Co2.94(MoO4)5.

Project description:Silver(I) aluminiun tricobalt(II) penta-kis-[tetra-oxidomolybdate(VI)], Ag0.90Al1.06Co2.94(MoO4)5, was synthesized using a solid-state reaction at 845 K. The structure can be described as a three-dimensional framework formed from dimeric M 2O10 (M = Co/Al) and trimeric M 3O14 units linked to MoO4 tetra-hedra by sharing corners, with the cavities occupied by disordered Ag(+) cations. It is shown that the Co and Al atoms occupy common positions with different occupancies. The Ag(+) cations are located at two different sites with occupancies of 0.486 (1) and 0.408 (1). The title coumpond is isotypic with NaMg3Al(MoO4)5 and NaFe4(MoO4)5. Differences and similarities with other related structures are discussed.

| S-EPMC4438844 | biostudies-literature

Structure cristalline et analyses thermique et de surface Hirshfeld du diperchlorate de 4-aza-niumyl-2,2,6,6-tetramethylpiperidin-1-ium.

Project description:The synthesis of 4-aza-niumyl-2,2,6,6-tetra-methyl-piperidin-1-ium diperchlorate, C9H22N22+·2ClO4-, was carried out from an aqueous reaction of perchloric acid with 4-amino-2,2,6,6-tetra-methyl-piperidine. This compound was characterized by TGA-DSC analysis and single-crystal X-ray diffraction. The piperidine ring of the dication adopts a chair conformation and the orientation of the C-NH3 bond is equatorial. One of the two crystallographically independent perchlorate anions exhibits disorder [occupancies 0.625 (7) and 0.375 (7)]. The crystal packing is constituted by a succession of mixed layers parallel to the (-102) plane, made up of C9H22N22+ dications and ClO4- anions. These ions are linked by normal and bifurcated N-H⋯O hydrogen bonds with R44(12) graph-set motifs, generating a two-dimensional network. The inter-molecular inter-actions in the crystal structure were qu-anti-fied and analysed using Hirshfeld surface analysis.

| S-EPMC5730294 | biostudies-literature

Unsymmetrical bimetallic complexes with M(II)-(?-OH)-M(III) cores (M(II)M(III) = Fe(II)Fe(III), Mn(II)Fe(III), Mn(II)Mn(III)): structural, magnetic, and redox properties.

Project description:Heterobimetallic cores are important units within the active sites of metalloproteins but are often difficult to duplicate in synthetic systems. We have developed a synthetic approach for the preparation of a complex with a Mn(II)-(?-OH)-Fe(III) core, in which the metal centers have different coordination environments. Structural and physical data support the assignment of this complex as a heterobimetallic system. A comparison with analogous homobimetallic complexes, Mn(II)-(?-OH)-Mn(III) and Fe(II)-(?-OH)-Fe(III) cores, further supports this assignment.

| S-EPMC3826960 | biostudies-other

Structure cristalline, caracterisation spectroscopique, calcul DFT et analyse de surface Hirshfeld du perchlorate de p-toluidinium.

Project description:The synthesis of p-toluidinium perchlorate (systematic name: 4-methyl-anilinium perchlorate), C7H10N+·ClO4-, was carried out from an aqueous reaction of perchloric acid with p-toluidine. This compound was characterized by powder XRD, IR and UV-Vis spectroscopy. The structure was further confirmed by a single-crystal X-ray diffraction study. The crystal structure is formed by a succession of two-dimensional mol-ecular layers consisting of perchlorate anions and organic cations parallel to the (100) plane and located at x = 2n + ½ (n ∈ Z). Each mixed layer is formed by infinite chains {C7H10N+·ClO4-} n parallel to the [010] direction and developing along the c axis, generating R24(8), R22(4) and R44(12) graph-set motifs. The results of a theoretical study using the DFT method at the B3LYP/6-311++G(d,p) level are in good agreement with the experimental data. Hirshfeld surface and fingerprint plots reveal that the structure is dominated by O⋯H/H⋯O (54.2%), H⋯H (26.9%) and C-H ⋯π (14.3%) contacts. The studied crystal was refined as a two-component twin.

| S-EPMC5956314 | biostudies-literature

New Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Zn(II), Cd(II), and Hg(II) Gibberellate Complexes: Synthesis, Structure, and Inhibitory Activity Against COVID-19 Protease.

Project description:Transition metals such as Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Zn(II), Cd(II), and Hg(II) have been reacted with gibberellic acid (HGA) to give novel complexes, and those have been characterized by physical, spectral and analytical methods. The plant hormone gibberellate acts as a deprotonated bidentate ligand in the complexation reaction with central metal ions in the ratio 1 : 2 (M n+ : GA). The complexes [M(GA)2(H2O)2], where [M = Mn(II), Co(II), and Ni(II)] form octahedral structures, while [M(GA)2] complexes [M = Zn(II), Cd(II), and Hg(II)] display four-coordination geometry. The octahedral structures of Cr(III) and Fe(III) complexes are characterized by the general formula [M(GA)2(H2O)(Cl)]. Computational study carried out has determined possible interactions of the complexes with COVID-19 (6LU7).

| S-EPMC8210501 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data