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Poly[[tetra-aquadi-?(3)-oxalato-?(2)-oxalato-diprasedymium(III)] dihydrate].

ABSTRACT: In the title compound, {[Pr(2)(C(2)O(4))(3)(H(2)O)(4)]·2H(2)O}(n), the three-dimensional network structure has the Pr(III) ion coordinated by nine O atoms in a distorted tricapped trigonal-prismatic geometry. The coordinated and uncoordinated water mol-ecules inter-act with the carboxyl-ate O atoms to consolidate the network via O-H?O hydrogen bonds.

SUBMITTER: Chen JH

PROVIDER: S-EPMC2980182 | biostudies-literature | 2009 Dec

REPOSITORIES: biostudies-literature

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Poly[[tetra-aquadi-μ(3)-oxalato-μ(2)-oxalato-diprasedymium(III)] dihydrate].

Chen Jian-Hong JH Fang Hua-Cai HC Jia Hong-Yang HY Li Shan-Shan SS Cai Yue-Peng YP

Acta crystallographica. Section E, Structure reports online 20091219 Pt 1

In the title compound, {[Pr(2)(C(2)O(4))(3)(H(2)O)(4)]·2H(2)O}(n), the three-dimensional network structure has the Pr(III) ion coordinated by nine O atoms in a distorted tricapped trigonal-prismatic geometry. The coordinated and uncoordinated water mol-ecules inter-act with the carboxyl-ate O atoms to consolidate the network via O-H⋯O hydrogen bonds. ...[more]

PMID: 21579975

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Poly[tetra-aquadi-?(4)-oxalato-lutetium(III)potassium].

Project description:In the title compound, [KLu(C(2)O(4))(2)(H(2)O)(4)](n), the Lu(III) ion lies on a site of [Formula: see text] symmetry in a dodeca-hedron defined by eight O atoms from four oxalate ligands. The K atom lies on another site of the same symmetry and is coordinated by four oxalate O atoms and four O water atoms. The mid-point of the C-C bond of the oxalate group lies on an inversion center. In the packing structure, each oxalate ligand links two Lu(III) and two K atoms, forming a three-dimensional open framework with channels running along [001]. Inter-molecular O-H?O hydrogen bonds occur.

| S-EPMC3247002 | biostudies-literature

Poly[tetra-aquadi-?(4)-oxalato-potassium-ytterbium(III)].

Project description:In the title compound, [KYb(C(2)O(4))(2)(H(2)O)(4)](n), the Yb(III) ion lies on a site of [Formula: see text] symmetry in a dodeca-hedral environment defined by eight O atoms from four oxalate ligands. The K atom lies on a different [Formula: see text] axis and is coordinated by four O atoms from four oxalate ligands and four water O atoms. The oxalate ligand has an inversion center at the mid-point of the C-C bond. The metal ions are linked by the oxalate ligands into a three-dimensional framework. O-H?O hydrogen bonding is present in the crystal structure.

| S-EPMC3238636 | biostudies-literature

Poly[[tetra-aquadi-?4-fumarato-?2-oxalato-dierbium(III)] tetra-hydrate].

Project description:The title compound, {[Er2(C4H2O4)2(C2O4)(H2O)4]·4H2O} n , was synthesized by the reaction of erbium nitrate hexa-hydrate with fumaric acid and oxalic acid under hydro-thermal conditions. The Er(3+) cation (site symmetry ..2) is eight-coordinated by six O atoms from four fumarate anions (site symmetry ..2) and one bidentate oxalate anion (site symmetry 222), and by two water mol-ecules. The complex exhibits a three-dimensional structure consisting of oxalate pillared Er-fumarate layers with channels occupied by coordinating and lattice water mol-ecules. The three-dimensional structure features by Owater-H?O hydrogen bonds involving both the coordinating and lattice water mol-ecules.

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Poly[[tetra-aqua-di-?(4)-oxalato-?(2)-oxalato-dineo-dymium(III)] dihydrate].

Project description:The title compound, {[Nd(2)(C(2)O(4))(3)(H(2)O)(4)]·2H(2)O}(n), was synthesized hydro-thermally in the presence of bis-(carb-oxy-ethyl-germanium) sesquioxide. It is isostructural with the corresponding Pr compound [Yang et al. (2009). Acta Cryst. E65, m1152-m1153]. The Nd(3+) cation is nine-coordinated and its coordination polyhedron can be described as a distorted tricapped trigonal prism. Two Nd(3+) ions are connected by two O atoms from two oxalate ions to give a dinuclear Nd(2) unit. The unit is further linked to four others via four oxalate ions yielding a layerparallel to (0-11). The linkages between the layers by neighbouring oxalate anions lead to a three-dimensional framework with channels along the c axis. The coordinating and free water mol-ecules are located in the channels and make contact with each other and the host framework by weak O-H?O hydrogen bonds.

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catena-Poly[[tetra-?(3)-isonicotinato-?(3)-oxalato-?(2)-oxalato-disamarium(III)disilver(I)] dihydrate].

Project description:In the title compound, {[AgSm(C(6)H(4)NO(2))(2)(C(2)O(4))]·H(2)O}(n), the asymmetric unit contains one Sm(III) ion, one Ag(I) ion, two unique isonicotinate (ina) ligands, two half oxalate (ox) ligands (one on an inversion centre, the other on a twofold axis) and one uncoordinated water mol-ecule. The central Sm(III) ion is nine-coordinated by four O-donor atoms from separate bidentate bridging ox ligands and five O-donor atoms from the two ina ligands (both bidentate) and a symmetry-related ina ligand [Sm-O = 2.389?(4)-2.791?(4)?Å], giving a distorted monocapped square anti-prismatic geometry. The Ag(I) ion is three-coordinated in a T-shaped geometry involving two ina N-donor atoms [Ag-N = 2.181?(6) and 2.185?(5)?Å] and a bridging oxalate O-donor atom [Ag-O = 2.620?(4)?Å]. The three-dimensional heterometallic Sm-Ag coordination polymer, having a unique (3,4,6)-connected five-nodal net topology, is constructed from two-dimensional samarium-oxalate layers and pillared Ag(ina)(2) subunits. Inter-molecular water-carboxyl-ate O-H?O hydrogen-bonding inter-actions are also present.

| S-EPMC2980152 | biostudies-literature

Poly[dimethyl-ammonium [aquadi-?(2)-oxalato-dysprosate(III)] trihydrate].

Project description:The title compound, {(C(2)H(8)N)[Dy(C(2)O(4))(2)(H(2)O)]·3H(2)O}(n), was obtained as an unexpected product under hydro-thermal conditions. The Dy(III) atom is chelated by four oxalate anions, two of which are situated on two different centres of inversion. The distorted tricapped trigonal-prismatic coordination sphere of the Dy(III) atom is completed by a water mol-ecule. The bridging mode of the anions results in the formation of a three-dimensional network with cavities where the ammonium cations and the uncoordinated water mol-ecules reside. The structure is stabilized by numerous N-H?O and O-H?O hydrogen-bonding inter-actions.

| S-EPMC3007264 | biostudies-literature

Poly[dimethyl-ammonium [aquadi-μ(2)-oxalato-yttriate(III)] trihydrate].

Project description:The title complex, {(C(2)H(8)N)[Y(C(2)O(4))(2)(H(2)O)]·3H(2)O}(n), was obtained accidentally under hydro-thermal conditions. The Y(III) atom is chelated by four oxalate ligands and one water mol-ecule resulting in a distorted tricapped trigonal-prismatic geometry. Each oxalate ligand bridges two Y(III) atoms, thus generating a three-dimensional network with cavities in which the ammonium cations and lattice water mol-ecules reside. Various O-H⋯O and N-H⋯O hydrogen-bonding inter-actions stabilize the crystal structure. The title complex is isotypic with the Eu and Dy analogues.

| S-EPMC3151934 | biostudies-literature

Crystal structure of poly[?6-adipato-di-aquadi-?2-oxalato-didysprosium(III)].

Project description:In the title coordination polymer, [Dy2(C6H8O4)(C2O4)2(H2O)2] n , the asymmetric unit consists of one Dy(3+) cation, one half of an adipate anion, two halves of oxalate anions and one coordinating water mol-ecule. The adipate and oxalate ions are located on centres of inversion. The Dy(3+) cation has a distorted tricapped trigonal-prismatic geometry and is coordinated by nine O atoms, four belonging to three adipate anions, four to two oxalate anions and one from an aqua ligand. The cations are bridged by adipate ligands, generating a two-dimensional network parallel to (010). This network is further extended into three dimensions by coordination of the rigid oxalate ligands and is further consolidated by O-H?O hydrogen bonds. A part of the adipate anion is disordered over two positions in a 0.75:0.25 ratio.

| S-EPMC4257430 | biostudies-literature

Poly[dimethyl-ammonium [aquadi-?(2)-oxalato-samarate(III)] trihydrate].

Project description:In the title complex, {(C(2)H(8)N)[Sm(C(2)O(4))(2)(H(2)O)]·3H(2)O}(n), the Sm(III) atom is chelated by four oxalate ligands and one water mol-ecule forming a distorted tricapped trigonal-prismatic geometry. Each oxalate ligand chelates to two Sm(III) atoms, generating a three-dimensional anionic network with cavities in which the ammonium cations and lattice water mol-ecules reside. Various O-H?O, N-H?O and C-H?O hydrogen-bonding inter-actions further stablize the crystal structure.

| S-EPMC3152119 | biostudies-other

Poly[[tetra-?(3)-acetato-hexa-?(2)-acetato-diaqua-?(2)-oxalato-tetra-lanthanum(III)] dihydrate].

Project description:The title compound, {[La(4)(CH(3)CO(2))(10)(C(2)O(4))(H(2)O)(2)]·2H(2)O}(n), exhibits a two-dimensional layered structure with the oxalate and acetate ligands acting as bridges. The asymmetric unit contains two crystallographically independent lanthanum(III) ions, half of an oxalate ligand, five acetate ligands, one coordinated water mol-ecule and one uncoordinated water mol-ecule. The coordination numbers of the two La ions are 9 and 10. Adjacent layers of the structure, which extend parallel to (100), are linked by O-H?O hydrogen bonds and are also held together by van der Waals inter-actions between the CH(3) groups of the acetate anions.

| S-EPMC3201431 | biostudies-other

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