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Poly[diaqua-?(2)-isonicotinato-?(2)-oxalato-terbium(III)].

ABSTRACT: In the crystal structure of the title complex, [Tb(C(6)H(4)NO(2))(C(2)O(4))(H(2)O)(2)](n), the Tb(III) ion is coordinated by two O atoms from two isonicotinate (inic) anions, four O atoms of two oxalate anions, and two water mol-ecules, displaying a distorted square-antiprismatic geometry. The Tb(III) ion, the inic anion and the water mol-ecules occupy general positions. One of the two crystallographically independent oxalate anions is located on a center of inversion, whereas the second is located on the twofold rotation axis. The carboxyl-ate groups of the inic and oxalate anions link the terbium metal centres into layers. These layers are connected by O-H?O and N-H?O hydrogen bonding into a three-dimensional network.

SUBMITTER: Fang ZQ

PROVIDER: S-EPMC2968019 | biostudies-literature | 2008 Dec

REPOSITORIES: biostudies-literature

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Poly[diaqua-μ(2)-isonicotinato-μ(2)-oxalato-terbium(III)].

Fang Zhan-Qiang ZQ Zeng Rong-Hua RH Li Yan-Ting YT Yang Shuo S Song Zhao-Feng ZF

Acta crystallographica. Section E, Structure reports online 20081220 Pt 1

In the crystal structure of the title complex, [Tb(C(6)H(4)NO(2))(C(2)O(4))(H(2)O)(2)](n), the Tb(III) ion is coordinated by two O atoms from two isonicotinate (inic) anions, four O atoms of two oxalate anions, and two water mol-ecules, displaying a distorted square-antiprismatic geometry. The Tb(III) ion, the inic anion and the water mol-ecules occupy general positions. One of the two crystallographically independent oxalate anions is located on a center of inversion, whereas the second is loca ...[more]

PMID: 21581482

Similar Datasets

Poly[diaqua-μ(2)-isonicotinato-μ(2)-oxalato-terbium(III)].

Project description:In the crystal structure of the title complex, [Tb(C(6)H(4)NO(2))(C(2)O(4))(H(2)O)(2)](n), the Tb(III) cation is coordinated by four O atoms from two oxalate ligands, two O atoms from two isonicotinate ligands and two O atoms from water mol-ecules within a distorted square-anti-prismatic coordination. The Tb(III) cation, the isonicotinate anion and the two crystallographically independent water mol-ecules occupy general positions, whereas one of the two crystallographically independent oxalate anions is located on a center of inversion, and the second oxalate anion is located on a twofold rotation axis. The Tb(III) cations are linked by the oxalate and isonicotinate anions into layers, which are connected via inter-molecular hydrogen-bonding and π-π stacking [with centroid-to-centroid distances of 3.509 (2) and 3.343 (3) Å] inter-actions into a three-dimensional network.

| S-EPMC2968018 | biostudies-literature

Poly[[diaqua-hemi-μ(4)-oxalato-μ(2)-oxalato-praseodymium(III)] monohydrate].

Project description:In the title complex, {[Pr(C(2)O(4))(1.5)(H(2)O)(2)]·H(2)O}(n), the Pr(III) ion, which lies on a crystallographic inversion centre, is coordinated by seven O atoms from four oxalate ligands and two O atoms from two water ligands; further Pr-O coordination from tetra-dentate oxalate ligands forms a three-dimensional structure. The compound crystallized as a monohydrate, the water mol-ecule occupying space in small voids and being secured by O-H⋯O hydrogen bonding as an acceptor from ligand water H atoms and as a donor to oxalate O-acceptor sites.

| S-EPMC2969896 | biostudies-literature

catena-Poly[[[diaqua-terbium(III)]-tri-?(2)-isonicotinato-?O:O'] tris(perchlorate) monohydrate].

Project description:In the title complex, {[Tb(C(6)H(5)NO(2))(3)(H(2)O)(2)](ClO(4))(3)·H(2)O}(n), the Tb(III) ion is coordinated by six O atoms from six isonicotinate (inic) ligands and two water mol-ecules, displaying a bicapped trigonal-prismatic geometry. The inic ligands, which are protonated at the pyridine N atom, link the metal centres, forming a polymeric chain running parallel to the a axis. The chains are further assembled via intra- and inter-molecular O-H?O and N-H?O hydrogen-bonding inter-actions into a three-dimensional supra-molecular network involving the inic ligands, the water mol-ecules and the perchlorate anions. One of the perchlorate ions is disordered over two sites with occupancies of 0.561?(17) and 0.439?(17).

| S-EPMC2962002 | biostudies-literature

Poly[diaqua-μ(2)-oxalato-di-μ(4)-terephthalato-diytterbium(III)].

Project description:The crystal structure of the title complex, [Yb(2)(C(8)H(4)O(4))(2)(C(2)O(4))(H(2)O)(2)](n), features an extended three-dimensional framework made up of Yb(3+) ions coordinated by terephthalate ligands, oxalate ligands and water mol-ecules. The Yb(3+) ion has a distorted square-anti-prismatic coordination formed by one aqua ligand, two O atoms from an oxalate ligand and five O atoms belonging to four terephthalate anions. Two symmetry-independent terephthalate anions, as well as the oxalate anion, occupy special positions on inversion centers. The water molecule participates in O-H⋯O hydrogen bonding with both terephthalate anions.

| S-EPMC3008045 | biostudies-literature

Poly[diaqua-μ(2)-oxalato-di-μ(4)-succinato-diyttrium(III)].

Project description:In the title compound, [Y(2)(C(4)H(4)O(4))(2)(C(2)O(4))(H(2)O)(2)](n), the flexible succinate anion assumes a gauche conformation and bridges the eight-coordinated Y atoms, generating two-dimensional layers parallel to (010). The coordination polymer layers are linked into a three-dimensional framework by the rigid oxalate ligands. The oxalate ions are located on a center of inversion. Inter-molecular O-H⋯O hydrogen bonds help to stabilize the crystal structure.

| S-EPMC2969986 | biostudies-literature

Poly[diaqua-μ-oxalato-μ-pyrazine-2-carbox-yl-ato-lanthanum(III)].

Project description:In the title complex, [La(C(5)H(3)N(2)O(2))(C(2)O(4))(H(2)O)(2)](n), the La(III) ion is coordinated by one N and three O atoms from two pyrazine-2-carboxylate ligands, by four O atoms from two oxalate ligands and by two O atoms of two water molecules, displaying a distorted bicapped square-anti-prismatic geometry. The carboxyl-ate groups of pyrazine-2-carboxyl-ate and oxalate ligands link the lanthanum metal centres, forming layers parallel to (10). The layers are further connected by inter-molecular O-H⋯O and N-H⋯O hydrogen-bonding inter-actions, forming a three-dimensional supra-molecular network.

| S-EPMC2967913 | biostudies-literature

Poly[diaqua-(μ-oxalato)(μ-2-oxidopyridinium-3-carboxyl-ato)lanthanum(III)].

Project description:In the title complex, [La(C(6)H(4)NO(3))(C(2)O(4))(H(2)O)(2)](n), the La(III) ion is coordinated by eight O atoms from two 2-oxido-pyridinium-3-carboxyl-ate ligands, two oxalate ligands and two water mol-ecules in a distorted bicapped square-anti-prismatic geometry. The carboxyl-ate groups link adjacent La(III) ions, forming two-dimensional layers that are further linked by N-H⋯O and O-H⋯O hydrogen bonds.

| S-EPMC2969809 | biostudies-literature

catena-Poly[{di-μ-isonicotinato-bis[di-aqua-isonicotinatoeuropium(III)]}-μ-isonicotinato-[diisonicotinatocopper(II)]-μ-isonicotinato].

Project description:The title compound, [CuEu(2)(C(6)H(4)NO(2))(8)(H(2)O)(4)](n), displays a one-dimensional chain structure. The four-coordinate Cu(II) ion (site symmetry ) adopts a trans-CuN(2)O(2) geometry and is bridged by two carboxyl-ate groups from two isonicotinate ligands. The Eu(III) ion adopts a distorted square-anti-prismatic geometry, being coordinated by four O atoms from bridging carboxyl-ate groups of four isonicotinate ligands, two O atoms from chelating carboxyl-ate groups of one isonicotinate ligand and two O atoms from coordinated water mol-ecules; adjacent Eu(III) ions in the chain are related by inversion. The water mol-ecules interact with the ligands via O-H⋯N hydrogen bonds [O⋯O = 2.782 (3)-2.881 (3) Å], which link the chains into a three-dimensional structure.

| S-EPMC2959990 | biostudies-literature

catena-Poly[[[diaqua-terbium(III)]-μ-6-carboxy-nicotinato-μ-pyridine-2,5-di-carboxyl-ato] dihydrate].

Project description:The title compound, {[Tb(C(7)H(3)NO(4))(C(7)H(4)NO(4))(H(2)O)(2)]·2H(2)O}(n), is isotypic with the analogous Tm(III) compound [Li, Zhang, Wang & Bai (2009). Acta Cryst. E65, m411]. The Tb(III) atom is octa-coordinated by two water mol-ecules and by four carboxyl-ate O atoms and two pyridyl N atoms from two pyridine-2,5-dicarboxyl-ate (2,5-pydc) and two 6-carboxy-nicotinate (2,5-Hpydc) ligands. The 2,5-pydc and 2,5-Hpydc ligands bridge Tb(III) atoms, generating helical coordination polymers along [001]. An extensive network of O-H⋯O hydrogen bonds is formed between the coordination polymers and the uncoordinated water mol-ecules. The refined Flack parameter of 0.54 (2) suggests inversion twinning.

| S-EPMC2968984 | biostudies-literature

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

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