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Catena-Poly[[diaqua-magnesium(II)]-bis-(μ-5-ammonio-isophthalato-κO:O)].

ABSTRACT: In the title compound, [Mg(C(8)H(6)NO(4))(2)(H(2)O)(2)](n), the Mg(II) ion lies on a twofold roatation axis and is coordinated in a slightly distorted octa-hedral environment. Pairs of bridging ammonium-isophthalate ligands connect symmetry-related Mg(II) ions, forming chains along [010]. In the crystal, inter-molecular O-H⋯O and N-H⋯O hydrogen bonds link these chains into a three-dimensional network. The centroids of pairs of symmetry-related benzene rings within a chain are separated by 3.5707 (12) Å.

SUBMITTER: Wu CY

PROVIDER: S-EPMC3009009 | biostudies-literature |

REPOSITORIES: biostudies-literature

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catena-Poly[[bis-(1-methyl-imidazole-κN)zinc(II)]-μ-isophthalato-κO:O].

Project description:In the solid state, the title compound, [Zn(C(8)H(4)O(4))(C(4)H(6)N(2))(2)](n), exhibits the existence of polymeric zigzag chains extending along the a axis. Each Zn(II) ion is coordinated by two N atoms [Zn-N = 1.996 (6) and 2.032 (5) Å] and two O atoms [Zn-O = 1.930 (4) and 1.976 (4) Å] in a distorted tetra-hedral geometry. Weak C-H⋯O inter-actions contribute to the crystal packing stability.

| S-EPMC2959463 | biostudies-literature

catena-Poly[[diaqua-bis-(isoquinoline-κN)cobalt(II)]-μ-succinato-κO:O].

Project description:In the title compound, [Co(C(4)H(4)O(4))(C(9)H(7)N)(2)(H(2)O)(2)](n), the Co(II) cation, located on an inversion center, is coordinated by two succinate anions, two isoquinoline ligands and two water mol-ecules in a distorted octa-hedral geometry. The succinate anion, located across another inversion center, bridges the Co cations, forming polymeric chains running along the b axis. The partially overlapped arrangement of parallel isoquinoline ring systems of adjacent polymeric chains and the shorter face-to-face distance of 3.402 (6) Å indicates the existence of weak π-π stacking in the crystal structure. Classical intra- and inter-molecular O-H⋯O hydrogen bonding and weak non-classical inter-molecular C-H⋯O hydrogen bonding help to stabilize the crystal structure.

| S-EPMC3006983 | biostudies-literature

catena-Poly[[diaqua-cobalt(II)]-bis-(μ-4-fluoro-benzoato-κO:O')].

Project description:The hydro-thermal reaction of CoCO(3) and 4-fluoro-benzoic acid afforded the title Co(II) complex, [Co(C(7)H(4)FO(2))(2)(H(2)O)(2)](n). The Co(II) atom is located on an inversion center and is coordinated by six O atoms from two water mol-ecules and four μ(2)-carboxyl-ate groups of 4-fluoro-benzoate anions, forming a distorted CoO(6) octa-hedron, with Co-O bond lengths in the range 2.071 (2)-2.130 (2) Å. All adjacent O-Co-O angles are in the range 84.78 (6)-95.22 (6)° and opposite angles are 180.0°. Each μ-carboxyl-ate group of the 4-fluoro-benzoate anions bridges two symmetry-related Co(II) atoms. Hydrogen-bonding inter-actions of the coordinated water mol-ecules further connect the cobalt-carboxyl-ate units, forming layers perpendicular to the a axis. The cobalt-oxygen layers are encased in a sandwich-like fashion by layers of π-stacked 4-fluoro-benzoate anions. Within these layers the benzene rings of the 4-fluoro-benzoate anions are π-stacked, with centroid-centroid distances of 3.432 (4) Å.

| S-EPMC2977626 | biostudies-literature

catena-Poly[cadmium(II)-(μ-3-ammonio-3-phenyl-propanoato-κO:O')-di-μ-chlorido].

Project description:The title compound, [CdCl(2)(C(9)H(11)NO(2))](n), is a coordination polymer prepared by the hydro-thermal reaction of cadmium(II) chloride and 3-amino-3-phenyl-propanoic acid. Geometric parameters are in the usual ranges. The cadmium cation is octa-hedrally coordinated by four Cl atoms at equatorial sites and two O atoms from two ligands at the axial sites. The material is composed of one-dimensional extended polymeric chains in which two Cl atoms bridge Cd atoms. The crystal structure is stabilized by an intra-molecular N-H⋯O hydrogen bond.

| S-EPMC2961993 | biostudies-literature

catena-Poly[[bis-(μ-3-carboxy-benzoato)bis-(1,10-phenanthroline)tricopper(II)]-di-μ(3)-isophthalato].

Project description:The title copper coordination polymer, [Cu(3)(C(8)H(4)O(4))(2)(C(8)H(5)O(4))(2)(C(10)H(8)N(2))(2)](n), was synthesized by reacting Cu(NO(3))(2), isophthalic acid and 1,10-phenanthroline under hydro-thermal conditions. The trinuclear unit presents a central almost planar CuO(4) chromophore with the cation on a symmetry center, and two symmetry-related CuN(2)O(3) groups with the metal centre in a distorted square-pyramidal environment. These units are bridged by isophthalate ligands into one-dimensional double-chain coordination polymers which are, in turn, connected by various π-π stacking inter-actions (face-to-face distance ca 3.45 Å) and O-H⋯O hydrogen bonds, forming a three-dimensional supra-molecular network.

| S-EPMC2959876 | biostudies-literature

catena-Poly[[[diaqua-bis(1H-indole-3-acetato-κO)cobalt(II)]-μ-4,4'-bipyridine-κN:N'] tetra-hydrate].

Project description:The 4,4'-bipyridine spacer in the title compound, [Co(C(10)H(8)NO(2))(2)(C(10)H(8)N(2))(H(2)O)(2)]·4H(2)O, links the diaqua-cobalt(II) dicarboxyl-ate units into a linear chain; the metal atom lies on a center of inversion in an octa-hedral environment. The coordinated and uncoordinated water mol-ecules inter-act through O-H⋯O hydrogen bonds to form a three-dimensional network.

| S-EPMC2961286 | biostudies-literature

catena-Poly[[[diaqua-cadmium(II)]-bis-[μ-3,5-bis-(isonicotinamido)benzoato]] tetra-hydrate].

Project description:The title compound, {[Cd(C(19)H(13)N(4)O(4))(2)(H(2)O)(2)]·4H(2)O}(n) or {[Cd(BBA)(2)(H(2)O)(2)]·4H(2)O}(n), where BBA is 3,5-bis-(iso-nicotin-amido)-benzoate, is isotypic with its Mn isologue [Chen et al. (2009 ▶). J. Coord. Chem.62, 2421-2428]. The cation sits on a twofold axis and is six-coordinated in a slightly distorted octa-hedral geometry; the polyhedra are linked into zigzag chains, which are further connected by N-H⋯O, O-H⋯O and O-H⋯N hydrogen bonds as well as π-π inter-actions [centroid-centroid distance of 3.639 (2) Å], giving a three-dimensional supra-molecular framework.

| S-EPMC2983169 | biostudies-literature

catena-Poly[[aqua-(2,2'-bipyridine-κN,N')copper(II)]-μ-5-nitro-isophthalato-κO,O:O].

Project description:In the asymmetric unit of the title compound, [Cu(C(8)H(3)NO(6))(C(10)H(8)N(2))(H(2)O)](n), there are two symmetry-independent one-dimensional coordination polymers related by a non-crystallographic inversion center. Within the polymers, the Cu(II )atoms, coordinated by the water mol-ecule and the chelating 2,2'-bipyridine ligands, are bridged by 5-nitro-benzene-1,3-dicarboxyl-ate dianions which act as tridentate ligands; the carboxyl-ate groups exhibit monodentate and symmetric bidentate coordination modes. The Cu(II) atoms show a strongly distorted octa-hedral coordination geometry. In the crystal structure, the two symmetry-independent coordination polymers form another one-dimensional polymeric structure via O-H⋯O hydrogen bonds between coordinated water mol-ecules and carboxyl-ate groups.

| S-EPMC2959803 | biostudies-literature

catena-Poly[(triaqua-cadmium)-μ-5-hy-droxy-isophthalato-κO,O:O].

Project description:The title compound, [Cd(C(8)H(4)O(5))(H(2)O)(3)](n), a one-dimensional chain complex of 5-hy-droxy-isophthalate with Cd(II), was prepared by a hydro-thermal reaction. The Cd(II) ion is coordinated by three water O atoms and three carboxyl-ate O atoms of two different 5-hy-droxy-isophthalate ligands, which act as bidentate and monodentate ligands. The crystal structure is stabilized by O-H⋯O hydrogen bonds.

| S-EPMC3246980 | biostudies-literature

Poly[[aqua-[μ-1,4-bis-(3-pyridylmeth-yl)piperazine-κN:N'](μ-isophthalato-κO:O)copper(II)].

Project description:In the title compound, [Cu(C(8)H(4)O(4))(C(16)H(20)N(4))(H(2)O)](n), square-pyramidally coordinated Cu(II) ions are linked into [Cu(H(2)O)(isophthalate)](n) coordination polymer chains by isophthalate dianions. These chains are connected into undulating [Cu(H(2)O)(isophthalate)(3-bpmp)](n) [3-bmp is bis-(3-pyridylmeth-yl)piperazine] layers by 3-bpmp tethering ligands. The pseudo three-dimensional structure of the title compound is fostered by inter-layer O-H⋯O hydrogen bonding between the aqua ligands and unligated isophthalate O atoms. The selected crystal was non-merohedrally twinned. Only reflections from the major twin component were used in the solution and refinement.

| S-EPMC2983567 | biostudies-literature

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