Browse
Submit Data
Databases
API
Help

Dataset Information

33 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

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

ACCESS DATA

Json Xml

Similar Datasets

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[[bis-(methanol-κO)bis-(pyridine-κN)nickel(II)]-μ-tetra-fluoro-terephthalato-κO:O'].

Project description:In the title compound, [Ni(C(8)F(4)O(4))(C(5)H(5)N)(2)(CH(4)O)(2)](n), the Ni(II) ion is located on an inversion center and is coordinated by four O atoms [Ni-O = 2.079 (4) Å] from two tetra-fluoro-terephthalate ligands and two methanol mol-ecules, and by two N atoms [Ni-N = 2.127 (4) Å] from two pyridine ligands in a distorted octa-hedral geometry. The Ni(II) ions are connected via the tetra-fluoro-terephthalate anions into a one-dimensional chain running along the crystallographic [011] direction.

| S-EPMC2961662 | 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[[tripyridine-nickel(II)]-μ-5-bromo-isophthalato].

Project description:The title compound, [Ni(C(8)H(3)BrO(4))(C(5)H(5)N)(3)], is the first structurally characterized complex with a transition metal coordinated by a 5-bromo-isophthalate anion. The Ni(II) ion is coordinated by three O atoms from the carboxyl-ate groups and three N atoms from three pyridine ligands in a distorted octa-hedral coordination geometry. The 5-bromo-isophthalate anion is planar within 0.057 (2) Å. The two carboxyl-ate groups of the ligand coordinate the Ni(II) ions in a chelating and monodentate mode, linking the metal atoms into infinite chains along the [010] direction. These chains are stacked together via strong π-π inter-actions between the pyridine rings [centroid-centroid distance 3.601 (4) Å], forming a three-dimensional motif.

| S-EPMC2961692 | 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