scholarly journals Poly[[diaquabis[μ4-5-nitroisophthalato-κ4O1:O1:O3:O3′]bis[μ3-pyridine-4-carboxylato-κ3O:O′:N]tricobalt(II)] tetrahydrate]

2012 ◽  
Vol 68 (4) ◽  
pp. m451-m452
Author(s):  
Xia Yin ◽  
Jun Fan ◽  
Jingling Xin ◽  
Shengrun Zheng ◽  
Weiguang Zhang
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Three Dimensional ◽  
Free Water ◽  
Water Molecules ◽  
Two Dimensional ◽  
Lattice Water ◽  
Free Water Molecule ◽  
Carboxylate Groups ◽  
Coordinated Water

The title compound, {[Co3(C6H4NO2)2(C8H3NO6)2(H2O)2]·4H2O}n, exhibits a two-dimensional layer-like structure in which the CoIIions exhibit two kinds of coordination geometries. One nearly octahedral CoIIion with crystallographic inversion symmetry is coordinated to six carboxylate O atoms from four bridging 5-nitroisophthalate (NIPH) ligands and two isonicotinate (IN) anions, while the other type of CoIIion binds with one N atom and one carboxylate O atom from two IN anions, two carboxylate O atoms from two different NIPH anions and one ligated water molecule, displaying a distorted square-pyramidal coordination geometry. Three adjacent CoIIions are bridged by six carboxylate groups from four NIPH ligands and two IN anions to form a linear trinuclear secondary building unit (SBU). Every trinuclear SBU is linked to its nearest neighbours in theabplane, resulting in a two-dimensional layer-like structure perpendicular to thecaxis. Along thea-axis direction neighbouring molecules are connected through carboxylate and pyridyl units of the IN anions, along thebaxis through carboxylate groups of the NIPH ligands. The H atoms of one free water molecule are disordered in the crystal in a 1:1 ratio. Typical O—H...O hydrogen bonds are observed in the lattice, which include the following contacts: (a) between coordinated water molecules and carboxylate O atoms of the NIPH anions, (b) between lattice water molecules and carboxylate O atoms of the NIPH anions, and (c) between coordinated and lattice water molecules. These intermolecular hydrogen bonds connect the two-dimensional layers to form a three-dimensional supramolecular structure.

scholarly journals catena-Poly[[(tetraaquacadmium)-μ-4,4′-bipyridine-κ2 N:N′] 4-hydroxy-3-sulfonatobenzoate monohydrate]

2012 ◽  
Vol 68 (6) ◽  
pp. m715-m715
Author(s):  
Shan Gao ◽  
Seik Weng Ng
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Lattice Water Molecule ◽  
Three Dimensional ◽  
Octahedral Geometry ◽  
Water Molecules ◽  
Lattice Water ◽  
Rotation Axes ◽  
Dimensional Network ◽  
Coordinated Water

The two independent CdII atoms in the polymeric title compound, [Cd(C10H8N2)(H2O)4](C7H4O6S)·H2O, lie on twofold rotation axes, and each is coordinated by four water molecules and the N atoms of two 4,4′-bipyridine molecules in an octahedral geometry. Bridging gives rise to chains along [101] and [-101]. The 4-hydroxy-3-sulfonatobenzoate dianions are not connected to the CdII atoms, but form hydrogen bonds to the coordinated water molecules as well as the lattice water molecule, generating a three-dimensional network.

scholarly journals Crystal structure of poly[diaquabis(μ5-benzene-1,3-dicarboxylato)(N,N-dimethylformamide)cadmium(II)disodium(I)]

2017 ◽  
Vol 73 (11) ◽  
pp. 1599-1602 ◽  
Author(s):  
Matimon Sangsawang ◽  
Kittipong Chainok ◽  
Nanthawat Wannarit
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Water Molecules ◽  
Asymmetric Unit ◽  
Carboxylate Groups ◽  
Benzene Rings ◽  
Coordinated Water ◽  
Coordinate Geometry

The title compound, [CdNa2(C8H4O4)2(C3H7NO)(H2O)2]nor [CdNa2(1,3-bdc)2(DMF)(H2O)2]n, is a new CdII–NaIheterobimetallic coordination polymer. The asymmetric unit consists of one CdIIatom, two NaIatoms, two 1,3-bdc ligands, two coordinated water molecules and one coordinated DMF molecule. The CdIIatom exhibits a seven-coordinate geometry, while the NaIatoms can be considered to be pentacoordinate. The metal ions and their symmetry-related equivalents are connectedviachelating–bridging carboxylate groups of the 1,3-bdc ligands to generate a three-dimensional framework. In the crystal, there are classical O—H...O hydrogen bonds involving the coordinated water molecules and the 1,3-bdc carboxylate groups and π–π stacking between the benzene rings of the 1,3-bdc ligands present within the frameworks.

scholarly journals Crystal structures of tetramethylammonium (2,2′-bipyridine)tetracyanidoferrate(III) trihydrate and poly[[(2,2′-bipyridine-κ2N,N′)di-μ2-cyanido-dicyanido(μ-ethylenediamine)(ethylenediamine-κ2N,N′)cadmium(II)iron(II)] monohydrate]

2016 ◽  
Vol 72 (5) ◽  
pp. 741-746
Author(s):  
Songwuit Chanthee ◽  
Wikorn Punyain ◽  
Supawadee Namuangrak ◽  
Kittipong Chainok
Keyword(s):  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Layer Structure ◽  
Three Dimensional ◽  
Building Blocks ◽  
Chain Structure ◽  
Water Molecules ◽  
Two Dimensional ◽  
Lattice Water ◽  
Π Stacking

The crystal structures of the building block tetramethylammonium (2,2′-bipyridine-κ2N,N′)tetracyanidoferrate(III) trihydrate, [N(CH3)4][Fe(CN)4(C10H8N2)]·3H2O, (I), and a new two-dimensional cyanide-bridged bimetallic coordination polymer, poly[[(2,2′-bipyridine-κ2N,N′)di-μ2-cyanido-dicyanido(μ-ethylenediamine-κ2N:N′)(ethylenediamine-κ2N,N′)cadmium(II)iron(II)] monohydrate], [CdFe(CN)4(C10H8N2)(C2H8N2)2]·H2O, (II), are reported. In the crystal of (I), pairs of [Fe(2,2′-bipy)(CN)4]−units (2,2′-bipy is 2,2′-bipyridine) are linked together through π–π stacking between the pyridyl rings of the 2,2′-bipy ligands to form a graphite-like structure parallel to theabplane. The three independent water molecules are hydrogen-bonded alternately with each other, forming a ladder chain structure withR44(8) andR66(12) graph-set ring motifs, while the disordered [N(CH3)4]+cations lie above and below the water chains, and the packing is stabilized by weak C—H...O hydrogen bonds. The water chains are further linked with adjacent sheets into a three-dimensional networkviaO—H...O hydrogen bonds involving the lattice water molecules and the N atoms of terminal cyanide groups of the [Fe(2,2′-bipy)(CN)4]−building blocks, forming anR44(12) ring motif. Compound (II) features a two-dimensional {[Fe(2,2′-bipy)(CN)4Cd(en)2]}nlayer structure (en is ethylenediamine) extending parallel to (010) and constructed from {[Fe(2,2′-bipy)(CN)4Cd(en)]}nchains interlinked by bridging en ligands at the Cd atoms. Classical O—H...N and N—H...O hydrogen bonds involving the lattice water molecule and N atoms of terminal cyanide groups and the N—H groups of the en ligands are observed within the layers. The layers are further connectedviaπ–π stacking interactions between adjacent pyridine rings of the 2,2′-bipy ligands, completing a three-dimensional supramolecular structure.

scholarly journals Tetrakis(dipropylammonium) tetrakis(oxalato-κ2O1,O2)stannate(IV) monohydrate: a complex with an eight-coordinate SnIVatom

2014 ◽  
Vol 70 (2) ◽  
pp. m49-m50 ◽  
Author(s):  
Ndongo Gueye ◽  
Libasse Diop ◽  
Helen Stoeckli-Evans
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Mirror Symmetry ◽  
Lattice Water Molecule ◽  
Three Dimensional ◽  
Water Molecules ◽  
Special Position ◽  
Lattice Water ◽  
Dimensional Network ◽  
Anions And Cations

In the title salt, [(CH3CH2CH2)2NH2]4[Sn(C2O4)4]·H2O, the SnIVatom of the stannate anion is located on a special position with -42msymmetry. It is eight-coordinated by four chelating oxalate anions. The dipropylammonium cation possesses mirror symmetry while the lattice water molecule is disordered about a position with -42msymmetry and has an occupancy of 0.25. In the crystal, the anions and cations are linked by N—H...O hydrogen bonds, forming a three-dimensional network. This network is futher stabilized by weak O—H...O hydrogen bonds involving the water molecules and oxalate O atoms. The crystal studied was refined as an inversion twin.

A two-dimensional cadmium(II) coordination polymer based on 5-(pyridin-4-yl)isophthalic acid: poly[[tetraaquabis[μ3-5-(pyridin-4-yl)isophthalato]dicadmium(II)] pentahydrate]

2015 ◽  
Vol 71 (9) ◽  
pp. 834-838 ◽  
Author(s):  
Fang Liu ◽  
Jing-Jing Zhang ◽  
Ming-Yuan Lei ◽  
Qing-Fu Zhang
Keyword(s):  
Hydrothermal Reaction ◽  
Layer Structure ◽  
Three Dimensional ◽  
Isophthalic Acid ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Two Dimensional ◽  
Hydrogen Bonding Interactions ◽  
Carboxylate Groups ◽  
Coordinated Water

The title CdIIcompound, {[Cd2(C13H7NO4)2(H2O)4]·5H2O}n, was synthesized by the hydrothermal reaction of Cd(NO3)2·4H2O and 5-(pyridin-4-yl)isophthalic acid (H2L). The asymmetric unit contains two crystallographically independent CdIIcations, two deprotonatedL2−ligands, four coordinated water molecules and five isolated water molecules. One of the CdIIcations adopts a six-coordinate octahedral coordination geometry involving three O atoms from one bidentate chelating and one monodentate carboxylate group of two differentL2−ligands, one N atom of anotherL2−ligand and two coordinated water molecules. The second CdIIcation adopts a seven-coordinate pentagonal–bipyramidal coordination geometry involving four O atoms from two bidentate chelating carboxylate groups of two differentL2−ligands, one N atom of anotherL2−ligand and two coordinated water molecules. EachL2−ligand bridges three CdIIcations and, likewise, each CdIIcation connects to threeL2−ligands, giving rise to a two-dimensional graphite-like 63layer structure. These two-dimensional layers are further linked by O—H...O hydrogen-bonding interactions to form a three-dimensional supramolecular architecture. The photoluminescence properties of the title compound were also investigated.

Adducts of 1,4,8,11-tetraazacyclotetradecane with carboxylic acids: hydrogen-bonded supramolecular structures in two or three dimensions

2004 ◽  
Vol 60 (1) ◽  
pp. 65-75 ◽  
Author(s):  
Choudhury M. Zakaria ◽  
Alan J. Lough ◽  
George Ferguson ◽  
Christopher Glidewell
Keyword(s):  
Carboxylic Acid ◽  
Hydrogen Bonds ◽  
Water Molecule ◽  
Carboxylic Acids ◽  
Rotation Axis ◽  
Three Dimensional ◽  
Supramolecular Structures ◽  
Three Dimensions ◽  
Water Molecules ◽  
Two Dimensional

Four solvated salt-type adducts derived from cyclam (1,4,8,11-tetraazacyclotetradecane) and carboxylic acids have been structurally characterized. In the salt derived from adamantane-1-carboxylic acid, 4,11-diaza-1,8-diazoniacyclotetradecane bis(adamantane-1-carboxylate) tetrahydrate, (1) (monoclinic, P21/c, Z′ = 0.5), where the cation lies across a centre of inversion, the anions and the water molecules form chains of edge-fused R_4^2(8) and R_6^6(16) rings, which are linked into sheets by the cations. In the 4-aminobenzoate salt, 4,11-diaza-1,8-diazoniacyclotetradecane bis(4-aminobenzoate) monohydrate, (2) (monoclinic, C2/c, Z′ = 0.5), where the cation lies across a centre of inversion and the water molecule lies across a twofold rotation axis, the cations and anions generate a three-dimensional framework, readily analysed in terms of two distinct two-dimensional substructures, viz. (10\overline 1) sheets of R_8^6(46) rings, and pairwise interwoven (100) sheets, reinforced by water molecules. The 3-hydroxybenzoate salt, 4,11-diaza-1,8-diazoniacyclotetradecane bis(3-hydroxybenzoate) dihydrate, (3) (monoclinic, Pc, Z′ = 1), contains a three-dimensional framework constructed from anions and water molecules only, which encapsulates large voids and within which the cations are linked to the anion–water framework via N—H...O hydrogen bonds. There are two independent cations in 4,11-diaza-1,8-diazoniacyclotetradecane 5-hydroxyisophthalate(2−) methanol solvate, (4) (monoclinic, P21/c, Z′ = 1), both lying across centres of inversion but with entirely different configurations. The anions alone form simple chains, and these chains are linked by the two types of cation into a three-dimensional framework from which the methanol molecules are pendent. Comparisons are made with carboxylate complexes of the [Ni(cyclam)]2+ cation and with carboxylate salts derived from meso-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane.

scholarly journals Piperazin-1-ium 4-aminobenzoate monohydrate

IUCrData ◽  
2016 ◽  
Vol 1 (5) ◽  
Author(s):  
P. Sivakumar ◽  
A. Mani ◽  
S. Sudhahar ◽  
S. Israel ◽  
G. Chakkaravarthi
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonds ◽  
Water Molecule ◽  
Three Dimensional ◽  
Chair Conformation ◽  
Water Molecules ◽  
Two Dimensional ◽  
Bond Forming ◽  
Hydrated Salt ◽  
Dimensional Network

The asymmetric unit of the title hydrated salt, C4H11N2+·C7H6NO2−·H2O, contains a piperazin-1-ium cation, a 4-aminobenzoate anion and a water molecule. One NH group of the piperazine ring is protonated and this ring adopts a chair conformation. The anion of this salt is generated by deprotonation of the OH group of the carboxylic acid substituent of 4-aminobenzoic acid. The benzene ring makes a dihedral angle of 2.6 (2)° with the carboxylate substituent. The anion and the solvent water molecule are linked by an N—H...O hydrogen bond. Additional N—H...O and O—H...O hydrogen bonds connect adjacent anions through the water molecules, generating a two-dimensional network parallel to (100), formingR33(12) ring motifs. Adjacent cations are linked by N—H...N hydrogen bonds into infinite chains along (001). These chains are linked to the two-dimensional network of anions and water molecules by another N—H...O hydrogen bond, forming a three-dimensional network.

A novel cadmium(II) coordination polymer containing two kinds of independent one-dimensional chain

2013 ◽  
Vol 69 (8) ◽  
pp. 829-832 ◽  
Author(s):  
Wei-Qiang Liao ◽  
Yi Zhang
Keyword(s):  
Three Dimensional ◽  
Water Molecules ◽  
Dimensional Chain ◽  
Two Dimensional ◽  
One Dimensional ◽  
Solvent Water ◽  
Carboxylate Groups ◽  
Chloride Ligand ◽  
Chloride Ligands ◽  
Coordinated Water

The structure of the title compound,catena-poly[[cadmium(II)-di-μ-chlorido-μ-(1,4-diazoniabicyclo[2.2.2]octane-1-carboxylato)] [[aquachloridocadmium(II)]-di-μ-chlorido] dihydrate], {[Cd(C8H15N2O2)Cl2][CdCl3(H2O)]·2H2O}n, contains two kinds of independent one-dimensional chain,viz.{[Cd(C8H15N2O2)Cl2]+}nand {[CdCl3(H2O)]−}n, and uncoordinated water molecules. Each CdIIcation in the {[Cd(C8H15N2O2)Cl2]+}nchain is octahedrally coordinated by two pairs of bridging chloride ligands and two O atoms from different bridging carboxylate groups. CdIIcations in the {[CdCl3(H2O)]−}nchain are also octahedrally surrounded by four bridging chloride ligands, one terminal chloride ligand and one coordinated water molecule. Hydrogen bonds between solvent water molecules and these two independent chains generate a three-dimensional framework containing two-dimensional zigzag layers.<!?tpb=18pt>

A three-dimensional polymeric potassium complex of 5-sulfonobenzene-1,2,4-tricarboxylic acid: poly[μ-aqua-aqua-μ9-(2,4-dicarboxy-5-sulfonatobenzoato)-dipotassium(I)]

2013 ◽  
Vol 69 (10) ◽  
pp. 1132-1135
Author(s):  
Wei-Lu Xiong ◽  
Yu-Ling Wang ◽  
Qing-Yan Liu
Keyword(s):  
Water Molecule ◽  
Title Compound ◽  
Three Dimensional ◽  
Water Molecules ◽  
Compound K ◽  
One Dimensional ◽  
Repeat Units ◽  
Carboxylate Groups ◽  
Coordinated Water ◽  
Thermal Stability Of

The asymmetric unit in the structure of the title compound, [K2(C9H4O9S)(H2O)2]n, consists of two eight-coordinated KIcations, one 2,4-dicarboxy-5-sulfonatobenzoate dianion (H2SBTC2−), one bridging water molecule and one terminal coordinated water molecule. One KIcation is coordinated by three carboxylate O atoms and three sulfonate O atoms from four H2SBTC2−ligands and by two bridging water molecules. The second KIcation is coordinated by four sulfonate O atoms and three carboxylate O atoms from five H2SBTC2−ligands and by one terminal coordinated water molecule. The KIcations are linked by sulfonate groups to give a one-dimensional inorganic chain with cage-like K4(SO3)2repeat units. These one-dimensional chains are bridged by one of the carboxylic acid groups of the H2SBTC2−ligand to form a two-dimensional layer, and these layers are further linked by the remaining carboxylate groups and the benzene rings of the H2SBTC2−ligands to generate a three-dimensional framework. The compound displays a photoluminescent emission at 460 nm upon excitation at 358 nm. In addition, the thermal stability of the title compound has been studied.

scholarly journals catena-Poly[[diaqua[μ2-4-(4-carboxyphenoxy)benzoato](μ2-4,4′-oxydibenzoato)praseodymium(III)] monohydrate]

2013 ◽  
Vol 69 (11) ◽  
pp. m586-m587
Author(s):  
Ping Li ◽  
Duo-Meng Su ◽  
Chang-Ge Zheng
Keyword(s):  
Carboxylic Acid ◽  
Hydrogen Bonds ◽  
Water Molecule ◽  
Network Structure ◽  
Three Dimensional ◽  
Water Molecules ◽  
Two Dimensional ◽  
Dimensional Network ◽  
Bidentate Chelate ◽  
Single Water Molecule

In the title compound, {[Pr(C14H8O5)(C14H9O5)(H2O)2]·H2O}n, the PrIIIcation is eight-coordinated by six carboxyl O atoms from both a monoanionic 4-(4-carboxyphenoxy)benzoate and a dianionic 4,4′-oxydibenzoate ligand (four bridging with two from a bidentate chelate interaction), and two O-atom donors from water molecules. A single water molecule of solvation is also present. The complex units are linked through carboxylO:O′ bridges giving a two-dimensional sheet polymer lying parallel to (001). An overall three-dimensional network structure is generated through intermolecular carboxylic acid and water O—H...O hydrogen bonds and weak C—H...O interactions.

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