scholarly journals Crystal structure of poly[μ2-aqua-aqua(μ2-4-nitro-2,5,6-trioxo-1,2,5,6-tetrahydropyridin-3-olato)hemi-μ4-oxalato-barium(II)]

2015 ◽  
Vol 71 (5) ◽  
pp. 459-462 ◽  
Author(s):  
Rusul Alabada ◽  
Olga Kovalchukova ◽  
Irina Polyakova ◽  
Svetlana Strashnova ◽  
Vladimir Sergienko
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Water Molecules ◽  
Two Dimensional ◽  
Supramolecular Framework ◽  
Screw Axis ◽  
Bond Lengths ◽  
Chelate Rings

In the title coordination polymer, [Ba(C5HN2O6)(C2O4)0.5(H2O)2]n, the tenfold coordination of the Ba centre consists of four O atoms from the two 4-nitro-2,5,6-trioxo-1,2,5,6-tetrahydropyridin-3-olate (L) anions, three O atoms of two oxalate anions and three water molecules. The Ba—O bond lengths fall in the range 2.698 (3)–2.978 (3) Å. TheLligand chelates two Ba atoms related by a screw axis, leading to formation of fused five- and six-membered chelate rings. Due to the bridging function of the ligands and water molecules, the complex monomers are connected into polymeric two-dimensional layers parallel to thebcplane. Intermolecular O—H...O hydrogen bonds link these layers into a three-dimensional supramolecular framework.

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 structure of bis(acetato-κ2 O,O′)diaqua[1-(pyridin-2-ylmethylidene-κN)-2-(pyridin-2-yl-κN)hydrazine-κN 1]terbium(III) nitrate monohydrate

2017 ◽  
Vol 73 (8) ◽  
pp. 1121-1124 ◽  
Author(s):  
NDiaye Mbossé Gueye ◽  
Dieng Moussa ◽  
Elhadj Ibrahima Thiam ◽  
Aliou Hamady Barry ◽  
Mohamed Gaye ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Title Compound ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Water Molecules ◽  
Coordination Environment ◽  
Bond Lengths ◽  
Nitrate Anions ◽  
Trigonal Prismatic

In the title compound, [Tb(C2H3O2)2(C11H10N4)(H2O)2]NO3·H2O, the Tb3+ ion is nine-coordinated in a distorted tricapped trigonal-prismatic geometry by the three N atoms of the tridentate 1-(pyridin-2-ylmethylidene)-2-(pyridin-2-yl)hydrazine ligand, four carboxylate O atoms of two chelating acetate groups and two O atoms of the coordinating water molecules. The organic hydrazine ligand is disordered over two orientations with a refined occupancy ratio of 0.52 (3):0.48 (3). All bond lengths in the coordination environment of the Tb3+ ion are slightly larger than those observed in the isostructural Y3+ and Er3+ complexes. In the crystal, the complex cations are linked by pairs of O—H...O hydrogen bonds into dimers. These dimers, nitrate anions and non-coordinating water molecules are joined by O—H...O and N—H...O hydrogen bonds into a three-dimensional structure.

Diaquabis(dicyanamido)bis[4-(2-pyridyl)-4H-1,2,4-triazole-κN 1]cobalt(II)

2006 ◽  
Vol 62 (7) ◽  
pp. m1479-m1481 ◽  
Author(s):  
Yu-Hong Ma ◽  
Pi-Zhuang Ma ◽  
Huan-Qin Zhu ◽  
Chang-Cheng Liu
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Title Complex ◽  
Water Molecules ◽  
Two Dimensional ◽  
Complex Molecules ◽  
Dimensional Network

The title complex, [Co(C2N3)2(C7H6N4)2(H2O)2] or [Co(dca)2(pytrz)2(H2O)2], where pytrz is 4-(2-pyridyl)-4H-1,2,4-triazole and dca is the dicyanamide monoanion, was prepared using pytrz, Na(dca) and CoCl2·6H2O. The CoII atom lies on a center of inversion and is coordinated in a slightly distorted octahderal geometry by two pytrz ligands, two dca ligands and two trans-oriented water molecules. In the crystal structure, complex molecules are linked by O—H...N hydrogen bonds into a two-dimensional network and further into a three-dimensional network via weak C—H...N hydrogen bonds.

scholarly journals Crystal structure of the two-dimensional coordination polymer poly[di-μ-bromido-bis(μ-tetrahydrothiophene)dicopper(I)]

2021 ◽  
Vol 77 (7) ◽  
pp. 744-748
Author(s):  
Michael Knorr ◽  
Lydie Viau ◽  
Yoann Rousselin ◽  
Marek M. Kubicki
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Two Dimensional ◽  
Different Types ◽  
Secondary Building Units ◽  
Mecn Solution ◽  
Bonding Mode

The polymeric title compound, [Cu2Br2(C4H8S)2] n , CP1, represents an example of a two-dimensional coordination polymer resulting from reaction of CuBr with tetrahydrothiophene (THT) in MeCN solution. The two-dimensional layers consist of two different types of rhomboid-shaped dinuclear Cu(μ2-Br)2Cu secondary building units (SBUs); one with a quite loose Cu...Cu separation of 3.3348 (10) Å and a second one with a much closer intermetallic contact of 2.9044 (9) Å. These SBUs are interconnected through bridging THT ligands, in which the S atom acts as a four-electron donor bridging each Cu(μ2-Br)2Cu unit in a μ2-bonding mode. In the crystal, the layers are linked by very weak C—H...·Br hydrogen bonds with H...Br distances of 2.95 Å, thus giving rise to a three-dimensional supramolecular network.

scholarly journals Crystal structure of the co-crystalfac-triaquatris(thiocyanato-κN)iron(III)–2,3-dimethylpyrazine (1/3)

2015 ◽  
Vol 71 (4) ◽  
pp. 374-376
Author(s):  
Olesia I. Kucheriv ◽  
Sergii I. Shylin ◽  
Tetiana A. Ilina ◽  
Sebastian Dechert ◽  
Il'ya A. Gural'skiy
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Title Compound ◽  
Rotation Axis ◽  
Three Dimensional ◽  
Water Molecules ◽  
Supramolecular Framework

In the crystal of the title compound, [Fe(NCS)3(H2O)3]·3C6H8N2, the FeIIIcation is located on a threefold rotation axis and is coordinated by three N atoms of the thiocyanate anions and three water molecules in afacarrangement, forming a slightly distorted N3O3octahedron. Stabilization within the crystal structure is provided by O—H...N hydrogen bonds; the H atoms from coordinating water molecules act as donors to the N atoms of guest 2,3-dimethylpyrazine molecules, leading to a three-dimensional supramolecular framework.

scholarly journals Crystal structure of a heterometallic coordination polymer: catena-poly[[[tetraaquacobalt(II)]-μ-pyridine-2,6-dicarboxylato-calcium(II)-μ-pyridine-2,6-dicarboxylato] dihydrate]

2018 ◽  
Vol 74 (6) ◽  
pp. 808-811
Author(s):  
Jie-Shuang Lin ◽  
Bing-Guang Zhang
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Octahedral Geometry ◽  
Water Molecules ◽  
Stacking Interactions ◽  
Polymeric Complex ◽  
Lattice Water ◽  
Polymeric Chains

In the crystal of the title polymeric complex, {[CoCa(C7H3NO4)2(H2O)4]·2H2O} n (1), the CoII ion is N,O,O′-chelated by two pyridine-2,6-dicarboxylate anions in a distorted N2O4 octahedral geometry, and two carboxylate O atoms of pyridine-2,6-dicarboxylate anions bridge tetraaquacalcium(II) units to form polymeric chains propagating along the b-axis direction. In the crystal, O—H...O and C—H...O hydrogen bonds, and offset π–π stacking interactions [intercentroid distances = 3.551 (1) and 3.746 (1) Å] involving inversion-related pyridine rings link the polymeric chains and lattice water molecules to form a supramolecular three-dimensional framework.

scholarly journals Crystal structure of bis(dimethylammonium) hexaaquanickel(II) bis(sulfate) dihydrate

2014 ◽  
Vol 70 (11) ◽  
pp. 403-405 ◽  
Author(s):  
Peter Held
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Metal Cations ◽  
Water Molecules ◽  
Bond Lengths ◽  
Complex Metal ◽  
Distorted Octahedral ◽  
Medium Strength

In the title salt, (C2H8N)2[Ni(H2O)6)](SO4)2·2H2O, the NiIIcation is located on a centre of inversion and exhibits a slightly distorted octahedral arrangement of water molecules. The Ni—O bond lengths in the complex [Ni(H2O)6]2+cation show a distribution as in the related Tutton salt (NH4)2[Ni(H2O)6](SO4)2, but are longer in average [2.056 (13)versus2.037 (12) Å]. The noncoordinating water molecules and dimethylammonium cations connect the sulfate and [Ni(H2O)6]2+octahedraviaO—H...O and N—H...O hydrogen bonds from weak up to medium strength into a three-dimensional framework whereby the complex metal cations and sulfate anions are arranged in sheets parallel (001).

scholarly journals Crystal structure of a three-dimensional neodymium(III) coordination polymer, [Nd2(H2O)6(glutarato)(SO4)2] n

2022 ◽  
Vol 78 (2) ◽  
Author(s):  
Saranphong Yimklan ◽  
Yothin Chimupala ◽  
Sutsiri Wongngam ◽  
Nippich Kaeosamut
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Microwave Heating ◽  
Three Dimensional ◽  
Two Dimensional ◽  
Coordination Network ◽  
Dinuclear Cluster ◽  
Trigonal Prismatic

A three-dimensional coordination polymer, poly[hexaaqua(μ4-glutarato)bis(μ3-sulfato)dineodymium(III)], [Nd2(H2O)6(glutarato)(SO4)2] n (glutarato2– = C5H6O4 2–), 1, consisting of cationic {Nd2(H2O)6(SO4)2} n 2n+ layers linked by bridging glutarate ligands, was synthesized by the microwave-heating technique within few minutes. The crystal structure of 1 consists of two crystallographically independent TPRS-{NdIIIO9} (TPRS is tricapped trigonal–prismatic geometry) units that form an edge-sharing dinuclear cluster interconnected to neighbouring dimers by the μ3-SO4 2– anions, yielding a cationic two-dimensional {Nd2(H2O)6(SO4)2} n 2n+ sheet. Adjacent cationic layers are then linked via the μ4-glutarato2– ligands into a three-dimensional coordination network. Strong O—H...O hydrogen bonds are the predominant interaction in the crystal structure.

scholarly journals In situsingle-crystal to single-crystal (SCSC) transformation of the one-dimensional polymercatena-poly[[diaqua(sulfato)copper(II)]-μ2-glycine] into the two-dimensional polymer poly[μ2-glycine-μ4-sulfato-copper(II)]

2014 ◽  
Vol 70 (11) ◽  
pp. 1057-1063 ◽  
Author(s):  
Helen Stoeckli-Evans ◽  
Olha Sereda ◽  
Antonia Neels ◽  
Sebastien Oguey ◽  
Catherine Ionescu ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Two Dimensional ◽  
Apical Position ◽  
Coordination Environment ◽  
One Dimensional ◽  
Carboxylate Groups ◽  
The One

The one-dimensional coordination polymercatena-poly[diaqua(sulfato-κO)copper(II)]-μ2-glycine-κ2O:O′], [Cu(SO4)(C2H5NO2)(H2O)2]n, (I), was synthesized by slow evaporation under vacuum of a saturated aqueous equimolar mixture of copper(II) sulfate and glycine. On heating the same blue crystal of this complex to 435 K in an oven, its aspect changed to a very pale blue and crystal structure analysis indicated that it had transformed into the two-dimensional coordination polymer poly[(μ2-glycine-κ2O:O′)(μ4-sulfato-κ4O:O′:O′′:O′′)copper(II)], [Cu(SO4)(C2H5NO2)]n, (II). In (I), the CuIIcation has a pentacoordinate square-pyramidal coordination environment. It is coordinated by two water molecules and two O atoms of bridging glycine carboxylate groups in the basal plane, and by a sulfate O atom in the apical position. In complex (II), the CuIIcation has an octahedral coordination environment. It is coordinated by four sulfate O atoms, one of which bridges two CuIIcations, and two O atoms of bridging glycine carboxylate groups. In the crystal structure of (I), the one-dimensional polymers, extending along [001], are linkedviaN—H...O, O—H...O and bifurcated N—H...O,O hydrogen bonds, forming a three-dimensional framework. In the crystal structure of (II), the two-dimensional networks are linkedviabifurcated N—H...O,O hydrogen bonds involving the sulfate O atoms, forming a three-dimensional framework. In the crystal structures of both compounds, there are C—H...O hydrogen bonds present, which reinforce the three-dimensional frameworks.

scholarly journals Crystal structure of dipotassiumN-carbodithioato-L-prolinate trihydrate

2017 ◽  
Vol 73 (9) ◽  
pp. 1375-1378 ◽  
Author(s):  
Phil Liebing
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Coordination Mode ◽  
Molecular And Crystal Structure ◽  
Water Molecules ◽  
Two Dimensional

The molecular and crystal structure of the L-proline-derived dithiocarbamate–carboxylate compound poly[tri-μ-aqua-(μ-2-carboxylatopyrrolidine-1-carbodithioato)dipotassium], [K2(C6H7NO2S2)(H2O)3]nor K2(SSC–NC4H7–COO)·3H2O, has been determined. The dithiocarbamate moiety displays a unique coordination mode, comprising a `side-on' π-coordinated K+cation besides a commonly σ-chelated K+cation. By bridging coordination of the CSS group, COO group and water molecules, the K+cations are linked into a two-dimensional coordination polymer extending parallel to theabplane. These layers are again interconnected by O—H...S hydrogen bonds.

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