scholarly journals Chlorido{μ-2,6-bis[(2-aminoethyl)iminomethyl]-4-chlorophenolato}-μ-oxido-dicopper(II) trihydrate

2012 ◽  
Vol 68 (6) ◽  
pp. m794-m795
Author(s):  
Jing-Jing Zhou ◽  
Wei Xiao ◽  
Jia-Wei Mao ◽  
Hong Zhou
Keyword(s):  
Complex Molecule ◽  
Three Dimensional ◽  
The Other ◽  
Dinuclear Complex ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Lattice Water ◽  
Dimensional Network ◽  
Apical Direction ◽  
Square Planar

In the title dinuclear complex, [Cu2(C14H20ClN4O)ClO]·3H2O, one CuII cation assumes a distorted square-planar coordination geometry and the other a distorted square-pyramidal coordination geometry. Both CuII cations are N,N′,O-chelated by one arm of the 2,6-bis[(2-aminoethyl)iminomethyl]-4-chlorophenolate anion, and one oxide anion bridges the two CuII cations, forming a dinuclear complex. One of the CuII cations is further coordinated by an Cl− anion in the apical direction. In the crystal, lattice water molecules are linked with the complex molecule via O—H...Cl hydrogen bonds while O—H...O hydrogen bonding occurs between lattice water molecules , forming three-dimensional network structure.

scholarly journals Bis[tris(propane-1,3-diamine-κ2N,N′)nickel(II)] diaquabis(propane-1,3-diamine-κ2N,N′)nickel(II) hexabromide dihydrate

2014 ◽  
Vol 70 (6) ◽  
pp. m227-m228 ◽  
Author(s):  
Aymen Yangui ◽  
Walid Rekik ◽  
Slim Elleuch ◽  
Younes Abid
Keyword(s):  
Hydrogen Bonds ◽  
Title Compound ◽  
General Position ◽  
Three Dimensional ◽  
The Other ◽  
Octahedral Coordination ◽  
Water Molecules ◽  
Coordination Environment ◽  
Lattice Water ◽  
Dimensional Network

In the title compound, [Ni(C3H10N2)3]2[Ni(C3H10N2)2(H2O)2]Br6·2H2O, one Ni2+cation, located on an inversion centre, is coordinated by four N atoms from two ligands and by two water O atoms. The other Ni2+cation, located in a general position, is coordinated by six N atoms from three ligands. In both cases, the Ni2+cation has an octahedral coordination environment. The overall structural cohesion is ensured by three types of hydrogen bonds, N—H...Br, O—H...Br and O—H...O, which connect the two types of complex cations, the bromide counter-anions and the lattice water molecules into a three-dimensional network.

scholarly journals Pentaaqua(4,6-dihydroxybenzene-1,3-disulfonato-κO1)zinc pentahydrate

2012 ◽  
Vol 68 (4) ◽  
pp. m492-m493
Author(s):  
Zhi-Biao Zhu ◽  
Shan Gao ◽  
Seik Weng Ng ◽  
Edward R. T. Tiekink
Keyword(s):  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Title Complex ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Lattice Water ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Hydroxy Groups

The ZnIIatom in the title complex, [Zn(C6H4O8S2)(H2O)5]·5H2O, is coordinated by five water molecules and an O atom of a 4,6-dihydroxybenzene-1,3-disulfonate dianion. The coordination geometry is distorted octahedral, with the Zn—Osulfonatebond relatively long compared to the Zn—Owaterbonds. The coordinated and lattice water molecules interact with each other and with the hydroxy groups and sulfonate ligand through O—H...O hydrogen bonds, generating a tightly held three-dimensional network.

scholarly journals Crystal structure of bis[(1-ammonio-1-phosphonoethyl)phosphonato]tetraaquacadmium dihydrate: a powder X-ray diffraction study

2015 ◽  
Vol 71 (4) ◽  
pp. 342-345 ◽  
Author(s):  
Mwaffak Rukiah ◽  
Thaer Assaad
Keyword(s):  
Complex Molecule ◽  
Three Dimensional ◽  
Distorted Octahedral Geometry ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Complex Molecules ◽  
Lattice Water ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Ring Motif

In the title compound, [CdL2(H2O)4]·2H2O [L= (1-ammonio-1-phosphonoethyl)phosphonate, C2H8NO6P2−], the CdIIion is situated on an inversion centre being coordinated by four aqua molecules in the equatorial plane and two phosphonate O atoms from two deprotonatedLligands in the axial positions in a distorted octahedral geometry. The asymmetric unit contains one-half of the complex molecule and one lattice water molecule. The ligandLexists in a zwitterionic form, with a positive charge on the NH3group and a negative charge on the O atom of the non-coordinating phosphonate group, and with an intramolecular O—H...O interaction forming anS(6) ring motif and two intramolecular N—H...O interactions each generating anS(5) ring motif. In the crystal, N—H...O and O—H...O hydrogen bonds link the complex molecules into a three-dimensional network in which the voids of 38 Å3are filled with ordered lattice water molecules, which are also involved in O—H...O hydrogen bonding.

scholarly journals Crystal structure oftrans-diaquabis(1H-pyrazole-3-carboxylato-κ2N,O)copper(II) dihydrate

2015 ◽  
Vol 71 (12) ◽  
pp. m232-m233 ◽  
Author(s):  
Santiago Reinoso ◽  
Beñat Artetxe ◽  
Oscar Castillo ◽  
Antonio Luque ◽  
Juan M. Gutiérrez-Zorrilla
Keyword(s):  
Hydrogen Bonds ◽  
Complex Molecule ◽  
Three Dimensional ◽  
Organic Ligands ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Complex Molecules ◽  
Carboxylate Ligands ◽  
Dimensional Network ◽  
Additional Hydrogen

In the title compound, [Cu(C4H3N2O2)2(H2O)2]·2H2O, the CuIIion is located on an inversion centre and exhibits an axially elongated octahedral coordination geometry. The equatorial plane is formed by twoN,O-bidentate 1H-pyrazole-3-carboxylate ligands in atransconfiguration. The axial positions are occupied by two water molecules. The mononuclear complex molecules are arranged in layers parallel to theabplane. Each complex molecule is linked to four adjacent species through intermolecular O—H...O and N—H...O hydrogen bonds that are established between the coordinating water molecules and carboxylate O atoms or protonated N atoms of the organic ligands. These layers are further connected into a three-dimensional network by additional hydrogen bonds involving solvent water molecules and non-coordinating carboxylate O atoms.

scholarly journals catena-Poly[[[bis(acetato-κ2 O,O′)aquacadmium]-μ-[(pyridin-3-yl)(pyridin-4-yl)methanone]-κ2 N:N′] dihydrate]

2012 ◽  
Vol 68 (6) ◽  
pp. m723-m723
Author(s):  
Zhi-Wei Wang ◽  
Ai-Min Li ◽  
Ya Zhang
Keyword(s):  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Title Complex ◽  
Infinite Chain ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Lattice Water ◽  
Metal Atoms ◽  
Dimensional Network

In the title complex, {[Cd(CH3COO)2(C11H8N2O)(H2O)]·2H2O} n , the CdII ion adopts an O5N2 pentagonal–bipyramidal coordination geometry with four acetate O atoms and one water O atom at the equatorial sites and two pyridine N atoms at the axial sites. The (pyridin-3-yl)(pyridin-4-yl)methanone ligand acts in a μ2-bridging mode, linking the metal atoms, leading to an infinite chain along [-110]. O—H...O hydrogen bonds involving the lattice water molecules connect these chains into a three-dimensional network.

scholarly journals Bis[μ-1,3-bis(1H-imidazol-1-yl)propane-κ2N3:N3′]bis(dichloridozinc) dihydrate

2014 ◽  
Vol 70 (5) ◽  
pp. m184-m184
Author(s):  
Xiao-Juan Wang ◽  
Yun-Long Feng
Keyword(s):  
Zinc Complex ◽  
Complex Molecule ◽  
Dimensional Structure ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Tetrahedral Coordination ◽  
Lattice Water ◽  
Bridging Ligand ◽  
Cl Atoms ◽  
Distorted Tetrahedral Coordination

The title hydrated complex, [Zn2Cl4(C9H12N4)2]·2H2O, is a discrete dinuclear zinc complex with 1,3-bis(1H-imidazol-1-yl)propane as the bridging ligand. The complex molecule lies about a crystallographic inversion centre. The ZnIIatom exhibits a distorted tetrahedral coordination geometry defined by two imidazole N atoms and two Cl atoms. O—H...Cl hydrogen bonding between the lattice water molecules and the terminal Cl atoms of the molecule lead to a two-dimensional structure extending parallel to (100).

scholarly journals Crystal structure of (2-amino-7-methyl-4-oxidopteridine-6-carboxylato-κ3O4,N5,O6)aqua(1,10-phenanthroline-κ2N,N′)zinc trihydrate

2015 ◽  
Vol 71 (9) ◽  
pp. m162-m163
Author(s):  
Siddhartha S. Baisya ◽  
Baidyanath Ghosh ◽  
Parag S. Roy
Keyword(s):  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Carboxylate Ligand ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Complex Molecules ◽  
Distorted Octahedral Coordination ◽  
Dimensional Network ◽  
Distorted Octahedral Coordination Geometry ◽  
Distorted Octahedral

In the title compound, [Zn(C8H5N5O3)(C12H8N2)(H2O)]·3H2O, a tridentate 2-amino-7-methyl-4-oxidopteridine-6-carboxylate ligand, a bidentate ancillary 1,10-phenanthroline (phen) ligand and a water molecule complete a distorted octahedral coordination geometry around the ZnIIatom. The pterin ligand forms two chelate rings. The phen and pterin ring systems are nearly perpendicular [dihedral angle = 85.16 (5)°]. Classical N—H...O, O—H...N and O—H...O hydrogen bonds and weak C—H...O hydrogen bonds link the complex molecules and lattice water molecules into a three-dimensional network. π–π stacking contacts are observed as well, with centroid-to-centroid distances of 3.5679 (14), 3.7004 (14), 3.6641 (15), 3.6974 (13) and 3.3412 (12) Å.

Darstellung und Kristallstruktur von K2Sb4S7 · H2O / Preparation and Crystal Structure of K2Sb4S7 · H2O

1979 ◽  
Vol 34 (3) ◽  
pp. 383-385 ◽  
Author(s):  
Brigitte Eisenmann ◽  
Herbert Schäfer
Keyword(s):  
Crystal Structure ◽  
Free Electron ◽  
Electron Pair ◽  
Three Dimensional ◽  
The Other ◽  
Water Molecules ◽  
Triclinic System ◽  
Dimensional Network ◽  
Free Electron Pair

Abstract K2Sb4S7 · H2O crystallizes in the triclinic system with a = 1171.4(5) pm, b = 952.0(5) pm, c = 715.6(5) pm and α = 99.36(5)°, β = 86.80(5)°, γ= 103.48(5)°. One half of the Sb atoms has three sulfur neighbours forming with the free electron pair a ψ-ShS3 tetrahedron, while the other half is coordinated by four S atoms to build a ψ-trigonal SbS4 bipyramid. These polyhedra are connected by common edges and corners to a three-dimensional network with two types of channels, in which either K+ ions only or K+ ions and water molecules are located.

scholarly journals Crystal structures of ZnCl2·2.5H2O, ZnCl2·3H2O and ZnCl2·4.5H2O

2014 ◽  
Vol 70 (12) ◽  
pp. 515-518 ◽  
Author(s):  
Erik Hennings ◽  
Horst Schmidt ◽  
Wolfgang Voigt
Keyword(s):  
Phase Diagram ◽  
Room Temperature ◽  
Three Dimensional ◽  
Water Molecules ◽  
Tetrahedral Coordination ◽  
Lattice Water ◽  
Octahedral Environment ◽  
Dimensional Network ◽  
Different Types ◽  
Solid Liquid

The formation of different complexes in aqueous solutions is an important step in understanding the behavior of zinc chloride in water. The structure of concentrated ZnCl2solutions is governed by coordination competition of Cl−and H2O around Zn2+. According to the solid–liquid phase diagram, the title compounds were crystallized below room temperature. The structure of ZnCl2·2.5H2O contains Zn2+both in a tetrahedral coordination with Cl−and in an octahedral environment defined by five water molecules and one Cl−shared with the [ZnCl4]2−unit. Thus, these two different types of Zn2+cations form isolated units with composition [Zn2Cl4(H2O)5] (pentaaqua-μ-chlorido-trichloridodizinc). The trihydrate {hexaaquazinc tetrachloridozinc, [Zn(H2O)6][ZnCl4]}, consists of three different Zn2+cations, one of which is tetrahedrally coordinated by four Cl−anions. The two other Zn2+cations are each located on an inversion centre and are octahedrally surrounded by water molecules. The [ZnCl4] tetrahedra and [Zn(H2O)6] octahedra are arranged in alternating rows parallel to [001]. The structure of the 4.5-hydrate {hexaaquazinc tetrachloridozinc trihydrate, [Zn(H2O)6][ZnCl4]·3H2O}, consists of isolated octahedral [Zn(H2O)6] and tetrahedral [ZnCl4] units, as well as additional lattice water molecules. O—H...O hydrogen bonds between the water molecules as donor and ZnCl4tetrahedra and water molecules as acceptor groups leads to the formation of a three-dimensional network in each of the three structures.

Structure of Hydrated Copper(II) Colchiceine

1999 ◽  
Vol 52 (4) ◽  
pp. 333 ◽  
Author(s):  
Maureen F. Mackay ◽  
Robert W. Gable ◽  
James D. Morrison ◽  
Lothar O. Satzke
Keyword(s):  
Hydrogen Bonding ◽  
Copper Atom ◽  
Three Dimensional ◽  
Water Molecules ◽  
R Factor ◽  
Bonding System ◽  
Dimensional Network ◽  
Square Planar ◽  
Hydrogen Bonding System ◽  
C 50

Hydrated crystals of copper(II) colchiceine belong to the tetragonal space group P 432I2 with a 13·415(1), c 50·169(8) Å and Z 8. The structure has been refined to a conventional R factor of 0·077 for 4560 observed data. The tropolonic oxygens from two colchiceine molecules are coordinated to the copper atom in this bis-chelated complex to form a square planar arrangement. The sites of three of the waters are clearly defined, but the others are disordered over seven partially occupied sites. An intricate hydrogen-bonding system links the complex and water molecules into a three-dimensional network in the crystal.

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