scholarly journals Reversible Water Ad-/Desorption Behavior of a 3D Polycatenation Network, [Zn(bpp)(BDC)]·1.5(H2O), Constructed by 2D Undulated Layered MOF

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 371
Author(s):  
Chih-Chieh Wang ◽  
Wei-Cheng Yi ◽  
Zi-Ling Huang ◽  
Wen-Chi Chien ◽  
Yu-Chun Chuang ◽  
...  
Keyword(s):  
Terephthalic Acid ◽  
Three Dimensional ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Coordination Geometry ◽  
Supramolecular Architecture ◽  
Weight Percentage ◽  
Weight Losses ◽  
One Step ◽  
Chemical Formulas

A three-dimensional (3D) polycatenation supramolecular network with chemical formulas, [Zn(bpp)(BDC)]·1.5H2O (1), (bpp = 1,3-bis(4-pyridyl)propane, BDC2- = dianion of terephthalic acid), was synthesized and structurally determined. In compound 1, the coordination geometry of Zn(II) ion is distorted tetrahedral, where its 2D undulated layered framework is constructed via the bridges of Zn(II) ions with bpp and BDC2− ligands. Adjacent 2D layers are arranged in a combined parallel and interpenetrated manner to complete its 3D polycatenation supramolecular architecture. Compound 1 shows a one-step dehydration process with the weight losses of 6.1 %, approximately equal to the weight percentage of losing 1.5 guest water molecules. The cyclic thermogravimetric analysis reveals that compound 1 shows reversible, sponge-like water de-/adsorption behavior during de-/rehydration processes. Compound 1 also exhibits significant water vapor hysteresis isotherm.

scholarly journals Crystal structure of di-μ-hydroxido-bis[aqua(1,10-phenanthroline-κ2N,N′)copper(II)] naphthalene-2,6-dicarboxylate hexahydrate

2015 ◽  
Vol 71 (4) ◽  
pp. 360-362 ◽  
Author(s):  
Daniela Arias-Zárate ◽  
María Fernanda Ballesteros-Rivas ◽  
Rubén A. Toscano ◽  
Jesús Valdés-Martínez
Keyword(s):  
Crystal Structure ◽  
Binuclear Complex ◽  
Complex Cation ◽  
Three Dimensional ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Supramolecular Architecture ◽  
Aromatic Rings ◽  
Phen Molecule ◽  
Lattice Water

In the title compound, [Cu2(OH)2(C12H8N2)2(H2O)2](C12H6O4)·6H2O, the two hydroxide groups bridge the two CuIIcations, forming a centrosymmetric binuclear complex cation, in which the CuIIcation is coordinated by a 1,10-phenanthroline (phen) molecule, one water molecule and two bridging hydroxide O atoms in a distorted N2O3square-pyramidal coordination geometry. The naphthalene-2,6-dicarboxylate anion is also located on an inversion centre. In the crystal, O—H...O hydrogen bonds link the cations, anions and lattice water molecules into a three-dimensional supramolecular architecture. Extensive π–π stacking is observed between the parallel or nearly parallel aromatic rings of adjacent phen ligands and naphthalenedicarboxylate anions, the centroid-to-centroid distances ranging from 3.4990 (16) to 3.8895 (16) Å.

Hydrothermal synthesis, crystal structure and electrochemical properties of a novel 3D Dawson-type polyoxometalate supramolecular network

2008 ◽  
Vol 2008 (11) ◽  
pp. 626-629
Author(s):  
LiHong Tian ◽  
ShiZhong Liu ◽  
NingHai Hu ◽  
HengQing Jia
Keyword(s):  
Crystal Structure ◽  
Cyclic Voltammetry ◽  
Title Compound ◽  
Three Dimensional ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Supramolecular Architecture ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
X Ray Crystallography

A novel Dawson-type polyoxometalate supramolecular architecture of the formula [4,4′-H2bipy]2.5·[4,4′-Hbipy]·[P2W18O62]·6.25H2O (4,4′-bipy = 4,4′-bipyridine) has been hydrothermally synthesised and characterised by means of elemental analysis, IR, CV and X-ray single-crystal diffraction. X-ray crystallography indicates that the title compound consists of Dawson-type polyoxoaions [P2W18O62]6-, water molecules and 4,4′-bipy units. The polyoxoanion clusters together with 4,4′-bipy units and water molecules to construct the three-dimensional supramolecular network through hydrogen bonds. The crystal structure analyses reveal that water molecules and 4,4′-bipy units play the important role on the packing arrangements of crystals. Cyclic voltammetry shows that the title compound exhibits three chemically reversible steps

scholarly journals Crystal structure ofcatena-poly[[diaquacobalt(II)]-bis[μ-5-(4-carboxyylatophenyl)picolinato]-κ3N,O2:O5;κ3O5:N,O2-[diaquacobalt(II)]-μ-1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole-κ2N3:N3′]

2015 ◽  
Vol 71 (7) ◽  
pp. m145-m146
Author(s):  
Guo-Wang Xu ◽  
Ye-Nan Wang ◽  
Hai-Bing Wang ◽  
Zhong-Long Wang
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
Polymeric Chain ◽  
Water Molecules ◽  
Coordination Geometry ◽  
Supramolecular Architecture ◽  
Asymmetric Unit ◽  
Polymeric Chains ◽  
Coordination Water ◽  
Binuclear Unit

The asymmetric unit of the title polymeric CoIIcomplex, [Co2(C13H7NO4)2(C12H10N4)(H2O)4]n, contains a CoIIcation, a 5-(4-carboxylatophenyl)picolinate dianion, two coordination water molecules and half of 1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole ligand. The CoIIcation is coordinated by two picolinate dianions, two water molecules and one 1-[4-(1H-imidazol-1-yl)phenyl]-1H-imidazole molecule in a distorted N2O4octahedral coordination geometry. The two picolinate dianions are related by an inversion centre and link two CoIIcations, forming a binuclear unit, which is further bridged by the imidazole molecules, located about an inversion centre, into the polymeric chain propagating along the [-1-11] direction. In the crystal, the three-dimensional supramolecular architecture is constructed by O—H...O hydrogen bonds between the coordinating water molecules and the non-coordinating carboxylate O atoms of adjacent polymeric chains.

Diaqua[N,N′-(o-phenylene)bis(pyridine-2-carboxamidato)-κ 4 N]manganese(III) perchlorate

2007 ◽  
Vol 63 (11) ◽  
pp. m2760-m2760
Author(s):  
Li-Fang Zhang
Keyword(s):  
Hydrogen Bonds ◽  
Equatorial Plane ◽  
Complex Cation ◽  
Three Dimensional ◽  
Maximum Deviation ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Coordination Geometry ◽  
Rotation Axes ◽  
The Mean

In the MnIII complex of the title compound, [MnIII(C18H12N4O2)(H2O)2]ClO4, the MnIII atom is coordinated by four N atoms from the bpb2− [1,2-bis(pyridine-2-carboxamido)benzene] ligand located in the equatorial plane and two O atoms of water molecules at axial positions, yielding a distorted MnN4O2 octahedral coordination geometry. The bpb2− ligand is nearly planar, with a maximum deviation of 0.2311 (3) Å from the mean plane. The MnIII complex cation and the perchlorate anion, both of which are located on twofold rotation axes, are connected by O—H...O and C—H...O hydrogen bonds into a three-dimensional supramolecular network structure.

Chloridobis(1,10-phenanthroline-κ2 N,N′)copper(I) hexahydrate

2007 ◽  
Vol 63 (3) ◽  
pp. m826-m828 ◽  
Author(s):  
H. Zhong ◽  
X.-R. Zeng ◽  
X.-M. Yang ◽  
Q.-Y. Luo ◽  
S.-Z. Xiao
Keyword(s):  
Three Dimensional ◽  
Water Molecules ◽  
Stacking Interactions ◽  
Coordination Geometry ◽  
Rotation Axes ◽  
Trigonal Bipyramidal ◽  
Distorted Trigonal Bipyramidal Coordination ◽  
Cl Atom ◽  
Phenanthroline Ligands ◽  
Distorted Trigonal Bipyramidal

The CuI atom in the title complex, [CuCl(C12H8N2)2]·6H2O, exists in a distorted trigonal-bipyramidal coordination geometry defined by one Cl atom and four N atoms of two 1,10-phenanthroline ligands. In the crystal structure, molecules are linked into a three-dimensional framework by O—H...O hydrogen bonds and π–π stacking interactions. Four water molecules lie on crystallographic twofold rotation axes.

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.

scholarly journals Crystal structure ofcatena-poly[[[tetraaquairon(II)]-trans-μ-1,2-bis(pyridin-4-yl)ethene-κ2N:N′] bis(p-toluenesulfonate) methanol disolvate]

2017 ◽  
Vol 73 (12) ◽  
pp. 1977-1980
Author(s):  
Volodymyr M. Hiiuk ◽  
Diana D. Barakhty ◽  
Sergiu Shova ◽  
Ruslan A. Polunin ◽  
Il'ya A. Gural'skiy
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Distorted Octahedral Geometry ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Polymeric Complex ◽  
Distorted Octahedral ◽  
Polymeric Chains ◽  
Coordinated Water

In the title polymeric complex, {[Fe(C12H10N2)2(H2O)4](CH3C6H4SO3)2·2CH3OH}n, the FeIIcation, located on an inversion centre, is coordinated by four water molecules in the equatorial positions and two 1,2-bis(pyridin-4-yl)ethene molecules in the axial positions. This results in a distorted octahedral geometry for the [N2O4] coordination polyhedron. The 1,2-bis(pyridin-4-yl)ethene molecules bridge the FeIIcations, forming polymeric chains running along thea-axis direction. Stabilization of the crystal structure is provided by O—H...O hydrogen bonds; these are formed by coordinated water molecules as donors towards the O atoms of the methanol molecules and tosylate anions as acceptors of protons, leading to the formation of a three-dimensional supramolecular network. Weak C—H...O hydrogen bonds are also observed in the crystal.

scholarly journals Crystal structure of tetraaquabis(1,3-dimethyl-2,6-dioxo-7H-purin-7-ido-κN7)cobalt(II)

2017 ◽  
Vol 73 (9) ◽  
pp. 1302-1304 ◽  
Author(s):  
Hicham El Hamdani ◽  
Mohammed El Amane ◽  
Carine Duhayon
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
Title Complex ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Coordination Environment ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Intramolecular Hydrogen ◽  
Distorted Octahedral Coordination Environment

The title complex, [Co(C7H7N4O2)2(H2O)4], comprises mononuclear molecules consisting of a CoIIion, two deprotonated theophylline ligands (systematic name: 1,3-dimethyl-7H-purine-2,6-dione) and four coordinating water molecules. The CoIIatom lies on an inversion centre and has a slightly distorted octahedral coordination environment, with two N atoms of twotrans-oriented theophylline ligands and the O atoms of four water molecules. An intramolecular hydrogen bond stabilizes this conformation. A three-dimensional supramolecular network structure is formed by intermolecular O—H...O and O—H...N hydrogen bonds.

A novel one-dimensional CoIIcoordination polymer:catena-poly[[hexaaquacobalt(II)] [[diaquabis(sulfato-κO)cobalt(II)]-μ-4,4′-bipyridine-κ2N:N′] [[triaqua(sulfato-κO)cobalt(II)]-μ-4,4′-bipyridine-κ2N:N′]]

2012 ◽  
Vol 68 (9) ◽  
pp. m265-m268 ◽  
Author(s):  
Kai-Long Zhong ◽  
Ming-Yi Qian
Keyword(s):  
Crystal Structure ◽  
Three Dimensional ◽  
The Other ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Sulfate Ion ◽  
Sulfate Ions ◽  
One Dimensional ◽  
The Third ◽  
Hydrogen Bonding Interactions

The title compound, {[Co(H2O)6][Co(SO4)(C10H8N2)(H2O)3][Co(SO4)2(C10H8N2)(H2O)2]}n, contains three crystallographically unique CoIIcentres, all of which are in six-coordinated environments. One CoIIcentre is coordinated by two bridging 4,4′-bipyridine (4,4′-bipy) ligands, one sulfate ion and three aqua ligands. The second CoIIcentre is surrounded by two N atoms of two 4,4′-bipy ligands and four O atoms,i.e.two O atoms from two monodentate sulfate ions and two from water molecules. The third CoIIcentre forms part of a hexaaquacobalt(II) ion. In the crystal structure, there are two different one-dimensional chains, one being anionic and the other neutral, and adjacent chains are arranged in a cross-like fashion around the mid-point of the 4,4′-bipy ligands. The structure features O—H...O hydrogen-bonding interactions between sulfate anions and water molecules, resulting in a three-dimensional supramolecular network.

scholarly journals Crystal structure of poly[[di-μ3-acetato-tetraaquabis(μ2-cyclohexane-1,4-dicarboxylato)dilanthanum(III)] dihydrate]

2017 ◽  
Vol 73 (12) ◽  
pp. 1926-1930
Author(s):  
R. Drisya ◽  
U. S. Soumya Mol ◽  
P. R. Satheesh Chandran ◽  
M. Sithambaresan ◽  
M. R. Sudarsankumar
Keyword(s):  
Crystal Structure ◽  
Coordination Mode ◽  
Three Dimensional ◽  
Raw Material ◽  
Water Molecules ◽  
Supramolecular Network ◽  
Formula Unit ◽  
Remarkable Feature ◽  
Two Component ◽  
Coordinated Water

The title compound, {[La2(CH3COO)2(C8H10O4)2(H2O)4]·2H2O}nor [La2(ac)2(e,a-cis-1,4-chdc)2(H2O)4]·2H2O, whereacis acetate and 1,4-chdc is cyclohexane-1,4-dicarboxylate anion, is a binuclear lanthanum(III) complex. Each metal atom is decacoordinated by four O atoms from two distinct 1,4-chdc2−ligands, four O atoms from three acetate groups and two O atoms from coordinated water molecules to form a distorted bicapped square-antiprismatic geometry. Two non-coordinated water molecules are also present in the formula unit. The most remarkable feature of this compound is that it possesses a onlycisconformation for cyclohexane-1,4-dicarboxylic acid, although the raw material consists of a mixture ofcisandtransisomers. The μ3-η2:η2coordination mode of the bridging acetate group and the flexible dicarboxylate fragments of 1,4-chdc2−results in the formation of infinite two-dimensional lanthanide–carboxylate layers within the crystal structure. The directionality of strong intermolecular O—H...O and weak C—H...O interactions provides robustness to the layers, which leads to the construction of a three-dimensional supramolecular network. The crystal studied was refined as a two-component twin.

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