A one-dimensional CdIIcoordination polymer constructed from 4-(dimethylamino)pyridinium-1-acetate ligands and thiocyanate coordination bridges

2015 ◽  
Vol 71 (7) ◽  
pp. 549-553 ◽  
Author(s):  
Hui-Ting Wang ◽  
Lin Zhou
Keyword(s):  
Supramolecular Network ◽  
Zigzag Chain ◽  
Cadmium Nitrate ◽  
Thiocyanate Complex ◽  
One Dimensional ◽  
Distorted Octahedral Coordination ◽  
Hydrogen Bond Interactions ◽  
Acetate Ligand ◽  
Distorted Octahedral ◽  
Nitrate Tetrahydrate

A new cadmium–thiocyanate complex, namelycatena-poly[1-carboxymethyl-4-(dimethylamino)pyridinium [cadmium(II)-tri-μ-thiocyanato-κ4N:S;κ2S:N] [[[4-(dimethylamino)pyridinium-1-acetate-κ2O,O′]cadmium(II)]-di-μ-thiocyanato-κ2N:S;κ2S:N]], {(C9H13N2O2)[Cd(NCS)3][Cd(NCS)2(C9H12N2O2)]}n, was synthesized by the reaction of 4-(dimethylamino)pyridinium-1-acetate, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, two types of CdIIatoms are observed in distorted octahedral coordination environments. One type of CdIIatom is coordinated by two O atoms from the carboxylate group of the 4-(dimethylamino)pyridinium-1-acetate ligand and by two N atoms and two S atoms from four different thiocyanate ligands, while the second type of CdIIatom is coordinated by three N atoms and three S atoms from six different thiocyanate ligands. Neighbouring CdIIatoms are linked by thiocyanate bridges to form a one-dimensional zigzag chain and a one-dimensional coordination polymer. Hydrogen-bond interactions are involved in the formation of the supramolecular network.

A two-dimensional cadmium(II) coordination polymer based on 1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane and thiocyanate ligands

2015 ◽  
Vol 71 (9) ◽  
pp. 763-767
Author(s):  
Hui-Ting Wang ◽  
Qiang Li ◽  
Lin Zhou
Keyword(s):  
Three Dimensional ◽  
Supramolecular Network ◽  
Cadmium Nitrate ◽  
Two Dimensional ◽  
Thiocyanate Complex ◽  
Distorted Octahedral Coordination ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Nitrate Tetrahydrate

A cadmium–thiocyanate complex, poly[(1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane-κ4N)octakis-μ2-thiocyanato-κ8N:S;κ8S:N-tricadmium(II)], [Cd3(C8H14N3)2(NCS)8]n, was synthesized by the reaction of 1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, there are two independent types of CdIIcation (one on a centre of inversion and one in a general position) and both are in distorted octahedral coordination environments, coordinated by N and S atoms from different ligands. Neighbouring CdIIcations are linked together by thiocyanate bridges to form a two-dimensional network. Hydrogen-bonding interactions are involved in the formation of a three-dimensional supramolecular network.

A two-dimensional cadmium(II) polymer based on nicotinic acid and thiocyanate ligands

2015 ◽  
Vol 71 (9) ◽  
pp. 820-823
Author(s):  
Lin Zhou ◽  
Hui-Ting Wang
Keyword(s):  
Nicotinic Acid ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Cadmium Nitrate ◽  
Two Dimensional ◽  
Thiocyanate Complex ◽  
Hydrogen Bond Interactions ◽  
Dimensional Network ◽  
Distorted Octahedral ◽  
Nitrate Tetrahydrate

A cadmium–thiocyanate complex, poly[[bis(nicotinic acid-κN)di-μ-thiocyanato-κ2N:S;κ2S:N-cadmium(II)] monohydrate], {[Cd(NCS)2(C6H5NO2)2]·H2O}n, was synthesized by the reaction of nicotinic acid, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, each CdIIcation is in a distorted octahedral coordination environment, coordinated by the N and S atoms of nicotinic acid and thiocyanate ligands. Neighbouring CdIIcations are linked together by thiocyanate bridges to form a two-dimensional network. Hydrogen-bond interactions between the uncoordinated solvent water molecules and the organic ligands result in the formation of the three-dimensional supramolecular network.

A new two-dimensional polymeric cadmium(II) complex containing dicyanamide bridging ligands

2017 ◽  
Vol 73 (11) ◽  
pp. 885-888 ◽  
Author(s):  
Yang Lu ◽  
Wei-Qiang Liao ◽  
Xiu-Ni Hua
Keyword(s):  
Distorted Octahedral Geometry ◽  
Supramolecular Network ◽  
Cadmium Nitrate ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Bridging Ligands ◽  
Hydrogen Bond Interactions ◽  
Anionic Layer ◽  
Distorted Octahedral ◽  
Nitrate Tetrahydrate

As part of an exploration of new coordination polymers, a cadmium-dicyanamide complex, namely poly[benzyltriethylammonium [tri-μ-dicyanamido-κ6 N 1:N 5-cadmium(II)]], {(C13H22N)[Cd(C2N3)3]} n , has been synthesized by the reaction of benzyltriethylammonium bromide, cadmium nitrate tetrahydrate and sodium dicyanamide in aqueous solution, and characterized by single-crystal X-ray diffraction at room temperature. In the crystal structure, each CdII cation is coordinated by six nitrile N atoms from six anionic dicyanamide (dca) ligands to furnish a slightly distorted octahedral geometry. Neighbouring CdII cations are linked by dicyanamide bridges to construct a two-dimensional anionic layer coordination polymer. One amide N atom in the bridging dca ligand is disordered over two sites. The cations lie between the anionic frameworks and there are no hydrogen-bond interactions between the cations and anions. The organic cations are not involved in the formation of the supramolecular network.

The two-dimensional coordination polymer poly[diaqua(μ2-1H-imidazo[4,5-f][1,10]phenanthroline)-μ4-sulfato-μ3-sulfato-dicadmium(II)]

2014 ◽  
Vol 70 (8) ◽  
pp. 770-772 ◽  
Author(s):  
Xiao-Min Hao ◽  
Gang Chen ◽  
Chang-Sheng Gu ◽  
Ji-Wei Liu
Keyword(s):  
Coordination Polymer ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
Two Dimensional ◽  
Coordination Environment ◽  
One Dimensional ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Trigonal Prismatic ◽  
Distorted Octahedral Coordination Environment

In the title coordination polymer, [Cd2(SO4)2(C13H8N4)(H2O)2]n, there are two crystallographically independent CdIIcentres with different coordination geometries. The first CdIIcentre is hexacoordinated by four O atoms of four sulfate ligands, one water O atom and one N atom of a 1H-imidazo[4,5-f][1,10]phenanthroline (IP) ligand, giving a distorted octahedral coordination environment. The second CdIIcentre is heptacoordinated by four O atoms of three sulfate ligands, one water O atom and two N atoms of one chelating IP ligand, resulting in a distorted monocappedanti-trigonal prismatic geometry. The symmetry-independent CdIIions are bridged in an alternating fashion by sulfate ligands, forming one-dimensional ladder-like chains which are connected through the IP ligands to form two-dimensional layers. These two-dimensional layers are linked by interlayer hydrogen bonds, leading to the formation of a three-dimensional supramolecular network.

scholarly journals Di-μ2-acetato-1:2κ2O:O′;2:3κ2O:O′-bis{μ2-4,4′-dichloro-2,2′-[2,2-dimethylpropane-1,3-diylbis(nitrilomethanylylidene)]diphenolato}-1:2κ6O,N,N′,O′:O,O′;2:3κ6O,O′:O,N,N′,O′-tricadmium

2013 ◽  
Vol 69 (12) ◽  
pp. m629-m630
Author(s):  
Koji Kubono ◽  
Keita Tani ◽  
Kunihiko Yokoi ◽  
Teruo Shinmyozu ◽  
Kenta Goto
Keyword(s):  
Chair Conformation ◽  
Trinuclear Complex ◽  
Supramolecular Network ◽  
Coordination Geometry ◽  
Schiff Base Ligands ◽  
Tetradentate Schiff Base ◽  
Distorted Octahedral Coordination ◽  
Acetate Ligand ◽  
Distorted Octahedral Coordination Geometry ◽  
Distorted Octahedral

In the title linear homo-trinuclear complex, [Cd3(C19H18Cl2N2O2)2(C2H3O2)2], the central CdIIatom is located on a centre of inversion and has a distorted octahedral coordination geometry formed by four O atoms from two bidentate/tetradentate Schiff base ligands and two O atoms from two bridging acetate ligands. The coordination geometry of the terminal CdIIatom is square-pyramidal with the tetradentate part of the ligand in the basal plane and one O atom from an acetate ligand occupying the apical site. The six-membered CdN2C3ring adopts a chair conformation. The acetate-bridged Cd...Cd distance is 3.3071 (2) Å. The crystal structure is stabilized by C—H...O hydrogen bonds, which formC(7) chain motifs and give rise to a two-dimensional supramolecular network structure lying parallel to theabplane.

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.

3-(Pyridin-4-yl)acetylacetone: CdII and HgII compete for nitrogen coordination

2017 ◽  
Vol 73 (9) ◽  
pp. 724-730 ◽  
Author(s):  
Khai-Nghi Truong ◽  
Carina Merkens ◽  
Ulli Englert
Keyword(s):  
Solid State ◽  
Hydrogen Bonds ◽  
Carbonyl Group ◽  
Coordination Sphere ◽  
Aqua Ligand ◽  
Polymeric Chain ◽  
One Dimensional ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
The One

3-(Pyridin-4-yl)acetylacetone (HacacPy) acts as a pyridine-type ligand towards CdII and HgII halides. With CdBr2, the one-dimensional polymer [Cd(μ-Br)2(HacacPy)Cd(μ-Br)2(HacacPy)2]∞ is obtained in which five- and six-coordinated CdII cations alternate in the chain direction. Reaction of HacacPy with HgBr2 results in [Hg(μ-Br)Br(HacacPy)]∞, a polymer in which each HgII centre is tetracoordinated. In both compounds, each metal(II) cation is N-coordinated by at least one HacacPy ligand. Equimolar reaction between these CdII and HgII derivatives, either conducted in ethanol as solvent or via grinding in the solid state, leads to ligand redistribution and the formation of the well-ordered bimetallic polymer catena-poly[[bromidomercury(II)]-μ-bromido-[aquabis[4-hydroxy-3-(pyridin-4-yl)pent-3-en-2-one]cadmium(II)]-di-μ-bromido], [CdHgBr4(C10H11NO2)2(H2O)] n or [{HgBr}(μ-Br){(HacacPy)2Cd(H2O)}(μ-Br)2]∞. HgII and CdII cations alternate in the [100] direction. The HacacPy ligands do not bind to the HgII cations, which are tetracoordinated by three bridging and one terminal bromide ligand. The CdII centres adopt an only slightly distorted octahedral coordination. Three bromide ligands link them in a (2 + 1) pattern to neighbouring HgII atoms; two HacacPy ligands in a cis configuration, acting as N-atom donors, and a terminal aqua ligand complete the coordination sphere. Classical O—H...Br hydrogen bonds stabilize the polymeric chain. O—H...O hydrogen bonds between aqua H atoms and the uncoordinated carbonyl group of an HacacPy ligand in a neighbouring strand in the c direction link the chains into layers in the (010) plane.

An organic–inorganic hybrid compound containing imidazolium cations and a one-dimensional lithium hexacyanidocobaltate-based anionic framework

2014 ◽  
Vol 70 (6) ◽  
pp. 603-605 ◽  
Author(s):  
Xiu-Dan Shao ◽  
Chun-Hua Yu
Keyword(s):  
Three Dimensional ◽  
Chain Structure ◽  
Supramolecular Network ◽  
Monoclinic Space Group ◽  
Zigzag Chain ◽  
Imidazolium Chloride ◽  
Hybrid Compound ◽  
Inorganic Hybrid ◽  
One Dimensional ◽  
Imidazolium Cations

An organic–inorganic hybrid compound,catena-poly[bis(3H-imidazol-1-ium) [[tetracyanido-κ4C-cobalt(III)]-μ-cyanido-κ2C:N-[diaqualithium(I)]-μ-cyanido-κ2N:C]], {(C3H5N2)2[CoLi(CN)6(H2O)2]}n, was synthesized by the reaction of Li3[Co(CN)6] with imidazolium chloride in aqueous solution. The compound crystallizes in the monoclinic space groupC2/c(data collected at 273 K). In the crystal structure, neighbouring [Co(CN)6]3−anionic units are linked by Li+cations through the cyanide groups in atransmode, forming a one-dimensional zigzag chain structure extending along thecaxis. A three-dimensional supramolecular network is formed through hydrogen-bonding interactions and is further stabilized by weak CN...π interactions between the cyanide groups and the imidazolium cations.

A mixed-valence complex of cobalt based on 3-methoxysalicylaldoxime

2014 ◽  
Vol 70 (4) ◽  
pp. 364-367 ◽  
Author(s):  
Tiantian Yao ◽  
Jing Lu ◽  
Dacheng Li ◽  
Jianmin Dou
Keyword(s):  
Magnetic Properties ◽  
Cobalt Complex ◽  
Mixed Valence ◽  
Ethanol Solution ◽  
Octahedral Coordination ◽  
Supramolecular Network ◽  
Two Dimensional ◽  
Distorted Octahedral Coordination ◽  
Distorted Octahedral ◽  
Mixed Valence Complex

A new tetranuclear mixed-valence cobalt complex, namely di-μ2-azido-diazidodiethanolbis{μ2-2-[(hydroxyimino)methyl]-6-methoxyphenolato}bis{μ3-6-methoxy-2-[(oxidoimino)methyl]phenolato}dicobalt(II)dicobalt(III) ethanol disolvate, [CoII2CoIII2(C8H7NO3)2(C8H8NO3)2(N3)4(C2H5OH)2]·2C2H5OH, has been synthesized by the reaction of Co(OAc)2·4H2O (OAc is acetate) with 3-methoxysalicylaldoxime (H2mosao) in an ethanol solution. In the complex, the four Co cations all display distorted octahedral coordination environments and they are bridged by two κ2,κ1,κ1;μ3-mosao2−ligands, two κ2,κ2;μ2-Hmosao−ligands and two μ2-N3−anions to form a tetranuclear [Co4N4O4] cluster. Adjacent clusters are connected through weak C—H...N and C—H...O interactions, resulting in a two-dimensional supramolecular network parallel to theacplane. The magnetic properties of the complex have also been studied.

scholarly journals catena-Poly[[(2-{[2-(dimethylammonio)ethyl]iminomethyl}pyridine-κ2N,N′)bis(thiocyanato-κN)manganese(II)]-μ-thiocyanato-κ2N:S]

2012 ◽  
Vol 68 (8) ◽  
pp. m1131-m1131
Author(s):  
Jun Wang ◽  
Wubiao Zhu ◽  
Jichang Li
Keyword(s):  
Schiff Base ◽  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Three Dimensional ◽  
Supramolecular Network ◽  
One Dimensional ◽  
Distorted Octahedral ◽  
Title One

In the title one-dimensional coordination polymer, [Mn(NCS)3(C10H16N3)]n, the MnIIatom is coordinated by anN,N′-bidentate Schiff base and four thiocyanate ligands in a distorted octahedral N5S geometry. Bridging thiocyanate ligands interconnect adjacent [Mn(NCS)2(C10H16N3)] units, giving rise to helical chains extending along thebaxis. The chains are further linked through N—H...S hydrogen bonds, leading to a three-dimensional supramolecular network.

Sign in / Sign up

Export Citation Format

Share Document