Structure–property relationships: Polymorphism, solvates, and clay behavior in the one-dimensional coordination polymer chains [Ag(L)(NO3)](H2O)n, L=ethanediyl bis(isonicotinate), n=0, and 2

2007 ◽  
Vol 360 (1) ◽  
pp. 212-220 ◽  
Author(s):  
Adeline Y. Robin ◽  
Jorge L. Sague Doimeadios ◽  
Antonia Neels ◽  
Tünde Vig Slenters ◽  
Katharina M. Fromm
Keyword(s):  
Coordination Polymer ◽  
Polymer Chains ◽  
Structure Property ◽  
One Dimensional ◽  
Structure Property Relationships ◽  
The One

scholarly journals Probing the structure of framework materials by high pressure and the example of a magnetic, non-porous coordination polymer

2015 ◽  
Vol 71 (3) ◽  
pp. 247-249 ◽  
Author(s):  
Francesca P. A. Fabbiani
Keyword(s):  
High Pressure ◽  
Coordination Polymer ◽  
Coordination Compounds ◽  
Functional Materials ◽  
Research Tool ◽  
Structure Property ◽  
Framework Materials ◽  
Porous Framework ◽  
Structure Property Relationships ◽  
Porous Coordination Polymer

High pressure has become an indispensable research tool in the quest for novel functional materials. High-pressure crystallographic studies on non-porous, framework materials based on coordination compounds are markedly on the rise, enabling the unravelling of structural phenomena and taking us a step closer to the derivation of structure–property relationships.

scholarly journals Mixed Ca/Sr salt forms of salicylic acid: tuning structure and aqueous solubility

2018 ◽  
Vol 74 (2) ◽  
pp. 131-138 ◽  
Author(s):  
Pamela Allan ◽  
Jean-Baptiste Arlin ◽  
Alan R. Kennedy ◽  
Aiden Walls
Keyword(s):  
Salicylic Acid ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Structural Feature ◽  
Structural Changes ◽  
Aqueous Solubility ◽  
Single Crystal Diffraction ◽  
One Dimensional ◽  
The One ◽  
Salt Forms

Ten isostructural single-crystal diffraction studies of mixed cation Ca/Sr salt forms of the salicylate anion are presented, namely catena-poly[[diaquacalcium(II)/strontium(II)]-bis(μ2-2-hydroxybenzoato)], [Ca1–x Sr x (C7H5O3)2(H2O)2] n , where x = 0, 0.041, 0.083, 0.165, 0.306, 0.529, 0.632, 0.789, 0.835 and 1. The structure of an isostructural Sr/Ba species, namely catena-poly[[diaquastrontium(II)/barium(II)]-bis(μ2-2-hydroxybenzoato)], [Sr0.729Ba0.271(C7H5O3)2(H2O)2], is also described. The Ca/Sr structures form a series where, with increasing Sr content, the unit cell expands in both the crystallographic a and c directions (by 1.80 and 3.18%, respectively), but contracts slightly in the b direction (−0.31%). The largest percentage structural expansion lies parallel to the direction of propagation of the one-dimensional coordination polymer that is the primary structural feature. This structural expansion is thus associated with increased M—O distances. Aqueous solubility measurements show that solubility generally increases with increasing Sr content. Thus, tuning the composition of these mixed counter-ion salt forms leads to systematic structural changes and allows solubility to be tuned to values between those for the pure Ca and Sr species.

scholarly journals catena-Poly[[[4-amino-3,5-bis(pyridin-2-yl)-4H-1,2,4-triazole-κ2N1,N5](dicyanamido-κN)copper(II)]-μ2-dicyanamido-κ2N:N′]: coordination polymer chains linked into a bilayer by hydrogen bonds and π–π stacking interactions

2014 ◽  
Vol 70 (4) ◽  
pp. 359-363 ◽  
Author(s):  
Zouaoui Setifi ◽  
Fatima Setifi ◽  
Mohamed Saadi ◽  
Djamil-Azzeddine Rouag ◽  
Christopher Glidewell
Keyword(s):  
Coordination Polymer ◽  
Hydrogen Bonds ◽  
Polymer Chains ◽  
Stacking Interactions ◽  
Terminal Ligand ◽  
One Dimensional ◽  
Bridging Ligand ◽  
Pyramidal Geometry ◽  
Π Stacking ◽  
Square Pyramidal Geometry

In the title compound, [Cu(C2N3)2(C12H10N6)]nor [Cu(dca)2(abpt)]n, where abpt is 4-amino-3,5-bis(pyridin-2-yl)-4H-1,2,4-triazole and dca is the dicyanamide anion, the CuIIcentre is five-coordinate with an approximately square-pyramidal geometry. One of the two dicyanamide ligands is a terminal ligand, but the other one acts as a μ1,5-bridging ligand between pairs of CuIIcentres, so generating a one-dimensional coordination polymer. A combination of N—H...N and C—H...N hydrogen bonds, augmented by π–π stacking interactions, links the coordination polymer chains into a bilayer structure. Comparisons are made with some related CuIIcomplexes containing dca ligands and heteroaromatic co-ligands.

One-dimensional CuIIcoordination polymers containingC2h-symmetric 1,1′:4′,1′′-terphenyl-3,3′-dicarboxylate linkers

2015 ◽  
Vol 71 (10) ◽  
pp. 929-935 ◽  
Author(s):  
Hyun-Chul Kim ◽  
Ja-Min Gu ◽  
Seong Huh ◽  
Chul-Hyun Yo ◽  
Youngmee Kim
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Polymer Chains ◽  
Water Molecules ◽  
Binding Modes ◽  
Bridging Ligands ◽  
One Dimensional ◽  
X Ray Crystallography ◽  
Dimensional Network ◽  
The One

Two new one-dimensional CuIIcoordination polymers (CPs) containing theC2h-symmetric terphenyl-based dicarboxylate linker 1,1′:4′,1′′-terphenyl-3,3′-dicarboxylate (3,3′-TPDC), namelycatena-poly[[bis(dimethylamine-κN)copper(II)]-μ-1,1′:4′,1′′-terphenyl-3,3′-dicarboxylato-κ4O,O′:O′′:O′′′] monohydrate], {[Cu(C20H12O4)(C2H7N)2]·H2O}n, (I), andcatena-poly[[aquabis(dimethylamine-κN)copper(II)]-μ-1,1′:4′,1′′-terphenyl-3,3′-dicarboxylato-κ2O3:O3′] monohydrate], {[Cu(C20H12O4)(C2H7N)2(H2O)]·H2O}n, (II), were both obtained from two different methods of preparation: one reaction was performed in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) as a potential pillar ligand and the other was carried out in the absence of the DABCO pillar. Both reactions afforded crystals of different colours,i.e.violet plates for (I) and blue needles for (II), both of which were analysed by X-ray crystallography. The 3,3′-TPDC bridging ligands coordinate the CuIIions in asymmetric chelating modes in (I) and in monodenate binding modes in (II), forming one-dimensional chains in each case. Both coordination polymers contain two coordinated dimethylamine ligands in mutuallytranspositions, and there is an additional aqua ligand in (II). The solvent water molecules are involved in hydrogen bonds between the one-dimensional coordination polymer chains, forming a two-dimensional network in (I) and a three-dimensional network in (II).

catena-Poly[[bis(di-4-pyridylamine-κN)(terephthalato-κ2 O,O′)nickel(II)]-μ-di-4-pyridylamine-κ2 N:N′]

2007 ◽  
Vol 63 (11) ◽  
pp. m2780-m2780
Author(s):  
Maxwell A. Braverman ◽  
Robert L. LaDuca
Keyword(s):  
Hydrogen Bonding ◽  
Coordination Polymer ◽  
Title Compound ◽  
Polymer Chains ◽  
Three Dimensions ◽  
Octahedral Coordination ◽  
One Dimensional ◽  
Axis Direction

In the title compound, [Ni(C8H4O4)(C10H9N3)3] n , an NiII atom with octahedral coordination is bound by one chelating terephthalate (tp) dianion, two monodentate di-4-pyridylamine (dpa) ligands, and two bridging dpa ligands. These link the Ni atoms into one-dimensional [Ni(tp)(dpa)3] n coordination polymer chains that propagate along the b-axis direction. Interweaving pairs of chains stack in three dimensions via N—H...O hydrogen bonding.

A new photoluminescent coordination polymer constructed with an N-donor ligand having extended coordination capabilities derived from quinoline and pyridine

2020 ◽  
Vol 76 (5) ◽  
pp. 500-506
Author(s):  
Kamil Twaróg ◽  
Małgorzata Hołyńska ◽  
Andrzej Kochel
Keyword(s):  
Coordination Polymer ◽  
Pyridyl Ring ◽  
Ligand Molecule ◽  
Hydrothermal Conditions ◽  
Absorption Bands ◽  
Donor Ligand ◽  
One Dimensional ◽  
The One ◽  
Chloride Monohydrate ◽  
Carboxylic Acid Ligand

Employment of the organic 2-(pyridin-4-yl)quinoline-4-carboxylic acid ligand with extended coordination capabilities leads to the formation of the one-dimensional copper(II) coordination polymer catena-poly[[diaquacopper(II)]-bis[μ-2-(pyridin-4-yl)quinoline-4-carboxylato]-κ2 N 2:O;κ2 O:N], {[Cu(C15H9N2O2)2(H2O)2]·2H2O} n , under hydrothermal conditions. The ligand, isolated as its hydrochloride salt, namely, 4-(4-carboxyquinolin-2-yl)pyridinium chloride monohydrate, C15H11N2O2 +·Cl−·H2O, reveals a pseudosymmetry element (translation a/2) in its crystal structure. The additional pyridyl N atom, in comparison with the previously reported analogues with an arene ring instead of the pyridyl ring in the present ligand molecule, promotes the formation of a one-dimensional coordination polymer, rather than discrete molecules. This polymer shows photoluminescent properties with bathochromic/hypsochromic shifts of the ligand absorption bands, leading to a single band at 479 nm. The CuII ions are involved in weak antiferromagnetic interactions within dimeric units, as evidenced by SQUID magnetometry.

catena-Poly[[bis(thiocyanato-κN)cobalt(II)]-μ-di-4-pyridylamine-κ2 N:N′]

2007 ◽  
Vol 63 (11) ◽  
pp. m2705-m2705 ◽  
Author(s):  
Caleb H. Springsteen ◽  
Robert L. LaDuca
Keyword(s):  
Coordination Polymer ◽  
Title Compound ◽  
Polymer Chains ◽  
Tetrahedral Coordination ◽  
One Dimensional ◽  
Axis Direction

In the title compound, [Co(NCS)2(C10H9N3)], a CoII atom with tetrahedral coordination is bound by two N-donor thiocyanate anions and two N-donor atoms from two crystallographically distinct di-4-pyridylamine (dpa) ligands whose central NH units lie on twofold axes. The dpa ligands link the Co atoms into one-dimensional [Co(NCS)2(dpa)] n coordination polymer chains that propagate along the b-axis direction.

scholarly journals catena-Poly[[di-tert-butyltin(IV)]-μ-oxalato]

2014 ◽  
Vol 70 (4) ◽  
pp. m133-m133 ◽  
Author(s):  
Martin Reichelt ◽  
Hans Reuter
Keyword(s):  
Nitric Acid ◽  
Coordination Polymer ◽  
Van Der Waals Interactions ◽  
Mirror Plane ◽  
Coordination Geometry ◽  
One Dimensional ◽  
Bond Lengths ◽  
The One ◽  
Oxalate Ion ◽  
Asymmetric Coordination

The title compound, [Sn(C4H9)2(C2O4)]n, an unexpected side product in the reaction of di-tert-butyltin(IV) oxide with nitric acid, represents the first diorganotin(IV) oxalate to be structurally characterized. The SnIVatom of the one-dimensional coordination polymer is located on a mirror plane and is coordinated by two chelating oxalate ions with two rather different Sn—O bond lengths of 2.150 (1) and 2.425 (1) Å, and twot-butyl groups with Sn—C bond lengths of 2.186 (2) and 2.190 (2) Å. The coordination polyhedron around the SnIVatom is a distorted tetragonal disphenoid. The centrosymmetric oxalate ion also has an asymmetric coordination geometry, as reflected by the two slightly different C—O bond lengths of 1.242 (2) and 1.269 (2) Å. The chains of the polymer propagate along theb-axis direction. Only van der Waals interactions are observed between the chains.

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