A novel two-dimensional network cadmium(II) coordination polymer containing one 1,4-bis(1,2,4-triazol-1-yl)butane and double dicyanamide bridges

Author(s):  
Bao-Zong Li ◽  
Xun-Gao Liu ◽  
Zhao-Hui Wang ◽  
Bao-Long Li ◽  
Yong Zhang
2009 ◽  
Vol 65 (3) ◽  
pp. m118-m120
Author(s):  
Olha Sereda ◽  
Helen Stoeckli-Evans

The title coordination polymer, [Cd3Co2(CN)12(C2H8N2)4]n, has an infinite two-dimensional network structure. The asymmetric unit is composed of two crystallographically independent CdIIatoms, one of which is located on a twofold rotation axis. There are two independent ethylenediamine (en) ligands, one of which bis-chelates to the Cd atom that sits in a general position, while the other bridges this Cd atom to that sitting on the twofold axis. The Cd atom located on the twofold rotation axis is linked to four equivalent CoIIIatomsviacyanide bridges, while the Cd atom that sits in a general position is connected to three equivalent CoIIIatomsviacyanide bridges. In this way, a series of trinuclear, tetranuclear and pentanuclear macrocycles are linked to form a two-dimensional network structure lying parallel to thebcplane. In the crystal structure, these two-dimensional networks are linkedviaN—H...N hydrogen bonds involving an en NH2H atom and a cyanide N atom, leading to the formation of a three-dimensional structure. This coordination polymer is only the second example involving a cyanometallate where the en ligand is present in both chelating and bridging coordination modes.


Author(s):  
Hang-Ju Zhao ◽  
Jian-Ping Ma ◽  
Qi-Kui Liu ◽  
Yu-Bin Dong

A new 1,3,4-oxadiazole-containing bispyridyl ligand, namely 5-(pyridin-4-yl)-3-[2-(pyridin-4-yl)ethyl]-1,3,4-oxadiazole-2(3H)-thione (L), has been used to create the novel complexes tetranitratobis{μ-5-(pyridin-4-yl)-3-[2-(pyridin-4-yl)ethyl]-1,3,4-oxadiazole-2(3H)-thione}zinc(II), [Zn2(NO3)4(C14H12N4OS)2], (I), andcatena-poly[[[dinitratocopper(II)]-bis{μ-5-(pyridin-4-yl)-3-[2-(pyridin-4-yl)ethyl]-1,3,4-oxadiazole-2(3H)-thione}] nitrate acetonitrile sesquisolvate dichloromethane sesquisolvate], {[Cu(NO3)(C14H12N4OS)2]NO3·1.5CH3CN·1.5CH2Cl2}n, (II). Compound (I) presents a distorted rectangular centrosymmetric Zn2L2ring (dimensions 9.56 × 7.06 Å), where each ZnIIcentre lies in a {ZnN2O4} coordination environment. These binuclear zinc metallocycles are linked into a two-dimensional network through nonclassical C—H...O hydrogen bonds. The resulting sheets lie parallel to theacplane. Compound (II), which crystallizes as a nonmerohedral twin, is a coordination polymer with double chains of CuIIcentres linked by bridgingLligands, propagating parallel to the crystallographicaaxis. The CuIIcentres adopt a distorted square-pyramidal CuN4O coordination environment with apical O atoms. The chains in (II) are interlinkedviatwo kinds of π–π stacking interactions along [0\overline 11]. In addition, the structure of (II) contains channels parallel to the crystallographicadirection. The guest components in these channels consist of dichloromethane and acetonitrile solvent molecules and uncoordinated nitrate anions.


2018 ◽  
Vol 73 (9) ◽  
pp. 655-660
Author(s):  
Fei-Hang Zhang ◽  
Nan-Nan Chai ◽  
Sheng-Chun Chen ◽  
Ming-Yang He ◽  
Qun Chen

AbstractA new zinc(II)-based coordination polymer {[Zn(5-fip)(tdbpy)]·(DMF)}n (1) {5-H2fip=5-fluoroisophthalic acid, tdbpy=4,4′-(2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diyl)bispyridine, DMF=dimethylformamide} has been solvothermally synthesized and structurally characterized. Single-crystal X-ray diffraction revealed that complex 1 shows a unique two-dimensional network architecture containing single-stranded [Zn(5-fip)]n and double-stranded helical [Zn(tdbpy)]n chains. The thermal and luminescence properties of complex 1 have also been studied.


2017 ◽  
Vol 73 (10) ◽  
pp. 828-832 ◽  
Author(s):  
Huai-Xia Yang ◽  
Yan-Qiu Yang ◽  
Di Cheng ◽  
Ya-Xue Li ◽  
Xiang-Ru Meng

In the construction of coordination polymers, many factors can influence the formation of the final architectures, such as the nature of the metal centres, the organic ligands and the counter-anions. In the coordination polymer poly[aqua(μ-benzene-1,2-dicarboxylato-κ4O1,O1′:O2,O2′)[μ-2-(1H-imidazol-1-ylmethyl)-6-methyl-1H-benzimidazole-κ2N2:N3]cadmium(II)], [Cd(C12H12N4)(C8H4O4)(H2O)]nor [Cd(immb)(1,2-bdic)(H2O)]n, each CdIIion is seven-coordinated by two N atoms from two symmetry-related 2-(1H-imidazol-1-ylmethyl)-6-methyl-1H-benzimidazole (immb) ligands, by four O atoms from two symmetry-related benzene-1,2-dicarboxylate (1,2-bdic2−) ligands and by one water molecule, leading to a CdN2O5distorted pentagonal bipyramidal coordination environment. The immb and 1,2-bdic2−ligands bridge CdIIions and form a two-dimensional network structure. O—H...O and N—H...O hydrogen bonds stabilize the structure. In addition, the IR spectroscopic properties, PXRD patterns, thermogravimetric behaviour and fluorescence properties of the title polymer have been investigated.


2015 ◽  
Vol 70 (8) ◽  
pp. 605-608
Author(s):  
Zhi-Guo Kong ◽  
Sheng-Nan Guo ◽  
Jia-Qi Miao ◽  
Miao An

AbstractA new Cd(II) coordination polymer, [Cd(CNA)]n (1) (H2CNA = 3-(carboxymethoxy)-2-naphthoic acid), was hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction. The crystals are monoclinic, space group P21/c with a = 16.9698(18), b = 7.8314(8), c = 8.9553(10) Å, β = 100.657(2)°, V = 1169.6(2) Å3, Z = 4, Dcalcd. = 2.03 g cm−3, μ(MoKα) = 1.9 mm−1, F(000) = 696 e, R = 0.0305, wR = 0.0784 for 172 refined parameters and 2285 data. Each CNA anion bridges three Cd(II) cations to give rise to a two-dimensional network structure. Topologically, if each CNA anion is regarded as a linker, and each Cd(II) atom considered as a 4-conencted node, the structure is simplified as a 4-connected (4,4) network. The solid state photoluminescent properties of the compound were also studied at room temperature.


2015 ◽  
Vol 71 (8) ◽  
pp. 701-705 ◽  
Author(s):  
Qiu-Ying Huang ◽  
Yi Yang ◽  
Xiang-Ru Meng

In the coordination polymer, poly[[{μ-1-[(1H-benzimidazol-2-yl)methyl]-1H-imidazole-κ2N:N′}(μ-5-carboxybenzene-1,3-dicarboxylato-κ2O1:O3)zinc(II)] dimethylformamide monosolvate pentahydrate], {[Zn(C9H4O6)(C11H10N4)]·C3H7NO·5H2O}n, the ZnIIion is coordinated by two N atoms from two symmetry-related 1-[(1H-benzimidazol-2-yl)methyl]-1H-imidazole (bmi) ligands and two O atoms from two symmetry-related 5-carboxybenzene-1,3-dicarboxylate (Hbtc2−) ligands in a slightly distorted tetrahedral geometry. The ZnIIions are bridged by Hbtc2−and bmi ligands, leading to a 4-connected two-dimensional network with the topological notation (44.62). Adjacent layers are further connected by 12 kinds of hydrogen bonds and also by π–π interactions, resulting in a three-dimensional supramolecular architecture in the solid state.


2015 ◽  
Vol 71 (4) ◽  
pp. 306-310 ◽  
Author(s):  
Qiu-Ying Huang ◽  
Yu-Hong Zhang ◽  
Xiang-Ru Meng

In the title coordination polymer,catena-poly[[bis[{1-[(1H-benzimidazol-2-yl-κN3)methyl]-1H-tetrazole}zinc(II)]-bis(μ4-pentane-1,5-dioato-1:2:1′:2′κ4O1:O1′:O5:O5′)] methanol disolvate], {[Zn(C5H6O4)(C9H8N6)]·CH3OH}n, each ZnIIion is five-coordinated by four O atoms from four glutarate ligands and by one N atom from a 1-[(1H-benzimidazol-2-yl)methyl]-1H-tetrazole (bimt) ligand, leading to a slightly distorted square-pyramidal coordination environment. Two ZnIIions are linked by four bridging glutarate carboxylate groups to generate a dinuclear [Zn2(CO2)4] paddle-wheel unit. The dinuclear units are further connected into a one-dimensional chainviathe glutarate ligands. The bimt ligands coordinate to the ZnIIions in a monodentate mode and are pendant on both sides of the main chain. In the crystal, the chains are linked by O—H...O and N—H...O hydrogen bonds into a two-dimensional layered structure. Adjacent layers are further packed into a three-dimensional network through van der Waals forces. A thermogravimetric analysis was carried out and the photoluminescent behaviour of the polymer was investigated.


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