Three isomorphous two-dimensional coordination polymers generated from a benzimidazole bridging ligand and ZnX2(X= Cl, Br and I)

2013 ◽  
Vol 69 (4) ◽  
pp. 367-371
Author(s):  
Yue-Feng Zhang ◽  
Jian-Ping Ma ◽  
Qi-Kui Liu ◽  
Yu-Bin Dong
Keyword(s):  
Solid State ◽  
Benzoic Acid ◽  
Coordination Polymers ◽  
Room Temperature ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Red Shift ◽  
Two Dimensional ◽  
Π Interactions ◽  
Bridging Ligand

A novel bridging asymmetric benzimidazole ligand, 4-{2-[3-(pyridin-4-yl)phenyl]-1H-benzimidazol-1-ylmethyl}benzoic acid, was used to construct three isomorphous two-dimensional coordination polymers, namelycatena-poly[chlorido(μ3-4-{2-[3-(pyridin-4-yl)phenyl]-1H-benzimidazol-1-ylmethyl}benzoato)zinc(II)], [Zn(C26H18N3O2)Cl]n, (I), and the bromide, (II), and iodide, (III), analogues. Neighbouring two-dimensional networks are stacked into three-dimensional frameworksviainterlayer π–π interactions. The luminescent properties of (I)–(III) were investigated and they display an obvious red-shift in the solid state at room temperature.

scholarly journals Structural and luminescent properties of co-crystals of tetraiodoethylene with two azaphenanthrenes

2020 ◽  
Vol 76 (3) ◽  
pp. 438-442 ◽  
Author(s):  
Yu-Jin Cui ◽  
Feng Su ◽  
Wei-Jun Jin
Keyword(s):  
Solid State ◽  
Room Temperature ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Two Dimensional ◽  
Halogen Bonds ◽  
One Dimensional ◽  
X Ray ◽  
X Ray Crystallography ◽  
Independent Molecules

Two new co-crystals, tetraiodoethylene–phenanthridine (1/2), 0.5C2I4·C13H9N (1) and tetraiodoethylene–benzo[f]quinoline (1/2), 0.5C2I4·C13H9N (2), were obtained from tetraiodoethylene and azaphenanthrenes, and characterized by IR and fluorescence spectroscopy, elemental analysis and X-ray crystallography. In the crystal structures, C—I...π and C—I...N halogen bonds link the independent molecules into one-dimensional chains and two-dimensional networks with subloops. In addition, the planar azaphenanthrenes lend themselves to π–π stacking and C—H...π interactions, leading to a diversity of supramolecular three-dimensional structural motifs being formed by these interactions. Luminescence studies show that co-crystals 1 and 2 exhibit distinctly different luminescence properties in the solid state at room temperature.

`0'- and `8'-shaped complexes generated from a nano-sized oxadiazole-containing organic ligand with CdI2and CuI

2013 ◽  
Vol 70 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Zhao-Cai Liu ◽  
Qi-Kui Liu ◽  
Yan-An Li ◽  
Jian-Ping Ma ◽  
Yu-Bin Dong
Keyword(s):  
Solid State ◽  
Mirror Symmetry ◽  
Room Temperature ◽  
Organic Ligand ◽  
Red Shift ◽  
Luminescence Properties ◽  
Two Dimensional ◽  
One Dimensional ◽  
Π Interactions ◽  
Dimensional Network

A new nano-sized rigid double-armed oxadiazole-bridged organic ligand, 2,5-bis{2-methyl-5-[2-(pyridin-3-yl)ethenyl]phenyl}-1,3,4-oxadiazole, C30H20N4O,Lor (I), which adopts acisconformation in the solid state, has been synthesized and used to create the two novel metallocycle complexes (2,5-bis{2-methyl-5-[2-(pyridin-3-yl-κN)ethenyl]phenyl}-1,3,4-oxadiazole)diiodidocadmium(II) dichloromethane monosolvate, [CdI2(C30H20N4O)]·CH2Cl2, (II), and di-μ-iodido-bis[(2,5-bis{2-methyl-5-[2-(pyridin-3-yl-κN)ethenyl]phenyl}-1,3,4-oxadiazole)copper(I)], [Cu2I2(C30H20N4O)2], (III). Molecules of complex (II) adopts a 20-membered `0'-shaped metallocycle structure with crystallographic mirror symmetry. The discrete units are linked into one-dimensional chains through intermolecular π–π and C—H...π interactions. In (III), the two I atoms and two CuIatoms form a {Cu2(μ-I)2} cluster. One {Cu2(μ-I)2} cluster and twoLligands form two 20-membered monometallic rings in a head-to-head fashion, leading to a discrete centrosymmetric `8'-shaped metallocyclic complex. These metallocycles stack togetherviatwo kinds of intermolecular π–π interactions to generate a two-dimensional network in theacplane. The luminescence properties of (I)–(III) were investigated in the solid state at room temperature and displayed an obvious red shift.

scholarly journals Different Benzendicarboxylate-Directed Structural Variations and Properties of Four New Porous Cd(II)-Pyridyl-Triazole Coordination Polymers

2020 ◽  
Vol 8 ◽  
Author(s):  
Ying Zhao ◽  
Jin Jing ◽  
Ning Yan ◽  
Min-Le Han ◽  
Guo-Ping Yang ◽  
...  
Keyword(s):  
Solid State ◽  
Coordination Polymers ◽  
Three Dimensional ◽  
Two Dimensional ◽  
Gas Sorption ◽  
Structural Variations ◽  
Benzenedicarboxylic Acid ◽  
Topological Framework ◽  
The Stability

Four new different porous crystalline Cd(II)-based coordination polymers (CPs), i. e., [Cd(mdpt)2]·2H2O (1), [Cd2(mdpt)2(m-bdc)(H2O)2] (2), [Cd(Hmdpt)(p-bdc)]·2H2O (3), and [Cd3(mdpt)2(bpdc)2]·2.5NMP (4), were obtained successfully by the assembly of Cd(II) ions and bitopic 3-(3-methyl-2-pyridyl)-5-(4-pyridyl)-1,2,4-triazole (Hmdpt) in the presence of various benzendicarboxylate ligands, i.e., 1,3/1,4-benzenedicarboxylic acid (m-H2bdc, p-H2bdc) and biphenyl-4,4′-bicarboxylate (H2bpdc). Herein, complex 1 is a porous 2-fold interpenetrated four-connected 3D NbO topological framework based on the mdpt− ligand; 2 reveals a two-dimensional (2D) hcb network. Interestingly, 3 presents a three-dimensional (3D) rare interpenetrated double-insertion supramolecular net via 2D ···ABAB··· layers and can be viewed as an fsh topological net, while complex 4 displays a 3D sqc117 framework. Then, the different gas sorption performances were carried out carefully for complexes 1 and 4, the results of which showed 4 has preferable sorption than that of 1 and can be the potential CO2 storage and separation material. Furthermore, the stability and luminescence of four complexes were performed carefully in the solid state.

A two-dimensional layered CdIIcoordination polymer with a three-dimensional supramolecular architecture incorporating mixed multidentateN- andO-donor ligands

2015 ◽  
Vol 71 (6) ◽  
pp. 474-478 ◽  
Author(s):  
Qiu-Ying Huang ◽  
Ming-Yang Su ◽  
Xiang-Ru Meng
Keyword(s):  
Solid State ◽  
Room Temperature ◽  
Three Dimensional ◽  
Fluorescence Emission ◽  
Good Choice ◽  
Donor Ligands ◽  
Supramolecular Architecture ◽  
Two Dimensional ◽  
Carboxylate Groups ◽  
Metal Organic

The combination of N-heterocyclic and multicarboxylate ligands is a good choice for the construction of metal–organic frameworks. In the title coordination polymer, poly[bis{μ2-1-[(1H-benzimidazol-2-yl)methyl]-1H-tetrazole-κ2N3:N4}(μ4-butanedioato-κ4O1:O1′:O4:O4′)(μ2-butanedioato-κ2O1:O4)dicadmium], [Cd(C4H4O4)(C9H8N6)]n, each CdIIion exhibits an irregular octahedral CdO4N2coordination geometry and is coordinated by four O atoms from three carboxylate groups of three succinate (butanedioate) ligands and two N atoms from two 1-[(1H-benzimidazol-2-yl)methyl]-1H-tetrazole (bimt) ligands. CdIIions are connected by two kinds of crystallographically independent succinate ligands to generate a two-dimensional layered structure with bimt ligands located on each side of the layer. Adjacent layers are further connected by hydrogen bonding, leading to a three-dimensional supramolecular architecture in the solid state. Thermogravimetric analysis of the title polymer shows that it is stable up to 529 K and then loses weight from 529 to 918 K, corresponding to the decomposition of the bimt ligands and succinate groups. The polymer exhibits a strong fluorescence emission in the solid state at room temperature.

Influence of Anions on the Self-assembly of Cd(II)-containing Coordination Polymers Based on the Flexible Ligand 2-((1H-1,2,4-Triazol-1-yl)methyl)-1H-benzimidazole

2012 ◽  
Vol 67 (1) ◽  
pp. 29-35
Author(s):  
Guanghua Jin ◽  
Yang Yang ◽  
Xiaoli Zhou ◽  
Xiangru Meng
Keyword(s):  
Solid State ◽  
Hydrogen Bonds ◽  
Coordination Polymers ◽  
Infrared Spectra ◽  
Self Assembly ◽  
Room Temperature ◽  
Luminescent Properties ◽  
The Self ◽  
Stacking Interactions ◽  
Flexible Ligand

Three Cd(II)-containing coordination polymers [CdCl2(tmb)]n (1) and two polymorphs of {[CdI2(tmb)]·DMF}n (2, 3) (tmb = 2-((1H-1,2,4-triazol-1-yl)methyl)-1H-benzimidazole) have been synthesized by the reactions of tmb with the cadmium salts. Polymer 1 exhibits an infinite · · ·Cd- (Cl1)2-Cd-(Cl2)2-Cd· · · chain with μ2Cl bridges, while polymers 2 and 3 are isomers, in which the Cd(II) ions are bridged by the bidentate tmb ligands leading to · · ·Cd-tmb-Cd· · · chains. The polymers form 3-D supramolecular frameworks through hydrogen bonds and π · · ·π stacking interactions. The different structures of polymers 1 - 3 indicate that the anions and the flexibility of the tmb ligand can influence the structures of the coordination polymers. The infrared spectra and luminescent properties of the polymers have been investigated in the solid state at room temperature

A calcium-bridged porphyrin coordination network

2002 ◽  
Vol 06 (06) ◽  
pp. 377-381 ◽  
Author(s):  
Margaret E. Kosal ◽  
Jun-Hong Chou ◽  
Kenneth S. Suslick
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Coordination Polymers ◽  
Three Dimensional ◽  
Pyridine Molecule ◽  
Two Dimensional ◽  
X Ray ◽  
Hydrogen Bonding Interactions ◽  
Dimensional Network ◽  
Polymeric Framework

The hydrothermal assembly of a very stable porphyrin network with nanoscale cavities is described. A tightly packed and interpenetrated, linear polymeric framework was observed in the solid-state X-ray structure of freebase 5,10,15,20-tetrakis-(4-carboxyphenyl)porphyrin coordinated to calcium(II) ions. Strong hydrogen-bonding interactions between the coordination polymers form a two-dimensional network. Perpendicular bands interpenetrate generating an unusual three-dimensional box that clathrates a pyridine molecule.

Syntheses, Structures and Photoluminescent Properties of the Two Novel Coordination Polymers [Cd(pydc)2(tu)]n and [Cd2(SO4)(nic)2(tu)1.5(H2O)2]n (pydc = Pyridine-2,3-dicarboxylate, nic = Nicotinate, tu = Thiourea)

2011 ◽  
Vol 66 (5) ◽  
pp. 459-464 ◽  
Author(s):  
Chao Xu ◽  
Sheng-Bo Liu ◽  
Taike Duan ◽  
Qun Chen ◽  
Qian-Feng Zhang
Keyword(s):  
Hydrogen Bonds ◽  
Coordination Polymers ◽  
Room Temperature ◽  
Three Dimensional ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
One Dimensional ◽  
X Ray ◽  
Dimensional Network

Two novel cadmium coordination polymers, [Cd(pydc)2(tu)]n (1) and [Cd2(SO4)(nic)2(tu)1.5 - (H2O)2]n (2) (pydc = pyridine-2,3-dicarboxylate, nic = nicotinate, tu = thiourea), have been synthesized under hydrothermal conditions and structurally characterized by X-ray diffraction analysis. 1 is a one-dimensional ladder coordination polymer in a two-dimensional network formed by hydrogen bonds. 2 consists of two kinds of Cd(II) centers in different coordination environments connected via nicotinate and sulfate to form a two-dimensional grid network integrated in a three-dimensional framework generated by hydrogen bonds. 2 shows intense fluorescent emission in the solid state at room temperature

A new two-dimensional ZnII coordination polymer based on 1,3-bis(2-methyl-1H-imidazol-1-yl)benzene and 5-nitrobenzene-1,3-dicarboxylic acid: synthesis, crystal structure and physical properties

2019 ◽  
Vol 75 (2) ◽  
pp. 196-199 ◽  
Author(s):  
Ning-Ning Chen ◽  
Jian-Ning Ni ◽  
Jun Wang ◽  
Jian-Qing Tao
Keyword(s):  
Solid State ◽  
Single Crystal ◽  
Dicarboxylic Acid ◽  
Three Dimensional ◽  
Acid Synthesis ◽  
Dimensional Structure ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Π Interactions

A novel two-dimensional (2D) ZnII coordination framework, poly[[μ-1,3-bis(2-methyl-1H-imidazol-1-yl)benzene](μ-5-nitrobenzene-1,3-dicarboxylato)zinc(II)], [Zn(C8H3NO6)(C14H14N4)] n or [Zn(NO2-BDC)(1,3-BMIB)] n [1,3-BMIB is 1,3-bis(2-methyl-1H-imidazol-1-yl)benzene and NO2-H2BDC is 5-nitrobenzene-1,3-dicarboxylic acid], has been prepared and characterized by IR, elemental analysis, thermal analysis and single-crystal X-ray diffraction. Single-crystal X-ray diffraction analysis revealed that the compound is a new 2D polymer with a 63 topology parallel to the (10\overline{2}) crystal planes based on left-handed helices, right-handed helical NO2-BDC–Zn chains and [Zn2(1,3-BMIB)2] n clusters. In the crystal, adjacent layers are further connected by C—H...O hydrogen bonds, C—H...π interactions, C—O...π interactions and N—O...π interactions to form a three-dimensional structure in the solid state. In addition, the compound exhibits strong fluorescence emissions in the solid state at room temperature.

Two one-dimensional coordination polymers generated from a new benzimidazole bridging ligand and CdX2(X= Br and I)

2013 ◽  
Vol 69 (5) ◽  
pp. 476-479 ◽  
Author(s):  
Yue-Feng Zhang ◽  
Jian-Ping Ma ◽  
Qi-Kui Liu ◽  
Yu-Bin Dong
Keyword(s):  
Hydrogen Bonds ◽  
Coordination Polymers ◽  
Three Dimensional ◽  
The Novel ◽  
Asymmetric Unit ◽  
One Dimensional ◽  
Π Interactions ◽  
Solvent Water ◽  
Bridging Ligand ◽  
Dimensional Network

The novel asymmetric bridging ligand 1-[(pyridin-3-yl)methyl]-2-[4-(pyridin-3-yl)phenyl]-1H-benzimidazole (L) has been used to construct the coordination polymerscatena-poly[[[dibromidocadmium(II)]-μ3-1-[(pyridin-3-yl)methyl]-2-[4-(pyridin-3-yl)phenyl]-1H-benzimidazole] monohydrate], {[CdBr2(C24H18N4)]·H2O}n, (I), andcatena-poly[[diiodidocadmium(II)]-μ3-1-[(pyridin-3-yl)methyl]-2-[4-(pyridin-3-yl)phenyl]-1H-benzimidazole], [CdI2(C24H18N4)]n, (II). Compounds (I) and (II) are closely related one-dimensional polymers based on 16- and 20-membered macrocycles along the chains, but they are not isomorphous. The chains are crosslinked into a two-dimensional networkviahydrogen bonds and π–π interactions in (I), and into a three-dimensional framework through π–π interactions in (II). One well-ordered solvent water molecule per asymmetric unit is included in (I) and forms O...Br hydrogen bonds.

One-dimensional coordination polymers generated from a new triazole bridging ligand and HgX2(X= Cl, Br and I): characterization and luminescent properties

2012 ◽  
Vol 68 (6) ◽  
pp. m147-m151 ◽  
Author(s):  
Na Qin ◽  
Chao-Wei Zhao ◽  
Jian-Ping Ma ◽  
Qi-Kui Liu ◽  
Yu-Bin Dong
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Coordination Complexes ◽  
The Other ◽  
Tridentate Ligand ◽  
Dimensional Structure ◽  
One Dimensional ◽  
Bridging Ligand ◽  
Solvent Molecules

The new 4-amino-1,2,4-triazole asymmetric bridging ligand 4-amino-5-(pyridin-3-yl)-3-[4-(pyridin-4-yl)phenyl]-4H-1,2,4-triazole (L) has been used to generate three novel isomorphic one-dimensional coordination polymers,viz. catena-poly[[tris[dichloridomercury(II)]-bis{μ3-4-amino-5-(pyridin-3-yl)-3-[4-(pyridin-4-yl)phenyl]-4H-1,2,4-triazole}] acetonitrile monosolvate], {[Hg3Cl6(C18H14N6)2]·CH3CN}n, (I), and the bromido, {[Hg3Br6(C18H14N6)2]·CH3CN}n, (II), and iodido, {[Hg3I6(C18H14N6)2]·CH3CN}n, (III), analogs. The asymmetric ligand acts as a tridentate ligand to coordinate the three different HgIIcenters (two of which are symmetry-related). Two ligands and two symmetry-related HgIIcenters form centrosymmetric rectangular units which are linked into one-dimensional chainsviathe other unique Hg atoms, which sit on mirror planes. The chains are elaborated into a three-dimensional structureviainterchain hydrogen bonds. The acetonitrile solvent molecules are located in ellipsoidal cavities. The luminescent character of these three coordination complexes was investigated in the solid state.

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