One-dimensional (1D) europium coordination polymer wires: Synthesis, characterization and photoluminescence properties

2010 ◽  
Vol 28 ◽  
pp. 106-110 ◽  
Author(s):  
Longfei LUO ◽  
Rong XU ◽  
Dong ZHAO ◽  
Shengliang ZHONG
2015 ◽  
Vol 71 (7) ◽  
pp. 534-538 ◽  
Author(s):  
Feng Su ◽  
Li-Ping Lu

The title coordination polymer, poly[[aqua(μ5-1,1′-biphenyl-2,2′,5,5′-tetracarboxylato)bis[μ2-1,4-bis(1H-imidazol-1-yl)benzene]dicadmium(II)] dihydrate], {[Cd2(C16H6O8)(C12H10N4)2(H2O)]·2H2O}n, was crystallized from a mixture of 1,1′-biphenyl-2,2′,5,5′-tetracarboxylic acid (H4bpta), 1,4-bis(1H-imidazol-1-yl)benzene (1,4-bib) and cadmium nitrate in water–dimethylformamide. The crystal structure consists of two crystallographically independent CdIIcations, with one of the CdIIcations possessing a slightly distorted pentagonal bipyramidal geometry. The second CdIIcentre is coordinated by carboxylate O atoms and imidazole N atoms from two separate 1,4-bib ligands, displaying a distorted octahedral CdN2O4geometry. The completely deprotonated bpta4−ligand, exhibiting a new coordination mode, bridges five CdIIcations to form one-dimensional chainsviaμ3-η1:η2:η1:η2and μ2-η1:η1:η0:η0modes, and these are further linked by 1,4-bib ligands to form a three-dimensional framework with a (42.64)(4.62)(43.65.72) topology. The structure of the coordination polymer is reinforced by intermolecular hydrogen bonding between carboxylate O atoms, aqua ligands and crystallization water molecules. The solid-state photoluminescence properties were investigated and the complex might be a candidate for a thermally stable and solvent-resistant blue fluorescent material.


2016 ◽  
Vol 72 (12) ◽  
pp. 960-965 ◽  
Author(s):  
Pattiya Krinchampa ◽  
Kittipong Chainok ◽  
Siriporn Phengthaisong ◽  
Sujittra Youngme ◽  
Filip Kielar ◽  
...  

One of most interesting systems of coordination polymers constructed from the first-row transition metals is the porous ZnIIcoordination polymer system, but the numbers of such polymers containingN-donor linkers are still limited. The title double-chain-like ZnIIcoordination polymer, [Ag2Zn(CN)4(C10H10N2)2]n, presents a one-dimensional linear coordination polymer structure in which ZnIIions are linked by bridging anionic dicyanidoargentate(I) units along the crystallographicbaxis and each ZnIIion is additionally coordinated by a terminal dicyanidoargentate(I) unit and two terminal 1-benzyl-1H-imidazole (BZI) ligands, giving a five-coordinated ZnIIion. Interestingly, there are strong intermolecular AgI...AgIinteractions between terminal and bridging dicyanidoargentate(I) units and C—H...π interactions between the phenyl rings of BZI ligands of adjacent one-dimensional linear chains, providing a one-dimensional linear double-chain-like structure. The supramolecular three-dimensional framework is stabilized by C—H...π interactions between the phenyl rings of BZI ligands and by AgI...AgIinteractions between adjacent double chains. The photoluminescence properties have been studied.


Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3358
Author(s):  
Sadaf Rauf ◽  
Agata Trzesowska-Kruszynska ◽  
Tomasz Sierański ◽  
Marcin Świątkowski

Three new copper coordination compounds derived from 2,2-bis(hydroxymethyl)propionic acid (dmpa) and hexamethylenetetramine (hmta) were obtained and their crystal structures were determined. The stoichiometry of the reagents applied in the syntheses reflects the metal to ligand molar ratio in the formed solid products. Due to the multiple coordination modes of the used ligands, wide structural diversity was achieved among synthesized compounds, i.e., mononuclear [Cu(dmp)2(hmta)2(H2O)] (1), dinuclear [Cu2(dmp)4(hmta)2] (2), and 1D coordination polymer [Cu2(dmp)4(hmta)]n (3). Their supramolecular structures are governed by O—H•••O and O—H•••N hydrogen bonds. The compounds were characterized in terms of absorption (UV-Vis and IR) and thermal properties. The relationships between structural features and properties were discussed in detail. Owing to discrepancies in the coordination mode of a dmp ligand, bidentate chelating in 1, and bidentate bridging in 2 and 3, there is a noticeable change in the position of the bands corresponding to the stretching vibrations of the carboxylate group in the IR spectra. The differences in the structures of the compounds are also reflected in the nature and position of the UV-Vis absorption maxima, which are located at lower wavelengths for 1.


2015 ◽  
Vol 71 (8) ◽  
pp. m148-m149
Author(s):  
Mohammad Iqbal ◽  
James Raftery ◽  
Peter Quayle

The title copper(II) complex, {(C27H37N2)[Cu4(CH3COO)8Cl]·3CH2Cl2}n, is a one-dimensional coordination polymer. The asymmetric unit is composed of a copper(II) tetraacetate paddle-wheel complex, a Cl−anion situated on a twofold rotation axis, half a 1,3-bis(2,6-diisopropylphenyl)imidazolium cation (the whole molecule being generated by twofold rotation symmetry) and one and a half of a dichloromethane solvent molecule (one being located about a twofold rotation axis). The central metal-organic framework comprises of a tetranuclear copper(II) acetate `paddle-wheel' complex which arises from the dimerization of the copper(II) tetraacetate core comprising of three μ2-bidentate acetate and one μ3-tridentate acetate ligands per binuclear paddle-wheel complex. Both CuIIatoms of the binuclear component adopt a distorted square-pyramidal coordination geometry (τ = 0.04), with a Cu...Cu separation of 2.6016 (2) Å. The apical coordination site of one CuIIatom is occupied by an O atom of a neighbouring acetate bridge [Cu—O = 2.200 (2) Å], while that of the second CuIIatom is occupied by a bridging chloride ligand [Cu...Cl = 2.4364 (4) Å]. The chloride bridge is slightly bent with respect to the Cu...Cu internuclear axis [Cu—Cl—Cu = 167.06 (6)°] and the tetranuclear units are located about a twofold rotation axis, forming the one-dimensional polymer that propagates along [101]. Charge neutrality is maintained by the inclusion of the 1,3-bis(2,6-diisopropylphenyl)imidazolium cation within the crystal lattice. In the crystal, the cation and dichloromethane solvent molecules are linked to the coordination polymer by various C—H...O and C—H...Cl hydrogen bonds. There are no other significant intermolecular interactions present.


Nanoscale ◽  
2016 ◽  
Vol 8 (3) ◽  
pp. 1456-1461 ◽  
Author(s):  
Ye Yuan ◽  
Mingguang Yao ◽  
Shuanglong Chen ◽  
Shijie Liu ◽  
Xigui Yang ◽  
...  

Unlike bulk iodine, iodine molecular chains formed inside one dimensional (1D) nanochannels of AlPO4-5 (AFI) single crystals show unexpected PL behavior.


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