Synthesis of coordination polymers with d10 metal ions and a new linear ligand: X-ray structural and luminescence studies

Polyhedron ◽  
2013 ◽  
Vol 52 ◽  
pp. 1145-1152 ◽  
Author(s):  
Musheer Ahmad ◽  
Parimal K. Bharadwaj
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
X Ray ◽  
D10 Metal

scholarly journals Structural Diversity of Six Coordination Polymers Based on the Designed X-Shaped Ligand 1,1,1,1-Tetrakis[(3-pyridiniourea)methyl]methane

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2292 ◽  
Author(s):  
Qi-Long Zhang ◽  
Qing Yu ◽  
Hai-Fang Xie ◽  
Bo Tu ◽  
Hong Xu ◽  
...  
Keyword(s):  
Metal Ions ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Coordination Polymers ◽  
Chain Complex ◽  
Structural Diversity ◽  
Structural Comparison ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
Loop Chain

In this study, six coordination polymers (CPs), {[Ag2(L)(CF3SO3)]·CF3SO3·2H2O·DMF}n (1), {[Ag(L)]·SbF6·4DMF·H2O}n (2), {[Zn(L)0.5(I)2]·3.75H2O}n (3), {[Cd2(L)(I)4(H2O)(DMF)]·4H2O·3DMF}n (4), {[Hg2(L)(I)4]·H2O·4DMF}n (5) and {[Hg2(L)(Cl)4]·2H2O·3DMF}n (6), were obtained based on the designed X-shaped urea-based ligand. X-ray single crystal diffraction analysis revealed that complex 1 displayed a 3D (3,4)-connected {6·82}{64·82}-tcj net. Complex 2 featured a 2D 4-connected {43·63} sheet. Complexes 3 and 5 exhibited a 1D polymeric loop chain. Complex 4 displayed a 1D polymeric fishbone chain. Complex 6 showed a 2D 4-connected {44·62}-sql sheet. Structural comparison revealed that not only the metal ions, but also the anions played crucial roles in the control of final structures.

Two coordination polymers based on 2,2′-biimidazoles and d10 metal ions: syntheses, structures, and luminescence

2011 ◽  
Vol 64 (16) ◽  
pp. 2912-2922 ◽  
Author(s):  
Li-Ning Yang ◽  
Yan-Xiang Zhi ◽  
Jia-Hui Hei ◽  
Jun Li ◽  
Feng-Xing Zhang ◽  
...  
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
D10 Metal

New homodinuclear tris(3-alkylpyrazolyl)borate complexes of CoIIand NiIIwith a tetraacetylethane dianion as a bridging ligand

2016 ◽  
Vol 72 (11) ◽  
pp. 777-785
Author(s):  
Elena A. Mikhalyova ◽  
Swiatoslaw Trofimenko ◽  
Matthias Zeller ◽  
Anthony W. Addison ◽  
Vitaly V. Pavlishchuk
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Molecular Structures ◽  
Polynuclear Complexes ◽  
X Ray ◽  
X Ray Crystallography ◽  
Coordination Sites ◽  
Borate Complexes ◽  
Capping Ligands

Polynuclear complexes and coordination polymers of 3dmetals have attracted significant interest evoked by a number of their unique properties. One of the most common approaches to the directed synthesis of coordination polymers is the linking of pre-prepared discrete coordination units by polydentate ligands. The formation of polynuclear complexes is usually a spontaneous process and precise prediction of the products of such reactions is virtually impossible in most cases. Tris(pyrazolyl)borates (Tp) act as tripodal `capping' ligands which form stable complexes with 3dmetal ions. In such 1:1 compounds, three metal-ion coordination sites are occupied by N atoms from a Tp anion. This limits the number of remaining coordination sites, and thus the number of additional ligands which may coordinate, and opens an attractive approach for the directed design of desirable structures by exploiting ligands with appropriate composition and topology. In the present study, Tp anions with neopentyl [TpNp, tris(3-neopentylpyrazolyl)borate] and cyclohexyl [TpCy, tris(3-cyclohexylpyrazolyl)borate] substituents were used as `capping' ligands and the dianion of tetraacetylethane (3,4-diacetylhexa-2,4-diene-2,5-diolate, tae2−) was employed as a bridge. The dinuclear complexes (μ-3,4-diacetylhexa-2,4-diene-2,5-diolato-κ4O2,O3:O4,O5)bis{[tris(3-cyclohexyl-1H-pyrazol-1-yl-κN2)borato]cobalt(II)} acetonitrile disolvate, [Co2(C27H40BN6)2(C10H12O4)]·2CH3CN, (I)·2CH3CN, and (μ-3,4-diacetylhexa-2,4-diene-2,5-diolato-κ4O2,O3:O4,O5)bis{[tris(3-neopentyl-1H-pyrazol-1-yl-κN2)borato]nickel(II)}, [Ni2(C24H40BN6)2(C10H12O4)], (II), were synthesized by the reaction of the mononuclear complexes TpCyCoCl or TpNpNiCl with H2tae (3,4-diacetylhexane-2,5-dione or tetraacetylethane) in the presence of NEt3as base. Compounds (I) and (II) were characterized by mass spectrometry, elemental analysis, and X-ray crystallography. They possess similar molecular structures, X-ray diffraction revealing them to be dinuclear in nature and composed of discrete Tp–Munits in which two metal ions are linked by a tae2−dianion. Each metal ion possesses a five-coordinate square-pyramidal environment. The interplanar angles between the acetylacetonate fragments are significantly smaller than the near-90° values commonly observed.

New coordination polymers of glyoxal bis(2-hydroxyanil)

1995 ◽  
Vol 7 (4) ◽  
pp. 433-441 ◽  
Author(s):  
Salah A EI-Shatoury
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Metal Ions ◽  
Coordination Polymers ◽  
Elemental Analysis ◽  
Electronic Spectra ◽  
Metal Content ◽  
X Ray ◽  
Dsc Analyses ◽  
Scanning Electron

Coordination polymers of [2,2'-(ethandiylidenedinitrilo) diphenol) have been prepared with the metal ions Cu(II), Ni(1I) and Cr(III). They were characterized by elemental analysis, IR and electronic spectra. The metal content in all polymers was found to be consistent with a 1:1 (metal:ligand) stoichiometry. The thermal behaviour of these coordination polymers has been studied by thermogravimetric and DSC analyses in air up to 500 C. The crystallinity of the formed polymers was determined by x-ray analysis. The morphological structures of these polymers were determined by scanning electron microscopy.

Different dimensional and structural variations in coordination polymers of d10 metal ions constructed from a benzimidazole based carboxylate linker

Polyhedron ◽  
2013 ◽  
Vol 50 (1) ◽  
pp. 22-30 ◽  
Author(s):  
Rupali Mishra ◽  
Musheer Ahmad ◽  
Madhav Ram Tripathi
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
Structural Variations ◽  
D10 Metal

scholarly journals Synthesis, Crystal Structure, and Luminescence of Cadmium(II) and Silver(I) Coordination Polymers Based on 1,3-Bis(1,2,4-triazol-1-yl)adamantane

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5400
Author(s):  
Roman D. Marchenko ◽  
Taisiya S. Sukhikh ◽  
Alexey A. Ryadun ◽  
Andrei S. Potapov
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Metal Ions ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Coordination Polymers ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray

Coordination polymers with a new rigid ligand 1,3-bis(1,2,4-triazol-1-yl)adamantane (L) were prepared by its reaction with cadmium(II) or silver(I) nitrates. Crystal structure of the coordination polymers was determined using single-crystal X-ray diffraction analysis. Silver formed two-dimensional coordination polymer [Ag(L)NO3]n, in which metal ions are linked by 1,3-bis(1,2,4-triazol-1-yl)adamantane ligands, coordinated by nitrogen atoms at positions 2 and 4 of 1,2,4-triazole rings. Layers of the coordination polymer consist of rare 18- and 30-membered {Ag2L2} and {Ag4L4} metallocycles. Cadmium(II) nitrate formed two kinds of one-dimensional coordination polymers depending on the metal-to-ligand ratio used in the synthesis. Coordination polymer [Cd(L)2(NO3)2]n was obtained in case of a 1:2 M:L ratio, while for M:L = 2:1 product {[Cd(L)(NO3)2(CH3OH)]·0.5CH3OH}n was isolated. All coordination polymers demonstrated ligand-centered emission near 450 nm upon excitation at 370 nm.

Luminescent Functionalised Supramolecular Coordination Polymers Based on an Aromatic Carboxylic Acid Ligand for Sensing Hg2+ Ions

2017 ◽  
Vol 70 (7) ◽  
pp. 786 ◽  
Author(s):  
Xiaojun Sun ◽  
Ping Yang ◽  
Guangfeng Hou ◽  
Jinzhi Wei ◽  
Xueliang Wang ◽  
...  
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
3D Structure ◽  
Crystallographic Analysis ◽  
X Ray ◽  
Luminescent Sensors ◽  
1D Chain ◽  
Supramolecular Coordination ◽  
Supramolecular Networks ◽  
Carboxylic Acid Ligand

Two luminescent functionalised supramolecular coordination polymers, namely, [Zn(TPDC-2CH3)(H2O)2]·H2O (1) and [Cd(TPDC-2CH3)(H2O)4]·H2O (2), were successfully synthesised by the reaction of 2′,5′-dimethyl-[1,1′:4′,1″-terphenyl]-4,4″-dicarboxylic acid (H2TPDC-2CH3) with Zn2+ and Cd2+ ions, respectively. X-Ray crystallographic analysis reveals that both compounds 1 and 2 exhibit fascinating 3D supramolecular networks, in which metal ions are linked by ligands to form a 1D chain which further extends to a 3D structure through the interaction of hydrogen bonding. The use of 1 and 2 as luminescent sensors for the optical detection of metal ions: Na+, K+, Hg2+, Ag+, Ca2+, Co2+, Ni2+, Mn2+, Cu2+, Zn2+, Cd2+, Pb2+, Mg2+, Al3+, Fe3+, Fe2+, In3+, Bi3+, and Cr3+ was carried out in aqueous solution, and the results indicated that compound 1 could effectively detect Hg2+ ions among various cations at room temperature, with a detection limit of 3.6 × 10−15 M.

scholarly journals 1D, 2D, and 3D Coordination Polymers based on 2,3‐Pyrazinedithiolate and d10 Metal Ions (Ag+, Zn2+)

2021 ◽  
Author(s):  
Stefan Henfling ◽  
Ozi Adi Saputra ◽  
Harald Krautscheid
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
D10 Metal ◽  
2D And 3D

Synthesis, crystal structure and biological properties of Cd and Zn coordination polymers based on a flexible tripodal ligand

2019 ◽  
Vol 75 (7) ◽  
pp. 1002-1010 ◽  
Author(s):  
Xia Wang ◽  
Ning Ling ◽  
Hanbing Li ◽  
Xiaohe Xiao ◽  
Yawen Zhang
Keyword(s):  
Metal Ions ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Radical Scavenging ◽  
Antidiabetic Activity ◽  
Distorted Octahedral Geometry ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Methyl Benzene

Two new coordination polymers, namely poly[[hexathiocyanatotetrakis{μ3-2,4,6-trimethyl-1,3,5-tris[(triazol-1-yl)methyl]benzene}tricadmium(II)] 3.5-hydrate], {[Cd3(SCN)6(C18H21N9)4]·3.5H2O} n (1), and poly[[hexathiocyanatotetrakis{μ3-2,4,6-trimethyl-1,3,5-tris[(triazol-1-yl)methyl]benzene}trizinc(II)] 3.5-hydrate], {[Zn3(SCN)6(C18H21N9)4]·3.5H2O} n (2), have been synthesized under hydrothermal conditions and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction analysis. From the X-ray analysis, it is noteworthy that polymers 1 and 2 are isostructural, with their three-dimensional structures composed of three kinds of four-connection metal ions and two kinds of three-connection 2,4,6-trimethyl-1,3,5-tris[(triazol-1-yl)methyl]benzene (TTTMB) ligand nodes. Each metal ion is six-coordinated in a slightly distorted octahedral geometry. The antioxidant activity against DPPH (2,2-diphenyl-1-picrylhydrazyl) and the antidiabetic activity against α-amylase of the synthesized compounds were evaluated in vitro. The results of the DPPH free-radical scavenging assay showed that polymers 1 and 2 exhibited strong antioxidant effects, with IC50 values of 3.81 and 2.56 mg ml−1, respectively. The IC50 value in the antidiabetic studies of polymer 1 was 3.94 mg ml−1, while polymer 2 exhibited no antidiabetic activity. Polymers 1 and 2 revealed different inhibitory activities on DPPH and α-amylase, which indicated that the metal ions play important roles in the biological activity of coordination polymers. In addition, the solid-state photoluminescence properties and thermal stability of 1 and 2 have been investigated.

A series of two-dimensional lanthanide coordination polymers: synthesis, structures, magnetism and selective luminescence detection for heavy metal ions and toxic solvents

2019 ◽  
Vol 75 (2) ◽  
pp. 221-230 ◽  
Author(s):  
Hongguo Hao ◽  
Hongyan Liu ◽  
Yuchen Wang ◽  
Suxian Yuan ◽  
Han Xu ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Metal Ions ◽  
Coordination Polymers ◽  
Double Layers ◽  
Antiferromagnetic Coupling ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrogen Bonding Interactions ◽  
Strong Luminescence

A series of two-dimensional (2D) coordination polymers (CPs), namely poly[[bis(μ-acetato)diaqua(μ6-biphenyl-3,3′,5,5′-tetracarboxylato)bis(N,N-dimethylacetamide)digadolinium(III)] N,N-dimethylacetamide monosolvate], {[Gd2(C16H6O8)(C2H3O2)2(C4H9NO)2(H2O)2]·C4H9NO} n (CP1), poly[[bis(μ-acetato)diaqua(μ6-biphenyl-3,3′,5,5′-tetracarboxylato)bis(N,N-dimethylacetamide)didysprosium(III)] N,N-dimethylacetamide monosolvate], {[Dy2(C16H6O8)(C2H3O2)2(C4H9NO)2(H2O)2]·C4H9NO} n (CP2), poly[bis(μ-acetato)diaqua(μ6-biphenyl-3,3′,5,5′-tetracarboxylato)bis(N,N-dimethylacetamide)dineodymium(III)], [Nd2(C16H6O8)(C2H3O2)2(C4H9NO)2(H2O)2] n (CP3), poly[bis(μ-acetato)diaqua(μ6-biphenyl-3,3′,5,5′-tetracarboxylato)bis(N,N-dimethylacetamide)disamarium(III)], [Sm2(C16H6O8)(C2H3O2)2(C4H9NO)2(H2O)2] n (CP4), has been synthesized from rigid biphenyl-3,3′,5,5′-tetracarboxylic acid under solvothermal conditions. Their structures have been determined by single-crystal X-ray diffraction analyses, elemental analyses, IR spectra, powder X-ray diffraction and thermogravimetric analyses, and CP1–CP4 crystallize in the monoclinic space group P21/n. CP1–CP4 are isomorphous and feature similar 2D double layers, which are further extended via interlayer hydrogen-bonding interactions into a three-dimensional (3D) supramolecular structure. Hydrogen-bonding interactions between N,N-dimethylacetamide molecules and carboxylate O atoms strengthen the packing of the layers. The organic ligands interconnect with metal ions to generate 2D layered structures with a (4,4)-connected net having {44.62} topology. CP1 has been investigated for its magnetic properties and magnetic susceptibility measurements were carried out in the range 2.0–300 K. The results of the magnetic measurements show weak antiferromagnetic coupling between the GdIII ions in CP1. Moreover, the strong luminescence of CP2 and CP4 can be selectively quenched by the Fe3+ ion and toxic solvents (e.g. acetone).

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