Design, Synthesis, and Photoluminescence Properties of One-, Two-, and Three-Dimensional Coordination Polymers: Anion-Assisted Argentophillic Interactions as Building Blocks

2014 ◽  
Vol 14 (10) ◽  
pp. 5164-5170 ◽  
Author(s):  
Kaustuv Banerjee ◽  
Sandipan Roy ◽  
Kumar Biradha
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Building Blocks ◽  
Photoluminescence Properties ◽  
Design Synthesis

A three-dimensional manganese(II) coordination polymer with two functional properties: magnetism and photochemical detection

2021 ◽  
Vol 77 (12) ◽  
Author(s):  
Dan Zhao ◽  
Yanyan An ◽  
Tingting Guo ◽  
Juanzhi Yan ◽  
Danmei Song
Keyword(s):  
Coordination Polymer ◽  
Hydrothermal Reaction ◽  
Three Dimensional ◽  
Building Blocks ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Detection Mechanism ◽  
Susceptibility Data ◽  
Dichromate Ions ◽  
Ditopic Ligand

Hydrothermal reaction of Mn2+ with the ditopic ligand 2,5-bis(1H-1,2,4-triazol-1-yl)benzoic acid (Hdtba) resulted in the complex poly[aqua[μ3-2,5-bis(1H-1,2,4-triazol-1-yl)benzoato-κ3 N 4:N 4′:O]chloridomanganese(II)] monohydrate], {[Mn(C11H7N6O2)Cl(H2O)]·H2O} n , (I). Coordination polymer I has been characterized by X-ray diffraction, IR spectroscopy, elemental analysis, thermogravimetry and susceptibility measurements. The topology of I corresponds to a three-dimensional (3,6)-conn net linked by {Mn2Cl2(COO)2} building blocks and dtba− anions. Significant antiferromagnetic exchange is observed within the dinuclear {Mn2Cl2(COO)2} subunits. A fit of the susceptibility data resulted in the magnetic parameters g = 1.93 and J = −1.52. Studies of the photoluminescence properties revealed that I represents a promising luminescence sensor for sensitively detecting dichromate ions in aqueous solution. The associated photochemical detection mechanism was studied in detail.

Structures and Photoluminescence Properties of Four Cadmium(II) Coordination Polymers Synthesized by Rigid Ligands and N-Donor Ligands

2015 ◽  
Vol 68 (5) ◽  
pp. 742 ◽  
Author(s):  
Qing-Guo Meng ◽  
Lin-Tong Wang ◽  
Ji-Tao Lu ◽  
Xin Wang ◽  
Wei Lu ◽  
...  
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Photoluminescence Properties ◽  
Thermal Stabilities ◽  
Structure Comparison ◽  
Layer Compound ◽  
Carboxylate Groups ◽  
Secondary Building Units ◽  
Coordinated Water ◽  
Dna 2

Four metal–organic coordination polymers, [Cd2(dna)2(2,2′-bpy)2]n (1), {[Cd4(dna)4(im)3]·5H2O}n (2), {[Cd2(dna)2(4,4′-bpy)(H2O)2]·2EtOH}n (3), and {[Cd4(dna)4(1,3-dpp)4(H2O)4]·2H2O}n (4) (H2dna = 4,6-dimethyl-5-nitroisophthalic acid; 2,2′-bpy = 2,2′-bipyridine; im = imidazole; 4,4′-bpy = 4,4′-bipyridine; 1,3-dpp = 1,3-di(4-pyridyl)propane; and EtOH = ethanol, have been solvothermally synthesized and characterized. Compound 1 displays a one-dimensional (1D) ladder structure and the neighbouring ladders are further stabilized by π···π interactions to form a two-dimensional (2D) layer. Compound 2 forms a 2D layer based on infinite 1D [Cd2(COO)4]n chain and the im ligands act as terminal ligands, preventing expansion of the dimensionality. Compound 3 features a 2D 44-sql layer based on binuclear [Cd2(COO)4] secondary building units as 4-connected nodes, and is further linked to be an unusual three-dimensional (3D) supramolecular architecture by hydrogen bonds involving the coordinated water molecules, carboxylate groups, and lattice ethanol molecules. Compound 4 possesses a 2-fold interpenetrated dia net. The diverse structures and topologies of compounds 1–4 indicate that the N-containing ligands have significant effects on the formation of the final network structures. In addition, the thermal stabilities, structure comparison, and photoluminescence properties of the complexes have been investigated.

Three Coordination Polymers Built by Methoxyphenyl Imidazole Dicarboxylate: Solvothermal Syntheses, Crystal Structures, and Properties

2015 ◽  
Vol 68 (6) ◽  
pp. 956 ◽  
Author(s):  
Ming-An Dang ◽  
Zi-Feng Li ◽  
Ying Liu ◽  
Gang Li
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Bridging Ligands ◽  
X Ray ◽  
Structures And Properties ◽  
Solvothermal Syntheses ◽  
Lattice Polymer ◽  
Imidazole Dicarboxylate

Three coordination polymers [Sr(p-H2MOPhIDC)2]n (1) (p-H3MOPhIDC = 2-p-methoxyphenyl-1H-imidazole-4,5-dicarboxylic acid), {[Cd2(p-HMOPhIDC)2(4,4′-bipy)]⋅H2O}n (4,4′-bipy = 4,4′-bipyridine) (2), and [Zn(p-HMOPhIDC)(4,4′-bipy)]n (3) have been solvothermally synthesized, and structurally characterized by single-crystal X-ray diffraction. Polymer 1 indicates a three-dimensional framework, which can be simplified as a 6-connected lattice. Polymer 2 is also a three-dimensional framework, and contains mixed bridging ligands HMOPhIDC2– and 4,4′-bipy. Polymer 3 exhibits a sheet structure bearing infinite rectangles. The coordination modes of the p-H3MOPhIDC ligand, and the thermal and solid-state photoluminescence properties of the polymers have been investigated as well.

Reversible recrystallization process of copper and silver thioacetamide–halide coordination polymers and their basic building blocks

CrystEngComm ◽  
2014 ◽  
Vol 16 (35) ◽  
pp. 8224-8231 ◽  
Author(s):  
J. Troyano ◽  
J. Perles ◽  
P. Amo-Ochoa ◽  
J. I. Martínez ◽  
F. Zamora ◽  
...  
Keyword(s):  
Coordination Polymers ◽  
Direct Synthesis ◽  
Three Dimensional ◽  
Building Blocks ◽  
Recrystallization Process

Three-dimensional [CuX(TAA)]n (X = Br (1), I (2)) and bi-dimensional [AgX(TAA)]n (X = Cl (3), Br (4)) coordination polymers have been isolated by the direct synthesis from copper(i) and silver(i) halides and thioacetamide (TAA).

Synthesis, crystal structures and magnetic characterisation of two 2p–3d metallic coordination polymers

2017 ◽  
Vol 41 (6) ◽  
pp. 365-369 ◽  
Author(s):  
Chongchong Xue ◽  
Jingwen Shi ◽  
Daopeng Zhang
Keyword(s):  
Magnetic Susceptibility ◽  
Coordination Polymers ◽  
Supramolecular Structure ◽  
Three Dimensional ◽  
Building Blocks ◽  
Chain Structure ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Dimensional Network

The coordination polymers {Mg[Fe(L)(CN)5]}n·0.5nH2O and {MgCu2(CH3COO)6}n [L = bis( N-imidazolyl)methane] have been synthesised. X-ray diffraction revealed that {Mg[Fe(L)(CN)5]}n·0.5nH2O has a one-dimensional neutral chain structure consisting of alternating [Mg(L)2(H2O)2)]2+ species and [Fe(L)(CN)5]2– building blocks, which can be further linked into a three-dimensional supramolecular structure by inter-chain p–p interactions. {MgCu2(CH3COO)6}n has a three-dimensional network with the [MgCu2(CH3COO)6] unit as neutral core extended by Mg–O bonds. Magnetic susceptibility studies on {MgCu2(CH3COO)6}n revealed antiferromagnetic interactions between adjacent Cu(II) ions.

Distinct 3D CdII Coordination Polymers with 1,2-Naphthalenedicarboxylate Regulated by Dipyridyl Co-Ligands with Different Spacers

2015 ◽  
Vol 68 (6) ◽  
pp. 906
Author(s):  
Zhuo-Wei Wang ◽  
Hui Zhao ◽  
Min Hu ◽  
Chun-Sen Liu
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Building Blocks ◽  
Metal Carboxylate ◽  
Two Dimensional ◽  
Coordination Networks ◽  
Hydrothermal Conditions ◽  
Porous Framework ◽  
3D Network ◽  
Structural Divergence

Two distinct three-dimensional (3D) CdII coordination polymers with 1,2-naphthalenedicarboxylate (ndc2–) and dipyridyl co-ligands have been synthesized under hydrothermal conditions. Interestingly, the slight difference in the two 4,4′-dipyridyl building blocks, namely, 1,2-bi(4-pyridyl)ethane (bpp) and 1,2-bi(4-pyridyl)ethene (bpe) with C–C or C=C spacers, results in the significant structural divergence of the resultant coordination polymers. Structural analysis reveals that complexes [Cd(ndc)(bpp)(H2O)]n (1) and {[Cd5(ndc)4(bpe)2(OH)2](H2O)1.5}n (2) are constructed by discrete metal–carboxylate dimeric units and metal–carboxylate chains, respectively, which are further extended by bpp or bpe linkers to form the inclined interpenetrated two-dimensional (2D)→3D network for 1 and the 3D porous framework for 2. This result reveals that the flexibility of auxiliary ligands plays an important role in the structural assemblies of coordination networks. The thermal and luminescence properties of both complexes were also investigated in solid state.

Structural Diversity and Fluorescence Regulation of Three ZnII Coordination Polymers Assembled from Mixed Ligands Tectons

2015 ◽  
Vol 68 (5) ◽  
pp. 758 ◽  
Author(s):  
Ling-Yun Xin ◽  
Guang-Zhen Liu ◽  
Lu-Fang Ma ◽  
Xue Zhang ◽  
Li-Ya Wang
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Emission Spectra ◽  
Structural Diversity ◽  
Double Layers ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Mixed Ligands ◽  
Structural Differences ◽  
Diffraction Patterns

By adopting a mixed-ligand strategy, three ZnII coordination polymers were prepared by hydrothermal reactions of zinc(ii) acetate with flexible 1,2-phenylenediacetic acid (H2phda) combining with three nitrogen-rich tectons namely, [Zn2(phda)2(bpo)2]n·2H2O (1), [Zn(phda)(pytz)]n (2), and [Zn(phda)(bib)]n·H2O (3) (where bpo = 2,5-bis(4-pyridyl)-1,3,4-oxadiazole, pytz = 3,5-di(4-pyridyl)-1,2,4-triazole, and bib = 1,4-bis(imidazol-1-yl)benzene). The single-crystal X-ray diffraction patterns reveal that the three compounds contain metal(ii)-carboxylate chains further extended by such nitrogen-rich co-ligands to afford a vast diversity of structures from two-dimensional (2D) stepwise grids (1), 2D double layers (2), to three-dimensional (3D)→3D 4-fold interpenetrating diamondoid networks. Furthermore, the structural differences in these complexes are primarily affected by the introduction of N-donor ancillary co-ligands so that their solid-state photoluminescence properties exhibit various emission spectra. Especially, compound 3 shows a guest-sensitive luminescence behaviour, which may be useful in applications as guest sensors.

Design, Synthesis and Bioactivity of Core 1 O-glycan and its Derivative on Human Gut Microbiota

2019 ◽  
Vol 16 (12) ◽  
pp. 1348-1353
Author(s):  
Huanhuan Qu ◽  
Baixue Li ◽  
Jingyi Yang ◽  
Huaiwen Liang ◽  
Meixia Li ◽  
...  
Keyword(s):  
Gut Microbiota ◽  
Initial Step ◽  
Building Blocks ◽  
Glycan Structure ◽  
Human Gut ◽  
Design Synthesis ◽  
The Core ◽  
Human Gut Microbiota ◽  
Biochemical Studies ◽  
Gut Symbionts

Background: Disaccharide core 1 (Galβ1-3GalNAc) is a common O-glycan structure in nature. Biochemical studies have confirmed that the formation of the core 1 structure is an important initial step in O-glycan biosynthesis and it is of great importance for human body. Objective: Our study will provide meaningful and useful sights for O-glycan synthesis and their bioassay. And all the synthetic glycosides would be used as intermediate building blocks in the scheme developed for oligosaccharide construction. Methods: In this article, we firstly used chemical procedures to prepare core 1 and its derivative, and a novel disaccharide was efficiently synthesized. The structures of the synthesized compounds were elucidated and confirmed by 1H NMR, 13C NMR and MS. Then we employed three human gut symbionts belonging to Bacteroidetes, a predominantphyla in the distal gut, as models to study the bioactivity of core 1 and its derivative on human gut microbiota. Results: According to our results, both core 1 and derivative could support the growth of B. fragilis, especially the core 1 derivative, while failed to support the growth of B. thetaiotaomicron and B. ovatus. Conclusion: This suggested that the B. fragilis might have the specificity glycohydrolase to cut the glycosidic bond for acquiring monosaccharide.

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