scholarly journals Synthesis, Crystal Structures and Luminescence Properties of Three New Cadmium 3D Coordination Polymers

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2465
Author(s):  
Hai-Yan Ju ◽  
Gang Zhang ◽  
Ming Yang ◽  
De-Zheng Liu ◽  
Yong-Sheng Yang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coordination Complexes ◽  
Luminescence Properties ◽  
Solvothermal Reaction ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Π Stacking Interaction ◽  
2D Network ◽  
3D Framework

The new rigid planar ligand 2,5-bis(3-(pyridine-4-yl)phenyl)thiazolo[5,4-d]thiazole (BPPT) has been synthesized, which is an excellent building block for assembling coordination polymer. Under solvothermal reaction conditions, cadmium ion with BPPT in the presence of various carboxylic acids including (1,1′-biphenyl)-4,4′-dicarboxylic acid (BPDC), isophthalic acid (IP), and benzene-1,3,5-tricarboxylic acid (BTC) gave rise to three coordination complexes, viz, [Cd(BPPT)(BPDA)](BPPT)n (1), [Cd(BPPT) (IP)] (CH3OH) (2), and [Cd3(BPPT)3(BTC)2(H2O)2] (3). The structures of 1, 2, and 3 were characterized by single crystal X-ray diffraction. The IR spectra as well as thermogravimetric and luminescence properties were also investigated. Complex 1 is a two-dimensional (2D) network and further stretched to a 3D supramolecular structure through π–π stacking interaction. The complexes 2 and 3 show 3D framework. The complexes 1, 2, and 3 exhibited luminescence property at room temperature.

Hydrothermal Syntheses, Crystal Structures, and Luminescent Properties of Two MnII Coordination Polymers: From Two-Fold Interpenetrated pcu Topological Net to Polycatenated 2D+2D→3D Framework

2015 ◽  
Vol 68 (2) ◽  
pp. 322 ◽  
Author(s):  
Wenlong Liu ◽  
Mengqiang Wu ◽  
Xueying Wang ◽  
Wei Wang ◽  
Dayu Liu ◽  
...  
Keyword(s):  
Dicarboxylic Acid ◽  
Coordination Polymers ◽  
Self Assembly ◽  
Room Temperature ◽  
Luminescent Properties ◽  
The Self ◽  
X Ray Diffraction ◽  
X Ray ◽  
3D Framework ◽  
Dimethyl Benzene

Using a hydrothermal synthesis, the self-assembly of MnII ions and 1,4-bis(1-imidazol-yl)-2,5-dimethyl benzene with two dicarboxylate ligands, 2-nitrobenzene-1,4-dicarboxylic acid (2-H2ata) and 5-methylbenzene-1,3-dicarboxylic acid (5-CH3-H2ip) constructed two interesting coordination polymers: [Mn(2-ata)(bimb)]n (1) and {[Mn(5-CH3-ip)(bimb)1.5]·2H2O}n (2), where bimb refers to 1,4-bis(1-imidazol-yl)-2,5-dimethyl benzene. Their structures were determined by single-crystal X-ray diffraction, elemental analysis, and infrared spectroscopy. Complex 1 exhibits a 2-fold interpenetrated pcu net. Complex 2 shows an unusual polycatenated 2D+2D→3D framework. In addition, the solid-state photoluminescent properties of 1 and 2 were investigated at room temperature.

Photoluminescence and photocatalytic activity of a 3D framework based on 4,4′-bis(1,2,4-triazol-1-ylmethyl)biphenyl as a ligand for cadmium

2019 ◽  
Vol 74 (7-8) ◽  
pp. 553-558
Author(s):  
Chen Zhang ◽  
Ning-Ning Chen ◽  
Jian-Qing Tao
Keyword(s):  
Thermal Analysis ◽  
Photocatalytic Activity ◽  
Phthalic Acid ◽  
Room Temperature ◽  
Three Dimensional ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coordination Framework ◽  
3D Framework

AbstractA novel three-dimensional Cd(II) coordination framework, [Cd(PTA)(BTBP)0.5 · H2O]n (1) (BTBP =  4,4′-bis(1,2,4-triazol-1-ylmethyl)biphenyl; H2PTA = p-phthalic acid), has been prepared and characterized through IR spectroscopy, elemental and thermal analysis, and single-crystal X-ray diffraction. The complex is a 5-connected network with the {45 · 66} topology based on Cd-μ2-H2O-Cd chains. It exhibits strong fluorescent emission in the solid state at room temperature. Moreover, complex 1 shows high photocatalytic activity in the degradation of methylene blue under UV irradiation.

Preparation and Characterization of Gold-Loaded Magnetite/Silica Core-Shell Composites

2016 ◽  
Vol 42 ◽  
pp. 47-52
Author(s):  
Dan Dan Huang ◽  
Zhao Dai ◽  
Kun Yang ◽  
Yuan Yuan Chu
Keyword(s):  
Room Temperature ◽  
Solvothermal Reaction ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
Silica Core ◽  
Shell Particles

The fabrication of gold-loaded magnetite/silica core-shell particles was presented in this paper. First, 250 nm of magnetic Fe3O4 nanoparticles were prepared by solvothermal reaction. Then, the Fe3O4 particles were coated by SiO2, and Au nanoparticles (AuNPs), respectively. The core-shell structure of these microspheres was confirmed by transmission electron microscopy (TEM) and Power X-ray diffraction (XRD). The magnetic property of the core-shell microspheres was investigated at room temperature. The results indicated that the core-shell composites had a well-retained high magnetic intensity, thus it can be easily separated from the mixture in less than a few minutes by simply using a magnet.

A Silver(I) Coordination Polymer Based on a Schiff Base Ligand: Synthesis, Crystal Structure and Luminescence Properties

2013 ◽  
Vol 68 (3) ◽  
pp. 284-288 ◽  
Author(s):  
Lin Yu Jin ◽  
Meng Meng Li ◽  
Dong Bin Dang ◽  
Yan Bai ◽  
Yan Ning Zheng
Keyword(s):  
Coordination Polymer ◽  
Room Temperature ◽  
Three Dimensional ◽  
Chain Structure ◽  
Luminescence Properties ◽  
Tridentate Ligand ◽  
Supramolecular Network ◽  
Zigzag Chain ◽  
X Ray Diffraction ◽  
X Ray

A new Ag(I) coordination polymer [AgL(NO3)]n 1 (L=4-(pyridine-2-yl)methyleneamino-1,2,4- trizaole) has been synthesized and characterized by IR spectroscopy, elemental analysis, powder and single-crystal X-ray diffraction. The Ag(I) atom has a seesaw environment with an N3O donor set from three N atoms of two ligands and one O atom of one NO-3 anion. Each twisted tridentate ligand is bound to two silver centers, and each silver atom is coordinated by two ligands thereby generating a zigzag chain structure. The chains interact with each other featuring a three-dimensional supramolecular network through multiple weak C-H···π interactions and C-H···O hydrogen bonds. The luminescence properties of the polymer 1 were investigated in the solid state at room temperature.

Synthesis of Monodisperse Fe3O4 Microspheres and Effect of the Precursor Concentration

2011 ◽  
Vol 183-185 ◽  
pp. 2327-2330 ◽  
Author(s):  
De Hui Sun ◽  
De Xin Sun ◽  
Ming Xing Han
Keyword(s):  
Room Temperature ◽  
Size Range ◽  
Precursor Concentration ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Xrd Pattern ◽  
X Ray ◽  
Magnetic Investigation ◽  
Cubic Structure ◽  
Average Size

In present work, we synthesized monodisperse Fe3O4microsphere using a free-surfactant solvothermal reduction route and investigated effect of the precursor concentration (FeCl3∙6H2O and NaAc) on microsphere sizes under other reaction conditions held constant. The morphologies, structures, and magnetism of the products were characterized by SEM, XRD, FTIR and VSM. The results showed that the Fe3O4 microsphere with a tunable average size range from 120 nm to 300 nm is composed of many Fe3O4collective nanoparticles. Their average diameters increased with increase of precursor FeCl3∙6H2O concentration but decreased with increase of precursor NaAc concentration. The X-ray diffraction (XRD) pattern confirmed that the Fe3O4microspheres belong to cubic structure. Magnetic investigation reveals that the Fe3O4microspheres have higher saturation magnetization and negligible coercivity at room temperature.

Synthesis and Characterization of Superparamagnetic Fe3O4 Nanoparticles

2013 ◽  
Vol 750-752 ◽  
pp. 340-343 ◽  
Author(s):  
De Hui Sun ◽  
Jiao Wu ◽  
Ji Lin Zhang
Keyword(s):  
Room Temperature ◽  
Thermal Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Xrd Pattern ◽  
X Ray ◽  
Magnetic Investigation ◽  
Average Size

We synthesized Fe3O4 nanoparticles using a solvent thermal method and characterized the morphologies, structures, surface properties, thermal stability and magnetism of the products by Field emission scanning electron microscopy (FE-SEM), Powder X-ray diffraction (XRD), Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA) and vibrating sample magnetometer (VSM). The experimental results showed that the Fe3O4 nanoparticles have a tunable average size range from 55 nm to 85 nm. Their diameters decreased with increase of precursor FeCl24H2O concentration or increase of the reaction time under other reaction conditions held constant. The XRD pattern confirmed that the Fe3O4 nanoparticles belong to cubic structure. Magnetic investigation reveals that the Fe3O4 nanoparticles have higher saturation magnetization and negligible coercivity at room temperature.

Syntheses, crystal structures and DNA-binding activities of divalent Fe, Cu, Zn and Cd complexes with 4′-(furan-2-yl)-2,2′:6′,2″-terpyridine

2017 ◽  
Vol 72 (10) ◽  
pp. 687-695
Author(s):  
Wei-Wei Fu ◽  
Dan Peng ◽  
Ya-Qian Li ◽  
Jing-Run Shen ◽  
Shuang-Hui Li
Keyword(s):  
Dna Binding ◽  
Room Temperature ◽  
Three Dimensional ◽  
Fluorescence Emission ◽  
Coordination Complexes ◽  
Dynamic Mode ◽  
X Ray Diffraction ◽  
X Ray ◽  
Face To Face ◽  
Intercalative Mode

AbstractFive coordination complexes [Fe(ftpy)2](ClO4)2·(H2O)2 (1), [Cu(ftpy)(NO3)(H2O)](NO3) (2), [Cu(ftpy)2]2(ClO4)4·(C2H5OH) (3), [Zn(ftpy)2]·(ClO4)2·(H2O)1.5 (4) and [Cd(ftpy)2]2(ClO4)4·(C2H5OH) (5) (ftpy=4′-(furan-2-yl)-2,2′:6′,2′-terpyridine) have been synthesized and characterized by IR, elemental analysis and single-crystal X-ray diffraction. With the exception of 4, all complexes adopt normal homoleptic [M(ftpy)2]2+ motifs. In the crystal, both hydrogen bonds and face-to-face interactions between furyl and pyridyl rings facilitate the construction of three-dimensional networks. The DNA-binding activities of the five complexes have been investigated by fluorescence emission titration at room temperature suggesting an intercalative mode for 1–3 with a relative order, 3>2>1, and a combined static and dynamic mode for 4 and 5.

Luminescence Properties of Europium Ion Doped Barium Borophosphate Phosphor

2015 ◽  
Vol 1107 ◽  
pp. 559-564
Author(s):  
Mukarramah M. Kamal ◽  
M. Nor M. Yusuf ◽  
N. Atiqah Jailani ◽  
S. Sholehah Hussein ◽  
R. Hussin ◽  
...  
Keyword(s):  
Solid State ◽  
Room Temperature ◽  
Solid State Reaction Method ◽  
Luminescence Properties ◽  
Broad Emission Band ◽  
X Ray Diffraction ◽  
X Ray ◽  
Europium Ion ◽  
Lighting Application ◽  
Pure Argon Atmosphere

A series of BaBPO5phosphors doped with different concentration of Eu2+ions were synthesized by solid state reaction method. The reduction of Eu3+to Eu2+ions were obtained by heating in pure argon atmosphere. The structural properties were analyzed by using X-ray diffraction (XRD). Luminescence properties were measured at room temperature using photoluminescence (PL) spectroscopy and the effects of europium ion in the phosphor were investigated. The XRD results showed that crystal structure of the phosphor is hexagonal single phases. The addition of europium ions exhibit a broad emission band in the violet region peaking at 383 nm corresponding to transition of configuration state 4f65d à 4f7(8S7/2) of Eu2+ions. The emission intensity is affected by the concentration of Eu2+. The optimum intensity is observed for 0.2 mol % of Eu2+ion. The occurrence of emission lines in violet region indicates that this phosphor has potential in solid-state lighting application.

Syntheses, Structures and Luminescence Properties of Two Cd(II) Complexes Based on 2-((1H-1,2,4-Triazol-1-yl)methyl)-1H-benzimidazole and Aromatic Polycarboxylate Ligands

2012 ◽  
Vol 67 (8) ◽  
pp. 783-790 ◽  
Author(s):  
Xiuxiu Wang ◽  
Xiao Han ◽  
Qiao ◽  
Guanghua Jin ◽  
Xiangru Meng
Keyword(s):  
Room Temperature ◽  
Luminescence Properties ◽  
X Ray Diffraction ◽  
Trans Conformation ◽  
X Ray ◽  
Carboxylate Groups ◽  
Benzenedicarboxylic Acid ◽  
In Trans ◽  
2D Structure ◽  
In Cis

Two new Cd(II) complexes, {[Cd(m-bdc)(tmb)(H2O)]·CH3OH}n (1) and {[Cd(t-bdc)(tmb)(H2O)] ·2H2O·DMF}n (2), have been prepared by using 2-((1H-1,2,4-triazol-1-yl)methyl)-1Hbenzimidazole (tmb) as a ligand in the presence of 1,3-benzenedicarboxylic acid (m-H2bdc) or 1,4-benzenedicarboxylic acid (t-H2bdc). Single-crystal X-ray diffraction exhibits that complex 1 displays a 2D structure constructed by tmb ligands in trans conformation and carboxylate groups in a chelating mode. The 2D structure of complex 2is different from that of 1, in that the tmb ligands are in cis conformation, and the carboxylate groups are in both unidentate or chelating coordination mode at the Cd(II) centers. The luminescence properties of 1and 2in the solid state at room temperature have been studied

Electron Microscopy of Human Gallstones

1971 ◽  
Vol 29 ◽  
pp. 296-297
Author(s):  
C. Wolpers ◽  
R. Blaschke
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Bile Pigment ◽  
X Ray Diffraction ◽  
Triclinic Crystal System ◽  
X Ray ◽  
Follow Up Study ◽  
Infra Red ◽  
Main Components

Scanning microscopy was used to study the surface of human gallstones and the surface of fractures. The specimens were obtained by operation, washed with water, dried at room temperature and shadowcasted with carbon and aluminum. Most of the specimens belong to patients from a series of X-ray follow-up study, examined during the last twenty years. So it was possible to evaluate approximately the age of these gallstones and to get information on the intensity of growing and solving.Cholesterol, a group of bile pigment substances and different salts of calcium, are the main components of human gallstones. By X-ray diffraction technique, infra-red spectroscopy and by chemical analysis it was demonstrated that all three components can be found in any gallstone. In the presence of water cholesterol crystallizes in pane-like plates of the triclinic crystal system.

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