The preparation and catalytic properties of copper(II) complexes derived from a pyrazole containing ligand. X-ray crystal structure of [Cu(pzmhp)(BF4)](BF4)

1997 ◽  
Vol 257 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Mitchell R. Malachowski ◽  
Josephine Carden ◽  
Marilyn G. Davidson ◽  
Willem L. Driessen ◽  
Jan Reedijk
Keyword(s):  
Crystal Structure ◽  
Catalytic Properties ◽  
X Ray

Synthesis of Au-SiO2 Composite Nanospheres and Their Catalytic Activity

2016 ◽  
Vol 16 (4) ◽  
pp. 3821-3826 ◽  
Author(s):  
Wang Dexuan ◽  
Li Guian ◽  
Han Qingyan ◽  
Wang Ziqiang ◽  
Pan Liping ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Photoelectron Spectroscopy ◽  
Au Nanoparticles ◽  
Catalytic Properties ◽  
Organic Dyes ◽  
Chemical Elements ◽  
X Ray ◽  
Transmission Electron ◽  
Environmentally Friendly Approach

We report a simple and environmentally friendly approach to the synthesis of Au-SiO2 composite nanospheres. Our method presents a route for the decoration of preformed amine functionalized SiO2 nanospheres by in situ formation of Au nanoparticles at three different concentrations of Au precursor (HAuCl4). Herein, the silane coupling agent (KH-550) is used as an intermediary to connect the Au nanoparticles to the surfaces of the SiO2 nanospheres, which helps avoid the aggregation of Au nanoparticles. The crystal structure, chemical elements, morphology and catalytic properties of the Au-SiO2 composite nanospheres were analyzed by transmission electron microscopy (TEM), X-Ray powder diffraction (XRD), UV-vis-spectrophotometer (UV-vis) and X-ray photoelectron spectroscopy (XPS). The analytical results demonstrate that the Au nanoparticles (4–9 nm) were homogeneously distributed on the surface of the SiO2 nanospheres, which had a good FCC crystal structure. Moreover, the Au-SiO2 composite nanospheres exhibited good catalytic properties, measured by their ability to reduce organic dyes. The Au-SiO2 composite nanospheres are promising candidates for applications in catalysis and wastewater treatment.

Crystal structure and physical properties of a new two-dimensional zinc coordination polymer based on 1,4-bis(4-(imidazole-1-yl)benzyl)piperazine and benzophenone-2,4′-dicarboxylate ligands

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Xin-Yue Zhang ◽  
Chen Zhang ◽  
Jun Wang ◽  
Xiao-Juan Xu
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Catalytic Properties ◽  
Gravimetric Analysis ◽  
Two Dimensional ◽  
Thermal Gravimetric ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zinc Coordination ◽  
Oriented Parallel

Abstract A new 2-dimensional (2D) zinc(II) coordination polymer based on a flexible bis(imidazole) ligand, namely, [Zn2(BIBP)(BPDC)2·DMF] n (1) BIBP is 1,4-bis(4-(imidazole-1-yl)benzyl)piperazine and H2BPDC is benzophenone-2,4′-dicarboxylic acid), has been synthesized and characterized through single-crystal X-ray diffraction, infrared (IR) spectroscopy, and elemental and thermal gravimetric analysis. Complex 1 exhibits a 2D framework oriented parallel to [0 2 1] based on [Zn(BPDC)] n chains. The fluorescence and catalytic properties of complex 1 for the photodegradation of methylene blue were investigated.

scholarly journals Synthesis, Crystal Structure, Catalytic Properties, and Luminescent of a Novel Eu(III) Complex Material with 4-Imidazolecarboxaldehyde-pyridine-2-carbohydrazone

2017 ◽  
Vol 12 (2) ◽  
pp. 185 ◽  
Author(s):  
Li-Hua Wang ◽  
Lei Liang ◽  
Peng-Fei Li
Keyword(s):  
Crystal Structure ◽  
Catalytic Properties ◽  
Coupling Reaction ◽  
Reaction Engineering ◽  
Orthorhombic Space Group ◽  
Single Crystal Diffraction ◽  
Complex Material ◽  
X Ray ◽  
A3 Coupling ◽  
Luminescent Spectrum

A novel Eu(III) complex, [Eu(L)2(H2O)4]·(NO3)·(H2O)4 (1) (H2L = 4-imidazolecarboxaldehyde-pyridine-2-carbohydrazide), was synthesized. Its structure has been characterized by elemental analysis, IR, and X-ray single crystal diffraction analysis. Complex 1 is of orthorhombic, space group Fdd2 with a = 29.471(6) A˚, b = 10.287(2) A˚, c = 24.340(5) A˚, V = 7379(3) A˚3, Z = 8, Mr = 902.58, Dc = 1.625 µg·m-3, µ = 1.789 mm-1, F(000) = 3656, GOOF = 1.099, the final R= 0.0517, ωR= 0.1292 for 3043 observed reflections with I > 2σ(I).  The A3 coupling reaction has been investigated using the complex 1 as catalyst. The luminescent spectrum of the complex 1 gives two weak peaks (448 nm and 491 nm) and two strong peaks (596 nm and 620 nm) from excitation at 279 nm. Copyright © 2017 BCREC Group. All rights reserved.Received: 11st November 2016; Revised: 10th February 2017; Accepted: 23rd February 2017How to Cite: Wang, L.H., Liang, L., Li, P.F. (2017). Synthesis, Crystal Structure, Catalytic Properties, and Luminescent of a Novel Eu(III) Complex Material with 4-Imidazolecarboxaldehyde-pyridine-2-carbohydrazone. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (2): 185-190 (doi:10.9767/bcrec.12.2.764.185-190)Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.2.764.185-190

Synthesis, crystal structure, and catalytic properties of 2,2’-bipyridyl-dicyano-palladium(II)

2015 ◽  
Vol 2 (2) ◽  
pp. 74-78
Author(s):  
Karthikeyan.V
Keyword(s):  
Crystal Structure ◽  
Hydrogen Peroxide ◽  
Catalytic Properties ◽  
Structural Parameters ◽  
In Situ Synthesis ◽  
Title Complex ◽  
Homogeneous Catalyst ◽  
X Ray ◽  
Solvothermal Condition

In the solvothermal condition, a Pd(II) complex with a in situ synthesis ligand, [Pd(2,2’-bipy)2(CN)2] (1) was obtained and characterized by elemental analysis, IR, UV, TG, and powder X-ray analysis. The single crystal X-ray analysis showed that the title complex is different from the reported 2,2’-bipyridyldicyano-palladium(II) (2) in crystal system and structural parameters. The catalytic investigation for the reactions of the disproportionation of hydrogen peroxide and oxidation of sulfide showed that the complex 1 is an active homogeneous catalyst in the presence of imidazole and 2-sulfobenzoic acid, respectively.

Hydrothermal Synthesis, Crystal Structure and Catalytic Properties of a Novel Polyoxometalate: (C5H7N2)3(AsMo12O40) ·2C5H6N2 · 1.5H2O

2010 ◽  
Vol 65 (9) ◽  
pp. 1101-1105 ◽  
Author(s):  
Tie-Jun Cai ◽  
Xiao-Ming Shen ◽  
Zhen-Shan Peng ◽  
Shu-Zi Lu ◽  
Qian Deng
Keyword(s):  
Crystal Structure ◽  
Continuous Flow ◽  
Catalytic Properties ◽  
Fixed Bed ◽  
High Catalytic Activity ◽  
Crystal Data ◽  
X Ray Diffraction ◽  
Initial Concentration ◽  
X Ray ◽  
Micro Reactor

(C5H7N2)3(AsMo12O40)・2C5H6N2・1.5H2O was hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction. Crystal data: monoclinic, P21/n, a = 13.310(3), b = 22.399(5), c = 19.820(4) A° , β = 99.99(3) ◦, V = 5819(2) °A3, Z = 1, wR(F2) = 0.1345. The structure consists of Keggin-type [AsMo12O40]3− polyoxoanions. The title compound has a high catalytic activity for the oxidation of acetone tested in a continuous-flow fixed-bed micro-reactor. When the initial concentration is 5.3 g m−3 in air and the flow rate is 2.5 mL min−1, the acetone is completely eliminated at 150 ◦C.

A study on α-RuCl3 crystal structure by scanning tunneling microscopy

1989 ◽  
Vol 47 ◽  
pp. 30-31
Author(s):  
H.-J. Cantow ◽  
H. Hillebrecht ◽  
S. Magonov ◽  
H. W. Rotter ◽  
G. Thiele
Keyword(s):  
Crystal Structure ◽  
Density Distribution ◽  
Scanning Tunneling Microscopy ◽  
Electron Density ◽  
Structure Determination ◽  
Electron Density Distribution ◽  
Scanning Tunneling ◽  
Monoclinic Space Group ◽  
Tunneling Microscopy ◽  
X Ray

From X-ray analysis, the conclusions are drawn from averaged molecular informations. Thus, limitations are caused when analyzing systems whose symmetry is reduced due to interatomic interactions. In contrast, scanning tunneling microscopy (STM) directly images atomic scale surface electron density distribution, with a resolution up to fractions of Angstrom units. The crucial point is the correlation between the electron density distribution and the localization of individual atoms, which is reasonable in many cases. Thus, the use of STM images for crystal structure determination may be permitted. We tried to apply RuCl3 - a layered material with semiconductive properties - for such STM studies. From the X-ray analysis it has been assumed that α-form of this compound crystallizes in the monoclinic space group C2/m (AICI3 type). The chlorine atoms form an almost undistorted cubic closed package while Ru occupies 2/3 of the octahedral holes in every second layer building up a plane hexagon net (graphite net). Idealizing the arrangement of the chlorines a hexagonal symmetry would be expected. X-ray structure determination of isotypic compounds e.g. IrBr3 leads only to averaged positions of the metal atoms as there exist extended stacking faults of the metal layers.

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