Synthesis and characterization of robust three-dimensional chiral metal sulfates

RSC Advances ◽  
2014 ◽  
Vol 4 (92) ◽  
pp. 50435-50442 ◽  
Author(s):  
J. N. Behera ◽  
Joydeep Bhattacharjee ◽  
Satoshi Horike ◽  
Subba R. Marri ◽  
Prem P. Dahiya
Keyword(s):  
Thermal Decomposition ◽  
High Temperature ◽  
First Principles ◽  
Three Dimensional ◽  
Ammonium Ion ◽  
Synthesis And Characterization ◽  
First Principles Calculations ◽  
X Ray Diffraction ◽  
X Ray

Chiral three-dimensional Mg(ii) and Mn(ii) sulfates have been synthesized, well characterized and studied from first-principles calculations. High temperature X-ray diffraction, thermogravimetric analysis and DFT calculations reveal that the structures of both the compounds remain intact even after the thermal decomposition of the ammonium ion.

scholarly journals High-pressure synthesis and characterization of the non-centrosymmetric scandium borate ScB6O9(OH)3

2020 ◽  
Vol 75 (6-7) ◽  
pp. 597-603
Author(s):  
Birgit Fuchs ◽  
Hubert Huppertz
Keyword(s):  
High Pressure ◽  
High Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature ◽  
Structure Solution ◽  
Temperature Experiment ◽  
Pressure Synthesis

AbstractThe non-centrosymmetric scandium borate ScB6O9(OH)3 was obtained through a high-pressure/high-temperature experiment at 6 GPa and 1473 K. Single-crystal X-ray diffraction revealed that the structure is isotypic to InB6O9(OH)3 containing borate triple layers separated by scandium layers. The compound crystallizes in the space group Fdd2 with the lattice parameters a = 38.935(4), b = 4.4136(4), and c = 7.6342(6) Å. Powder X-ray diffraction and vibrational spectroscopy were used to further characterize the compound and verify the proposed structure solution.

Synthesis and Characterization of Co Nanoparticles by Solventless Thermal Decomposition

2007 ◽  
Vol 119 ◽  
pp. 71-74 ◽  
Author(s):  
Yan Li ◽  
Xiao Li Zhang ◽  
Young Hwan Kim ◽  
Young Soo Kang
Keyword(s):  
Crystal Structure ◽  
Thermal Decomposition ◽  
Synthesis And Characterization ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Structure Of Nanoparticles ◽  
Co Nanoparticles

Co nanoparticles were synthesized via a solventless thermal decomposition of Co2+-oleate2. The crystalline structure is strongly affected by the thermal treatment of the Co nanoparticles. Further, the annealing also results in the decomposition of surfactant around Co particles. The size of nanoparticles was confirmed by transmission electron microscopy (TEM). The crystal structure of nanoparticles was characterized by X-ray diffraction pattern (XRD). The magnetic properties were characterized by vibrating sample magnetometer (VSM).

Synthesis and Characterization of a Three-dimensional Porous Compound: [Cu(H2O)6][{Cu(H2O)2}2{Cu(H2O)4H4W12O42}] · 12H2O

2008 ◽  
Vol 63 (2) ◽  
pp. 187-192 ◽  
Author(s):  
Chun-jing Zhang ◽  
Ya-guang Chen ◽  
Dong-mei Shi ◽  
Hai-jun Pang
Keyword(s):  
Aqueous Solution ◽  
Magnetic Susceptibility ◽  
Elemental Analysis ◽  
3D Structure ◽  
Three Dimensional ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vis Spectroscopy

A novel transition metal polyoxotungstate, [Cu(H2O)6][{Cu(H2O)2}2{Cu(H2O)4H4W12O42}] · 12H2O (1), has been synthesized in aqueous solution and characterized by single-crystal X-ray diffraction, elemental analysis, IR and UV/vis spectroscopy, and TG analysis. The paradodecatungstate anions [H2W12O42]10− are linked by CuO6 octahedra, forming a three-dimensional (3D) structure. The magnetic susceptibility of compound 1 in the temperature range 2 - 300 K shows the presence of antiferromagnetic interactions within the uniform Cu2・ ・ ・Cu3 chains

The Synthesis and Characterization of NiCo2O4 Nanoparticles

2012 ◽  
Vol 512-515 ◽  
pp. 2467-2470 ◽  
Author(s):  
Hong Xiao Zhao ◽  
Bao Ming He ◽  
Jing Li ◽  
Hui Min Jia ◽  
Li Wei Mi
Keyword(s):  
Thermal Decomposition ◽  
Hydrothermal Method ◽  
Physical Adsorption ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Preparation Methods ◽  
Oxalate Precursor ◽  
X Ray ◽  
Scanning Electron

In this paper, NiCo2O4 nanoparticles were synthesized by three different methods. The applied preparation methods in this research are thermal decomposition of a mixed oxalate precursor, combustion synthesis and hydrothermal method. The crystalline phase, morphology and specific surface area (BET) of the resultant samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and nitrogen physical adsorption, respectively. The research found that the hydrothermal method is a promising method to prepare NiCo2O4 nanoparticles.

Synthesis and Characterization of a Cubic Iron Hydroxy Boracite

2011 ◽  
Vol 66 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Stephanie C. Neumair ◽  
Johanna S. Knyrim ◽  
Oliver Oeckler ◽  
Reinhard Kaindl ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Single Crystals ◽  
Room Temperature ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Pressure High Temperature

The cubic iron hydroxy boracite Fe3B7O13OH・1.5H2O was synthesized from Fe2O3 and B2O3 under high-pressure/high-temperature conditions of 3 GPa and 960 °C in a modified Walker-type multianvil apparatus. The crystal structure was determined at room temperature by X-ray diffraction on single crystals. It crystallizes in the cubic space group F4̄3c (Z = 8) with the parameters a = 1222.4(2) pm, V = 1.826(4) nm3, R1 = 0.0362, and wR2 = 0.0726 (all data). The B-O network is similar to that of other cubic boracites.

scholarly journals Synthesis and Characterization of the Amidomanganates Rb2[Mn(NH2)4] and Cs2[Mn(NH2)4]

Crystals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 676
Author(s):  
Christian Bäucker ◽  
Soeren Bauch ◽  
Rainer Niewa
Keyword(s):  
High Temperature ◽  
Single Phase ◽  
Inert Atmosphere ◽  
High Temperature Phase ◽  
Synthesis And Characterization ◽  
Temperature Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ir Spectroscopic

We report the successful synthesis of Rb2[Mn(NH2)4] and Cs2[Mn(NH2)4] from ammonothermal conditions at 723 K and pressures above 850 bar. Both compounds were obtained single phase according to powder X-ray diffraction. The crystal structures were determined by single crystal X-ray diffraction. For Rb2[Mn(NH2)4] we have obtained the high-temperature phase. The structures are analyzed with respect to the earlier reported alkali metal amidomanganates. Upon heating in inert atmosphere Cs2[Mn(NH2)4] decomposes to manganese nitrides. IR spectroscopic results are reported.

Synthesis and characterization of three new rare-earth orthoborates: Ba2MgY2(BO3)4, Ba2CdY2(BO3)4, and Ba2CdSc(BO3)3

2020 ◽  
Vol 49 (31) ◽  
pp. 10874-10879
Author(s):  
Runqing Liu ◽  
Hongping Wu ◽  
Hongwei Yu ◽  
Zhanggui Hu ◽  
Jiyang Wang ◽  
...  
Keyword(s):  
Rare Earth ◽  
High Temperature ◽  
Solution Method ◽  
Synthesis And Characterization ◽  
High Temperature Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Solution ◽  
First Time

Three rare-earth orthoborates Ba2MgY2(BO3)4, Ba2CdY2(BO3)4, and Ba2CdSc(BO3)3 were synthesized via a high-temperature solution method and their structures were determined by single crystal X-ray diffraction for the first time.

Synthesis and structural characterization of Ca12Ge17B8O58

2016 ◽  
Vol 71 (11) ◽  
pp. 1141-1146
Author(s):  
Sebastian Bräuchle ◽  
Klaus Wurst ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Temperature ◽  
Solid State ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Open Structure ◽  
X Ray ◽  
Tetragonal Crystal ◽  
Tetragonal Crystal System

AbstractCa12Ge17B8O58 was prepared by high-temperature solid state synthesis at 1100°C in a platinum crucible from calcium carbonate, boric acid, and germanium(IV) oxide. The compound crystallizes in the tetragonal crystal system in the space group P4̅ (No. 81) isotypically to Cd12Ge17B8O58. The structure was refined from single-crystal X-ray diffraction data: a = 15.053(8), c = 4.723(2) Å, V = 1070.2(2) Å3, R1 = 0.0151, and wR2 = 0.0339 for all data. The crystal structure of Ca12Ge17B8O58 consists of [Ge4O12]n chains composed of GeO4 tetrahedra and GeO6 octahedra. The chains are interconnected into a [Ge4O10.5]n network via corner sharing. By additional [Ge(B2O7)4]28– clusters, these units are connected to a three-dimensional [Ge17B8O58]24– framework. The open structure forms three types of tunnels with five-, six-, and seven-membered rings (MRs) along the c axis, where the Ca2+ are located.

Synthesis and Characterization of Nickel-Based Monolithic Aerogel via Sol-Gel Method

2011 ◽  
Vol 335-336 ◽  
pp. 368-371 ◽  
Author(s):  
Yu Tie Bi ◽  
Hong Bo Ren ◽  
Bo Wei Chen ◽  
Lin Zhang
Keyword(s):  
Electron Microscopy ◽  
Polyacrylic Acid ◽  
Sol Gel ◽  
Three Dimensional ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method

The synthesis and characterization of nickel-based aerogel prepared using nickel chloride as the precursor via sol-gel method is described. The addition of the polyacrylic acid as an template to the solution of NiCl2•6H2O can guide the gelation in the reaction to build a three dimensional open structure. The aerogel has been characterized using field emission scanning electron microscopy (FESEM), highresolution transmission electron microscopy (HRTEM), nitrogen adsorption desorption analysis and powder X-ray diffraction (XRD). The results indicate that the nickel-based aerogel has a typical three dimensional structure made up of spherical particles with an open porous network and has high surface area about 192 m2/g, average pore diameter about 40nm. The X-ray diffraction (XRD) patterns show that the aerogel prepared at room temperature belongs to amorphous material. The synthesis of nickel-based aerogel, using polyacrylic acid as an template, is especially unique in our experiment.

Synthesis and characterization of Na2Ba4Ga2Sb6 and Li13Ba8GaSb12

2006 ◽  
Vol 221 (5-7) ◽  
Author(s):  
Iliya Todorov ◽  
Slavi C. Sevov
Keyword(s):  
High Temperature ◽  
Single Crystal ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray

AbstractThe title compounds were synthesized from the elements by heating the corresponding stoichiometric mixtures at high temperature. Their structures were determined from single-crystal X-ray diffraction. Na

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