scholarly journals Metal Complexes of Mixed Nucleobases. Part I: Synthesis and Characterization of Copper(II), Zinc(II), Cadmium(II) and Mercury(II) Complexes of Adenine and Uracil

2016 ◽  
Vol 64 (2) ◽  
pp. 127-133
Author(s):  
Humaira Yeasmin ◽  
MS Rahman ◽  
AA Shaikh ◽  
Pradip K Bakshi
Keyword(s):  
Aqueous Solution ◽  
Cyclic Voltammetry ◽  
Magnetic Susceptibility ◽  
Redox Properties ◽  
Synthesis And Characterization ◽  
Bidentate Ligands ◽  
Cadmium Complexes ◽  
X Ray ◽  
Metal Contents

The complexes of Cu(II), Zn(II), Cd(II) and Hg(II) with adenine (AdeH) and uracil (UraH) have been synthesized and characterized by a combination of metal contents estimation, IR, UV-vis spectral data, thermogravimetric analysis (QSTG, TG and DSC) and magnetic susceptibility measurement. All the complexes are micro-crystalline, slightly soluble in water and decompose at high temperature. Both adenine and uracil deprotonated under experimental condition and then ligated to the metal ions as bidentate ligands through N(3) and N(9) of adeninato (Ade), and through N(3) and C(2)=O of uracilato (Ura) anions. On the basis of the metal contents, the complexes are formulated as [M(C5H4N5O)(C5H4N5)(H2O)2] [M = Cu(II), Zn(II) and Hg(II)] and [Cd(C5H4N5)(C4H3N2O2)(H2O)2].2H2O. The redox properties of copper and cadmium complexes were examined in aqueous solution by cyclic voltammetry. The voltammograms show quasi-reversible behavior for both the complexes. The X-ray powder diffraction study of the copper complex indicates that it is poorly crystalline in nature. Dhaka Univ. J. Sci. 64(2): 127-133, 2016 (July)

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

Synthesis and Characterization of T12Ba2CaCu2O8 and T12Ba2Ca2Cu3O10

1989 ◽  
Vol 169 ◽  
Author(s):  
Lauren E. H. McMills ◽  
Shu Li ◽  
Zhen Zhang ◽  
Martha Greenblatt
Keyword(s):  
Magnetic Susceptibility ◽  
Powder Diffraction ◽  
Single Phase ◽  
Synthesis And Characterization ◽  
Synthetic Method ◽  
Superconducting Properties ◽  
X Ray ◽  
Preparation Conditions ◽  
The Relationship

AbstractSingle-phase samples of T12Ba2CaCu2O8 and T12Ba2Ca2Cu3O10 have been prepared using a reliable and simple synthetic method. Samples were characterized by x-ray powder diffraction, magnetic susceptibility and four probe resistivity methods. The TcR=0 values for T12Ba2CaCu2O8 ranged from 100 to 105K, whereas those for T12Ba2Ca2Cu3O10 ranged from 96 to 107K. The relationship between the superconducting properties and the various preparation conditions are discussed.

Darstellung und Charakterisierung des Silber(I,II,III)-oxidclathrates Ag7O8HCO3 / Synthesis and Characterization of the Silver(I,II,III) Oxide Clathrate Ag7O8HCO3

2000 ◽  
Vol 55 (9) ◽  
pp. 882-886 ◽  
Author(s):  
Martin Jansen ◽  
Sascha Vensky
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Magnetic Susceptibility ◽  
Solid State Nmr ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The silver(I,II,III) oxide clathrate Ag7O8HCO3 was synthesized by anodic oxidation of silver(I) in a suspension of Ag2CO3 in an aqueous AgF solution. The title compound was characterized by single crystal X-ray diffraction (cubic, Fm3̄m, a = 9.8085(3) Å, Z = 4), scanning electron microscopy, thermal analysis, IR spectroscopy, 1H-solid state-NMR and measurement of the magnetic susceptibility

Synthesis and Characterization of Magnetic Rubidium Superoxide, RbO2

2019 ◽  
Vol 966 ◽  
pp. 237-242
Author(s):  
Fahmi Astuti ◽  
Mizuki Miyajima ◽  
Takahito Fukuda ◽  
Masashi Kodani ◽  
Takehito Nakano ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Spin Relaxation ◽  
Powder Diffraction ◽  
Solution Method ◽  
Muon Spin ◽  
Muon Spin Relaxation ◽  
Synthesis And Characterization ◽  
X Ray

Polycrystalline rubidium superoxide (RbO2) has been synthesized by using solution method followed by the reaction process under the cooling condition of-40 °C. X-ray Powder Diffraction (XRD) spectra showed that RbO2 was successfully synthesized by this method. The magnetic susceptibility and pulsed muon spin relaxation (μSR) measurements were carried out in order to study the magnetic properties of RbO2.

Synthesis and characterization of a new Keggin anion: [BeW12O40]6−

2014 ◽  
Vol 50 (65) ◽  
pp. 9083-9085 ◽  
Author(s):  
Alexander V. Anyushin ◽  
Anton I. Smolentsev ◽  
Dmitry A. Mainichev ◽  
Cristian Vicent ◽  
Artem L. Gushchin ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Cyclic Voltammetry ◽  
Synthesis And Characterization ◽  
Keggin Anion ◽  
X Ray ◽  
Esi Mass Spectrometry

The first berillododecatungstate [BeW12O40]6− has been synthesized and characterized by X-ray analysis, cyclic voltammetry, ESI-mass spectrometry, and 9Be and 183W NMR.

scholarly journals Regioselective synthesis and characterization of monovanadium-substituted β-octamolybdate [VMo7O26]5−

2019 ◽  
Vol 75 (7) ◽  
pp. 872-876
Author(s):  
Lukáš Krivosudský ◽  
Alexander Roller ◽  
Annette Rompel
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
The Other ◽  
Synthesis And Characterization ◽  
One Pot ◽  
X Ray ◽  
Composition And Structure ◽  
Elemental Analyses ◽  
Crystallization Solution

The monovanadium-substituted polyoxometalate anion [VMo7O26]5−, exhibiting a β-octamolybdate archetype structure, was selectively prepared as pentapotassium [hexaikosaoxido(heptamolybdenumvanadium)]ate hexahydrate, K5[VMo7O26]·6H2O (VMo7 ), by oxidation of a reduced vanadomolybdate solution with hydrogen peroxide in a fast one-pot approach. X-ray structure analysis revealed that the V atom occupies a single position in the cluster that differs from the other positions by the presence of one doubly-bonded O atom instead of two terminal oxide ligands in all other positions. The composition and structure of VMo7 was also confirmed by elemental analyses and IR spectroscopy. The selectivity of the synthesis was inspected by a 51V NMR investigation which showed that this species bound about 95% of VV in the crystallization solution. Upon dissolution of VMo7 in aqueous solution, the [VMo7O26]5− anion is substantially decomposed, mostly into [VMo5O19]3−, α-[VMo7O26]4− and [V2Mo4O19]4−, depending on the pH.

Chemical synthesis and characterization of polyaniline-molybdenum trisulfide composite

1999 ◽  
Vol 14 (5) ◽  
pp. 1805-1813 ◽  
Author(s):  
Florence Fusalba ◽  
Daniel Bélanger
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Chemical Polymerization ◽  
X Ray ◽  
Scanning Electron

A novel polyaniline-molybdenum trisulfide composite has been prepared by chemical polymerization from an acidic (1 M HCl) aqueous solution containing aniline and ammonium tetrathiomolybdate. The presence of molybdenum trisulfide in the polyaniline matrix induces morphological change to the polymer as evidenced by scanning electron micrographs. X-ray diffraction and differential scanning calorimetry indicate that polyaniline-molybdenum trisulfide is slightly less crystalline than polyaniline-HCl. X-ray photoelectron spectroscopy (XPS) and elemental analysis have been used to confirm the presence of molybdenum trisulfide in the polymer matrix. The XPS data also confirm that molybdenum trisulfide and tetrathiomolybdate anions are present with polyaniline to form a new inorganic-organic composite.

Synthesis and characterization of the pentadentate macrobicyclic ligand, 14-thia-1,4,8,11-tetraazabicyclo[9.5.3]nonadecane (L1) and its nickel(II) complexes. X-ray crystal structure of [Ni(L1)(ClO4)](ClO4)·2[Ni(L1)(OH2)](ClO4)2·6H2O

2001 ◽  
Vol 79 (5-6) ◽  
pp. 930-937 ◽  
Author(s):  
Kevin R Coulter ◽  
Alexander McAuley ◽  
Steven Rettig
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
Axial Symmetry ◽  
Synthesis And Characterization ◽  
High Dilution ◽  
Subsequent Reduction ◽  
X Ray ◽  
Frozen Solution ◽  
Reversible Redox

The pentadentate macrobicycle,14-thia-1,4,8,11-tetraazabicyclo[9.5.3]nonadecane (L1), has been synthesized by high dilution cyclization of 1-thia-4,8-diazacyclododecane ([10]aneN2S) (2) with N,N'-bis(α-chloro acetamido) propane (3) and subsequent reduction of the di-oxo intermediate. The structure of the [Ni(L1)(ClO4)](ClO4)·2[Ni(L1)(OH2)](ClO4)2·6H2O complex (monoclinic, P21/c, a = 13.9261(4) Å, b = 30.279(2) Å, c = 17.1248(3) Å, β = 94.5065(3)°) at R = 0.039 (Rw = 0.034) for 911 parameters using 18 266 reflections with I > 3σI has been determined. The ligand adopts a trans-III configuration. The Ni(II) ion is pseudooctahedral with Ni-S = 2.3896(10) Å in [Ni(L1)(ClO4)]+ and 2.4193(10) Å, 2.4225(10) Å, in the two [Ni(L1)(H2O)]2+ cations. Both nickel(II) and nickel(III) complexes are six-coordinate in solution. Oxidation of the [Ni(L1)(OH2)]2+ complex with K2S2O8 in aqueous solution yielded an ESR active Ni(III) species and the frozen solution spectrum displayed axial symmetry with g[Formula: see text] = 2.159 and g|| = 2.024. In CH3CN, the [Ni(L1)(solv)]2+ complex showed two reversible redox waves corresponding to the Ni2+/+ couple at E1/2 = -1.807 V vs. Fc+/0 and Ni3+/2+ couple at E1/2 = 0.715 V vs. Fc+/0.Key words: synthesis, structure, polydentate macrobicycle, nickel(II).

Tp*WIVO(S2CNEt2): the Missing Member of the Series

2004 ◽  
Vol 57 (3) ◽  
pp. 269 ◽  
Author(s):  
Aston A. Eagle ◽  
Charles G. Young ◽  
Edward R. T. Tiekink
Keyword(s):  
Crystal Structure ◽  
Mass Spectrometry ◽  
Cyclic Voltammetry ◽  
1H Nmr Spectroscopy ◽  
Octahedral Complex ◽  
Synthesis And Characterization ◽  
Oxygen Atom Transfer ◽  
X Ray ◽  
Distorted Octahedral

The missing member of the series Tp*ME(S2CNEt2) (M = Mo, W; E = O, S), namely Tp*WO(S2CNEt2), has been synthesized by oxygen-atom transfer from pyridine N-oxide to Tp*W(S2CNEt2)(CO)2. The air-stable, blue-purple complex was characterized by microanalysis, mass spectrometry (m/z 645 (100%), [M]+), cyclic voltammetry, and IR and 1H NMR spectroscopy. Solutions of the complex are dichroic and solvatochromic. The X-ray crystal structure of the complex revealed a six-coordinate, distorted octahedral complex with axial oxo (W = O 1.680(5) Å), ‘equatorial’ dithiocarbamate (W—S 2.3962(17) and 2.4102(17) Å), and facial tridentate Tp* ligands. The synthesis and characterization of Tp*WCl3 are also reported.

scholarly journals Synthesis and characterization of the new two-dimensional Heisenberg antiferromagnet double perovskite BaLaCuSbO6

2015 ◽  
Vol 44 (23) ◽  
pp. 10860-10866 ◽  
Author(s):  
M. Cecilia Blanco ◽  
Sergio Alexis Paz ◽  
Vivian M. Nassif ◽  
Julio J. Guimpel ◽  
Raúl E. Carbonio
Keyword(s):  
Magnetic Susceptibility ◽  
Double Perovskite ◽  
Synthesis And Characterization ◽  
Two Dimensional ◽  
Heisenberg Antiferromagnet ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffraction Patterns

Powder X-ray diffraction patterns, magnetic susceptibility as a function of temperature, and polyhedral representation along the c-axis of the BaLaCuSbO6 double perovskite have been reported.

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