scholarly journals Formation of Tetranuclear Nickel(II) Complexes with Schiff-Bases: Crystal Structures and Magnetic Properties

Crystals ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 592 ◽  
Author(s):  
Zhonglu You ◽  
Yingying Luo ◽  
Susan Herringer ◽  
Yanmin Li ◽  
Silvio Decurtins ◽  
...  
Keyword(s):  
Bond Angle ◽  
Binding Mode ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Structural Correlation ◽  
Magnetization Data ◽  
Coupling Parameters ◽  
Nonzero Spin

The cubane-type structure is a typical representative of tetranuclear coordination compounds. In this work, two anionic Schiff-base ligands, (L1)2− and (L2)2−, each offering an O^N^O coordination pocket, ligate four NiII ions into a [Ni4O4] cubane core. The ligands are H2L1 = 2−[[(3-ethoxy-2−hydroxyphenyl) methylene]amino]benzenemethanol and H2L2 = 2−[[(5-fluoro-2−hydroxyphenyl)methylene]amino]benzenemethanol. In both compounds, [Ni4(L1)4(EtOH)4] (1) and [Ni4(L2)4(MeOH)4] (2), alkoxy oxygens of the ligands act in a bridging μ3-O binding mode. Magnetic susceptibility and magnetization data for compounds 1 and 2 are presented. The Ni–O–Ni bond angles of the cubane core determined from single crystal X-ray diffraction data play a key role for a magneto-structural correlation. Dominant intracube ferromagnetic behavior is observed, and the coupling parameters were determined for both compounds, leading to nonzero spin ground states in accordance with the broadly accepted bond angle guideline.

New Copper Compounds with Antiplatelet Aggregation Activity

2019 ◽  
Vol 15 (8) ◽  
pp. 850-862
Author(s):  
Mirthala Flores-García ◽  
Juan Manuel Fernández-G. ◽  
Cristina Busqueta-Griera ◽  
Elizabeth Gómez ◽  
Simón Hernández-Ortega ◽  
...  
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Thrombotic Event ◽  
X Ray Diffraction ◽  
Nmr Studies ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Antiplatelet Aggregation ◽  
Aggregation Activity ◽  
L1 And L2

Background: Ischemic heart disease, cerebrovascular accident, and venous thromboembolism have the presence of a thrombotic event in common and represent the most common causes of death within the population. Objective: Since Schiff base copper(II) complexes are able to interact with polyphosphates (PolyP), a procoagulant and potentially prothrombotic platelet agent, we investigated the antiplatelet aggregating properties of two novel tridentate Schiff base ligands and their corresponding copper( II) complexes. Methods: The Schiff base ligands (L1) and (L2), as well as their corresponding copper(II) complexes (C1) and (C2), were synthesized and characterized by chemical analysis, X-ray diffraction, mass spectrometry, and UV-Visible, IR and far IR spectroscopy. In addition, EPR studies were carried out for (C1) and (C2), while (L1) and (L2) were further analyzed by 1H and 13C NMR. Tests for antiplatelet aggregation activities of all of the four compounds were conducted. Results: X-ray diffraction studies show that (L1) and (L2) exist in the enol-imine tautomeric form with a strong intramolecular hydrogen bond. NMR studies show that both ligands are found as enol-imine tautomers in CDCl3 solution. In the solid state, the geometry around the copper(II) ion in both (C1) and (C2) is square planar. EPR spectra suggest that the geometry of the complexes is similar to that observed in the solid state by X-ray crystallography. Compound (C2) exhibited the strongest antiplatelet aggregation activity. Conclusion: Schiff base copper(II) complexes, which are attracting increasing interest, could represent a new approach to treat thrombosis by blocking the activity of PolyP with a potential anticoagulant activity and, most importantly, demonstrating no adverse bleeding events.

Synthesis of an Unprecedented H-stitched Binuclear Crystal Structure Based on Selective Fluorescence Recognition of Zn2+ in Newly Synthesized Schiff Base Ligand with DFT and Imaging Application in Living Cells

2021 ◽  
Author(s):  
SOUMYA SUNDAR MATI ◽  
Dr. SAUGATA KONAR ◽  
BOBY SAMAI
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Elemental Analysis ◽  
Schiff Base Ligand ◽  
Binuclear Complex ◽  
Living Cells ◽  
X Ray Diffraction ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Imaging Application

A zinc coordinated rare binuclear complex was synthesised and characterized by elemental analysis and single-crystal X-ray diffraction. Two mononuclear units formed by two Schiff base ligands 2-((2-(pyrimidin-2-yl)hydrazono)methyl)phenol (PHP) coordinated with...

Nitrido-und Oxochlorokomplexe des Vanadiums(V); die Kristallstruktur von AsPh4 [V0C14] Nitrido and Oxochloro Complexes of Vanadium(V); the Crystal Structure of AsPh4[VOCl4]

1980 ◽  
Vol 35 (5) ◽  
pp. 522-525 ◽  
Author(s):  
Gisela Beindorf ◽  
Joachim Strähle ◽  
Wolfgang Liebelt ◽  
Kurt Dehnicke
Keyword(s):  
Crystal Structure ◽  
Ir Spectra ◽  
Bond Length ◽  
Bond Angle ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Linear Arrangement ◽  
Space Group ◽  
X Ray ◽  
Complex Anions

The complexes AsPh4[Cl4V = N-Cl] and AsPh4[VOCl4] are prepared by the reaction of AsPh4Cl with Cl3VNCl and VOCl3, respectively. The IR spectra indicate C4v symmetry for the complex anions with multiple VN and VO bonds and a linear arrangement for the VNCl-group. AsPh4[VOCl4] crystallizes in the tetragonal space group P4/n with two formula units in the unit cell. The crystal structure was solved by X-ray diffraction methods (R = 0,062, 1096 observed, independent reflexions). The structure consists of AsPh4+ cations and [VOCl4]- anions with symmetry C4v. The extremely short VO bond length corresponds with a VO triple; its steric requirements cause the relatively large bond angle OVCl of 103.4°.

Synthesis and Properties of YBaSrCu3O6.9 Prepared from Soluble Precursors

1988 ◽  
Vol 121 ◽  
Author(s):  
Paul J. Nigrey ◽  
J. F. Kwak ◽  
E. L. Venturini ◽  
M. O. Eatough ◽  
R. J. Baughman
Keyword(s):  
Solid Solution ◽  
Solution Chemistry ◽  
X Ray Diffraction ◽  
Oxygen Annealing ◽  
X Ray ◽  
Resistivity Measurements ◽  
Superconducting Ceramics ◽  
Magnetization Data ◽  
Zero Resistance ◽  
Superconducting Onset Temperature

ABSTRACTSolution chemistry routes have been used to prepare single-phased superconducting ceramics of YBaSrCu3O6.9 (1113). Resistivity measurements on air annealed samples showed a superconducting onset temperature of 85 K with zero resistance at 78 K which improves to 81 K upon oxygen annealing. Magnetization data show ca. 78% flux exclusion at 5 K for 1113. X-ray diffraction experiments revealed that an orthorhombic to tetragonal transition occurs near 590°C when 1113 was heated in air. This work has demonstrated that such techniques can be utilized to prepare solid solution material with properties similar to those observed in YBa2Cu3Ox (123).

Ferromagnetic Homogeneous Polycrystalline Zn1-xCoxO Oxides

2006 ◽  
Vol 45 ◽  
pp. 2520-2527
Author(s):  
Yue Bin Zhang ◽  
Sean Li
Keyword(s):  
Single Phase ◽  
Nearest Neighbor ◽  
Ferromagnetic Behavior ◽  
Additional Contribution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxygen Ions ◽  
Random Manner ◽  
Single Phase Wurtzite Structure ◽  
Single Phase Wurtzite

In this work, the structural and magnetic properties of polycrystalline Zn1-xCoxO (x = 0, 0.02, 0.05, 0.0625, 0.10 and 0.15) oxides were studied in detail. Rietveld refinement of x-ray diffraction spectra indicates that a single-phase wurtzite structure was formed in Zn1-xCoxO samples for x up to 0.10. The magnetization for x = 0.02 can be fitted to a model with a paramagnetic Curie term and a diamagnetic constant which could arise from spins of isolated free Co ions and a diamagnetic background, respectively. For x > 0.02, however, an additional antiferromagnetic Curie-Weiss term needs to employ for fitting. This is due to an additional contribution from clustered Co ions that are in nearest neighbor positions through oxygen ions. Results show that the substitution of Co at the Zn site does not occur in a completely random manner but Co ions appear to have a tendency for clustering. In addition, the homogenous ZnO:Co thin film prepared by Pulsed Laser Deposition on SiO2/Si substrate shows ferromagnetic behavior at room temperature.

Hydrothermal Synthesis and Room Temperature Ferromagnetism of Ni-Doped Rod-Like ZnO Particles

2014 ◽  
Vol 934 ◽  
pp. 71-74
Author(s):  
Lian Mao Hang ◽  
Zhao Ji Zhang ◽  
Zhi Yong Zhang
Keyword(s):  
Quantum Interference ◽  
Room Temperature ◽  
Room Temperature Ferromagnetism ◽  
Hexagonal Wurtzite Structure ◽  
Ferromagnetic Behavior ◽  
Secondary Phases ◽  
Superconducting Quantum Interference Device ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zno Particles

Ni-doped rod-like ZnO particles with doping concentration of 1 at.% were synthesized at 200°C by hydrothermal method and characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and superconducting quantum interference device (SQUID). The results show that the as-synthesized samples are pure hexagonal wurtzite structure without metallic Ni or other secondary phases and display rod-like shape with smooth surface. The magnetization measurements reveal that the Ni-doped rod-like ZnO particles show ferromagnetic behavior at room temperature. The saturation magnetization and coercive field are 0.0046 emu/g and 15 Oe, respectively.

Powder X-ray diffraction and Rietveld analysis of La1−xBaxCoO3 (0

2006 ◽  
Vol 21 (4) ◽  
pp. 304-306 ◽  
Author(s):  
Wanju Luo ◽  
Fangwei Wang
Keyword(s):  
Phase Transformation ◽  
Bond Length ◽  
Structural Properties ◽  
Powder Diffraction ◽  
Bond Angle ◽  
Structural Phase ◽  
Rietveld Analysis ◽  
X Ray Diffraction ◽  
Structural Phase Transformation ◽  
X Ray

Detailed structural properties of La1−xBaxCoO3 (LBCO) have been investigated by means of X-ray powder diffraction and Rietveld analysis. A structural phase transformation from R3c to Pm3m at x=0.30–0.35 has been detected based on a comparison between the refinements of R3c and Pm3m. The Co–O bond length of the CoO6 octahedron expanded rapidly with increasing Ba content when x<0.1, and then it leveled off and kept constant at 0.1⩽x⩾0.35, where the Co–O–Co bond angle reaches 180°. The Co–O bond length expansion resumed with increasing Ba content beyond x=0.35.

The effect of coordinated water on the connectivity of uranium(IV) sulfatex-hydrate: [U(SO4)2(H2O)5]·H2O and [U(SO4)2(H2O)6]·2H2O, and a comparison with other known structures

2014 ◽  
Vol 70 (7) ◽  
pp. 726-731 ◽  
Author(s):  
Alexander D. Burns ◽  
Brian O. Patrick ◽  
Anita E. Lam ◽  
David Dreisinger
Keyword(s):  
Raman Spectroscopy ◽  
Binding Mode ◽  
Three Dimensions ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
Anhydrous Compound ◽  
Coordinated Water ◽  
Ir And Raman ◽  
Sulfate Complexes

Two new solid-state uranium(IV) sulfatex-hydrate complexes (wherexis the total number of coordinated plus solvent waters), namelycatena-poly[[pentaaquauranium(IV)]-di-μ-sulfato-κ4O:O′] monohydrate], {[U(SO4)2(H2O)5]·H2O}n, and hexaaquabis(sulfato-κ2O,O′)uranium(IV) dihydrate, [U(SO4)2(H2O)6]·2H2O, have been synthesized, structurally characterized by single-crystal X-ray diffraction and analyzed by vibrational (IR and Raman) spectroscopy. By comparing these structures with those of four other known uranium(IV) sulfatex-hydrates, the effect of additional coordinated water molecules on their structures has been elucidated. As the number of coordinated water molecules increases, the sulfate bonds are displaced, thus changing the binding mode of the sulfate ligands to the uranium centre. As a result, uranium(IV) sulfatex-hydrate changes from being fully crosslinked in three dimensions in the anhydrous compound, through sheet and chain linking in the tetra- and hexahydrates, to fully unlinked molecules in the octa- and nonahydrates. It can be concluded that coordinated waters play an important role in determining the structure and connectivity of UIVsulfate complexes.

scholarly journals ENHANCED FERROELECTRICITY AND FERROMAGNETISM OF (Y, Ni) CO-DOPED BiFeO3 MATERIALS

2018 ◽  
Vol 56 (1A) ◽  
pp. 219
Author(s):  
Dao Viet Thang
Keyword(s):  
Ferroelectric Properties ◽  
Sol Gel ◽  
Rhombohedral Structure ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co Doping ◽  
Saturation Polarization ◽  
Perovskite Type ◽  
Co Doped

In this study, multiferroicMultiferroic Bi1-xYxFe0.975Ni0.025O3 (x = 0.00, 0.05, 0.10, and 0.15) called as (Y, Ni)                co-doped BiFeO3 materials were synthesized by a sol-gel method.  and characterized by X-ray diffraction diagrams and(XRD), energy-dispersive X-ray (EDX) and vibrating sample magnetization (VSM) measurements demonstrated. The result showed that Bi1-xYxFe0.975Ni0.025O3all investigated materials waspresent a single phase of the perovskite-type rhombohedral structure. Ferromagnetism and ferroelectricity of the Bi1-xYxFe0.975Ni0.025O3 materials have been investigated. Results showed that the co-doping by (Y, Ni) for (Bi, Fe)  have affected in enhancing by the (Y, Ni) co-doping, as a result the ferroelectric polarization and magnetization of BiFeO3. The magnetic characterization indicated that the ferromagnetic behavior wasthe initial BiFeO3 materialwere enhanced with increasing concentration of Y3+ for (Y, Ni) co-substituted of BiFeO3. Which could beion. It is attributed to the defferentdifference of the magnetic momentmoments of Ni2+ and Fe3+, and+ ions, as well as the Y3+-Fe3+,+ and Y3+-Ni2+ super-exchange interaction. Theinteractions. The characteristics of the investigated materials, such as remanent magnetization (Mr), saturation magnetization (Ms), remanent polarization (2Pr) and saturation polarization (2Ps) continuously increase upon increasing in the range of x from 0.00 to 0.15. When x = 0.15, the values of Mr and Ms are 0.078 and 0.794 emu/g, respectively. The values of 2Pr and 2Ps are 16.58 and 27.99 µC/cm2, respectively. Origin of ferromagnetic and ferroelectric properties of Bi1-xYxFe0.975Ni0.025O3 materials will be discussed in this paper.

Electron optical studies of the formation of vanadium pentoxide catalyst

1987 ◽  
Vol 45 ◽  
pp. 354-355
Author(s):  
A. Legrouri
Keyword(s):  
Electron Microscopy ◽  
Vanadium Pentoxide ◽  
High Resolution Electron Microscopy ◽  
X Ray Diffraction ◽  
Optical Studies ◽  
X Ray ◽  
Physicochemical Changes ◽  
Structural Correlation ◽  
Resolution Electron ◽  
Xrd Techniques

The oxides of vanadium, especially vanadium pentoxide, have been extensively studied because of their interesting physical properties particularly in catalysis. Vanadium pentoxide is generally used in the oxidation and ammoxidation of hydrocarbons.This catalyst has been prepared via the thermal decomposition of ammonium metavanadate (AMV) in air. Thermogravimetric analysis (TGA), infrared spectroscopy (IRS) and x-ray diffraction (XRD) techniques together with high resolution electron microscopy (HREM) and scanning electron microscopy (SEM) have enabled us to elucidate the physicochemical changes occurring during the decomposition process.According to TGA results, the decomposition of AMV commences at 150°C and is complete by 320°C leading to vanadium pentoxide by loss of ammonia and water with the formation of two intermediate compounds, namely at 190°C, ammonium bivanadate: (NH4)2V4 O11, and at 230°C, ammonium hexavanadate AHV: (NH4)2V6O16 . Samples for structural correlation studies were prepared by heating AMV in a stream of air for 2 hours at selected temperatures of 140, 190, 230, 320 and 400°C.

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