New Copper(II) and Nickel(II) Complexes with Bifunctional Tetrazolate-5-carboxylate Ligands: Syntheses, Crystal Structures, and Magnetic Properties

2009 ◽  
Vol 62 (12) ◽  
pp. 1622 ◽  
Author(s):  
A-Qing Wu ◽  
Qi-Yong Chen ◽  
Mei-Feng Wu ◽  
Fa-Kun Zheng ◽  
Feng Chen ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Variable Temperature ◽  
Supramolecular Network ◽  
X Ray Diffraction ◽  
Carboxylate Ligands ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Variable Temperature Magnetic Susceptibility ◽  
Network Variable

Four new complexes with bifunctional tetrazolate-5-carboxylate ligands of 1H-tetrazole-5-formic acid (H2tzf) and 1H-tetrazole-5-acetic acid (H2tza), namely two dinuclear [M(tzf)(H2O)3]2·2H2O (M = Cu 1, Ni 2) and two mononuclear [Cu(tzf)(2,2′-bipy)2]·5H2O 3 and Cu(tza)(2,2′-bipy)H2O 4, were prepared and structurally characterized by single-crystal X-ray diffraction. Two different coordination modes of tetrazolate-5-carboxylate ligands exist: a tridentate N,O-chelated-N-bridged mode in 1 and 2, and a bidentate N,O-chelated mode in 3 and 4, which was first observed for the tetrazolate-5-carboxylate complexes. Extensive hydrogen bonds play an important role in the construction of the supramolecular network. Variable-temperature magnetic susceptibility data show the presence of antiferromagnetic interactions in 1 and 2. The thermogravimetric analyses of complexes 1–4 are also discussed.

Manganese(II) Oxazolidine Nitroxide Chelates: Structure, Magnetism, and Redox Properties

2014 ◽  
Vol 67 (11) ◽  
pp. 1618 ◽  
Author(s):  
Ian A. Gass ◽  
Mousa Asadi ◽  
David W. Lupton ◽  
Boujemaa Moubaraki ◽  
Alan M. Bond ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Intramolecular Interaction ◽  
Variable Temperature ◽  
Field Measurements ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Variable Temperature Magnetic Susceptibility ◽  
Radical Interaction

The mononuclear oxazolidine nitroxide complex [MnII(L•)2](ClO4)2 (1) (L•, 4-dimethyl-2,2-di(2-pyridyl)oxazolidine N-oxide) has been synthesized and investigated using single-crystal X-ray diffraction, variable-temperature magnetic susceptibility measurements, and electrochemistry. The structural analysis reveals bond lengths compatible with a linear L•–MnII–L• arrangement where the ligands are in the neutral ligand form and the central MnII ion is high spin (S = 5/2). Although analysis of the variable-temperature magnetic susceptibility data suggests a strong antiferromagnetic metal–radical interaction, the radical–radical intramolecular interaction could not be determined unambiguously from such fits. The resultant isolated S = 3/2 ground state is confirmed by low-temperature magnetization versus field measurements. Electrochemical studies reveal similar square schemes and redox intermediates to the previously reported analogues [FeII(L•)2][BF4]2 and [CoII(L•)2][NO3]2.

A new binuclear NiII complex with tetrafluorophthalate and 2,2′-bipyridine ligands: synthesis, crystal structure and magnetic properties

2019 ◽  
Vol 74 (11-12) ◽  
pp. 833-838 ◽  
Author(s):  
Jun-Xia Li ◽  
Zhong-Xiang Du ◽  
Xun Feng
Keyword(s):  
Variable Temperature ◽  
Ferromagnetic Coupling ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Variable Temperature Magnetic Susceptibility ◽  
Niii Complex ◽  
Weak Ferromagnetic ◽  
Dinuclear Structure

AbstractA new NiII compound, [Ni2(tfpa)2(bipy)2(H2O)4] (1) with tetrafluorophthalate (tfpa2−) and 2,2′-bipyridine (abbreviated as bipy) ligands, has been synthesized and structurally characterized. The single-crystal X-ray diffraction analysis reveals that the tfpa2− anions act as bis-monodentate linkers connecting NiII centers to form the dinuclear structure of 1. The dimeric units are stabilized by intramolecular π–π stacking and are further connected into a layer through O–HLO hydrogen bonding. Variable-temperature magnetic susceptibility data in the 10–200 K temperature range indicate weak ferromagnetic coupling between the two NiII ions.

Synthesis, Structures and Magnetic Properties of a Family of One-Dimensional Oxides

1996 ◽  
Vol 453 ◽  
Author(s):  
H.-C. Zur Loye ◽  
P. Núñez ◽  
M. A. Rzeznik
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Rietveld Refinement ◽  
Diffraction Data ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
One Dimensional ◽  
X Ray ◽  
Susceptibility Data ◽  
The One

AbstractThe one-dimensional compounds Sr3MgPtO6, Sr3MgIrO6, Sr3MgRhO6, Sr3GdRhO6, have been synthesized and structurally characterized by Rietveld refinement of powder X-ray diffraction data. All four compounds are isostructural with the rhombohedral K4CdCl6-type structure. The structure consists of infinite one-dimensional chains of alternating face-shared MO6 octahedra (M = Pt, Ir, Rh) and M′O6 (M′ = Gd, Mg) trigonal prisms. The strontium cations are located in a distorted square antiprismatic environment. Magnetic susceptibility data show that both Sr3MgIrO6 and Sr3MgRhO6 obey the Curie-Weiss law with θ = −6(1) K, and θ= −15(3)K, respectively. Sr3GdRhO6 obeys the Curie law with μeff = 7.80 B.M, consistent with an oxidation state of +3 for both rhodium and gadolinium.

scholarly journals A 3D Silverton-Type Polyoxomolybdate Based on {PrMo12O42}: Synthesis, Structure, Photoluminescence and Magnetic Properties

2021 ◽  
Vol 9 ◽  
Author(s):  
Yanxin Zhao ◽  
Xiaopeng Sun ◽  
Yanfang Ji ◽  
Hui Kong ◽  
Shumin Chen ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Variable Temperature ◽  
Three Dimensional ◽  
Magnetic Behavior ◽  
X Ray Diffraction ◽  
Red Emission ◽  
X Ray ◽  
Variable Temperature Magnetic Susceptibility ◽  
Elemental Analyses ◽  
Inorganic Building Block

A three-dimensional (3D) Silverton-type polyoxomolybdate (POMo) with the formula of NH4{Mn4[PrMo12O42]}·18H2O (1) was successfully isolated and well characterized by single crystal X-ray diffraction, X-ray powder diffraction pattern, infrared spectrum, thermogravimetric and elemental analyses. The inorganic building block {PrMo12O42} has formed 3D frameworks via the {MnO6} linker. The excitation of compound 1 in solid state at 375 nm displays red emission. Moreover, variable temperature magnetic susceptibility measurements indicate that the magnetic behavior in compound 1 is dominated by antiferromagnetic interactions.

Synthesis, crystal structure, and magnetic properties of the complex [(CH3)3NH]2 [Co(NCS)4]

2018 ◽  
Vol 73 (8) ◽  
pp. 571-575
Author(s):  
Yang Jie ◽  
Huang Yuan ◽  
Zhong YouQuan ◽  
Fang Ting ◽  
Hao Fan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Infrared Spectroscopy ◽  
Magnetic Measurements ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Ferromagnetic Interactions

AbstractA new complex [(CH3)3NH]2[Co(NCS)4], in which zero-dimensional [Co(NCS)4]n2− anions are balanced by 2n [(CH3)3NH]+ cations, was synthesized. The complex has been characterized by single X-ray diffraction, infrared spectroscopy, elemental analysis, and magnetic measurements. Magnetic susceptibility data indicate ferromagnetic interactions among the CoII ions.

Crystal Structures and Magnetic Properties of (2,2'-Dipyridyl)-(3-methoxysalicylaldiminato)copper(II) Perchlorate and (2,2'-Dipyridyl)-(4-methoxysalicylaldiminato)copper(II) Perchlorate

2002 ◽  
Vol 57 (5) ◽  
pp. 519-523 ◽  
Author(s):  
Y. Elerman ◽  
A. Elmali ◽  
I. Svoboda
Keyword(s):  
Magnetic Properties ◽  
Crystal Structures ◽  
Effective Magnetic Moment ◽  
Variable Temperature ◽  
Mixed Ligand ◽  
Dinuclear Complexes ◽  
Magnetic Susceptibility Data ◽  
Susceptibility Data ◽  
Variable Temperature Magnetic Susceptibility ◽  
Dimeric Unit

The mixed-ligand dinuclear complexes (2,2'-dipyridyl)-(3-methoxysalicylaldiminato)copper( II) perchlorate (1) and (2,2'-dipyridyl)-(4-methoxysalicylaldiminato)copper(II) perchlorate (2)were synthesized and their crystal structures determined. Both structures consist of a dimeric unit involving a planar Cu2O2 group. In both structures, the coordination sphere of the Cu atoms can be described as an elongated octahedron where the basal plane is formed by the twoN atoms of the 2,2'-dipyridyl molecule and the two O atoms of the salicylaldehyde anion. The phenoxo O atom is the negative ligand of the monomeric unit. Two apical Cu-O contacts complete the 4+2 coordination of the Cu atoms. They correspond to one of the O atoms of the perchlorate anion and to the O atom of the nearest salicylaldehyde molecule. Variable-temperature magnetic susceptibility data obey the Curie-Weiss law with Θ = -10.3(2) K for 1 and -10.1(2) K for 2. The decrease of the effective magnetic moment from 1.89(7) μB at 300 K to 1.77(7) μB at 70 K for 1 and from 1.88(8) μB at 300 K to 1.76(8) μB at 70 K for 2 and the negative Weiss constants indicate weak antiferromagnetic interactions between the two copper atoms in the dimeric units.

Syntheses, Crystal Structures and Magnetic Properties of Cr(NCNH2)4Cl2 and Mn(NCNH2)4Cl2

2012 ◽  
Vol 67 (11) ◽  
pp. 1205-1211 ◽  
Author(s):  
Xiaojuan Tang ◽  
Manfred Speldrich ◽  
Andrei L. Tchougréeff ◽  
Richard Dronskowski
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Quantum Theory ◽  
Transition Metal Ions ◽  
Chloride Ions ◽  
Many Body ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data

The two isotypic compounds Cr(NCNH2)4Cl2 and Mn(NCNH2)4Cl2 have been synthesized and characterized by X-ray diffraction. They crystallize in the cubic space group Im3̄m (Z = 6) with a = 12:643(2) Å for Cr(NCNH2)4Cl2 and a = 12:821(1) Å for Mn(NCNH2)4Cl2. The divalent transition metal ions are octahedrally coordinated by four H2NCN molecules in equatorial and two chloride ions in axial positions. The magnetic susceptibility data of the four Curie-paramagnetic compounds Cr(NCNH2)4Cl2, Mn(NCNH2)4Cl2, Co(NCNH2)4Cl2, and Ni(NCNH2)4Cl2 have been analyzed in greater detail, including many-body quantum theory.

The Effect of Partial Substitution of Non-Magnetic Impurity Zn on the Magnetic Moments of Eu1.88Ce0.12Cu1-yZnyO4+α-δ

2021 ◽  
Vol 1028 ◽  
pp. 15-20
Author(s):  
Muhammad Abdan Syakuur ◽  
Yati Maryati ◽  
Togar Saragi ◽  
Risdiana
Keyword(s):  
Magnetic Properties ◽  
Magnetic Susceptibility ◽  
Magnetic Impurity ◽  
Magnetic Moments ◽  
Magnetic Behavior ◽  
Partial Substitution ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
Susceptibility Data ◽  
Volume Unit

Structure and magnetic properties of electron-doped superconducting cuprates have been investigated in order to study the effect of magnetic impurity to its physical properties. Here, we reported structure and magnetic properties of Eu1.88Ce0.12Cu1-yZnyO4+α-δ (ECCZO) with y = 0 and 0.03. The properties of ECCZO have been studied from X-ray diffraction data and temperature dependence of magnetic susceptibility data, to elucidate the effect of partial substitution of non-magnetic impurity Zn for Cu to its structure, Tc and the value of magnetic moments per unit volume extracted from susceptibility data in normal state. Magnetic-susceptibility measurements were carried out down to 2 K on-field cooling at 5 Oe for Eu1.88Ce0.12Cu1-yZnyO4+a-d with y = 0 and 0.03. For ECCZO sample with y = 0 and d = 0.0669 indicated the change of magnetic behavior from paramagnetic to diamagnetic below 12 K which is addressed to the Tc onset of this samples. Diamagnetic behavior is observed starting from about 12 K. Above 12 K, all samples show paramagnetic behavior with the values of the magnetic moment in every volume unit increased with increasing Zn.

Ferromagnetic interactions in a dicyanamide-bridged multinuclear metal-organic framework [Pr3NH]+ [Mn(dca)3]−·H2O

2019 ◽  
Vol 74 (6) ◽  
pp. 485-489
Author(s):  
Yuan Huang ◽  
Xiu-feng Yu ◽  
Zhen Rong ◽  
Yi-chun Ai ◽  
Kun Qian ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Magnetic Measurements ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Metal Organic ◽  
Ferromagnetic Interactions

AbstractA new complex [Pr3NH]+ [Mn(dca)3]− · H2O (dicyanamide = dca−) was synthesized, in which the Mn2+ cations are bridged by end-to-end dca anions to form three-dimensional [Mn(dca)3]nn− networks and tripropylammonium cations reside in the cavities of these networks. The complex has been characterized by single-crystal X-ray diffraction, infrared spectroscopy, elemental analysis, and magnetic measurements. Magnetic susceptibility data indicate ferromagnetic interactions among the MnII ions.

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