Synthesis, X-Ray Crystal Structure and Magnetic Characterization of the First “Ni3S4N3” Nickel Thiolate Cluster

1995 ◽  
Vol 128 (2) ◽  
pp. 125-129 ◽  
Author(s):  
Albrecht Berkessel ◽  
Jan W. Bats ◽  
Martina Hüber ◽  
Wolfgang Haase ◽  
Thomas Neumann ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Characterization ◽  
X Ray

Structural and magnetic characterization of Ho3SbO7 and Dy3SbO7

2001 ◽  
Vol 79 (11-12) ◽  
pp. 1415-1419 ◽  
Author(s):  
T Fennell ◽  
S T Bramwell ◽  
M A Green
Keyword(s):  
Crystal Structure ◽  
Experimental Investigation ◽  
Rare Earth Ions ◽  
X Ray Diffraction ◽  
Magnetic Characterization ◽  
X Ray ◽  
Structural And Magnetic Properties ◽  
Ice Model ◽  
Magnetic Rare Earth

We present an experimental investigation of the structural and magnetic properties of Ho3SbO7 and Dy3SbO7. These compounds adopt the Y3TaO7 structure, space group C2221. The magnetic rare-earth ions occupy an intricate lattice related to the pyrochlore lattice that occurs in Ho2Ti2O7 and Dy2Ti2O7. The crystal structure of Ho3SbO7 is determined by Rietveld refinement of the powder X-ray diffraction pattern at ambient temperature, and that of the Dy analogue is inferred to be similar. Magnetic susceptibility measurements show that Ho3SbO7 and Dy3SbO7 have negative Curie–Weiss temperatures: –8.4 K (Ho) and –9.2 K (Dy). Magnetic transitions have been detected at 2.0 K (Ho) and 3.0 K (Dy). We discuss the results in terms of the ``dipolar spin ice model'' that has been used to describe Ho2Ti2O7 and Dy2Ti2O7. PACS Nos.: 75.25+z, 75.50Ee, 61.10Nz

Synthesis, Structure and Magnetic Characterization of a New Phosphate K1.84Fe1.42Nb0.58(PO4)3 with the Langbeinite- type Structure

2008 ◽  
Vol 63 (3) ◽  
pp. 345-348 ◽  
Author(s):  
Artem A. Babaryk ◽  
Igor V. Zatovsky ◽  
Nikolay S. Slobodyanik ◽  
Ivan V. Ogorodnyk
Keyword(s):  
Crystal Structure ◽  
Low Temperatures ◽  
Structure Type ◽  
The Self ◽  
Magnetic Characterization ◽  
X Ray ◽  
Complex Phosphate ◽  
Cubic System ◽  
The Relationship

A new complex phosphate K1.84Fe1.42Nb0.58(PO4)3 has been synthesized by the self-flux technique. The X-ray single crystal structure and magnetic properties were studied. The compound crystallizes in the cubic system with space group P213 (a = 9.9404(10) Å ) and belongs to the langbeinite structure type. The structure contains [M2P3O18] building units. “Closed” fragments [M8P9O60] provide space for location of two potassium atoms. Antiferromagnetic interactions were detected at low temperatures which originate from superexchange through a M(1)-O-P-O-M(2) pathway with corresponding J = −5.5(1) cm−1. The relationship between the UV/vis absorption and the structure is discussed.

Synthesis, crystal structure and magnetic characterization of a cyanide-bridged Mo–Ni nanosized molecular wheel

2015 ◽  
Vol 70 (8) ◽  
pp. 527-531 ◽  
Author(s):  
Daopeng Zhang ◽  
Lingqian Kong ◽  
Hongyan Zhang ◽  
Ping Wang
Keyword(s):  
Crystal Structure ◽  
Magnetic Properties ◽  
Ir Spectroscopy ◽  
Structure Determination ◽  
Building Blocks ◽  
Antiferromagnetic Coupling ◽  
X Ray Diffraction ◽  
Magnetic Characterization ◽  
X Ray

AbstractBy using K4[Mo(CN)8] and [Ni(L)(H2O)2][ClO4]2 as reagents (L = 2,12-dimethyl-3,7,11,17-tetraazabicyclo [11.3.1]heptadeca-1(17),13,15-triene), a new cyanide-bridged Mo–Ni complex containing the building blocks [Ni(H2O)(L)]2+ and [Ni(L)]2+ bridged by [Mo(CN)8]4− units has been obtained. The complex with the formula {[Ni(H2O)(L)][Ni(L)][Mo(CN)8]}6 · 36H2O · 2CH3OH (1) was characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. The structure determination reveals an octadecanuclear cluster in the form of a 36-membered macrocycle, in which the largest intramolecular W···W and Ni···Ni distances are 16.5 and 14.4 Å, respectively, indicating that complex 1 is a nanosized molecular wheel. Investigation of its magnetic properties has shown weak antiferromagnetic coupling between the adjacent Ni(II) ions bridged by the diamagnetic [Mo(CN)8]4− ions.

The preparation and characterization of Pt(Se3PPh)(PR3)2; the X-ray crystal structure of Pt(Se3PPh)(dppe)·CH2Cl2

Polyhedron ◽  
1990 ◽  
Vol 9 (7) ◽  
pp. 987-990 ◽  
Author(s):  
Ivan P. Parkin ◽  
Mark J. Pilkington ◽  
Alexandra M.Z. Slawin ◽  
David J. Williams ◽  
J.Derek Woollins
Keyword(s):  
Crystal Structure ◽  
X Ray

Synthesis, crystal structure and magnetic characterization of two Mn(III) chains with Schiff-base ligands

2013 ◽  
Vol 1033 ◽  
pp. 8-13 ◽  
Author(s):  
Cong-Ming Zhang ◽  
Xi-Feng Gao ◽  
Mei Zhu ◽  
Yun-Gai Li ◽  
Qing-Lun Wang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Schiff Base Ligands ◽  
Magnetic Characterization

Structural Systematics of Rare Earth Complexes. VII. Crystal Structure of Bis(2,2'/6',2␛-Terpyridinium) Octaaquaterbium(III) Heptachloride Hydrate

1994 ◽  
Vol 47 (2) ◽  
pp. 391 ◽  
Author(s):  
CJ Kepert ◽  
BW Skeleton ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Single Crystal ◽  
Structural Characterization ◽  
Title Compound ◽  
Room Temperature ◽  
Chloride Ions ◽  
Full Matrix ◽  
X Ray

The room-temperature single-crystal X-ray structural characterization of the title compound (tpyH2)2[Tb(OH2)8]Cl7.~2⅓H2O is recorded. Crystals are triclinic, Pī , a 17.063(5), b 16.243(3), c 7.878(3) Ǻ, α 84.78(2), β 84.39(3), γ 87.81(2)°, Z = 2 formula units; 3167 'observed' diffractometer reflections were refined by full-matrix least-squares procedures to a residual of 0.057. Notable features of interest of the compound are the 'chelation' of chloride ions by the terpyridinium cations , and the existence of a free [Tb(OH2)8]2+ cation in the presence of an abundance of chloride ions.

scholarly journals STRUCTURAL CHARACTERIZATION OF THE NEW DIAMOND-LIKE SEMICONDUCTOR CuNbGaSe3

2018 ◽  
Vol 15 (29) ◽  
pp. 228-233
Author(s):  
J. A. FLORES-CRUZ ◽  
G. E. DELGADO ◽  
J. E. CONTRERAS ◽  
M. QUINTERO ◽  
L. NIEVES ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Magnetic Behavior ◽  
Secondary Phase ◽  
Chalcopyrite Structure ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters ◽  
Chalcogenide Compound ◽  
Semiconductor Type

The chalcogenide compound CuNbGaSe3, belonging to the system I-II-III-VI3, has been investigated by means of X-ray powder diffraction and its crystal structure has been refined by the Rietveld method.This is a material of the semiconductor type, which improves the properties of a simple semiconductor like CuGaSe2 because it ads spintronic applications due to its magnetic behavior. The powder pattern was composed by 94.2% of the principal phase CuNbGaSe3 and 5.8% of the secondary phase Cu0.667NbSe2. This material crystallizes with a CuFeInSe3-type structure in the tetragonal space group P4 2c (Nº 112), unit cell parameters a = 5.6199(4) Å, c = 11.0275(2) Å, V = 348.28(4) Å3, with a normal adamantane-structure where occurs a degradation of symmetry from the chalcopyrite structure I4 2d to a related structure P4 2c.

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