X-Ray diffraction and magnetic studies on a series of isostructural divalent metal chloranilates with zigzag polymeric chain structures and on a dinuclear iron(III) chloranilate †

2000 ◽  
pp. 1793-1797 ◽  
Author(s):  
Brendan F. Abrahams ◽  
Kevin D. Lu ◽  
Boujemaa Moubaraki ◽  
Keith S. Murray ◽  
Richard Robson
Keyword(s):  
Divalent Metal ◽  
Polymeric Chain ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
X Ray ◽  
Dinuclear Iron

Synthesis, IR spectrum, thermal behaviour and crystal structure of a novel one-dimensional cyano-bridged zinc(II)/nickel(II) complex

2005 ◽  
Vol 220 (1) ◽  
Author(s):  
Ahmet Karadag ◽  
Hümeyra Pasaoglu ◽  
Gökhan Kastas ◽  
Orhan Büyükgüngör
Keyword(s):  
Crystal Structure ◽  
Thermal Analysis ◽  
Coordination Polymer ◽  
Single Crystal ◽  
Ir Spectrum ◽  
Polymeric Chain ◽  
X Ray Diffraction ◽  
Bimetallic Complex ◽  
One Dimensional ◽  
X Ray

AbstractThe cyano-bridged heteronuclear coordination polymer of zinc(II)/nickel(II) has been prepared by N-(2-hydroxyethyl)-ethylendiamine (hydet-en), alternatively named 2-(2-aminoethylamino)-ethanol and characterised by IR and thermal analysis. In the bimetallic complex, the decomposition of hydet-en ligands is seen to be endothermic whereas that of the cyano ligands is found to be exothermic. The crystal structure of the complex has been determined by single-crystal X-ray diffraction. The crystal structure of the zinc(II)-nickel(II) complex consists of a one-dimensional polymeric chain –Zn(hydet-en)

scholarly journals Quasi-Isostructural Co(II) and Ni(II) Complexes with Mefenamato Ligand: Synthesis, Characterization, and Biological Activity

Molecules ◽  
2020 ◽  
Vol 25 (13) ◽  
pp. 3099 ◽  
Author(s):  
Michał Gacki ◽  
Karolina Kafarska ◽  
Anna Pietrzak ◽  
Izabela Korona-Głowniak ◽  
Wojciech M. Wolf
Keyword(s):  
Absorption Spectrometry ◽  
Hirshfeld Surface ◽  
Polymeric Chain ◽  
X Ray Diffraction ◽  
Intermolecular Hydrogen Bonds ◽  
X Ray ◽  
Gram Positive Bacteria ◽  
Flame Atomic Absorption ◽  
Intermolecular Contacts ◽  
Antioxidant And Antimicrobial Activity

Three metal complexes of mefenamato ligand 1 were synthesized: [Co2(mef)4(EtOH)2(H2O)4]: 2; [Co(mef)2(MeOH)4]∙2MeOH: 3; and [Ni(mef)2(MeOH)4]∙2MeOH: 4. Their compositions and properties were investigated by elemental analysis (EA), flame atomic absorption spectrometry (FAAS), Fourier-transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). Crystal structures were determined by the single crystal X-ray diffraction technique. Additionally, their antioxidant and antimicrobial activity were established, thus proving good/moderate bioactivity against Gram-positive bacteria and yeasts. In the crystal structure of 2, an apical water molecule is shared between two adjacent cobalt(II) ions, resulting in the formation of a polymeric chain extending along the [100] direction. Meanwhile, structures 3 and 4 have strong intermolecular hydrogen bonds with diverse topologies that yield unique quasi-isostructural arrangements. The packing topology is reflected by the Hirshfeld surface analysis of intermolecular contacts.

X-ray diffraction and magnetic studies of altered ilmenite and pseudorutile

1980 ◽  
Vol 43 (329) ◽  
pp. 659-663 ◽  
Author(s):  
M. J. Wort ◽  
M. P. Jones
Keyword(s):  
Magnetic Susceptibility ◽  
Western Australia ◽  
Wide Distribution ◽  
Diffraction Spectrum ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
Subsequent Work ◽  
Secondary Alteration ◽  
X Ray ◽  
Magnetic Spin

SynopsisIT was not until 1966 that pseudorutile was first defined. Earlier, its X-ray diffraction spectrum had been confused with that of futile and, to a lesser degree, with those of hematite and ilmenite. Subsequent work has shown that pseudorutile has a world-wide distribution in detrital ilmenite-bearing heavy mineral deposits. The present work has confirmed its magnetic susceptibility and density. In addition pseudorutile is shown to be a magnetic spin glass with a peak susceptibility at 23 °K.Altered ilmenites, in which pseudorutile occurs as a secondary alteration product, display a range of chemical composition and magnetic susceptibility. The most highly magnetic fractions are not necessarily those containing the least-altered ilmenite, and in material from Capel, Western Australia, the most highly magnetic fractions were those containing grains of ferrimagnetic ferrian ilmenite.Quantitative X-ray diffraction has shown that West Australian altered ilmenite contains significant amounts of amorphous ilmenite, pseudorutile, and rutile. The magnetic susceptibility of paramagnetic fractions of altered ilmenite from Capel, Western Australia, can be calculated from normative compositions based on chemical analyses.

Synthese und Koordinationschemie eines neuartigen Bistetrazols: Ein 1D-Metallopolymer durch Selbstorganisation koordinativ ungesättigter Zink(II)-M4onomere [1] / Synthesis and Coordination Chemistry of a New Bistetrazole: A 1D-Metallopolymer via Self-Assembly of Monomeric Zinc(II)-Buildingblocks

1995 ◽  
Vol 50 (4) ◽  
pp. 642-648 ◽  
Author(s):  
Rolf W. Saalfrank ◽  
Klaus Schobert ◽  
Stefan Trümmer ◽  
Alexander Wolski
Keyword(s):  
Coordination Chemistry ◽  
Self Assembly ◽  
Intermediate Formation ◽  
The Self ◽  
Polymeric Chain ◽  
X Ray Diffraction ◽  
Bridging Ligands ◽  
Subsequent Formation ◽  
X Ray ◽  
Polymeric Compounds

The new bistetrazole 13 has been obtained by subsequent formation of the two heterocyclic units. In methanolic solution 13 reacts with zinc(II) acetate to yield the pseudo-meso-1 D-coordination polymer [ZnL2(MeOH)]n (n = ∞) 14. The structure of 14 was established by single crystal X-ray diffraction. The generation of the polymeric chain 14 is understandable, if intermediate formation of coordinatively unsaturated zinc(II) buildingblocks (Δ)-15 and (Λ)-15 is assumed. Alternating linkage of the self-complementary chiral monomers 15, across one cyanofunction each, leads to 14 with zinc being essentially octahedrally coordinated. Compared with polymeric compounds of similar bridging ligands, the Zn ··· N≡C-distance in 14 (225,7 pm) is short.

Two CoII coordination polymers of biphenyl-2,2′,5,5′-tetracarboxylic acid with flexible N-donor ligands: syntheses, structures and magnetic properties

2019 ◽  
Vol 75 (8) ◽  
pp. 1073-1083 ◽  
Author(s):  
Feng Su ◽  
Cheng-Yong Zhou ◽  
Lin-Tao Wu ◽  
Xi Wu ◽  
Jing Su ◽  
...  
Keyword(s):  
Coordination Polymers ◽  
Three Dimensional ◽  
Donor Ligands ◽  
Tetracarboxylic Acid ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
Orbital Contribution ◽  
X Ray ◽  
3D Network ◽  
Methyl Benzene

Two CoII-based coordination polymers, namely poly[(μ4-biphenyl-2,2′,5,5′-tetracarboxylato){μ2-1,3-bis[(1H-imidazol-1-yl)methyl]benzene}dicobalt(II)], [Co2(C16H6O8)(C14H14N4)2] n or [Co2(o,m-bpta)(1,3-bimb)2] n (I), and poly[[aqua(μ4-biphenyl-2,2′,5,5′-tetracarboxylato){1,4-bis[(1H-imidazol-1-yl)methyl]benzene}dicobalt(II)] dihydrate], {[Co2(C16H6O8)(C14H14N4)2(H2O)2]·4H2O} n or {[Co2(o,m-bpta)(1,4-bimb)2(H2O)2]·4H2O} n (II), were synthesized from a mixture of biphenyl-2,2′,5,5′-tetracarboxylic acid, i.e. [H4(o,m-bpta)], CoCl2·6H2O and N-donor ligands under solvothermal conditions. The complexes were characterized by IR spectroscopy, elemental analysis, single-crystal X-ray diffraction and powder X-ray diffraction analysis. The bridging (o,m-bpta)4− ligands combine with CoII ions in different μ4-coordination modes, leading to the formation of one-dimensional chains. The central CoII atoms display tetrahedral [CoN2O2] and octahedral [CoN2O4] geometries in I and II, respectively. The bis[(1H-imidazol-1-yl)methyl]benzene (bimb) ligands adopt trans or cis conformations to connect CoII ions, thus forming two three-dimensional (3D) networks. Complex I shows a (2,4)-connected 3D network with left- and right-handed helical chains constructed by (o,m-bpta)4− ligands. Complex II is a (4,4)-connected 3D novel network with ribbon-like chains formed by (o,m-bpta)4− linkers. Magnetic studies indicate an orbital contribution to the magnetic moment of I and II due to the longer Co...Co distances. An attempt has been made to fit the χM T results to the magnetic formulae for mononuclear CoII complexes, the fitting indicating the presence of weak antiferromagnetic interactions between the CoII ions.

Thermally stable coordination compounds intercalated in montmorillonite clay mineral

1992 ◽  
Vol 70 (7) ◽  
pp. 1927-1931 ◽  
Author(s):  
N. K. Labhsetwar ◽  
O. P. Shrivastava
Keyword(s):  
Clay Mineral ◽  
Coordination Compounds ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
Swelling Properties ◽  
X Ray ◽  
Good Thermal Stability ◽  
Intercalated Compounds ◽  
Layered Clay

Montmorillonite is a natural layered clay mineral having myriad applications due mainly to its remarkable ion exchange, intercalation, and swelling properties. It can act as a good host for several compounds. Two intercalated coordination compounds of Cu(II) and Ni(II) with 2,2′-bipyridyl have been prepared in the interlayer spaces of montmorillonite structure. They are characterized on the basis of elemental analysis, infrared spectroscopy, magnetic studies, and X-ray diffraction. Both compounds show similarity in their structure and properties with the respective normal complexes of similar composition. These compounds show good thermal stability. The present intercalated compounds might be useful for their nitrogen-immobilizing properties and high-temperature applications.

Magnetoelectric and magnetic studies of the Bi1–xCaxFeO3 multiferrioc system

2014 ◽  
Vol 92 (5) ◽  
pp. 389-394 ◽  
Author(s):  
S.F. Mansour ◽  
N.I. Abu-Elsaad ◽  
T.A. Elmosalami
Keyword(s):  
Room Temperature ◽  
Energy Levels ◽  
Resonance Field ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
X Ray ◽  
Transmission Electron ◽  
Spin Resonance ◽  
Particle Size And Shape ◽  
Combustion Technique

Bi1–xCaxFeO3 was prepared by the flash autocombustion combustion technique. X-ray diffraction analysis showed a Rhombohedrally distorted hexagonal perovskite structure with space group R3c. The particle size and shape were studied by transmission electron microscope. Magnetization studies at room temperature showed superparamagnetic behavior for the prepared nanoparticles. Magnetoelectric coefficient characterized as magnetic field – induced polarization was investigated. The Lande factor (g), resonance field (Br), relaxation time (τ), and the energy between two adjacent degenerate spin energy levels (ΔE) were estimated from the electron spin resonance spectra.

scholarly journals The structural diversity of DNA–neutral phospholipids–divalent metal cations aggregates: a small-angle synchrotron X-ray diffraction study

2006 ◽  
Vol 36 (4-5) ◽  
pp. 363-375 ◽  
Author(s):  
Daniela Uhríková ◽  
Adrián Lengyel ◽  
Mária Hanulová ◽  
Sérgio S. Funari ◽  
Pavol Balgavý
Keyword(s):  
Diffraction Study ◽  
Small Angle ◽  
Metal Cations ◽  
Structural Diversity ◽  
Divalent Metal ◽  
X Ray Diffraction ◽  
X Ray ◽  
Divalent Metal Cations

Divalent Metal Complexes of 2-Formylphenoxyacetic Acid: The Crystal Structures of 2-Formylphenoxyacetic Acid, and the Isomorphous Cobalt(II) and Zinc(II) 2-Formylphenoxyacetates

1985 ◽  
Vol 38 (9) ◽  
pp. 1381 ◽  
Author(s):  
CHL Kennard ◽  
EJ O'Reilly ◽  
G Smith ◽  
TCW Mak
Keyword(s):  
Metal Complexes ◽  
Crystal Structures ◽  
Divalent Metal ◽  
Carboxyl Groups ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Planar Molecules ◽  
Divalent Metal Complexes ◽  
Monoclinic Cell

The crystal structures of 2-formylphenoxyacetic acid ( ofpaH ), tetraaquabis (2-formylphenoxyacetato)-cobalt(II) (1) and tetraaquabis (2- formylphenoxyacetato )zinc(II) (2) have been determined by X-ray diffraction and refined to residuals R 0.039, 0.058 and 0.045 for 1197, 1178 and 1230 observed reflections respectively. 2-Formylphenoxyacetic acid crystallizes in a monoclinic cell, space group P21/n with a 8.066(2), b 7.375(1), c 14.206(2) Ǻ, β 98.12(1)° and Z 4. The planar molecules form unusual hydrogen-bonded chain polymers (O…O 2.694(3)Ǻ] linked through the carboxyl groups. The complexes (1) and (2) are isomorphous, the comparative cells being a 5.036(1), b 13.463(3), c 15.083(4) Ǻ, β 96.88(2)° for (1), and a 5.044(1), b 13.481(3), c 15.055(4) Ǻ, β 96.95(2)° for (2), with Z 2 and space group P21. The complexes have four waters and two trans-related carboxyl oxygens [mean M-O distances 2.129(5) and 2.117(3) Ǻ respectively] completing almost regular octahedral stereochemistries . The nickel(II) complex [Ni( ofpa )(H2O)4] is probably not isostructural with (1) and (2), and the copper(II) complex is also different, with formula [Cu( ofpa )2(H2O)2].

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