Search results for "Oxalate"

Synthesis and Characterization of a Soluble Bimetallic Oxalate-Based Bidimensional Magnet:  [K(18-crown-6)]3[Mn3(H2O)4{Cr(ox)3}3]

2006

The "templating" K crown ether cation allows for the preparation of soluble layered oxalate-based bimetallic magnets, as in [K(18-crown-6]3{Mn3(H2O)4[Cr(ox)3]3}, with an unprecedented bidimensional polymeric anionic network that involves both oxalato bridges and H bonds. As in other 2D oxalate-bridged compounds, the compound behaves as a soft ferromagnet, with the onset of magnetic ordering occurring at 3.3 K.

Crystal structure of isobutylammonium hydrogen oxalate hemihydrate

2014

In the title hydrated molecular salt, C4H12N+·C2HO4−·0.5H2O, the O atom of the water molecule lies on a crystallographic twofold axis. The dihedral angle between the CO2and CO2H planes of the anion is 18.47 (8)°. In the crystal, the anions are connected to each other by strong near-linear O—H...O hydrogen bonds. The water molecules are located between the chains of anions and isobutylamine cations; their O atoms participate as donors and acceptors, respectively, in O—H...O and N—H...O hydrogen bonds, which form channels (dimensions = 4.615 and 3.387 Å) arranged parallel to [010].

Crystal structure of 2-methyl-1H-imidazol-3-ium aquatrichlorido(oxalato-κ2O,O′)stannate(IV)

2015

N—H⋯O, N—H⋯Cl and O—H⋯O hydrogen bonds between cations and anions in the complex salt (C4H7N2)+[Sn(H2O)Cl3(C2O4)]− are responsible for the formation of a three-dimensional network structure.

ChemInform Abstract: Multifunctionality in Hybrid Magnetic Materials Based on Bimetallic Oxalate Complexes

2011

This tutorial review illustrates the design of multifunctional oxalate-based magnetic materials through the combination of the intrinsic magnetism of the metal–organic framework and the additional properties introduced by several organic/inorganic functional cations.

Ethyldimethylammonium oxalate

2006

The title crystal structure, C4H12N+·C2HO4−, contains discrete ethyl­dimethyl­ammonium cations and oxalate monoanions. Linear chains of oxalate monoanions are formed by strong O—H⋯O hydrogen bonds. These chains are further connected by N—H⋯O and C—H⋯O hydrogen bonds through ethyl­dimethyl­ammonium cations, forming channels along the a axis.

Cover Picture: Insertion of a Single-Molecule Magnet inside a Ferromagnetic Lattice Based on a 3D Bimetallic Oxalate Network: Towards Molecular Analo…

2014

Diethylammonium hydrogen oxalate

2006

The structure of the title compound, C4H12N+·C2HO4−, consists of discrete oxalate monoanions and diethyl­ammonium cations. The N atom lies on a crystallographic twofold rotation axis and the oxalate ion is centrosymmetric. The oxalate monoanions are present as hydrogen-bonded linear chains. Conformationally extended diethyl­ammonium cations link the linear chains through three–centre N–H⋯O hydrogen bonds.

Increasing the Coercivity in Layered Molecular-based Magnets A[MIIMIII(ox)3] (MII = Mn, Fe, Co, Ni, Cu; MIII = Cr, Fe; ox = oxalate; A = organic or o…

1999

Oxalate-based 2D magnets: the series [NBu4][MIIMnIII(ox)3] (MII= Fe, Co, Ni, Zn; ox = oxalate dianion)

2006

The synthesis, structure and physical properties of the bimetallic oxalate-based molecular magnets containing MnIII of formula [NBu4][MIIMn(ox)3] (MII = Fe, Co, Ni, Zn; ox = oxalate dianion) are presented here. All compounds are isostructural, containing two-dimensional honeycomb bimetallic networks formed by alternating MII and MIII ions connected by oxalate anions. These compounds exhibit antiferromagnetic interactions that give rise to ferrimagnets or weak ferromagnets ordering at critical temperatures up to 21 K.

Electrochemical Syntheses of Carboxylic Acids from Carbon Dioxide

1987

The first report on the reduction of carbon dioxide is due to the venerable name of Hermann Kolbe, who, in 1861, published with R. Schmitt the reduction of carbon dioxide to formate with metallic potassium (1). Seven years later he introduced to the Chemical Society in London his assistant E. Drechsel, who “after many unsuccessful experiments, made during several years” (2) at the end succeeded in reducing carbon dioxide to oxalate with metallic sodium or with potassium amalgam in anhydrous conditions. Soon afterwards Beketov (3) and Royer (4) opened the series of papers dealing with the direct involvement of carbon dioxide in electrolytic processes. Since then the reduction of carbon dioxi…