Search results for "Oxalate"

Tris(cyclo-hexyl-ammonium) cis-di-chlorido-bis-(oxalato-κ(2) O (1),O (2))stann-ate(IV) chloride monohydrate.

2013

The crystal structure of the title compound, (C6H14N)3[Sn(C2O4)2Cl2]Cl·H2O, contains three cyclohexylammonium cations, one stannate(IV) dianion, one isolated chloride anion and one lattice water molecule. The cyclohexylammonium cations adopt chair conformations. In the complex anion, two bidentate oxalate ligands and two chloride anions incispositions coordinate octahedrally to the central SnIVatom. The cohesion of the molecular entities is ensured by the formation of N—H...O, O—H...O, O—H...Cl and N—H...Cl interactions involving cations, anions and the lattice water molecule, giving rise to a layer-like arrangement parallel to (010).

Ethylammonium hydrogen oxalate–oxalic acid (2/1)

2019

The reaction between ethylamine and oxalic acid in water in a 1:1 molar ratio afforded the title salt, C2H8N+·C2HO4 −·0.5C2H2O4. The hydrogen oxalate anions interact through hydrogen bonding and are organized into a chains propagating along the c-axis direction. The chains are connected to the neighbouring cations and oxalic acid molecules by N—H...O and O—H...O hydrogen bonds and N...O dipole–dipole contacts, leading to a supramolecular three-dimensional network.

CCDC 1835272: Experimental Crystal Structure Determination

2021

Related Article: Mamadou Ndiaye, Mouhamadou Birame Diop, Abdoulaye Samb, Libasse Diop, Allen G. Oliver, Laurent Plasseraud|2020|Zeitschrift fuer Naturforschung, Teil B. Anorganische Chemie, Organische Chemie|75|815 |doi:10.1515/znb-2020-0097

Anion-Assisted Crystallization of a Novel Type of Rhenium(IV)-Based Salt

2016

A novel rhenium(IV)–manganese(II) double salt of formula (NBu4)10[{ReCl4(ox)}3Mn]2[ReCl6] (1) (NBu4+ = tetra-n-butylammonium cation and ox2– = oxalate dianion) has been prepared through the simultaneous use of two different anionic ReIV complexes, namely, [ReCl4(ox)]2– and [ReCl6]2–, in the presence of MnII ion, the [ReCl6]2– anion playing a key role in the crystallization process. 1 has been magnetically characterized and its crystal structure determined by single-crystal X-ray diffraction. The study of the magnetic properties reveals the occurrence of intramolecular antiferromagnetic exchange between ReIV and MnII ions. Remarkably, 1 is the first reported example of ReIV salt based on two…

2D and 3D bimetallic oxalate-based ferromagnets prepared by insertion of MnIII-salen type complexes

2013

The syntheses, structures and magnetic properties of the compounds of formulae [Mn((R)-salmen)(CH3OH)(CH3CN)][MnCr(ox)3](CH3OH)0.5(CH3CN)1.25 ((R)-1), [Mn((S)-salmen)(CH3OH)(CH3CN)][MnCr(ox)3](CH3OH)0.5(CH3CN)1.25 ((S)-1), [Mn((R)-salmen)(CH3OH)2][MnCr(ox)3](CH2Cl2)0.375(CH3OH)0.125(H2O)0.375 ((R)-2) and [Mn((S)-salmen)(CH3OH)2][MnCr(ox)3](CH2Cl2)0.375(CH3OH)0.375(H2O)0.125 ((S)-2) (ox = oxalate, salmen2− = N,N′-(1-methylethylene)bis(salicylideneiminate)), [Mn(salpn)(CH3OH)1.5(CH3CN)0.5][MnCr(ox)3](CH3OH)0.82(H2O)0.93 (3) (salpn2− = N,N′-(propane)bis(salicylideneiminate)) and [Mn(saltmen)(CH3OH)(CH3CN)][MnCr(ox)3](CH3OH) (4) (saltmen2− = N,N′-(1,1,2,2-tetramethylethylene)bis(salicylideneimi…

Controlling the dimensionality of oxalate-based bimetallic complexes: The ferromagnetic chain {[K(18-crown-6)][Mn(bpy)Cr(ox)3]}∞(18-crown-6=C12H24O6,…

2007

Abstract The bimetallic ferromagnetic chain {[K(18-crown-6)][Mn(bpy)Cr(ox)3]}∞ (1) has been synthesized and characterized. It crystallizes in the orthorhombic chiral space group P212121 [a = 9.0510(2) A, b = 14.4710(3) A, c = 26.8660(8) A, V = 3510.97(1) A3, Z = 2]. Compound 1 is made up by anionic [Mn(bpy)Cr(ox)3]− 1D chains and cationic [K(18-crown-6)]+ complexes. The magnetic exchange within the chain is ferromagnetic [J = +7.8(7) cm−1]. In the solid state, the ferromagnetic chains are well isolated magnetically and no long range magnetic ordering has been observed above 2 K.

2,2'-BIPYRIMIDINEOXALATOCOPPER(II) COMPLEXES - FROM THE MONONUCLEAR COMPLEX TO THE 2D SHEET-LIKE POLYMER

1993

Isolation From Human Calcium Oxalate Renal Stones of Nephrocalcin, a Glycoprotein Inhibitor of Calcium Oxalate Crystal Growth. Evidence That Nephroca…

1987

We have determined that the organic matrix of calcium oxalate kidney stones contains a glycoprotein inhibitor ofcalcium oxalate crystal growth (nephrocalcin) that resembles nephrocalcin present in the urine of patients with calcium oxalate stones and differs from nephrocalcin from the urine of normal people. Pulverized calcium oxalate renal stones were extracted with 0.05M EDTA, pH 8.0; nephrocalcin eluted in five peaks using DEAE-cellulose column chromatography, and each peak was further resolved by Sephacryl S-200 column chromatography. Four ofthe fiveDEAE peaks corresponded to those usually found in nephrocalcin from urine; the fifth eluted at a lower ionic strength than any found in uri…

Solid-state dinuclear-to-trinuclear conversion in an oxalato-bridged chromium(III)-cobalt(II) complex as a new route toward single-molecule magnets.

2011

A novel bis(oxalato)chromium(III) salt of a ferromagnetically coupled, oxalato-bridged dinuclear chromium(III)-cobalt(II) complex of formula [CrL(ox)(2)CoL'(H(2)O)(2)][CrL(ox)(2)]·4H(2)O (1) has been self-assembled in solution using different aromatic α,α'-diimines as blocking ligands, such as 2,2'-bipyridine (L = bpy) and 2,9-dimethyl-1,10-phenanthroline (L' = Me(2)phen). Thermal dehydration of 1 leads to an intriguing solid-state reaction between the S = 3/2 Cr(III) anions and the S = 3 Cr(III)Co(II) cations to give a ferromagnetically coupled, oxalato-bridged trinuclear chromium(III)-cobalt(II) complex of formula {[CrL(ox)(2)](2)CoL'} (2). Complex 2 possesses a moderately anisotropic S =…

Hybrid Organic/Inorganic Molecular Materials Formed by Tetrathiafulvalene Radicals and Magnetic Trimeric Clusters of Dimetallic Oxalate‐Bridged Compl…

2003

The first examples of trimeric, dimetallic, pure oxalate-bridged complexes [ox = (C2O4)2−] have been synthesized and characterized structurally and magnetically for the two new series of crystalline molecular assemblies formulated as (TTF)4{MII(H2O)2[MIII(ox)3]2}·nH2O [for MIII = Cr; MII = Mn (1), Fe (2), Co (3), Ni (4), Cu (5) and Zn (6); for MIII = Fe; MII = Mn (7), Fe (8), Co (9), Ni (10) and Zn (11)]. Both series (Cr2M and Fe2M) are isostructural. The crystal structure of (TTF)4{Mn(H2O)2[Cr(ox)3]2}⋅14H2O (1) [monoclinic, space group C2/c (no. 15), a = 13.240(5) A, b = 19.450(5) A, c = 27.690(5) A, β = 97.63(5)°, V = 7068(3) A3 and Z = 4] shows alternating layers of the organic radical T…