Search results for "oxalate"

showing 10 items of 215 documents

Preparation and crystal structure of the oxalato-bridged CrIII–AgItwo-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (dpa = 2,2′-dipyridylamin…

2004

The reaction of the mononuclear complex [Cr(dpa)(ox)2]− (dpa = 2,2-dipyridylamine) with Ag+ in aqueous solution affords the two-dimensional compound {Ag3(H2O)[Cr(dpa)(ox)2]3}n·2nH2O (1) whose structure has been determined by single-crystal X-ray diffraction. Six crystallographically independent metal atoms (three chromium and three silver atoms) occur in 1. The three [Cr(dpa)(ox)2]− units in 1 act as ligands towards the silver atoms through the two oxalate groups. Each oxalate group acts as bridging ligand adopting five coordination modes: bis-bidentate, bis-bidentate/monodentate (outer), bis-bidentate/monodentate (inner), bidentate/bis-monodentate (outer) and bidentate/monodentate (outer).…

DenticityAqueous solutionInorganic chemistrychemistry.chemical_elementBridging ligandGeneral ChemistryCrystal structureCondensed Matter PhysicsBlock (periodic table)OxalateMetalCrystallographychemistry.chemical_compoundChromiumchemistryvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceCrystEngComm
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A solution study of complex formation between iron(III) and oxalate in dimethylsulphoxide

1991

The complex formation between iron(III) and oxalic acid (ethanedioic acid, H2ox) has been studied by potentiometry in dimethylsulphoxide (dmso) solution. H2ox behaves as a weak diprotic acid in such a solvent, with overall association constants: log βj1=8.551(3) and log βj2=14.242(3) at 25°C and 0.1 Mn-Bu4NClO4. A reliable set of overall stability constants for the iron(III)-oxalato complexes, log β11=13.16(4), log β12=23.66(4) and log β13=30.75(4), have been obtained for the first time under identical conditions. The electrochemical behaviour of such complexes was studied in dmso at a platinum electrode. The coordination ability of oxalate towards iron(III) in dmso and water media is compa…

Oxalic acidInorganic chemistryMetals and Alloyschemistry.chemical_elementDiprotic acidOxalateInorganic ChemistrySolventchemistry.chemical_compoundchemistryMaterials ChemistryChemical stabilityCarboxylateCyclic voltammetryPlatinumTransition Metal Chemistry
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Crystal structure of bis(cyclohexylammonium) diphenyldioxalatostannate(IV)

2015

In the title salt, (CyNH3)2[Sn(Ph2)(C2O4)2] (Cy is cyclo­hexyl and Ph is phen­yl), the SnPh2 moiety is chelated by two oxalate anions, leading to a cis arrangement within the distorted octa­hedral coordination sphere of the SnIV atom.

crystal structureStereochemistryOxalic acidcyclo­hexyl­ammoniumorganotin(IV) compoundSalt (chemistry)Crystal structureMedicinal chemistryOxalateResearch CommunicationsCrystalchemistry.chemical_compoundMoietyGeneral Materials ScienceCoordination geometrychemistry.chemical_classificationCrystallographycis arrangementHydrogen bondoxalate ligandsGeneral ChemistryCondensed Matter PhysicschemistryQD901-999N—H...O hydrogen bondingN—H⋯O hydrogen bondingcyclohexylammoniumActa Crystallographica Section E: Crystallographic Communications
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Incommensurate nature of the multilayered molecular ferromagnetic metals based on bis(ethylenedithio)tetrathiafulvalene and bimetallic oxalate comple…

2004

The salt [ET]x[MnRh(ox)(3)].CH(2)Cl(2) (x = 2.526(1)) has been obtained and characterized. This paramagnetic metal is essentially isostructural to the ferromagnetic metal [ET]y[MnCr(ox)(3)].CH(2)Cl(2) (y approximately equal to 3) and provides a definite answer on the origin of the structural disorder present on such systems. As in the ferromagnetic analogue, this material shows high electrical conductivity at room temperature (13 S.cm(-1)) and metallic behavior.

ChemistryMineralogyOxalateInorganic ChemistryMetalParamagnetismchemistry.chemical_compoundCrystallographyFerromagnetismElectrical resistivity and conductivityvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryIsostructuralBimetallic stripTetrathiafulvaleneInorganic chemistry
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The effect of oxalate-based desensitizers on the microleakage and shear bond strength of resin modified glass ionomer

2017

Background The first line of intervention to alleviate tooth sensitivity is to use dentin desensitizers such as oxalate-based desensitizers. When the dentin sensitivity continues even after application of desensitizers the next intervention would be restoration of the lesion. The aim of this in vitro study was to investigate the effect of prior application of oxalate-based desensitizer on the marginal microleakage and shear bond strength of resin modified glass ionomer (RMGI) restorations. Material and methods In order to prepare the specimens for microleakage test standard class v cavities were prepared on buccal surfaces of 45 teeth. The specimens were randomly divided into three equal gr…

Materials scienceGlass ionomer cementDentistryOxalateOperative Dentistry and Endodontics03 medical and health scienceschemistry.chemical_compound0302 clinical medicinestomatognathic systemStereo microscopeDentinmedicine030212 general & internal medicineGeneral DentistryDentin SensitivityEnamel paintbusiness.industryResearch030206 dentistry:CIENCIAS MÉDICAS [UNESCO]medicine.diseasestomatognathic diseasesmedicine.anatomical_structurechemistryvisual_artTooth SensitivityUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumDentin hypersensitivitybusinessJournal of Clinical and Experimental Dentistry
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Self-assembly of a chiral three-dimensional manganese(II)-copper(II) coordination polymer with a double helical architecture

2013

The use of the anionic dicopper(ii) complex, [CuII(mpba) 2]4- [mpba = N,N′-1,3-phenylenebis(oxamate)], as tetrakis(bidentate) metalloligand toward MnII ions in the presence of oxalate and the chiral (S)-trimethyl-(1-phenylethyl)ammonium cation affords the first example of a mixed oxalato/oxamato-based chiral 3D metal-organic polymer. © 2013 The Royal Society of Chemistry.

chemistry.chemical_classificationDenticityCoordination polymerInorganic chemistrychemistry.chemical_elementGeneral ChemistryPolymerManganeseCondensed Matter PhysicsCopperOxalateIonchemistry.chemical_compoundchemistryPolymer chemistryGeneral Materials ScienceSelf-assemblyCrystEngComm
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First Reactions of 2,2′-Bisindolyls with Electrophilic Azo Compounds and Diethyl Mesoxalate

1992

Conformations and some electronic properties of the 2,2′-bisindolyls 6 were calculated for the prediction of probable Diels-Alder reactivity, in analogy to previous work on 2-vinylindoles. First reactions with dienophiles revealed that compounds 6 did not participate in [4 + 2]cycloadditions but rather underwent simple electrophilic substitutions at the enamine function with, above all, some heterodienophiles. Erste Reaktionen von 2,2′-Bisindolylen mit elektrophilen Azoverbindungen und Diethylmesoxalat Zur Vorhersage moglicher Diels-Alder-Reaktionen an 2,2′-Bisindolylen 6 werden Berechnungen zur Konformation und uber elektronische Eigenschaften durchgefuhrt. Die erstmals durchgefuhrten Reak…

Electrophilic substitutionDiethyl mesoxalateBicyclic moleculeChemistryDrug DiscoveryElectrophilePharmaceutical ScienceMedicinal chemistryArchiv der Pharmazie
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The odd association of a C3h trisamidinium cation and tosylate anion with a series of linear oxalate-bridged trinuclear heterometallic complexes

2013

A series of six isostructural heterometallic trinuclear oxalate-bridged complexes of the formula (TDbenz)(2)(TsO)(2)[M(II)(H(2)O)(2){(μ-ox)M(III)(ox)(2)}(2)]·6H(2)O·2CH(3)OH (TDbenz = 1,3,5-tris[2-(1,3-diazolinium)]benzene; TsO = 4-methylbenzenesulfonate; ox = oxalate; M(III) = Fe, M(II) = Mn (1), Fe (2), Co (3); M(III) = Cr, M(II) = Mn (4), Fe (5), Co (6)) have been synthesized from (NH(4))(3)[M(III)(ox)(3)]·3H(2)O, the chloride salts of the divalent metal ions and the tosylate salt of 1,3,5-tris[2-(1,3-diazolinium)]benzene (trisamidinium). Whereas the crystal structures of compounds 2, 3, 4 and 5 have been investigated by single-crystal X-ray diffraction, the structures of 1 and 6 have be…

Coordination sphere010405 organic chemistryChemistryHydrogen bondInorganic chemistryCrystal structure010402 general chemistry01 natural sciencesOxalate0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyOctahedron[CHIM]Chemical SciencesMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryIsostructuralCoordination geometryDalton Transactions
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Suitability of non-glucose-carbohydrates for parenteral nutrition

1975

Postoperative parenteral nutrition can only be optimally effective if the characteristics of post-traumatic metabolism are taken into account. Two main possibilities are discussed for the carbohydrate component of parenteral nutrition during this phase: glucose with high doses of insulin or non-glucose carbohydrates (sugar substitutes) possibly in a suitable combination with glucose. The risks as well as the technical and organisational problems involved in the use of them are discussed and the authors prefer the second of the two alternatives. Possible side effects of non-glucose carbohydrates are pointed out and it is shown how these can be avoided by observing dose guidelines. So far a c…

Parenteral Nutritionmedicine.medical_treatmentBlood sugarPhysiologyFructoseCarbohydrate metabolismCritical Care and Intensive Care MedicineXylitolElectrolyteschemistry.chemical_compoundPregnancyDietary CarbohydratesmedicineHumansSugarXylitolOxalatesAdenine Nucleotidesbusiness.industryInsulinProteinsBilirubinGeneral MedicineMetabolismCarbohydrateLipid MetabolismUric AcidGlucoseParenteral nutritionBiochemistrychemistryLactatesFemaleParenteral Nutrition TotalbusinessEuropean Journal of Intensive Care Medicine
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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.

chemistry.chemical_compoundMolecular magnetsFerromagnetismchemistryMagnetInorganic chemistryMaterials ChemistryAntiferromagnetismGeneral ChemistryIsostructuralBimetallic stripOxalateIonJ. Mater. Chem.
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