Search results for "Oxalate"

showing 10 items of 215 documents

Sensitive determination of aliphatic amines in water by high-performance liquid chromatography with chemiluminescence detection.

2004

A sensitive method has been developed for liquid chromatographic determination of short aliphatic amines in water samples. Analytes are preconcentrated and dansylated on solid sorbents (C18 solid-phase extraction cartridges). The dansyl derivatives are chromatographed and post-column mixed with peroxyoxalate (TCPO) and H2O2 in order to perform chemiluminescence detection. Optimal results have been obtained using a sample volume of 5 ml. The method has been applied to the quantification or screening of several aliphatic amines: methylamine, ethylamine, butylamine, diethylamine, pentylamine and hexylamine. The screening procedure has been developed including also polyamines (putrescine, cadav…

DiethylamineDetection limitChromatographyOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyPeroxyoxalateSensitivity and SpecificityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSpectrometry FluorescencechemistrylawHexylamineLuminescent MeasurementsSpectrophotometry UltravioletEthylaminePentylamineAminesChromatography High Pressure LiquidChemiluminescenceJournal of chromatography. A
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Antiferromagnetic Interactions in Copper(II) µ-Oxalato Dinuclear Complexes: The Role of the Counterion

2018

We report the preparation, crystal structure determination, magnetic properties and DFT calculations of five oxalato-bridged dicopper(II) complexes of formula [Cu-2(bpy)(2-)(H2O)(2)(C2O4)](CF3SO3)(2) (1), [Cu-2(bpy)(2)(C2O4)](PF6)(2) (2), [Cu-2(bpy)(2)(C2O4)](ClO4)(2) (3), [Cu-2(bpy)(2)Cl-2(C2O4)]center dot H2O (4) and [Cu-2(bpy)(2)(NO2)(2)(C2O4)] (5) (bpy = 2,2'-bipyridine and C2O42-= oxalate). Compounds 1, 2, 4 and 5 crystallize in the monoclinic system and 3 crystallizes in the triclinic system. The oxalate ligands in 1-5 adopt the bis-bidentate coordination mode and the two bpy molecules act as terminal ligands. The coordination of the counterions and the surroundings of the copper(II) …

Dinuclear complexesMatériauxFerromagnetismechemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistryTriclinic crystal system010402 general chemistry01 natural sciencesOxalateInorganic Chemistrychemistry.chemical_compoundOxalatoMagnetic propertiesAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryGénie des procédéschemistry.chemical_classificationCoure010405 organic chemistryPropietats magnètiquesCopper0104 chemical sciences3. Good healthCrystallographyDensity functional calculationschemistryFerromagnetismCounterionCopperMonoclinic crystal system
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Synthesis of porous indium phosphide with nickel oxide crystallites on the surface

2022

Y. Suchikova, S. Kovachov, I. Bohdanov, І. Bardus show their appreciation to the Ministry of Education and Science of Ukraine for its support, in particular: grant 0122U000129 “Search for Optimal Conditions for the Synthesis of Nanostructures on the Surface of Semiconductors A3B5, A2B6 and Silicon for Photonics and Solar Energy,” and grant 0121U109426 “Theoretical and Methodological Principles of Systemic Fundamentalization of Intended Specialist Training in the Field of Nanophase Materials Science for Productive Professional Activity”.

EDX spectrumcoating:NATURAL SCIENCES::Physics [Research Subject Categories]annealingelectrochemical etchingNickel oxalate
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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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Face-selective adhesion of calcium oxalate dihydrate crystals to renal epithelial cells

1996

The interaction between the most common urinary crystal, calcium oxalate dihydrate (COD) and the surface of monkey renal epithelial cells of the BSC-1 line was investigated. The [100] face of exogenous COD crystals bound selectively and rapidly to the kidney cell surface. Cellular processes extended preferentially over the [100] face initially, and then progressively covered the crystal so that by 24 hours some crystals were observed beneath the plasma membrane. When nucleated from solution onto the surface of the cell monolayer, COD crystals oriented preferentially so that their [100] faces were in direct contact with the cell surface. In contrast, when siliconized glass was used as a subs…

Endocrinology Diabetes and MetabolismCrystallography X-RayKidneyEpitheliumCell LineCrystalKidney CalculiEndocrinologyChlorocebus aethiopsMonolayerCell AdhesionAnimalsOrthopedics and Sports MedicineKidney Tubules CollectingCalcium OxalateChemistryCell MembraneSubstrate (chemistry)AdhesionMolecular arrayKidney cellModels StructuralCrystallographyMembraneMicroscopy Electron ScanningCalcium oxalate dihydrate crystalsCrystallizationCalcified Tissue International
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The Preparation and Characterization of New Antazoline Salts with Dicarboxylic Acids

2015

New antazoline salts with organic acids (fumaric acid, oxalic acid, and maleic acid) were prepared. The effect of the crystallization solvent and mechanochemical treatment on the crystalline forms of these salts was studied. Two polymorphs of antazoline hydrogen maleate were identified and their relative stability was determined. The molecular structures of antazoline hydrogen oxalate and antazoline hydrogen maleate showed differences in antazoline cation conformation. In crystal structures of all salts both imidazoline nitrogens of antazoline cation are involved in hydrogen bond formation with carboxyl groups of the acid.

Fumaric acidMaleic acidHydrogen bondOxalic acidGeneral ChemistryCondensed Matter PhysicsOxalateSolventchemistry.chemical_compoundchemistryPolymorphism (materials science)Polymer chemistryAntazolinemedicineOrganic chemistryGeneral Materials Sciencemedicine.drugMolecular Crystals and Liquid Crystals
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Bis(glycylglycinium) oxalate at 100 K.

2003

The structure of the title compound, 2C(4)H(9)N(2)O(3)(+).C(2)O(4)(2-), which has been determined by X-ray diffraction, contains discrete glycylglycine (HGly-Gly)(+) cations in general positions and oxalate anions which lie across centres of inversion. Although the geometry of the (HGly-Gly)(+) cation is not significantly different compared with other structures containing this residue, a few changes in conformation are observed which indicate the presence of molecular interactions. The molecular network in the crystal consists of one nearly linear O-H...O, five N-H...O and two weak C-H.O hydrogen bonds.

GlycylglycineOxalatesbiologyMolecular StructureHydrogen bondStereochemistryGlycylglycineMolecular ConformationHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyOxalateCrystalCold Temperaturechemistry.chemical_compoundCrystallographychemistryCationsbiology.proteinMoleculeCarboxylateOrganic anionActa crystallographica. Section C, Crystal structure communications
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Chromium(III) complexes with 2-(2′-pyridyl)imidazole: Synthesis, crystal structure and magnetic properties

2011

Abstract The preparation, crystal structure and variable temperature-magnetic investigation of three 2-(2′-pyridyl)imidazole-containing chromium(III) complexes of formula PPh4[Cr(pyim)(C2O4)2]·H2O (1), AsPh4[Cr(pyim)(C2O4)2]·H2O (2) and [Cr2(pyim)2(C2O4)2(OH2)2]·2pyim · 6H2O (3) [pyim = 2-(2′-pyridyl)imidazole, C 2 O 4 2 - = dianion of oxalic acid , PPh 4 + = tetraphenylphosphonium cation and AsPh 4 + = tetraphenylarsonium cation ] are reported herein. The isomorphous compounds are made up of discrete [Cr(pyim)(C2O4)2]− anions, XPh 4 + cations [X = P (1) and As (2)] and uncoordinated water molecules. The chromium environment in 1 and 2 is distorted octahedral with Cr–N and Cr–O bond distanc…

Hydrogen bondStereochemistrychemistry.chemical_elementCrystal structureMagnetic susceptibilityOxalateInorganic Chemistrychemistry.chemical_compoundChromiumCrystallographychemistryIntramolecular forceMaterials ChemistryImidazoleMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu 2 IM](HC 2 O 4 ) as CO 2 shuttle

2017

International audience; This manuscript describes the using of biosourced L-valine, oxalic acid and glyoxal to produce a biobased imidazolium hydrogen oxalate [iBu(2)IM](HC2O4) which is converted to its related hydrogen carbonate salt by a simple electrolysis without using strong base. The addition of weak protic acids to the latter compound leads to a rapid and quantitative CO2 release with formation of the starting hydrogen oxalate salt or a new halide free bio-based ionic liquid [iBu(2)IM](AcO) which is able to adsorb reversibly the CO2 at room temperature. The protonation reactions, combined with electrolysis, could then be a promising alternative solution for storage and transport of C…

HydrogenOxalic acidInorganic chemistryHalideSalt (chemistry)chemistry.chemical_elementProtonation010402 general chemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesOxalatelaw.inventionefficientionic liquidschemistry.chemical_compoundlawstabilized phosphenium adductsEnvironmental Chemistry[CHIM]Chemical Scienceselectrochemical reductioncaptureacidsmethanolchemistry.chemical_classificationElectrolysis010405 organic chemistrycrystal-structurePollution0104 chemical scienceschemistrydimethyl-sulfoxideIonic liquid
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Characterization of a new, nonpathogenic mutant of Botrytis cinerea with impaired plant colonization capacity.

2006

International audience; Botrytis cinerea is a necrotrophic pathogen that attacks more than 200 plant species.Here, the nonpathogenic mutant A336, obtained via insertional mutagenesis, was characterized.Mutant A336 was nonpathogenic on leaves and fruits, on intact and wounded tissue, while still able to penetrate the host plant. It grew normally in vitro on rich media but its conidiation pattern was altered. The mutant did not produce oxalic acid and exhibited a modified regulation of the production of some secreted proteins (acid protease 1 and endopolygalacturonase 1). Culture filtrates of the mutant triggered an important oxidative burst in grapevine ( Vitis vinifera ) suspension cells, a…

Hypersensitive responsehypersensitive responsePhysiology[SDV]Life Sciences [q-bio]colonisationMutantArabidopsisConidiationPlant ScienceMicrobiologyInsertional mutagenesisFungal Proteins03 medical and health sciencesPlasmidGene Expression Regulation FungalOnionsBotrytis cinerea; endopolygalacturonase BcPG1; hypersensitive responseVitismutantoxidative burstPathogenGene030304 developmental biologyBotrytis cinereaPhaseolus0303 health sciencesoxalateendopolygalacturonase BcPG1biology030306 microbiologyOxalic Acidfungifood and beveragesHydrogen-Ion Concentrationbiology.organism_classificationImmunity Innatenonpathogenic mutantEnzymesPlant LeavesMutagenesis Insertionalnonaspartyl acid protease ACP1Mutationbotrytis cinerea;endopolygalacturonase BcPG1;hypersensitive response;nonaspartyl acid protease ACP1;nonpathogenic mutant;oxalate;oxidative burstBotrytisbotrytis cinereaReactive Oxygen SpeciesThe New phytologist
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