Search results for "Oxalate"

showing 10 items of 215 documents

Solid Contact Potentiometric Sensors Based on a New Class of Ionic Liquids on Thiacalixarene Platform

2018

New solid-contact potentiometric sensors have been developed for hydrogen phosphate recognition on the basis of ionic liquids containing tetrasubstituted derivatives of thiacalix[4]arene in cone and 1,3-alternate conformations with trimethyl- and triethylammonium fragments at the lower rim substituents. The recognition of selected anions including carbonate, hydrogen phosphate, perchlorate, oxalate, picrate, and EDTA was conducted using electrochemical impedance spectroscopy with ferricyanide redox probe. For the potentiometric sensor assembling, the ionic liquids were stabilized by multiwalled carbon nanotubes and carbon black deposited on the glassy carbon electrode. The influence of supp…

PicratePotentiometric titrationInorganic chemistry02 engineering and technology01 natural sciencesOxalatelcsh:Chemistrychemistry.chemical_compoundPerchloratePotentiometric sensorThiacalixareneOriginal Researchionic liquidsolid-contact potentiometric sensorcarbon nanotubes010401 analytical chemistrythiacalix[4]areneGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistryphosphate determinationchemistrylcsh:QD1-999Ionic liquidFerricyanide0210 nano-technologyFrontiers in Chemistry
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A novel oxalate-based three-dimensional coordination polymer showing magnetic ordering and high proton conductivity

2017

A novel three-dimensional (3D) coordination polymer with the formula (C3N2H5)4[MnCr2(ox)6]·5H2O (2), where ox = oxalate and C3N2H5 = imidazolium cation, is reported. Single crystal X-ray diffraction reveals that this porous coordination polymer adopts a chiral three-dimensional quartz-like architecture, with the guest imidazolium cations and water molecules being hosted in its pores. This novel multifunctional material exhibits both a ferromagnetic ordering at TC = 3.0 K, related to the host MnCr2 network, and high proton conductivity [1.86 × 10−3 S cm−1 at 295 K and 88% relative humidity (RH)] due to the presence of the acidic imidazolium cations and free water molecules. The similarity of…

ProtonChemistryCoordination polymerInorganic chemistry02 engineering and technologyConductivity010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxalate0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundFerromagnetismMolecule[CHIM]Chemical SciencesAmmonium0210 nano-technologySingle crystalComputingMilieux_MISCELLANEOUS
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Post-elution processing of 44Ti/44Sc generator-derived 44Sc for clinical application

2009

The (44)Ti/(44)Sc (T(1/2)(44)Ti=60a) generator provides cyclotron-independent access to positron-emitting (44)Sc (T(1/2)=3.97d) for PET imaging. This work aims to post-elution processing of initial (44)Sc generator eluates in order to reduce its volume, HCl concentration and remove the oxalate anions. The on-line adsorption of (44)Sc on cationic resin AG 50W-X8 (200-400 mesh, H(+)-form) is achieved with >98% efficacy. Subsequently, the purified (44)Sc is desorbed by using 3ml of 0.25M ammonium acetate (pH=4.0). The post-processing takes 10min. The overall yield of the post-processing reached 90%, which is referred to the (44)Sc obtained from the (44)Ti/(44)Sc generator. In addition to the c…

RadioisotopesTitaniumRadiationElutionIon chromatographyAnalytical chemistryCationic polymerizationchemistry.chemical_elementOxalatechemistry.chemical_compoundAdsorptionchemistryIsotope LabelingPositron-Emission TomographyYield (chemistry)ScandiumRadiopharmaceuticalsScandiumAmmonium acetateNuclear chemistryApplied Radiation and Isotopes
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Reactivity of β-amino alcohols against dialkyl oxalate: synthesis and mechanism study in the formation of substituted oxalamide and/or morpholine-2,3…

2012

The reactivity of various β-amino alcohols with dialkyl oxalates, in several reaction conditions, has been investigated. Linear disubstituted oxalamides were obtained with primary β-amino alcohols and linear tetrasubstituted oxalamides, or a mixture of linear tetrasubstituted oxalamides and cyclic morpholine-2,3-diones were obtained with N-substituted β-amino alcohols. A DFT study of the possible mechanism has been made. The theoretical results indicate that these reactions are not kinetically controlled, there is an equilibrium between all species and therefore follow a thermodynamic control. The different behavior between the primary β-amino alcohols and N-methyl β-amino alcohols is due t…

Reaction conditionschemistry.chemical_compoundPrimary (chemistry)ChemistryMorpholineOrganic ChemistryDrug DiscoveryPolymer chemistryOxalate synthesisReactivity (chemistry)BiochemistryMedicinal chemistryTetrahedron
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1,2,4-Triazole Schiff base directed synthesis of polynuclear iron complexes: Investigating the magnetic properties going from a dimer to a 1D chain t…

2018

Abstract Based on two functionalized Schiff base ligands 4-(1H-imidazol-5-ylmethylene-amino)-4H-1,2,4-triazole (imztrz) and 4-(p-tolylidene-amino)-4H-1,2,4-triazole (toltrz), a series of three triazole based polynuclear Fe complexes has been prepared. Compounds {[FeII(toltrz)2(C2O4)]·10H2O}n (1) and {[FeII(5-imztrz)(C2O4)]·2H2O}n (2) are oxalate bridged FeII complexes with 1 showing a linear 1D chain structure and 2 exhibiting a zigzag chain based 3D interpenetrating framework. Both structures show rather big voids in the 3D architecture (∼15% of the crystal volume). Compound (5-imztrzH)2[FeIII2(cit4−)2(H2O)2]·6H2O (3) is a binuclear FeIII complex bridging by two citrate ligands to form a f…

Schiff base010405 organic chemistryDimerExchange interactionTriazole124-Triazole010402 general chemistry01 natural sciencesMagnetic susceptibilityOxalate0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryPolyhedron
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Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts

2012

[EN] Ni-Sn-O mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500 degrees C for 2 h. These materials have been characterized by several techniques (N-2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and O-18/O-16 isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80-90%). Thus, high selectivity to et…

SnO2-promotedInorganic chemistrychemistry.chemical_elementInfrared spectroscopyTin oxideCatalysisOxalateCatalysisEthane ODHNiO catalystsEthane oxidationchemistry.chemical_compoundNickelEthyleneTin oxidechemistryDehydrogenationPhysical and Theoretical ChemistryTemperature-programmed reductionTinOxidative dehydrogenation of ethaneNickel oxideCatalyst characterization (XPS HREM oxygen isotope exchange FTIR CO adsorbed)
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Charge transfer salts of tetrathiafulvalene derivatives with magnetic iron(III) oxalate complexes: [TTF]7[Fe(ox)3]2·4H2O, [TTF]5[Fe2(ox)5]·2PhMe·2H2O…

2000

Three novel TTF (tetrathiafulvalene) and TMTTF (tetramethyltetrathiafulvalene) radical salts of monomeric and dimeric iron(III) oxalate magnetic complexes, [TTF]7[Fe(ox)3]2·4H2O 1, [TTF]5[Fe2(ox)5]·2PhMe·2H2O 2 and [TMTTF]4[Fe2(ox)5]·PhCN·4H2O 3, have been synthesized, and their structures and physical properties investigated. The structures for these semiconducting salts feature monodimensional stackings of the radical cations interleaved by the complexes [Fe(ox)3]3− and [Fe2(ox)5]4−, and solvent molecules. For the novel dinuclear complex [Fe2(ox)5]4− antiferromagnetic exchange between the two iron atoms through the oxalate bridge was found.

SolventCrystallographychemistry.chemical_compoundMonomerchemistryInorganic chemistryAntiferromagnetismMoleculeCharge (physics)General ChemistryOxalateTetrathiafulvaleneJournal of the Chemical Society, Dalton Transactions
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CCDC 1835271: 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

Space GroupCrystallography14-diazabicyclo[2.2.2]octane-14-di-ium bromide hydrogen oxalateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1491387: Experimental Crystal Structure Determination

2016

Related Article: M.B. Diop, L. Diop, L. Plasseraud, H. Cattey|2016|Acta Crystallogr.,Sect.E:Cryst.Commun.|72|1113|doi:10.1107/S2056989016011038

Space GroupCrystallography2-methyl-1H-imidazol-3-ium hydrogen oxalate dihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1402187: Experimental Crystal Structure Determination

2015

Related Article: Georges Mouchaham, Marion Gualino, Nans Roques, Carine Duhayon, Stéphane Brandès, Jean-Pascal Sutter|2015|CrystEngComm|17|8906|doi:10.1039/C5CE01070E

Space GroupCrystallography4-{3-(pyridinium-4-yloxy)-22-bis[(pyridinium-4-yloxy)methyl]propoxy}pyridinium bis(oxalate) pentahydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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