Search results for "Ammonium Cation"

showing 9 items of 9 documents

Chemical speciation of nucleotide 5′-monophosphates in the presence of biogenic amines

2001

The interaction of adenosine-, uridine-, inosine- and guanosine-5’-monophosphates with protonated ethylenediamine, putrescine, cadaverine, spermidine and spermine, was studied potentiometrically, a...

CadaverineChemical Health and SafetyStereochemistryHealth Toxicology and MutagenesisSpermineEthylenediamineToxicologyMedicinal chemistryBiogenic PolyaminesUridineSpermidinechemistry.chemical_compoundchemistrynucleotide 5′-monophosphates; biogenic polyamines; nucleotide 5′-monophosphate-polyammonium cation complexes; speciationmedicinePutrescineInosinemedicine.drug
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Tetraalkylammonium Cations Conduction through a Single Nanofluidic Diode: Experimental and Theoretical Studies

2017

[EN] We describe experimentally and theoretically the concentration-dependent conduction of tetraalkylammonium (TAA+) cations through a nanofluidic diode fabricated in a polymer membrane via asymmetric track-etching techniques. This single-pore membrane exhibits current rectification characteristics because of the ionized carboxylate groups on the pore surface. We use aqueous solutions of potassium (K+ ), ammonium (A+ ), tetramethylammonium (TMA+ ), tetraethylammonium (TEA+ ), and tetrabutylammonium (TBA+ ) ions with concentrations ranging from 50 to 500 mM under acidic (pH 3.5) and physiological (pH 6.5) conditions. Compared with the K+ and A+ ions, the TMA+ , TEA+ , and TBA+ ions show rel…

General Chemical EngineeringInorganic chemistryAnalytical chemistry02 engineering and technology010402 general chemistry01 natural sciencesIonchemistry.chemical_compoundAdsorptionElectrochemistryNernst-Planck equationCarboxylateSurface chargeAlkylTetraalkyammonium cationsTetramethylammoniumchemistry.chemical_classificationAqueous solutionBiomimetic nanoporeCurrent rectification021001 nanoscience & nanotechnology0104 chemical sciencesMembraneNanofluidic diodechemistryFISICA APLICADA0210 nano-technology
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A novel supramolecular assembly in an iron(III) compound exhibiting magnetic ordering at 70 K

2004

Ethyl-substituted ammonium cation allows the preparation of an unprecedented oxo- and oxalato-bridged supramolecular three-dimensional network. The compound exhibits magnetic ordering with Tc = 70 K due to a weak spin canting. Julve Olcina, Miguel, Miguel.Julve@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es

Materials scienceMagneticUNESCO::QUÍMICAIronMetals and AlloysSupramolecular chemistryNanotechnologyGeneral ChemistryUNESCO::QUÍMICA::Química macromolecular:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSupramolecular assemblyNovel ; Iron ; Magnetic ; SupramolecularCrystallographySupramolecularMaterials ChemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]Ammonium CationNovelSpin canting
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Binding of fluoride and carbonate by open chain polyammonium cations

2004

The formation of open chain polyammonium cation-fluoride and -carbonate complexes was studied by potentiometric and calorimetric techniques at t=25 degrees C. Several species of H(i)AL (A=amine; L=F(-), CO(3)(2-)) are formed in both systems with a mean stability log K=1.0zeta (zeta=|z(anion)xz(cation)|) and log K=2.0zeta for fluoride and carbonate, respectively. The comparison with analogous systems (chloride and acetate for fluoride and hydrogenphosphate, sulfate and malonate for carbonate) showed that fluoride and carbonate form the most stable species with open chain polyammonium cations, among low molecular weight anions. The N-alkyl substitution does not play negligible role in the sta…

Open chain polyammonium cationCarbonatePotentiometric titrationInorganic chemistryComplex formationCalorimetryThermodynamic parametersMedicinal chemistryChlorideAnalytical Chemistrychemistry.chemical_compoundMalonatechemistryPotentiometrymedicineCarbonateSettore CHIM/01 - Chimica AnaliticaAmmoniumAmine gas treatingSulfateFluorideFluorideAnion coordination chemistrymedicine.drugTalanta
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Dependence of the distortion of the square pyramids in N,N-dimethylethylenediammonium pentachloroantimonate(III) on the geometry of hydrogen bonds

2001

Abstract N ,N-Dimethylethylenediammonium pentachloroantimonate(III) crystallizes in the monoclinic system, in space group P21/c (a = 12.460(2), b = 10.252(2), c = 10.330(2) Å, β = 97.75(3)°, V = 1307.5(4) Å3, Z = 4, dc = 1.997, dm = 1.99(2) g/cm3). The crystal structure of [(CH3)2NH(CH2)2NH3][SbCl5] consists of isolated [SbCl5]2- anions and [(CH3)2NH(CH2)2NH3]2+ cations. The [SbCl5]2- anion has a distorted square pyramidal geometry, presenting one short axial and four long equatorial Sb-Cl bonds. The square pyramids are characteristically stacked one close to the other, parallel to the c axis. The voids between the anionic sublattice are filled by [(CH3)2NH(CH2)2NH3]2+ cations. The five non…

chloroantimonate(III)CrystallographyHydrogen bondChemistryDistortionN-dimethylethylenediammonium cationGeneral ChemistryNMolecular physicsSquare (algebra)Zeitschrift Fur Naturforschung Section B = A Journal of Chemical Sciences
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Phase transitions and distortion of [BiCl6]3– octahedra in (C3H5NH3)3[BiCl6] – DSC and single-crystal X-Ray diffraction studies

2004

The DSC diagram of tris(allylammonium) hexachlorobismuthate(III), (C3H5NH3)3[BiCl6], revealed three anomalies at 152, 191 and 299 K. The structure of the salt was determined at 200 and 315 K, below and above the high-temperature phase transition at 299 K. In both phases the crystals are monoclinic. At 200 K the space group is C2/c whereas at 315 K it is C2/m. The structures, at both temperatures, are composed of [BiCl6]3− octahedra and allylammonium cations. The organic and inorganic moieties are attracted to each other by a network of the N-H. . .Cl hydrogen bonds. The relationship between corresponding parameters of the unit cells has been found. The phase transition at 299 K, of the orde…

chlorobismuthates(III)phase transitionallylammonium cationdisorderoctahedral distortionZeitschrift Fur Naturforschung Section B = A Journal of Chemical Sciences
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Crystal structure of the bis(cyclohexylammonium) succinate succinic acid salt adduct

2015

The title salt adduct comprises two cyclo­hexyl­ammonium cations, one succinate anion and one mol­ecule of succinic acid, linked together through inter­molecular hydrogen-bonding inter­actions giving a two-dimensional layer-like self-assembly lying parallel to (010).

crystal structureDenticityStereochemistryCyclohexane conformationSalt (chemistry)cyclo­hexyl­ammonium cationCrystal structureMedicinal chemistryResearch CommunicationsAdductchemistry.chemical_compoundsuccinic acidGeneral Materials Sciencecyclohexylammonium cationchemistry.chemical_classificationCrystallographymolecular adductHydrogen bondChemistryGeneral ChemistryCondensed Matter PhysicssuccinateAmmonium SuccinateSuccinic acidQD901-999hydrogen bondsorganic saltmol­ecular adductActa Crystallographica Section E: Crystallographic Communications
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Preparation, crystal structure at 298 and 90 K and phase transition in (C2H5NH3) 2[SbBr5] studied by the single crystal X-Ray diffraction method

2004

The reaction of antimony(III) oxide with ethylamine, in molar ratios from 1:1 to 1:10, in concentrated hydrobromic acid leads to the formation of one product – bis(ethylammonium) pentabromoantimonate(III). The structure of (C2H5NH3)2[SbBr5] was determined at 298 and 90 K, below and above the phase transition that occurs at about 158.5 K. The orthorhombic system was found in both phases, space groups Cmca and Pbca at 298 and 90 K, respectively. At both temperatures the structure consists of [SbBr6] 3− octahedra connected via cis bromine atoms forming one-dimensional zig-zag [{SbBr5}2−]n chains. The ethylammonium cations fill the space between polyanionic chains. The organic and inorganic sub…

phase transitionbromoantimonates(III)octahedral distortionethylammonium cationZeitschrift Fur Naturforschung Section B = A Journal of Chemical Sciences
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Two new organic-selenate salts: syntheses and crystal structures of bis(di-iso-propylammonium) selenate and di-n-butylammonium hydrogenoselenate

2017

Abstract Two new dialkyammonium selenate salts [i-Pr2NH2]2[SeO4] (1) and [n-Bu2NH2][HSeO4] (2) have been isolated and characterized by single-crystal X-ray diffraction. Salt 1 crystallizes in the monoclinic system, space group P21/n with a=8.7190(5), b=8.8500(4), c=22.5953(9) Å, β=94.6290(17)°, V=1737.84(14) Å3 and Z=4. Salt 2 crystallizes in the monoclinic system space group P21/n with a=10.9328(9), b=8.1700(6), c=13.8095(11) Å, β=97.130(3)°, V=1223.94(17) Å3 and Z=4. In both salts, dialkylammonium cations and selenate anions are connected through NH···O and OH···O hydrogen bonds. In the crystal structure, 1 and 2 are organized in layer-like arrangements. Structural characterizations were …

spectroscopyGeneral ChemistryCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesSelenatedialkylammonium cation[ CHIM ] Chemical Scienceshydrogen bonding networkNMR0104 chemical sciencesCrystallographychemistry.chemical_compoundchemistryX-ray crystallographyorganic-selenate salt[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSX-ray crystallography
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