Search results for "ionic"

showing 10 items of 2016 documents

1980

Using a bifunctional initiator such as the tetrameric dianion of α-methylstyrene for the anionic polymerization of methyl methacrylate the rate constant is found to increase with conversion approaching that observed with a monofunctional initiator while the tacticity of the polymers obtained changes from that of an almost ideally atactic to a highly syndiotactic polymer. The results are explained by the assumption of an intramolecular association of the two terminal ion pairs yielding a new active species and gradually dissociating with increasing degree of polymerization of the chain. Using a polymeric dianion of α-methylstyrene as an initiator the association phenomenon is not observed.

Kinetic chain lengthchemistry.chemical_compoundAnionic addition polymerizationBulk polymerizationChemistryPolymer chemistryPrecipitation polymerizationDegree of polymerizationMethyl methacrylatePhotochemistryIonic polymerizationLiving anionic polymerizationDie Makromolekulare Chemie
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Some kinetic effects in the polymerization of 1,3,5-trioxane

1960

Kinetic chain lengthchemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationPolymer chemistryCationic polymerizationPrecipitation polymerizationChain transferPhotochemistryIonic polymerization135-TrioxaneJournal of Polymer Science
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Ordering kinetics in synthetic Mg(Al,Fe3+)2O4 spinels: Quantitative elucidation of the whole Al-Mg-Fe partitioning, rate constants, activation energi…

2014

A novel procedure, based on the application of the kinetics simulator Gepasi, has been successfully applied for modeling the cation ordering process in two synthetic Mg(Al2-yFe3+y)O4 spinels (y~ 0.39 and 0.54, samples F39 and F54, respectively). The kinetic profiles suggested a two-stage mechanism, with rapid inter-site exchange of Fe3+ with Mg followed by slow exchange of Al with Mg. The trial to apply the classical approaches, based on the explicit solutions of the differential equations corresponding to single-cation (Sha-Chappel model) or two-cation (Müller model) exchange reactions, proved not feasible in the whole time range, thus implying a lack of information about the exchange proc…

KineticSettore GEO/06 - MineralogiaspinelChemistryKineticsCationic polymerizationMineralogyActivation energyRate equationKinetic energyintersite cation exchangeKineticsGeophysicsReaction rate constantIntersite cation exchange spinels kinetics rate constant activation energy geothermometersactivation energyGeochemistry and PetrologyIron contentintersite cation exchange; spinels; Kinetics; activation energy; geothermometerPhysical chemistryspinelsgeothermometerTime rangeSettore CHIM/02 - Chimica Fisica
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Ionic liquids and microwave irradiation as synergistic combination for polar Diels–Alder reactions using properly substituted heterocycles as dienoph…

2012

For the DA reactions between nitropyrrole derivatives and isoprene, the combination of microwave irradiation and protic ionic liquid, has a notable synergistic effect. DFT calculations suggest that a supplementary energy ranking in the IR region of 1700-1400 cm-1 can favour the structural changes in the reactants to reach the TS. Fil: Mancini, Pedro Maximo Emilio. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Departamento de Química; Argentina Fil: Ormachea, Carla. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa F…

LIQUIDOS IONICOSChemistryOrganic ChemistryCiencias QuímicasSynergistic combinationPhotochemistryBiochemistryDIELS-ALDERchemistry.chemical_compoundQuímica OrgánicaDrug DiscoveryIonic liquidMicrowave irradiationDiels alderPolarMicrowaveIsopreneCIENCIAS NATURALES Y EXACTAS
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Occurrence of (+)-6-desoxyandalusol in Stachys ionica and Stachys distans

2002

Labdanechemistry.chemical_compoundbiologychemistryBotanyStachys distansLamiaceaeStachysDiterpenebiology.organism_classificationBiochemistryEcology Evolution Behavior and SystematicsStachys ionicaBiochemical Systematics and Ecology
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Molecular organization of a water-insoluble iridium(III) complex in mixed monolayers.

2007

Abstract In this work, organized mixed monolayers containing a cationic water-insoluble iridium(III) complex, Ir-dye, [Ir(ppy)2(tmphen)]PF6, (tmphen = 3,4,7,8-tetramethyl-1,10-phenanthroline, and ppy = 2-phenylpyridine), and an anionic lipid matrix, DMPA, dimyristoyl-phosphatidic acid, with different molar proportions, were formed by the co-spreading method at the air–water interface. The presence of the dye at the interface, as well as the molecular organization of the mixed films, is deduced from surface techniques such as π – A isotherms, Brewster angle microscopy (BAM) and reflection spectroscopy. The results obtained remark the formation of an equimolar mixed film, Ir-dye/DMPA = 1:1. B…

LangmuirBrewster's angleChemistryCationic polymerizationAnalytical chemistryInfrared spectroscopychemistry.chemical_elementSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialssymbols.namesakeCrystallographyColloid and Surface ChemistryTransition metalMonolayersymbolsIridiumFourier transform infrared spectroscopyJournal of colloid and interface science
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D2/H2 adsorption selectivity on FAU zeolites at 77.4 K: Influence of Si/Al ratio and cationic composition

2018

Abstract Equilibrium D2/H2 adsorption selectivity was determined at 77.4 K below 1000 hPa for a series of FAU type zeolites X exchanged with different cations (Li+, Na+, K+, Mg2+, Ca2+, Ba2+ and Mn2+). In addition NaY, DAY (dealuminated Y) and pure silica CHA and MFI zeolites were studied. Two experimental approaches were used to determine the D2/H2 adsorption selectivity: direct determination at the thermodynamic equilibrium from manometric coadsorption experiments and calculations by Ideal Adsorbed Solution Theory (IAST) from single gas adsorption isotherms. While these two approaches are not in quantitative agreement, they reveal similar trends. At low loading (  MnX > LiX > CaX ≈ NaX > …

LangmuirThermodynamic equilibriumChemistryCationic polymerizationHigh loading02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences7. Clean energy0104 chemical sciencesAdsorption selectivity[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAdsorption13. Climate actionMechanics of MaterialsPhysical chemistry[CHIM]Chemical SciencesGeneral Materials ScienceComposition (visual arts)0210 nano-technologySelectivityComputingMilieux_MISCELLANEOUS
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Mobility of the Singly-Charged Lanthanide and Actinide Cations: Trends and Perspectives

2020

The current status of gaseous transport studies of the singly-charged lanthanide and actinide ions is reviewed in light of potential applications to superheavy ions. The measurements and calculations for the mobility of lanthanide ions in He and Ar agree well, and they are remarkably sensitive to the electronic configuration of the ion, namely, whether the outer electronic shells are 6s, 5d6s or 6s$^2$. The previous theoretical work is extended here to ions of the actinide family with zero electron orbital momentum: Ac$^+$ (7s$^2$, $^1$S), Am$^+$ (5f$^7$7s $^9$S$^\circ$), Cm$^+$ (5f$^7$7s$^2$ $^8$S$^\circ$), No$^+$ (5f$^{14}$7s $^2$S) and Lr$^+$ (5f$^{14}$7s$^2$ $^1$S). The calculations rev…

LanthanideAtomic Physics (physics.atom-ph)Ab initioFOS: Physical sciences02 engineering and technologyElectroninteraction potential010402 general chemistry7. Clean energy01 natural sciencesPhysics - Atomic PhysicsIonlcsh:Chemistryion mobilityAtomlanthanideselectronic configurationOriginal ResearchPhysicsIonic radiussuperheavy ionsactinidesGeneral ChemistryActinide021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesChemistrylcsh:QD1-999ddc:540Electron configurationAtomic physics0210 nano-technology
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Limiting transport properties of lanthanide and actinide ions in pure water

2003

Summary The limiting transport properties, i.e. the limiting ionic conductivity (λ°) and the limiting diffusion coefficient (D°), of lanthanide and actinide ions at 298.15K have been calculated by means of the microscopic version of the Stokes–Einstein law involving (i) the effective charge and the ionic radius of the ions and (ii) the ion micro-viscosity, i.e. the viscosity of the hydrated water molecules in the vicinity of the ion. The latter quantity was derived from the variation of the dynamic properties of the water molecules in the first hydration shell with the surface charge density of common mono-atomic cations of various charges. The obtained results were found to be consistent w…

LanthanideIonic radiusSolvation shellChemistryChemical physicsInorganic chemistryMoleculeIonic conductivityCharge densityPhysical and Theoretical ChemistryEffective nuclear chargeIonRadiochimica Acta
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Characterization of Flux-Grown SmxNd1–xVO4 Compounds and High-Pressure Behavior for x = 0.5

2019

The crystal structure and the vibrational and optical characteristics of flux-grown mixed lanthanide vanadate compounds SmxNd1–xVO4 (x = 0, 0.1, 0.25, 0.5, 0.75 and 1) are reported. A linear, monot...

LanthanideMaterials scienceAnalytical chemistryPHONON02 engineering and technologyCrystal structure010402 general chemistryPRVO401 natural sciencesRAMANX-RAY-DIFFRACTIONLATTICE-DYNAMICSCONTRACTIONSPECTRAVanadateEFFECTIVE IONIC-RADIICRYSTAL-STRUCTURESPhysical and Theoretical Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)X-RAY-DIFFRACTION; EFFECTIVE IONIC-RADII; CRYSTAL-STRUCTURES; LATTICE-DYNAMICS; ENERGY-TRANSFER; RAMAN; PHONON; CONTRACTION; SPECTRA; PRVO4General EnergyHigh pressure0210 nano-technologyENERGY-TRANSFERFlux (metabolism)
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