Search results for "Ammonium iodide"

showing 10 items of 12 documents

Para-Localization Energy (Free-Electron Molecular-Orbital Method) and Polarographic Half-Wave Potentials of some Polynuclear Hydrocarbons

1957

POLYNUCLEAR aromatic hydrocarbons in 75 per cent dioxane solution which contains 0.175 M tetrabutyl ammonium iodide are reducible in the dropping mercury electrode1. As shown by the corresponding polarograms, it is a two-electron addition step process, and it is similar to the reduction of these compounds by alkali metals or their amalgams and alcohol2, a fact which can be easily explained.

Free electron modelPolarographychemistry.chemical_compoundMultidisciplinarychemistryInorganic chemistrychemistry.chemical_elementMolecular orbitalHalf waveAlkali metalAmmonium iodideMercury (element)Nature
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Deuteron NMR investigations of glass and phase transitions in(KI)1−x(ND4I)xmixed crystals

1998

Powdered potassium ammonium iodide mixed crystals with ammonium concentrations of 20% and 70% have been studied using deuteron NMR techniques. For the less doped sample the deuteron line starts to broaden and the spin-lattice relaxation time ${T}_{1}$ becomes nonexponential below about 20 K. These observations indicate the breakdown of ergodicity and the onset of orientational glass freezing. At the lowest temperatures ${T}_{1}$ reaches a plateau value. For the 70% sample a relatively abrupt onset of two-phase behavior at $Tl35\mathrm{K}$ is inferred from measurements of the spin-spin and spin-lattice relaxation times. These observations are taken to indicate an order-disorder transition to…

Phase transitionMaterials scienceCondensed matter physicsRelaxation (NMR)DopingAnalytical chemistryAmmonium iodidechemistry.chemical_compoundDeuteriumchemistryLattice (order)Condensed Matter::Strongly Correlated ElectronsAmmoniumOrientational glassPhysical Review B
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CCDC 244862: Experimental Crystal Structure Determination

2005

Related Article: S.Busi, M.Lahtinen, H.Mansikkamaki, J.Valkonen, K.Rissanen|2005|J.Solid State Chem.|178|1722|doi:10.1016/j.jssc.2005.03.008

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersDiethyl-di-n-butylammonium iodideExperimental 3D Coordinates
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CCDC 692125: Experimental Crystal Structure Determination

2008

Related Article: M.Albrecht, C.Wessel, M.de Groot, K.Rissanen, A.Luchow|2008|J.Am.Chem.Soc.|130|4600|doi:10.1021/ja800219g

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterspentafluorophenyl(propan-2-ylidene)ammonium iodideExperimental 3D Coordinates
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CCDC 1005288: Experimental Crystal Structure Determination

2014

Related Article: Michael Giese, Markus Albrecht, Arto Valkonen, Kari Rissanen|2015|Chemical Science|6|354|doi:10.1039/C4SC02762K

Space GroupCrystallographyCrystal SystemCrystal StructureN-(Pentafluorobenzyl)triethylammonium iodideCell ParametersExperimental 3D Coordinates
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CCDC 244864: Experimental Crystal Structure Determination

2005

Related Article: S.Busi, M.Lahtinen, H.Mansikkamaki, J.Valkonen, K.Rissanen|2005|J.Solid State Chem.|178|1722|doi:10.1016/j.jssc.2005.03.008

Space GroupCrystallographyCrystal SystemDiethyl-di-n-propylammonium iodideCrystal StructureCell ParametersExperimental 3D Coordinates
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Quantum correlations in generalized spin star system

2006

The problem of detecting quantum signatures in the correlations formed in dynamical evolution of quantum bipartite systems receives a lot of attention in current literature. Generally speaking, the occurrence of correlations between two observables of a system does not necessarily reflect nonclassical behaviour. In this paper, the exact dynamics of a pair of uncoupled spins 1/2 interacting with a common spin 1/2 bath is investigated. Starting from a separable initial condition, the ability of the system to develop purely quantum correlations is brought to light. Physical interpretation of the concurrence function as well as a suggestion on how to measure it are given.

Statistics and ProbabilityPhysicsDISSOCIATION-CONSTANTSQuantum discordQuantum dynamicsTETRAETHYLAMMONIUM IODIDEStatistical and Nonlinear PhysicsObservable25 DEGREES CSODIUM-CHLORIDEHEAT-CAPACITIESIONIC-STRENGTH DEPENDENCEMOLECULAR-WEIGHTQuantum mechanicsQuantum processQuantum operationQuantum algorithmACTIVITY-COEFFICIENTSIONIZATION-CONSTANTQuantumCOMPLEX-FORMATIONMathematical PhysicsSpin-½
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Acid−Base Properties of Synthetic and Natural Polyelectrolytes: Experimental Results and Models for the Dependence on Different Aqueous Media

2008

Protonation constants of several natural and synthetic humates and fulvates were determined by ISE-H+ potentiometry in different ionic media (alkali metal halides and tetraethylammonium iodide) at different ionic strengths and T ) 298.15 K. Experimental data obtained in previous studies of different synthetic (polyacrylates, polymethacrylates, polyacrylate-co-maleate) and naturally occurring (alginate, humic substances) polycarboxylates were also taken into account in the general analysis of acid-base properties of polyelectrolytes. Protonation constants were expressed as a function of the dissociation degree (R) using three models, namely, a simple linear model, the Ho¨gfeldt three-paramet…

acid-base properiteAcrylate polymerdiprotic-like modelTetraethylammonium iodideGeneral Chemical EngineeringInorganic chemistryHalideIonic bondingProtonationGeneral ChemistryUronic acidAlkali metalPolyelectrolytethermodynamicchemistry.chemical_compoundchemistrySettore CHIM/01 - Chimica AnaliticapolyelectrolyteJournal of Chemical & Engineering Data
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The Synergetic Interplay of Weak Interactions in the Ion-Pair Recognition of Quaternary and Diquaternary Ammonium Salts by Halogenated Resorcinarenes

2013

The influence of halogens on the noncovalent interactions of different upper-rim-substituted hexylresorcinarenes with quaternary and diquaternary ammonium iodide salts was investigated in the gas phase by electrospray ionization Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometry and in solution by 1H NMR titration studies. The electronic nature of the substituents on the upper rim of the resorcinarene was directly reflected in the order of binding strengths of the hosts towards quaternary and diquaternary ammonium cations in the gas phase. In solution, the opposite trend was observed, with generally higher binding constants for the diquaternary over the quaternary salts…

chemistry.chemical_classificationHydrogen bondElectrospray ionizationOrganic ChemistryInorganic chemistryResorcinareneAmmonium iodidechemistry.chemical_compoundchemistryComputational chemistryHalogenProton NMRNon-covalent interactionsAmmoniumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Salt effects on the protonation of l-histidine and l-aspartic acid: a complex formation model

1991

Abstract Protonation constants of l -histidine (histidinate: his − ) and l -aspartic acid (aspartate: asp 2− ) were determined potentiometrically, using the (H + ) glass electrode, in aqueous tetraethylammonium iodide (Et 4 NI), calcium chloride and sodium chloride solutions, at 0 −3 and 10 ⩽, T ⩽, 45 ° C. Differences in protonation constants determined in different salt media were explained by a complex formation model and, according to this model, the presence of the following species was hypothesized: Ca(his) + , CaH(his) 2+ , CaH 2 (his) 3+ Na(his) 0 , H 3 (his)X + , H 2 (his)X 0 , Et 4 N(his) 0 , Et 4 NH(his) + , Ca(asp) 0 , CaH(asp) + , CaH 2 (asp) 2+ , Na(asp) − , NaH(asp) 0 , H 3 (a…

chemistry.chemical_classificationTetraethylammonium iodideAqueous solutionendocrine system diseasesSodiumInorganic chemistrychemistry.chemical_elementProtonationCondensed Matter PhysicsMedicinal chemistrychemistry.chemical_compoundDicarboxylic acidchemistryIonic strengthAspartic acidPhysical and Theoretical ChemistryInstrumentationHistidineThermochimica Acta
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