Search results for "bonding"

showing 10 items of 996 documents

Bis(5-tert-butyl-2-hydroxy-3-methylbenzyl)(6-hydroxyhexyl)ammonium chloride monohydrate, an anion receptor complex

2007

In the title compound, C(30)H(48)NO(3)(+) x Cl(-) x H(2)O, the cation acts with a water molecule as a chloride ion receptor. The chloride ion forms three strong intramolecular hydrogen bonds. The water molecule forms both an intramolecular bridge between one phenol H atom and the chloride ion, and an intermolecular link to the aliphatic alcohol O atom. Weak intermolecular C-H...Cl and C-H ...O hydrogen bonds provide additional packing interactions.

AnionsModels Molecularinorganic chemicalsBenzylaminesStereochemistryChemistryHydrogen bondIntermolecular forceHydrogen BondingGeneral MedicineCrystallography X-RayChlorideMedicinal chemistryAmmonium ChlorideGeneral Biochemistry Genetics and Molecular BiologyIonchemistry.chemical_compoundIntramolecular forcemedicineMoleculePhenolAmmonium chloridemedicine.drugActa Crystallographica Section C Crystal Structure Communications
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Conductance of potassium halides near the temperature of maximum density of water

1981

The conductances of dilute aqueous solutions of KCl, KBr, and KI have been measured over the temperature range 2 to 8°C and have been analyzed by the Fuoss-Hsia equation. The ionic Walden products at infinite dilution have been discussed in terms of local viscosity. The temperature dependence of these products suggest that near the temperature of maximum density of water, the structure-breaking ability of these ions changes in a regular way.

Aqueous solutionChemistryBiophysicsAnalytical chemistryIonic bondingHalideConductanceAtmospheric temperature rangeBiochemistryDilutionViscosityMaximum densityPhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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On the Creeping of Saturated Salt Solutions

2013

Creeping is a well-known but annoying phenomenon in the preparation of crystals from solution, where growing crystallites gradually extend up the walls of the growth vessel. In this process, solution is transported toward the tip of the creeping crystallites, where solvent evaporation takes place and solid material is deposited. In this study, the growth of crystal aggregates extending from evaporating droplets of saturated aqueous solutions of ionic salts, placed on different substrate materials, has been investigated using optical microscopy. It is shown that the rate determining step of the crystallization process is the evaporation of solution, following Fick’s laws. Fresh solution, nec…

Aqueous solutionChemistryEvaporationIonic bondingGeneral ChemistrySubstrate (electronics)Solid State ChemistryCondensed Matter Physicslaw.inventionCrystalCrystallographyChemical engineeringOptical microscopelawGeneral Materials ScienceCrystalliteCrystallizationCrystal Growth & Design
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Speciation of Organic Matter in Natural Waters-interaction of polyacrylates and polymethacrylates with major cation components of seawater

2004

Abstract The speciation of some high molecular weight polycarboxylates was studied in different ionic media. Polyacrylates here investigated ( W =2.0, 5.1 and 20.0 kDa) form weak species with alkali metal cations ( K =10 2 mol l −1 , t =25 °C, I =0 mol l −1 ) and quite stable complexes with alkaline earth metal cations ( K >10 6 mol l −1 , t =25 °C, I =0 mol l −1 ). Results are reported from experiments performed in a multicomponent electrolyte solution simulating the major composition of seawater (artificial seawater). Protonation constants in this medium are expressed as a polynomial function of S 1/2 ( S =salinity) and the sharp lowering with respect to values obtained in non-interacting…

Aqueous solutionChemistryInorganic chemistryIonic bondingArtificial seawaterProtonationGeneral ChemistryElectrolyteOceanographyAlkali metalDissociation (chemistry)Environmental ChemistrySeawaterWater Science and Technology
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The interaction of amino acids with the major constituents of natural waters at different ionic strengths

2000

Abstract The interaction of amino acids with the major constituents of natural waters has been studied potentiometrically by determining protonation constants at different ionic strengths (e.g., I ≤5.6 mol (kg H 2 O) −1 (NaCl)) and in artificial seawater (containing Na + , K + , Ca 2+ , Mg 2+ , Cl − and SO 4 2− ) at different salinities. For glycine determinations in mixed NaCl–MgCl 2 , electrolyte solutions were also performed. The data included in this work, together with some already published, make it possible to calculate parameters for dependence on ionic strength using different models, i.e. an extended Debye–Huckel type equation and Pitzer equations. The results can be interpreted b…

Aqueous solutionChemistryInorganic chemistryIonic bondingArtificial seawaterProtonationGeneral ChemistryOceanographyIonic strengthStability constants of complexesEnvironmental ChemistryPitzer equationsSeawaterWater Science and Technology
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Hydrolysis of dioxouranium(VI): a calorimetric study in NaClaq and NaClO4aq, at 25°C

2004

Abstract We report the results of a calorimetric study on the hydrolysis of UO 2 2+ in different ionic media (NaClO 4 aq , NaCl aq ) at 25 °C. Experiments in NaCl were performed at different ionic strength, at I ≤1 mol l −1 . The species considered in both ionic media were UO 2 (OH) + , (UO 2 ) 2 (OH) 2 2+ and (UO 2 ) 3 (OH) 5 + , and in addition (UO 2 ) 3 (OH) 4 2+ and (UO 2 ) 3 (OH) 7 − in NaCl aq . The dependence on ionic strength of enthalpy changes in NaCl aq was expressed by the simple linear equation Δ H pq =Δ H ° pq + aI 1/2 ( a , empirical parameter). Comparison with literature findings is given and some recommended values are reported.

Aqueous solutionChemistryIonic strength dependenceEnthalpyInorganic chemistryIonic bondingCalorimetryCalorimetryCondensed Matter PhysicsSodium perchlorateUranylchemistry.chemical_compoundHydrolysisReaction enthalpyIonic strengthPhysical chemistrySettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryHydrolysis of UO22+InstrumentationThermochimica Acta
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Polyacrylate Protonation in Various Aqueous Ionic Media at Different Temperatures and Ionic Strengths

2000

The protonation constants of the polyacrylate anion (molecular mass 2000 Da) in Et4NI, Me4NCl, LiCl, LiNO3, NaCl, NaNO3, and KCl aqueous solution, were determined in a wide range of ionic strengths. A three-parameter approximation was used to express protonation constants as a function of the dissociation degree α, and their dependence on ionic strength was considered using a simple polynomial expansion. Differences in log KH between different data in different media were interpreted in terms of weak complex formation between polyacrylate and alkali metal cations. Measurements were also performed at different temperatures (15 ≤ T/°C ≤ 55) in order to calculate enthalpy and entropy changes f…

Aqueous solutionChemistryIonic strengthGeneral Chemical EngineeringEnthalpyInorganic chemistryIonic bondingProtonationGeneral ChemistryAlkali metalPolyelectrolyteIonJournal of Chemical & Engineering Data
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Protonation thermodynamics of 2,2'-bipyridyl in aqueous solution. Salt effects and weak complex formation

1993

Abstract Protonation constants of 2,2'-bipyridyl (bipy) have been determined potentiometrically, using (H + )-glass electrode, in different aqueous media (alkali and alkaline earth chlorides, tetramethylammonium chloride and tetramethylammonium iodide) at different temperatures and ionic strengths. The differences in log K H values are explained using a complex formation model. Formation thermodynamic parameters are given.

Aqueous solutionEnthalpyInorganic chemistryIonic bondingProtonationCondensed Matter PhysicsAlkali metalStandard enthalpy of formationchemistry.chemical_compoundchemistryIonic strengthTetramethylammonium chloridePhysical and Theoretical ChemistryInstrumentationThermochimica Acta
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Thermodynamic parameters for the formation of glycine complexes with magnesium(II), calcium(II), lead(II), manganese(II), cobalt(II), nickel(II), zin…

1995

Abstract Protonation constants and Mg 2+ , Ca 2+ , Pb 2+ , Mn 2+ -, Co 2+ , Ni 2+ , Cu 2+ , Zn 2+  and Cd 2+ glycine complex formation constants have been determined in different aqueous media at different temperatures. Salt effects are explained by a complex formation model which takes into account the formation of weak species. From the temperature dependence of the formation constants, thermodynamic parameters ΔH θ (and in some cases ΔC θ p ) have been obtained. A rigorous analysis of literature data, together with experimental findings, allows recommended formation parameters, in the ranges 0 ≤ I e ≤ 1 mol l −1 ( I e is the effective ionic strength) and 5°C ≤ T ≤ 45°C, to be obt…

Aqueous solutionEnthalpyInorganic chemistrychemistry.chemical_elementIonic bondingProtonationManganeseCondensed Matter PhysicsNickelchemistryStability constants of complexesIonic strengthPhysical chemistryPhysical and Theoretical ChemistryInstrumentationThermochimica Acta
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Cobalt Metal-Organic Framework Based on Layered Double Nanosheets for Enhanced Electrocatalytic Water Oxidation in Neutral Media

2020

A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that are strongly connected by intermolecular bonds has been developed. Its 3D structure is held together by π-π stacking interactions between the labile pyridine ligands of the nanosheets. In aqueous solution, the axial pyridine ligands are exchanged by water molecules, producing a delamination of the material, where the individual double nanosheets preserve their structure. The original 3D layered structure can be restored by a solvothermal process with pyridine, so that the material shows a "memory effect"during the delamination-pillarization process. Electrochemical activation of a 2D-Co-MOF@Nafi…

Aqueous solutionOxygen evolutionStackingIonic bondingchemistry.chemical_elementGeneral ChemistryCobaltQuímicaOverpotential010402 general chemistryElectrochemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryQUIMICA ORGANICAchemistryChemical engineeringPyridineQUIMICA ANALITICACobalt
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