Search results for "Solvent effects"

showing 10 items of 164 documents

Static and dynamic screening effects in the electrostatic self-assembly of nano-particles.

2014

In the description of charge screening in the electrostatic self-assembly of nanoparticles (molecules) embedded into a polar solvent, the static screening effects (a contribution associated with the rapid spatial redistribution of small and highly mobile ions of a solvent) are traditionally treated phenomenologically, using the Yukawa short-range potential for describing the interaction between these particles. However, this model has a limited range of applicability being valid only for infinitely diluted systems and high salt concentrations. During a slow self-assembling process with nanoparticle formation, very dense structural elements (aggregates) are formed, in which the distances bet…

ChemistryYukawa potentialGeneral Physics and AstronomyNon-equilibrium thermodynamicsNanoparticleIonsymbols.namesakeChemical physicssymbolsPhysical chemistryMoleculeSelf-assemblyPhysical and Theoretical ChemistrySolvent effectsDebye lengthPhysical chemistry chemical physics : PCCP
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Effect of solvents on the selectivity of terbutylazine imprinted polymer sorbents used in solid-phase extraction

2002

A solid-phase extraction sample preparation method using a molecularly imprinted polymer (MIP) selective for the triazine type pesticide terbutylazine has been developed. The method involves preconcentration from large volumes of water samples on a C18 disk coupled to selective clean-up on the MIP. The method has been optimised by studying the recovery and retention of terbutylazine and some other structurally related triazine derivates as a function of the selective washing solvent used. The effect of the water content of the selective washing solvent was also investigated on the recovery of the MIP. River water samples were analysed with the coupled technique, and efficient clean-up of th…

ChromatographyPolymersTriazinesOrganic ChemistryExtraction (chemistry)Molecularly imprinted polymerGeneral MedicineBiochemistryAnalytical ChemistrySolventchemistry.chemical_compoundchemistrySolventsSample preparationSolid phase extractionSolvent effectsMolecular imprintingTriazineJournal of Chromatography A
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Modeling ?-lactam interactions in aqueous solution through combined quantum mechanics-molecular mechanics methods

1999

Computational MathematicsMolecular dynamicschemistry.chemical_compoundAqueous solutionChemistryComputational chemistryβ lactamsLactamDensity functional theoryGeneral ChemistrySolvent effectsMolecular mechanicsJournal of Computational Chemistry
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A DFT study of the role of the Mg complex formation on the mechanism of the 1,3-dipolar cycloadditions of benzonitrile oxides with acryloylpyrazolidi…

2010

Abstract The role of the Mg complex formation on the mechanism, the reaction rate and regioselectivity of the 1,3-dipolar cycloaddition (13DC) reactions of benzonitrile oxides (BNOs) towards electron-deficient acryloylpyrazolidinones has been theoretically studied using DFT methods at the 6-31G* level. These 13DC reactions have asynchronous concerted mechanism with a non-polar character. These cycloadditions present a slight 5-regioselectivity induced by a steric repulsion between the phenyl substituent of the BNOs and the pyrazolidinone appendage present on the acryloyl derivative, which increases with the formation of the bulky Mg–acryloylpyrazolidinone complex. The present DFT study poin…

Concerted reactionSubstituentRegioselectivityCondensed Matter PhysicsBiochemistryCycloadditionReaction ratechemistry.chemical_compoundBenzonitrilechemistryComputational chemistryPhysical and Theoretical ChemistrySolvent effectsDerivative (chemistry)Journal of Molecular Structure: THEOCHEM
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Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.

2010

The experimental ultrafast photophysics of thioxanthone in several aprotic organic solvents at room temperature is presented, measured using femtosecond transient absorption together with high-level ab initio CASPT2 calculations of the singlet- and triplet-state manifolds in the gas phase, including computed state minima and conical intersections, transition energies, oscillator strengths, and spin-orbit coupling terms. The initially populated singlet pi pi* state is shown to decay through internal conversion and intersystem crossing processes via intermediate n pi* singlet and triplet states, respectively. Two easily accessible conical intersections explain the favorable internal conversio…

Conical intersectionsChemistryTransition statesQuantum yieldInternal conversion (chemistry)Atomic and Molecular Physics and OpticsPhotophysicsIntersystem crossingExcited stateddc:540Solvent effectsUltrafast laser spectroscopySinglet fissionAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet stateChemphyschem : a European journal of chemical physics and physical chemistry
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Structural and Electrochemical Studies of Copper(I) Complexes with Diethoxyphosphoryl-1,10-phenanthrolines

2014

Two series of copper(I) complexes with diethoxyphosphoryl-substituted 1,10-phenanthroline ligands were synthesized and characterized in the solid state and in solution. The first comprised mixed-ligand CuI complexes with phenanthroline and triphenylphosphine. The second series includes bis-chelates with two phenanthroline ligands. According to the X-ray data for the six complexes, the ditopic phenanthroline ligands exhibit bidentate coordination to the copper(I) atom through two nitrogen atoms in both series. Solution equilibria involving different phenanthroline copper(I) species were studied by 1H and 31P NMR spectroscopy, electrochemistry, and spectroelectrochemistry. The solution specia…

Coordination sphereDenticityLigandPhenanthrolineInorganic chemistrySubstituentchemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistry[CHIM]Chemical SciencesSolvent effectsTriphenylphosphineComputingMilieux_MISCELLANEOUS
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Cover Picture: Source of Selectivity in Oxidative Cross-Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3-Hexafluoropropan-2-ol (Chem. Eur. J. 35/20…

2015

Coupling (electronics)Hydrogen bondChemistryOrganic ChemistryOrganic chemistryGeneral ChemistrySolvent effectsSelectivityMedicinal chemistryCatalysisChemistry - A European Journal
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17O NMR and molecular mechanical studies of arylmethylenemalonaldehydes

1990

The 17O NMR spectra of six different arylmethylenemalonaldehydes were measured for various solvents and temperatures. The 17O NMR chemical shifts and line widths of the carbonyl oxygens of the malonaldehyde fragment show a clear variation in the series of monoaryl compounds studied. The differences between the 17O NMR chemical shifts of the formyl oxygens correlate well with two conformationally dependent 1H–1H and 1H–13C coupling constants for the same compounds. Molecular mechanical calculations were also performed in order to relate the present data with the conformational preferences of the malonaldehyde fragment of the arylmethylenemalonaldehydes.

Coupling constantTertiary amineCarbon-13 NMR satelliteStereochemistryChemical shiftInternal rotationEtherGeneral ChemistrySpectral lineCrystallographychemistry.chemical_compoundchemistryGeneral Materials ScienceSolvent effectsMagnetic Resonance in Chemistry
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Kinetic control in the chiral recognition of three-bladed propellers

2010

The ion pair of the stereolabile C(3)-symmetric, i(+)o proton complex [1H](+) of diaza-macropentacycle 1 and the configurationally stable Delta-TRISPHAT ([Delta-3](-)) anion exists in the form of two diastereomers, namely, [Delta-(1.H)][Delta-3] and [Lambda-(1.H)][Delta-3], the ratio of which, in terms of diastereomeric excess (de) decreases in the order [D(8)]THF (28%)CD(2)Cl(2) (22%)CDCl(3) (20%)[D(8)]toluene (16%)C(6)D(6) (7%)[D(6)]acetone (0%) at thermodynamic equilibrium. Except in the case of [D(6)]acetone, the latter is reached after a period of time that increases from 1 h ([D(8)]THF) to 24 h (CDCl(3)). Moreover, the initial value of the de of [1.H][Delta-3] in CDCl(3), before the t…

CryptandsIon pairsProtonStereochemistryOrganic ChemistryKineticsDiastereomerProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyTolueneCatalysischemistry.chemical_compoundCrystallographyKineticsDeprotonationchemistryddc:540Solvent effectsSolvent effectsHelical structures
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MÖSSBAUER EFFECT STUDY ON THE HIGH-SPIN (5T2) ⇌ LOW SPIN (1A1) TRANSITION IN [Fe(2-pic)3]Cl2. DILUTION EFFECT IN [FexZn1-x(2-pic)3] Cl2. EtOH AND CRY…

1976

CrystalMössbauer effectChemistryGeneral EngineeringMineralogyPhysical chemistrySolvent effectsSpin-½DilutionLe Journal de Physique Colloques
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