Search results for "transition"

showing 10 items of 3988 documents

Stereoselective Synthesis of α-Arylalkylamines by Glycosylation-induced Asymmetric Addition of Organometallic Compounds to Imines

2009

Arylalkylamines are of interest as building blocks for the synthesis of biologically active compounds and as chiral ligands or chiral auxiliaries in stereoselective syntheses [1]. Their stereoselective synthesis has been achieved by enantioselective reduction of ketimines using chiral reagents [2], as for example Corey’s oxaborolidines [3], or proline-derived triacyloxyborohydrides [4]. Particularly efficient asymmetric syntheses of chiral arylalkylamines have been accomplished by Noyori et al. [5] through enantioselective catalysis of hydrogen transfer reactions using a chiral 1,2-diphenyl-ethylenediamine ruthenium catalyst. Enantioselective transferhydrogenationshave also been achieved us…

chemistry.chemical_classificationSteric effectsAldiminechemistryTransition metalAsymmetric hydrogenationEnantioselective synthesisStereoselectivityGeneral ChemistryCombinatorial chemistryGroup 2 organometallic chemistryCatalysisZeitschrift für Naturforschung B
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Mukaiyama–Michael Reactions with trans-2,5-Diarylpyrrolidine Catalysts: Enantioselectivity Arises from Attractive Noncovalent Interactions, Not from …

2013

The scope of the enantioselective Mukaiyama-Michael reactions catalyzed by trans-2,5-diphenylpyrrolidine has been expanded to include both α- and β-substituted enals. However, the rationalization of the observed enantioselectivity is far from obvious since the catalyst is not very sterically hindered. DFT calculations were carried out to rationalize the observed stereoselectivities. Transition states of the C-C bond formation between iminium intermediates and silyloxyfurans were located and their relative energies were used to estimate the stereoselectivity data. We find excellent agreement between the predicted and observed stereoselectivities. The analysis of intermolecular forces reveals…

chemistry.chemical_classificationSteric effectsStereochemistryOrganic ChemistryIntermolecular forceEnantioselective synthesisIminiumGeneral ChemistryCatalysisTransition statechemistryComputational chemistryOrganocatalysisNon-covalent interactionsStereoselectivityta116Chemistry: A European journal
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Relaxations Below Glass Transition Temperature in Bread and Its Components

1999

ABSTRACT Dry glassy bread, cooked gluten, and gelatinized wheat starch-sucrose mixtures were prepared. Dielectric properties were studied as a function of temperature at different frequencies ranging from 100 to 1,000 kHz. Both bread and starch samples exhibited a tan δ peak at -53°C at 10 kHz, which is associated with a secondary relaxation characterized by an activation energy of 50 kJ/mol. The gluten sample did not show any relaxation in the temperature range studied. The magnitude of the relaxation peak was sensitive to the sucrose concentration of the starch sample. The higher the sucrose content, the greater the amplitude of the peak. Such an effect is attributed to a greater β-relaxa…

chemistry.chemical_classificationSucroseChemistryStarchOrganic ChemistryAnalytical chemistryfood and beveragesMineralogyDielectricActivation energyAtmospheric temperature rangeGlutenchemistry.chemical_compoundRelaxation (physics)Glass transitionFood ScienceCereal Chemistry Journal
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Fragmentation reactions of realgar caused by early transition metal hydrides

2012

Abstract The reaction of realgar with [Cp′2MH3] in boiling toluene gave [Cp′2M2As2S6] (Cp′ = t-BuC5H4; M = Nb: 1; Ta: 2), while [Cp2WH2] (Cp = C5H5) reacted with As4S4 to give [Cp2W(H)(η1-As5S2)] (6). The structures were determined by X-ray crystallography. Compounds 1 and 2 are dimers in which two Cp′M units are symmetrically bridged by a μ,η2:2-AsS3 ligand, a sulfide ligand and a heteroallylic μ,η2:2-AsS2 ligand. The structure of 6 belongs to the type of bent metallocenes in which tungsten is surrounded tetrahedrally by two Cp ligands, a crystallographically found hydride atom and the new As5S2 cage. The reaction of 1 with W(CO)5THF gave [Cp′2Nb2As2S6·W(CO)5] (3) and [Cp′2Nb2As2S6W(CO)3·W…

chemistry.chemical_classificationSulfideLigandHydrideIodideElectrochemistryTolueneCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographyTransition metalchemistryMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Dynamical heterogeneities in glass-forming materials

1996

ABSTRACTCooperative dynamics around the glass transition leads to complex motional behavior of the individual molecules, resulting in non-exponential relaxation. The nature of this non-exponentiality is clarified theoretically as well as experimentally. The non-exponentiality may be due to heterogeneous relaxation (superposition of exponential processes with different rate constants) or homogeneous relaxation (identical intrinsically non-exponential processes). A precise definition of both limits is given. It is shown that the type of relaxation, i.e. to which degree heterogeneous and homogeneous contributions are present, reflects geometrical properties of the dynamics. The heterogeneous c…

chemistry.chemical_classificationSuperposition principleMaterials scienceOrder (biology)Distribution (mathematics)chemistryRelaxation (physics)PolymerStatistical physicsType (model theory)Glass transitionExponential functionMRS Proceedings
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Transition metal–saccharide chemistry: synthesis, characterization and solution stability studies of cis-dioxomolybdenum saccharide complexes

1998

Six cis-dioxomolybdenum(VI) complexes of simple monosaccharides (D-glucose, D-fructose, D-galactose, D-mannose, D-ribose and D-xylose) have been synthesized and characterized by a variety of analytical and spectral methods. Both the solution and solid-state studies have supported the presence of dimeric structures, formed through the cis-MoO2 moieties and the bridging saccharide units. Solution stability of these complexes as a function of time has also been addressed.

chemistry.chemical_classificationThermal AnalysisCircular dichroismSpectrometersStereochemistryCircular DichroismOrganic ChemistryMannoseFructoseGeneral MedicineXyloseBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryTransition metalGalactoseRiboseOrganic chemistryMonosaccharideCyclic VoltammetryIndraStra Global
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Computer simulations of undercooled fluids and the glass transition

2000

Abstract Two model studies are presented that attempt to describe the static and dynamic properties of glass-forming fluids via molecular dynamics simulations: The first model is an atomistically realistic model of SiO 2 , the second model provides a coarse-grained description of polymer liquids, i.e., typical `fragile' glassformers, while SiO 2 is the prototype of a `strong glassformer'. For both models, attention is given to the questions as to which range of temperatures are properties in equilibrium, and whether such simulations can help to interpret experiments and/or check theoretical predictions. While in the simulation of SiO 2 using the potential of van Beest, Kramer and van Santen…

chemistry.chemical_classificationThermodynamicsSodium silicatePolymerAtmospheric temperature rangeCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMolecular dynamicsMonomerchemistryMaterials ChemistryCeramics and CompositesGlass transitionPolymer meltMacromoleculeJournal of Non-Crystalline Solids
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Thermal properties of e-beam cured epoxy/thermoplastic matrices for advanced composite materials

2007

The aim of this work is to investigate the possibility to improve the thermal behaviour of epoxy based systems, cured by ionizing radiation, in order to produce matrices for advanced carbon fibres composites. Blends of two epoxy monomers, difunctional and trifunctional, have been polymerized by e-beam irradiation and the dynamic mechanical thermal properties have been investigated. The increase of the concentration of the trifunctional epoxy monomer in the blend causes a marked increase of the Tg, but strongly decreases the reactivity. Subsequently, blends of the same epoxy monomers with a high Tg thermoplastic toughening agent have been considered and their reactivity and the thermal prope…

chemistry.chemical_classificationThermoplasticMaterials sciencePolymers and PlasticsOrganic Chemistrythermal propertiesEpoxyCondensed Matter Physicscomposite materialelectron beam irradiationepoxy resinchemistry.chemical_compoundMonomerPolymerizationchemistryvisual_artAdvanced composite materialsMaterials Chemistryvisual_art.visual_art_mediumElectron beam processingReactivity (chemistry)Settore CHIM/07 - Fondamenti Chimici Delle TecnologieComposite materialGlass transition
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Stereoselective synthesis of unsaturated and functionalized L-NHBoc amino acids, using Wittig reaction under mild phase-transfer conditions.

2012

The stereoselective synthesis of a new amino acid phosphonium salt was described by quaternization of melting triphenylphosphine with the γ-iodo NHBoc-amino ester, derived from L-aspartic acid. The deprotection of the carboxylic acid function to afford the phosphonium salt with a free carboxylic acid group was achieved by a palladium-catalyzed desallylation reaction. This phosphonium salt was used in the Wittig reaction with aromatic or aliphatic aldehydes and trifluoroacetophenone, under solid-liquid phase-transfer conditions in chlorobenzene and in the presence of K(3)PO(4) as weak base, to afford the corresponding unsaturated amino acids without racemization. Thus, the reaction with subs…

chemistry.chemical_classificationTrifluoromethylDieneCarboxylic acidOrganic ChemistryMolecular ConformationPhosphonium saltStereoisomerismPhase TransitionAmino acidchemistry.chemical_compoundchemistryWittig reactionOrganic chemistryTriphenylphosphineAmino AcidsRacemizationThe Journal of organic chemistry
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Pressure effect studies in molecular magnetism

2004

We report on temperature dependent magnetic susceptibility and Mossbauer effect studies of the influence of hydrostatic pressure (up to 1.2 GPa) on dynamic electronic structure phenomena in 3d transition metal coordination compounds. The systems under investigation are mononuclear spin crossover compounds of iron (II) and chromium (II), dinuclear complexes of iron (II) exhibiting coexistence of intramolecular antiferromagnetic coupling and thermal spin crossover, 1D, 2D and 3D polynuclear spin crossover complexes of iron (II), a valence tautomeric system of cobalt (II) showing a thermal transition from a high spin [CoII (semiquinone)] to a low spin [CoII (catecholate)] species on lowering t…

chemistry.chemical_classificationValence (chemistry)Condensed matter physicsChemistryMagnetismGeneral Chemical EngineeringHydrostatic pressureGeneral ChemistryCondensed Matter PhysicsMagnetic susceptibilityCoordination complexCrystallographyElectron transferFerromagnetismTransition metalSpin crossoverCondensed Matter::Strongly Correlated ElectronsGeneral Materials ScienceJournal of Physics: Condensed Matter
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