Search results for "Density"

showing 10 items of 4402 documents

Reactivity of the carbon-carbon double bond towards nucleophilic additions. A dft analysis

2004

Abstract The global and local electrophilicity indexes have been used to characterize the reactivity pattern of the CC double bond towards nucleophilic addition reactions. A wide family of molecules including ketones, esters, anhydrides, nitriles and nitrocompounds containing appropriate substitution on the CC double bond have been classified within an unique scale of reactivity. The predictive capability of the theoretical model is tested against a series of benzylidenemalononitriles and substituted α-nitrostilbenes.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryReinforced carbon–carbonBiochemistrychemistryNucleophileComputational chemistryDrug DiscoveryElectrophileOrganic chemistryMoleculeDensity functional theoryReactivity (chemistry)
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A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
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The nucleophilic addition of nitrones to carbonyl compounds: insights on the nature of the mechanism of the l-proline induced asymmetric reaction fro…

2004

Abstract The mechanism of the l -proline induced asymmetric nitrone–aldol reaction of N -methyl- C -ethylnitrone with dimethyl ketomalonate has been studied by using density functional theory at B3LYP/6-31G** level. The reaction was initialized by the addition of l -proline to the nitrone to form an aminal, which by elimination of the hydroxylamine gave a chiral enamine. The nucleophilic addition of this chiral enamine to dimethyl ketomalonate corresponds to stereoselective C–C bond-formation step. Further nucleophilic addition of hydroxylamine to the zwitterionic intermediate formed in the enamine addition gave a second aminal, which by l -proline elimination afforded the corresponding β-h…

chemistry.chemical_classificationNucleophilic additionStereochemistryOrganic ChemistryCatalysisEnamineNitroneInorganic Chemistrychemistry.chemical_compoundHydroxylaminechemistryAminalDensity functional theoryStereoselectivityProlinePhysical and Theoretical ChemistryTetrahedron: Asymmetry
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The triplet excited state of the biocative compound thiabendazole. Characterization and suitability as reporter for cyclodextrin complexation

2012

Fluorescence spectroscopy, laser flash photolysis (LPF), and density functional theory calculations have been performed to characterize the photobehavior of thiabendazole (1). Direct LFP of 1 results in the generation of a transient absorbing at λmax = 570 nm identified as the triplet excited state (31∗). The intersystem crossing quantum yield is 0.91, and the triplet energy is 288 kJ mol−1. The singlet–triplet energy gap is 84 kJ mol−1. The behavior of thiabendazole within CDs results in a marked enhancement of the triplet lifetime, this change is attributed to the mobility restrictions of included 1 imposed by the cyclodextrin cavities.

chemistry.chemical_classificationOptimizationCyclodextrinBeta-CyclodextrinGeneral Physics and AstronomyQuantum yieldHuman-SerumDensityProteinsPhotochemistryPolarizable continuum modelBenzimidazoleFluorescence spectroscopyIntersystem crossingQUIMICA ORGANICAchemistryExcited stateSolventTransitionFlash photolysisPolarizable continuum modelDensity functional theoryPhysical and Theoretical ChemistryApproximation
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Stabilisation of LDPE cross-linked in the presence of peroxides III. Mass spectrometric study of chemical changes taking place in the n-octadecane–di…

2000

Abstract An attempt was made to identify the products of the reaction between dicumyl peroxide and Irganox 1081, carried out in n -octadecane (saturated hydrocarbon), in conditions of fast decomposition of the peroxide (180°C, 5 min). Mass spectrometry (MS) was employed to find m/z values of molecular and fragment ions in analyses of the components ( n -octadecane, dicumyl peroxide, Irganox 1081) and of the following systems: n -octadecane–dicumyl peroxide, n -octadecane–Irganox 1081 and n -octadecane–dicumyl peroxide–Irganox 1081, after holding them at a temperature of 180°C for 5 min. The tendency of sulphur in Irganox 1081 to oxidise, specifically in the presence of dicumyl peroxide, was…

chemistry.chemical_classificationOrganic peroxidePolymers and PlasticsChemistryConcentration effectCondensed Matter PhysicsMass spectrometryDecompositionPeroxidechemistry.chemical_compoundLow-density polyethyleneHydrocarbonOctadecaneMechanics of MaterialsPolymer chemistryMaterials ChemistryPolymer Degradation and Stability
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On the compatibilization of PET/HDPE blends through a new class of copolyesters

2000

Polyethyleneterephthalate (PET) and polyethylene are incompatible polymers and their blends show, in general, poor properties. Compatibilization is then a necessary step to obtain blends with good mechanical and barrier properties. In this work different compatibilizing agents were used, i.e. a maleic anhydride elastomer and some new products containing graft-copolymers having polyester segments grafted onto polyethylene backbone chains. Both the functionalized elastomer and the new products drastically improve the morphology and the ductility of the blend. In the case of the modified elastomer the compatibilizing action has been attributed to the formation of H-bonds whereas the copolymers…

chemistry.chemical_classificationPOLYETHYLENEMaterials sciencecompatibilizationPolymers and PlasticsOrganic ChemistryPET/HDPE blendsMaleic anhydridePolymerCompatibilizationPolyethyleneElastomercopolyestersLIQUID-CRYSTALLINE POLYMERPolyesterchemistry.chemical_compoundPET/HDPE blends; copolyesters; compatibilization; LIQUID-CRYSTALLINE POLYMER; POLYETHYLENEchemistryChemical engineeringMaterials ChemistryPolymer blendHigh-density polyethyleneComposite materialPolymer
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A bonding evolution theory study of the mechanism of [3+2] cycloaddition reactions of nitrones with electron-deficient ethylenes

2015

The mechanism of zw-type [3+2] cycloaddition (32CA) reactions of nitrones with electron-deficient (ED) ethylenes has been studied using density functional theory (DFT) methods at the MPWB1K/6-31G(d) level of theory. An exploration of the potential energy surfaces associated with the four competitive reactive channels of the 32CA reaction between C-phenyl-N-methyl nitrone and acrolein indicates that the cycloaddition reaction takes place through a one-step mechanism. This cycloaddition reaction presents a moderate meta regioselectivity and a complete endo stereoselectivity, which is diminished in dichloromethane. Analysis of the DFT reactivity indices of the reagents allows an explanation of…

chemistry.chemical_classificationPericyclic reactionGeneral Chemical EngineeringRegioselectivityGeneral ChemistryPhotochemistryCycloadditionNitronechemistryNucleophileComputational chemistrySingle bondDensity functional theoryLone pairRSC Advances
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Long Range Bond-Bond Correlations in Dense Polymer Solutions

2004

The scaling of the bond-bond correlation function $C(s)$ along linear polymer chains is investigated with respect to the curvilinear distance, $s$, along the flexible chain and the monomer density, $\rho$, via Monte Carlo and molecular dynamics simulations. % Surprisingly, the correlations in dense three dimensional solutions are found to decay with a power law $C(s) \sim s^{-\omega}$ with $\omega=3/2$ and the exponential behavior commonly assumed is clearly ruled out for long chains. % In semidilute solutions, the density dependent scaling of $C(s) \approx g^{-\omega_0} (s/g)^{-\omega}$ with $\omega_0=2-2\nu=0.824$ ($\nu=0.588$ being Flory's exponent) is set by the number of monomers $g(\r…

chemistry.chemical_classificationPhysicsLinear polymerGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyPolymerCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPower lawOmega0104 chemical sciencesChemical bondchemistryDensity dependentExponentSoft Condensed Matter (cond-mat.soft)Statistical physicsAtomic physics0210 nano-technologyScaling[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]61.25.Hq 05.10.Ln 05.40.Fb
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Phase transitions in a single polymer chain: A micro-canonical analysis of Wang–Landau simulations

2008

Abstract We present simulation results for the phase behavior of a single chain for a flexible lattice polymer model using the Wang–Landau sampling idea. Using the micro-canonical density of states obtained with this method we will discuss the ability of an analysis in the micro-canonical ensemble to locate the coil-globule (continuous) and liquid–solid (first-order) transitions found for this problem using a canonical analysis.

chemistry.chemical_classificationPhysicsPhase transitionMonte Carlo methodGeneral Physics and AstronomyPolymerSingle chainCanonical analysischemistryHardware and ArchitectureLattice (order)Density of statesStatistical physicsPhase diagramComputer Physics Communications
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Constant stretching rate experiments on low density polyethylene

1985

A simple apparatus for elongational test of molten polymers is presented. Its realiability is demonstrated by means of stress growth in constant stretching rate experiments and relaxation test on a low density polyethylene sample.

chemistry.chemical_classificationPolymers and PlasticsChemistryTesting equipmentRelaxation testGeneral ChemistryPolymerCondensed Matter PhysicsStress (mechanics)Low-density polyethyleneMolten statePolymer chemistryMaterials ChemistryComposite materialConstant (mathematics)Polymer Bulletin
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