Search results for "ALK"

showing 10 items of 4314 documents

Acid- and Base-Catalysis in the Mononuclear Rearrangement of Some (Z)-arylhydrazones of 5-Amino-3-benzoyl-1,2,4-oxadiazole in Toluene: Effect of Subs…

2011

The reaction rates for the rearrangement of eleven (Z)-arylhydrazones of 5-amino-3-benzoyl-1,2,4-oxadiazole 3a-k into the relevant (2-aryl-5-phenyl-2H-1, 2,3-triazol-4-yl)ureas 4a-k in the presence of trichloroacetic acid or of piperidine have been determined in toluene at 313.1 K. The results have been related to the effect of the aryl substituent by using Hammett and/or Ingold-Yukawa-Tsuno correlations and have been compared with those previously collected in a protic polar solvent (dioxane/water) as well as with those on the analogous rearrangement of the corresponding (Z)-arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole 1a-k in benzene. Some light can thus be shed on the general di…

SubstituentOxadiazoleAlkaliesMedicinal chemistryCatalysisDioxanesStructure-Activity RelationshipAcid catalysischemistry.chemical_compoundPiperidinesUreaOrganic chemistryAminesTrichloroacetic AcidBenzeneBiological ProductsOxadiazolesMolecular StructureArylMRH acid- and base-catalysis kinetic measurementsOrganic ChemistryHydrazonesTemperatureWaterSettore CHIM/06 - Chimica OrganicaTolueneSolventKineticschemistryMononuclear rearrangements of heterocycles; (Z)-Arylhydrazones; acid catalysis; base catalysis.PiperidineHydrophobic and Hydrophilic InteractionsToluene
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N1-Functionalized Indole-Phosphane Oxazoline (IndPHOX) Ligands in Asymmetric Allylic Substitution Reactions

2012

N-Functionalized IndPHOX ligands bearing various groups have been synthesized and the effects of the N1-substituent on the reaction rate, yield, and asymmetric induction in a palladium-catalyzed allylic substitution reaction are reported. The presence of an oxygen atom in the ligands, namely an N-MOM or N-THP group, led to enhancement of the enantioselectivity in the allylic amination reaction. In addition, a ligand with a chiral oxazoline ring at C-1 and a phosphane substituent at C-2 provided high enantioselectivity in good yield in an asymmetric allylic alkylation reaction.

Substitution reactionAllylic rearrangementChemistryorganic chemicalsOrganic ChemistrySubstituentfood and beveragesOxazolineAlkylationAsymmetric inductionMedicinal chemistrychemistry.chemical_compoundTsuji–Trost reactionPhysical and Theoretical Chemistryta116AminationEuropean Journal of Organic Chemistry
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Site Preference in Multimetallic Nanoclusters: Incorporation of Alkali Metal Ions or Copper Atoms into the Alkynyl-Protected Body-Centered Cubic Clus…

2016

The synthesis, structure, substitution chemistry, and optical properties of the gold-centered cubic monocationic cluster [Au@Ag8@Au6(C≡CtBu)12]+ are reported. The metal framework of this cluster can be described as a fragment of a body-centered cubic (bcc) lattice with the silver and gold atoms occupying the vertices and the body center of the cube, respectively. The incorporation of alkali metal atoms gave rise to [MnAg8−nAu7(C≡CtBu)12]+ clusters (n=1 for M=Na, K, Rb, Cs and n=2 for M=K, Rb), with the alkali metal ion(s) presumably occupying the vertex site(s), whereas the incorporation of copper atoms produced [CunAg8Au7−n(C≡CtBu)12]+ clusters (n=1–6), with the Cu atom(s) presumably occup…

Substitution reactiongold-silver nanoclustersta114Chemistry010405 organic chemistrySuperatomInorganic chemistrychemistry.chemical_elementGeneral ChemistryGeneral MedicineCubic crystal systemAlkali metal010402 general chemistryCopper01 natural sciencesCatalysisIonNanoclusters0104 chemical sciencesCrystallographycopperCluster (physics)ta116superatomsalkalai metalsAngewandte Chemie
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ChemInform Abstract: Highly Enantioselective Zinc/Binol-Catalyzed Alkynylation of N-Sulfonyl Aldimines.

2008

Sulfonylchemistry.chemical_classificationAldiminechemistryAlkynylationEnantioselective synthesischemistry.chemical_elementOrganic chemistryGeneral MedicineZincCatalysisChemInform
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Supported iridium catalysts for the total oxidation of short chain alkanes and their mixtures: Influence of the support

2021

13 figures, 3 tables.-- Supplementary information available.-- © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

SupportsGeneral Chemical EngineeringTotal oxidationchemistry.chemical_element02 engineering and technologyIridium oxide010402 general chemistryIridium01 natural sciencesIndustrial and Manufacturing EngineeringCatalysislaw.inventionsymbols.namesakeAdsorptionX-ray photoelectron spectroscopylawAlkanesEnvironmental ChemistryCalcinationIridiumVOCsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringsymbols0210 nano-technologyRaman spectroscopy
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Geminal Imidazolium Salts: A new Class of Gelators

2012

The gelling behavior of some geminal diimidazolium salts was investigated in solvents differing in polarity and hydrogen bond donor ability. The used salts, namely the 3,3'-di-n-decyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(decim)(2)][Br](2) (1), the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(dodecim)(2)][Br](2) (2), and the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium ditetrafluoroborate [p-Xyl-(dodecim)(2)][BF(4)](2) (3), differ in the alkyl chain length and in the anion properties, such as size, shape, and coordination ability. In all cases in which gelation process was observed, the obtained gels were characteri…

Supramolecular chemistrychemistry.chemical_compoundBromidePolymer chemistryElectrochemistryMoleculeOrganic chemistryGeneral Materials ScienceSpectroscopyAlkylchemistry.chemical_classificationMolecular StructureGeminalHydrogen bondChemistryImidazolesHydrogen BondingSurfaces and InterfacesSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsResonance (chemistry)Geminal imidazolium salts Low molecular weight gelator OrganogelThermodynamicsSaltsChemical stabilityGelsOrganogels Hydrogels imidazolium salts
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Effects of Crystal Field Splitting and Surface Faceting on the Electronic Shell Structure

1992

The shell structure of the valence electrons is clearly observed in all alkali and noble metal clusters containing up to hundreds of atoms[1 – 4]. It is seen in the abundances of the clusters, in the ionization potential and in the polarizability. The shell structure of the valence electrons is closely related to the shell model of nuclei, but is simpler owing to the negligibly small spin-orbit interaction. The ability to produce all sizes of metal clusters has made the metal clusters a test ground for the super-shell structure[5].

Surface (mathematics)Materials scienceNuclear Theoryengineering.materialAlkali metalMolecular physicsFacetingCrystal field theoryPolarizabilityPhysics::Atomic and Molecular ClustersengineeringCondensed Matter::Strongly Correlated ElectronsNoble metalIonization energyAtomic physicsValence electron
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Mechanical desorption of a single chain: unusual aspects of phase coexistence at a first-order transition.

2012

The phase transition occurring when a single polymer chain adsorbed at a planar solid surface is mechanically desorbed is analyzed in two statistical ensembles. In the force ensemble, a constant force applied to the nongrafted end of the chain (that is grafted at its other end) is used as a given external control variable. In the $z$-ensemble, the displacement $z$ of this nongrafted end from the surface is taken as the externally controlled variable. Basic thermodynamic parameters, such as the adsorption energy, exhibit a very different behavior as a function of these control parameters. In the thermodynamic limit of infinite chain length the desorption transition with the force as a contro…

Surface (mathematics)Models MolecularPhase transitionMaterials sciencePolymersSurface PropertiesThermodynamicsAdhesivenessRandom walkDisplacement (vector)Phase TransitionChain (algebraic topology)Energy TransferModels ChemicalPhase (matter)DesorptionThermodynamic limitThermodynamicsComputer SimulationAdsorptionPhysical review. E, Statistical, nonlinear, and soft matter physics
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Reply to "comment on 'Monte Carlo simulations for a Lotka-type model with reactant surface diffusion and interactions' ".

2002

As is well known, a wide class of physical problems, including the kinetics of heterogeneous catalytic reactions, is traditionally described in terms of the master equations ~ME!. The definition of ME allows us not only to perform Monte Carlo ~MC! simulations, but also to develop at the same time appropriate analytical methods @mean field~MF!, cluster approximations, etc. #@ 1#. ME is formally defined when all possible states of a system and the transition rates between these states are specified. This is enough to define only the transition rates K(i! j ) for such elementary processes as particle adsorption, desorption, diffusion, reaction, etc., from the initial state i to the final state…

Surface diffusionMonte Carlo methodMaster equationCluster (physics)State (functional analysis)Statistical physicsType (model theory)Diffusion (business)Random walkMathematicsPhysical review. E, Statistical, nonlinear, and soft matter physics
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Surfactant self-assembling in gas phase: positively monocharged sodium alkanesulfonate clusters

2009

Surfactant self-assemblingAlkanesulfonate clusters
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