Search results for "SELE"

showing 10 items of 4721 documents

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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Hyperbranched polyethylenimine-supported copper(II) ions as a macroliganted homogenous catalyst for strict click reactions of azides and alkynes in w…

2019

Abstract Loading hyperbranched polyethylenimine (PEI) with copper(II) ions leads to the formation of a new water-soluble metallodendritic polymer Cu(II)-PEI that has been found to effectively catalyze the clickable azide-alkyne [3 + 2] cycloaddition reactions in water under ambient conditions, in the lack of any external reducing agent. A positive dendritic effect on the catalyst activity was observed in the click of 1,2,3-triazole by lowering the reduction potential of copper(II) into the in-situ generation of the catalytically active species copper(I). The reaction proceeds straightforwardly to afford the corresponding 1,4-disubstituted-1,2,3-triazole derivatives in a regioselective manne…

chemistry.chemical_classificationPolyethylenimine010405 organic chemistryReducing agentChemistryOrganic ChemistryRegioselectivitychemistry.chemical_elementHomogeneous catalysisPolymer010402 general chemistry01 natural sciencesBiochemistryCopperCycloaddition0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Alkene epoxidations catalysed by Mo(VI) supported on Merrifield's polymer

1999

High conversion and epoxide selectivity from alkenes is achieved with tert-butyl hydroperoxide and a polystyrene-grafted Mo(VI) catalyst, with no noticeable leaching of Mo from the support.

chemistry.chemical_classificationPolymers and PlasticsAlkeneGeneral Chemical EngineeringCatalyst supportEpoxideGeneral ChemistryBiochemistryEnolCatalysischemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryEnvironmental ChemistrySelectivityCycloalkeneAminationReactive and Functional Polymers
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Polycyclic Aromatic Hydrocarbons in Sediments of Marine Coastal Lagoons in Messina, Italy: Extraction and GC/MS Analysis, Distribution and Sources

2004

The content of 21 polycyclic aromatic hydrocarbons (PAHs) has been determined in 16 samples of sediments collected from Ganzirri and Faro marine coastal lagoons in Messina (Italy). Analysis was performed by gas chromatography/mass spectrometry (GC/MS) in selected ion monitoring (SIM) mode. The total concentration of polycyclic aromatic hydrocarbons (PAHs) ranged from 74 to 5755 ...g/Kg of dry matrix. The resulting distributions and molecular ratios of specific compounds have been discussed in terms of sampling location and origin of organic matter. The results obtained show that levels of contamination are not homogeneous throughout the stations, while the relative distributions of PAH are…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryExtraction (chemistry)ContaminationMass spectrometrypolycyclic aromatic hydrocarbons sediments organic matter content coastal marine lagoonsSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Environmental chemistryMaterials ChemistrySettore CHIM/01 - Chimica AnaliticaSelected ion monitoringOrganic matterGas chromatographyGas chromatography–mass spectrometryPolycyclic Aromatic Compounds
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Synthesis and properties of aromatic ionenes

1993

Cationic polyelectrolytes with aromatic segments can be synthesized by a repetitive alkylation reaction. The structure of the products, their synthesis and their solubility are described. All ionenes are not, or only in small amounts, water soluble. The best solubility can be achieved by mixtures of polar protic and aprotic solvents. Variations of the counterion produces sufficient solubility in THF. All ionenes show a typical polyelectrolyte effect. The thermal stability of aromatic ionenes and the glass transition temperature is dominated by the nature of the counterion. The molecular weight of oligomers can be described by using a combination of a conductive titration method and an ion s…

chemistry.chemical_classificationPolymers and PlasticsOrganic Chemistryfood and beveragesAlkylationPolyelectrolyteIon selective electrodechemistryPolymer chemistryMaterials ChemistryTitrationThermal stabilityCounterionSolubilityGlass transitionPolymer International
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The effect of potassium on the selective oxidation ofn-butane and ethane over Al2O3-supported vanadia catalysts

1995

The catalytic properties of undoped and K-doped (K/V atomic ratio of 0.5) Al2O3-supported vanadia catalysts (∼4.5 wt% of V2O5) for the oxidation ofn-butane and ethane were studied. Isolated tetrahedral V5+ species are mainly observed in both undoped and K-doped samples. The incorporation of potassium decreases both the reducibility of surface vanadium species and the number of surface acid sites. Potassium-free vanadium catalysts show a high selectivity during the oxidative dehydrogenation (ODH) of ethane but a low selectivity during the ODH ofn-butane. However, the presence of potassium on the vanadium catalysts strongly influences their catalytic properties, increasing the selectivity to …

chemistry.chemical_classificationPotassiumInorganic chemistrychemistry.chemical_elementVanadiumButaneGeneral ChemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundHydrocarbonchemistryDehydrogenationSelectivityCatalysis Letters
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Complexation Selectivities of Pillar[5]arenes with Primary Ammonium Salts

2013

The complexation of alkyl-substituted pillar[5]arenes with primary ammonium salts is investigated. 1,4-Bis(methoxy)pillar[5]arene (MeP5) can form strong complexes with the primary ammonium salts in CDCl3. However, 1,4-bis(ethoxy)pillar[5]arene (EtP5) shows weak interaction with these guests, and 1,4-bis(butoxy)pillar[5]arene (BuP5) can not form such a complex at all. These results indicate that the modified alkyl chains of pillar[5]arene play an important role in the complexation selectivity.

chemistry.chemical_classificationPrimary (chemistry)Binding propertiesPillarGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistryAmmoniumSelectivityHost–guest chemistryAlkylChinese Journal of Chemistry
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A new synthesis of soluble poly(1,4-phenylenevinylene)s and poly(2,5-pyrimidinylenevinylene)s

1991

Abstract Alkoxy-substituted 4-methylbenzylideneanilines 2a-f and their pyrimidine analogues 2g,h show an efficient selfcondensation in the alkaline medium KOC(CH 3 ) 3 /DMF. The totally stereoselective reaction yields 3a-h which are transformed by acidic work-up to 4a-h . A narrow distribution of the molecular weight can be achieved.

chemistry.chemical_classificationPyrimidine analoguechemistryOrganic ChemistryDrug DiscoveryPolymer chemistryOrganic chemistryStereoselectivityPolymerSelf-condensationBiochemistryTetrahedron Letters
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Pattern-recognising Polymer Adsorption on Structured Surfaces: Gaussian Polymers vs. Freely Jointed Chains

2014

Abstract Selective adsorption of homopolymers is exploited as a model for pattern recognition. To this end the strong adsorption regime of Gaussian polymers adsorbed on a regularly structured surface is investigated for square and triangular lattices within a discrete Edwards model. The equilibrium behaviour of the specific heat, the gyration tensor and the (nematic) bond order tensor are analysed and compared to the properties for adsorbed freely jointed polymer chains.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencepattern recognitionGyration tensorPolymerPolymer adsorptionPhysics and Astronomy(all)Bond orderMonte Carlo simulationsCondensed Matter::Soft Condensed MatterPolymer adsorptionCondensed Matter::Materials ScienceAdsorptionchemistryLiquid crystalChemical physicsSelective adsorptionTensorPhysics::Chemical PhysicsPhysics Procedia
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Separation of lanthanides and actinides using magnetic silica particles bearing covalently attached tetra-CMPO-calix[4]arenes

2004

Calix[4]arene tetraethers in the cone conformation bearing four –NH–CO–CH2–P(O)Ph2 (= CMPO) residues on their wide rim and one, two or four ω-amino alkyl residues of various lengths at the narrow rim were synthesized. Reaction with dichlorotriazinyl (DCT) functionalized magnetic particles led to complete coverage of the available surface by covalently linked CMPO-calix[4]arenes in all cases. Magnetically assisted removal of Eu(III) and Am(III) from acidic solutions was distinctly more efficient with these particles in comparison to analogous particles bearing the same amount of analogous single-chain CMPO-functions. The best result, an increase of the extraction efficiency by a factor of 14…

chemistry.chemical_classificationRange (particle radiation)biologyOrganic ChemistryExtraction (chemistry)Actinidebiology.organism_classificationBiochemistrychemistryCovalent bondPolymer chemistryMagnetic nanoparticlesTetraOrganic chemistryPhysical and Theoretical ChemistrySelectivityAlkylOrg. Biomol. Chem.
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