Search results for "Selectivity"

showing 10 items of 1148 documents

Catalytic activity of large-pore high Si/Al zeolites: Cracking of heptane on H-Beta and dealuminated HY zeolites

1987

Abstract The catalytic activity, selectivity, catalyst decay, thermal and hydrothermal stability, and acidity of H-Beta and HY zeolites with Si Al ratios of 7.5 and 10, respectively, have been studied during cracking of n-heptane at 450 °C and atmospheric pressure. It has been found that the H-Beta zeolite is more active and decays more slowly than HY. H-Beta presents a higher steric hindrance for dibranched molecules and therefore its open structure should be smaller than that of HY. A lower hydrogen transfer activity and hydrothermal stability is observed for H-Beta in comparison with the corresponding HY.

Heptanechemistry.chemical_compoundChemistryInorganic chemistryPhysical and Theoretical ChemistryZeoliteFluid catalytic crackingSelectivityChemical reactionPyrolysisCatalysisHydrothermal circulationCatalysisJournal of Catalysis
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Silver Ion-Selective Electrodes Based on π-Coordinating Ionophores Without Heteroatoms

2002

Ion-selective electrodes (ISEs) were constructed by using spherical hydrocarbons (cyclophanes) as π-coordinating ionophores in solvent polymeric membranes. Four structurally similar cyclophanes, i. e., [2.2.2]p,p,p-cyclophane, [2.2.2]m,p,p-cyclophane, [2.2.1]p,p,p-cyclophane and [2.2.1]m,p,p-cyclophane were studied as ionophores for Ag+. The ion-selective membranes were composed of the corresponding ionophore (1%), potassium tetrakis(4-chlorophenyl)borate (0.5%), 2-nitrophenyl octyl ether (65–66%) and PVC (32–33%). The ion-selective membrane was placed on top of a layer of the conducting polymer, poly(3,4-ethylenedioxythiophene) (PEDOT), working as ion-to-electron transducer. The selectivit…

HeteroatomInorganic chemistryIonophoreEtherAnalytical ChemistryIon selective electrodeSolventchemistry.chemical_compoundMembranechemistryPolymer chemistryElectrochemistrySelectivityCyclophaneElectroanalysis
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A Stereocontrolled Protocol to Highly Functionalized Fluorinated Scaffolds through a Fluoride Opening of Oxiranes

2016

A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesis of various fluorine-containing, highly functionalized cycloalkane derivatives. The method involves the stereoselective epoxidation of some unsaturated cyclic beta-amino acid derivatives as model compounds, followed by a regioselective fluoride opening of oxiranes under various conditions with Deoxofluor and XtalFluor-E reagents, thereby offering an insight into this new epoxide opening methodology with fluoride.

Hydrocarbons FluorinatedPharmaceutical ScienceEpoxideAlkenesstereoselectivity010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Fluorideschemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistryamino acidsSulfur Compoundsoxirane; fluorination; amino acids; stereoselectivity; regioselectivity010405 organic chemistryOrganic ChemistryRegioselectivityStereoisomerismfluorination0104 chemical sciencesCycloalkanechemistryChemistry (miscellaneous)oxiraneregioselectivityReagentEpoxy CompoundsMolecular MedicineStereoselectivityFluorideMolecules
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New Cathepsin Inhibitors to Explore the Fluorophilic Properties of the S 2 Pocket of Cathepsin B: Design, Synthesis, and Biological Evaluation

2011

5 páginas, 1 figura, 2 tablas -- PAGS nros. 5256-5260

Hydrocarbons FluorinatedStereochemistryStereoisomerismhydrolasesstereoselectivityCatalysisCathepsin BCathepsin BNitrilesinhibitorsCombinatorial Chemistry TechniquesHumansMoleculefluorinated ligandsBiological evaluationCathepsinMolecular StructureCombinatorial Chemistry TechniquesligandsChemistryOrganic ChemistryStereoisomerismDipeptidesGeneral Chemistryfluorinated fluorinatedDesign synthesisDrug DesignpeptidesStereoselectivityChemistry – A European Journal
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The Reaction of 4-Amino-2-oxazolines with Isocyanates and Isothiocyanates. Synthesis and X-Ray Structures of Polysubstituted 2-Imidazolidinones, 1,3-…

2006

Abstract Reactions of 4-alkylamino-2-phenyl-2-oxazolines 1 with isocyanates and isothiocyanates provide unprecedented efficient and regioselective heterocycle–heterocycle transformations. Compounds 1 reacted rapidly with tosyl isocyanate yielding directly 3-alkyl-4-benzamido-1-tosyl-2-imidazolidinones 4 in almost quantitative yields. The corresponding ureido intermediates 2 were not isolable species. However, the reactions with non-sulfonylated isocyanates or isothiocyanates were slower, leading to the expected ureido and thioureido derivatives 5, which were easily and efficiently transformed to either polysubstituted 2-imino-1,3-oxazolidine or 2-imino-1,3-thiazolidine hydrochlorides 7, res…

HydrochlorideThiazolidinesOrganic ChemistryX-rayRegioselectivityHydrochloric acidGeneral MedicineBiochemistryMedicinal chemistryIsocyanatechemistry.chemical_compoundchemistryTosylDrug DiscoveryOrganic chemistryChemInform
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Combined study of anion recognition by a carbazole-based neutral tripodal receptor in a competitive environment

2012

Anion recognition studies have been carried out on a series of neutral synthetic receptors in which carbazole-2-carboxamide has been used as building block. Different ligands which include one to three carbazole units in their structure have been prepared. Binding experiments have been performed under competitive conditions in DMSO and DMSO-water solutions. The tripodal receptor offered a better host-guest association due to the synergistic effect of a well arranged set of hydrogen bonds. A selective response towards the biologically important pyrophosphate anion has been achieved. This selectivity is enhanced when studies are carried out with an increasing water content, which gets as high…

Hydrogen bondCarbazoleStereochemistryOrganic ChemistryMass spectrometryBiochemistryCombinatorial chemistryPyrophosphateIonchemistry.chemical_compoundchemistryProton NMRPhysical and Theoretical ChemistryAbsorption (chemistry)SelectivityOrganic & Biomolecular Chemistry
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Valorization of alginate for the production of hydrogen via catalytic aqueous phase reforming

2018

Abstract Alginate, a carbohydrate abundant in the outer cell wall of macroalgae, was subjected to catalytic aqueous phase reforming (APR) to produce hydrogen using a 3% Pt/C commercial catalyst. The performance of the process was evaluated according to the conversion of the carbon to gas, the hydrogen yield and the hydrogen selectivity. The catalyst and feed amount, temperature, reaction time, pH and the presence of H2 were modified to understand the dependence of the outcome of the process on these parameters. The presence of the catalyst was fundamental in order to increase the hydrogen yield compared to the uncatalyzed reaction, and it can be reused without activity loss. In addition, it…

Hydrogen010405 organic chemistryAlginateChemistry (all)Aqueous two-phase systemchemistry.chemical_elementAqueous phase reformingGeneral ChemistrySettore ING-IND/27 - Chimica Industriale E TecnologicaCarbohydrate010402 general chemistry01 natural sciencesCatalysisCatalysi0104 chemical sciencesCatalysischemistryChemical engineeringYield (chemistry)Hydrogen productionMoleculeSelectivityCarbonPlatinumCatalysis Today
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Regioselective acylation of aminoresorcinarenes

2007

Abstract The acid catalyzed hydrolytic cleavage of the oxazine rings in the readily available tetraoxazine derivatives of resorcinarenes results in tetraaminoresorcinarenes. A similar process applied to C2-symmetrical bisoxazine resorcinarene tetratosylates affords C2v-symmetrical resorcinarenediamines. The mild acylation of these resorcinareneamines with BOC-anhydride or para-nitrophenyl ester proceeds selectively at the nitrogen atoms without affecting the hydroxyl groups. Most of the resulting resorcinareneamides are thus obtained in preparative yields and can be easily purified by simple crystallizations. In the crystalline state the compounds obtained are found to bind chloride anions …

HydrogenChemistryHydrogen bondOrganic ChemistryRegioselectivitychemistry.chemical_elementResorcinareneCleavage (embryo)BiochemistryChlorideAcylationHydrolysisDrug DiscoveryPolymer chemistrymedicineOrganic chemistrymedicine.drugTetrahedron
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NO reduction by CO in the presence of water over gold supported catalysts on CeO2-Al2O3 mixed support, prepared by mechanochemical activation

2007

Abstract The reduction of NO by CO was studied on gold catalysts supported on ceria-alumina, prepared by mechanochemical activation. The samples were characterized by means of XRD, TPR, XPS and Raman spectroscopy. The influence of water in the feed on the catalytic activity was evaluated as well. It was established that the addition of hydrogen and water improves NO reduction activity by CO. The role of water was connected to the hydrogen production by WGS. The role of oxygen vacancies created in ceria structure in the presence of alumina was also discussed. The 100% selectivity to N2 at about 200 8C was kept in all cases of catalytic measurements, making the studied gold catalysts promisin…

HydrogenProcess Chemistry and TechnologyInorganic chemistryBinary compoundchemistry.chemical_elementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryTransition metalSelectivityGeneral Environmental ScienceHydrogen productionCarbon monoxideApplied Catalysis B: Environmental
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Selectivity in the direction of photoisomerization reactions in liquid-crystalline guest-host systems

1995

E ⇄ Z photoisomerization reactions of stilbenes la-c were studied in liquid-crystalline (LC) phases and in the corresponding isotropic melts. Whereas viscosity has a moderate influence on the photostationary states, a strong effect caused by the regular incorporation of the stilbene molecules in the LC phases was observed. The direction of the isomerization can be reversed, up to the case of a one-way isomerization Z E for the tailored guest-host system 1b/BS. Such an LC-matrix effect is of typical highly ordered (smectic) phases with free volumina which are strictly limited by hydrophobic interactions; it could not be detected in a much more mobile nematic phase. Textures based on the bire…

Hydrophobic effectCrystallographyAbsorption spectroscopyPhotoisomerizationLiquid crystalChemistryPhase (matter)MoleculeGeneral ChemistrySelectivityPhotochemistryIsomerizationRecueil des Travaux Chimiques des Pays-Bas
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