Search results for "Heptane"

showing 10 items of 103 documents

Calorimetric investigation on the formation of palladium nanoparticles in water/AOT/n-heptane microemulsions

1995

The formation enthalpy of palladium nanoparticles in water/sodium bis(2-ethylhexyl) sulfosuccinate (AOT)n-heptane microemulsions as a function of the waterAOT molar ratio (R = [water][AOT]) was measured by a calorimetric technique. The results indicate that at R < 10 the energetic state of the palladium nanoparticles compartmentalized within the reversed AOT micelles is signficantly different from that in bulk water. Effects due to the small size of the palladium nanoparticles and to interactions between nanoparticles and the waterAOT interface are discussed.

HeptaneTernary numeral systemChemistryEnthalpyNanoparticlechemistry.chemical_elementCalorimetryCondensed Matter PhysicsMicellechemistry.chemical_compoundPhysical chemistryMicroemulsionPhysical and Theoretical ChemistryInstrumentationPalladiumThermochimica Acta
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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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Hydrocracking ofn-heptane with a NiO-MoO3/HYUS zeolite as catalyst. Kinetic study

1988

The hydrocracking of n-heptane has been carried out in a fixed bed reactor at 2.45 MPa pressure and with a H2/n-heptane molar ratio of 5.0 using a 4 wt% NiO - 8 wt% MO3/HYUS zeolite as a catalyst. The W/F10 ratio was varied between 75.3 and 1624 kg · s/kmol at different reaction temperatures: 573, 588, 603 and 623 K. The kinetics of the reaction has been studied by two different procedures due to the slight deactivation of the catalyst. One of them uses the conversion and yield values extrapolated at time on stream to zero and the other uses a kinetic equation where the deactivation of the catalyst has been included. The experimental data were fit well by a pseudo-first order kinetic equati…

Heptanechemistry.chemical_compoundchemistryStereochemistryGeneral Chemical EngineeringYield (chemistry)Non-blocking I/OPhysical chemistryKinetic constantActivation energyKinetic energyZeoliteCatalysisThe Canadian Journal of Chemical Engineering
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A new potential toxaphene congener: synthesis, GC/EI-MS study, crystal structure, NMR analysis, and ab initio calculations of 3-endo,5-endo-dichloro-…

2001

Abstract A new potential toxaphene congener 3- endo ,5- endo -dichloro-7,7-bis-chloromethyl-4-dichloromethyl-tricyclo[2.2.1.0 2,6 ]heptane 2 has been isolated from reaction mixture obtained by the chlorination of 2- exo ,10,10-trichlorobornane 1 . The X-ray structural analysis of 2 revealed an unusual tricyclic structure, where the two chlorine atoms occupying endo -positions are in close spatial proximity with each other and near to the neighbouring CHCl 2 group. Further, it revealed that the symmetry of the molecule is distorted. The 1 H and 13 C NMR spectra of 2 have been assigned by means of 1 H, 1 H d ouble- q uantum f iltered co rrelation s pectroscop y (DQF COSY), PFG 1 H, 13 C HMQC …

InsecticidesMagnetic Resonance SpectroscopyEnvironmental EngineeringHealth Toxicology and MutagenesisAnalytical chemistryAb initioCrystal structureGas Chromatography-Mass Spectrometrychemistry.chemical_compoundAb initio quantum chemistry methodsEnvironmental ChemistryMoleculeToxapheneHeptaneChemistryTemperaturePublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryModels TheoreticalCarbon-13 NMRPollutionCrystallographyProton NMRMass spectrumEnvironmental PollutantsChemosphere
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Determination and separation of diarylheptanoids from alder growing in Latvia

2015

The composition of diarylhepatnoids fraction isolated from bark of two alder species (grey alder and black alder) was studied. The efficiency of three extraction methods used for isolation of diarylhepatnoids from alder bark was compared. Two diarylhepatnoids: 1,7-bis-(3,4-dihydroxyphenyl)-heptan- 3-one-5-O-β-D-xylopyronoside (oregonin) and 1,7-bis-(3,4-dihydroxyphenyl)-3-hydroxyheptane-5-O-β-D- xylopyranoside were isolated from the bark of grey alder. The phenolic components of the extracts were analyzed by high-performance liquid chromatography (HPLC). Quantitative determination of oregonin was performed using an internal standard method. The results obtained show that alder barks are ric…

Internal standardbiologyChemistryalnus species; bark extracts; diarylheptanoids; oregonin; 1; 7-bis-(3; 4-dihydroxyphenyl)-3- hydroxyheptane-5-O-β-D-xylopbiology.organism_classificationHigh-performance liquid chromatographyAlderQuantitative determinationvisual_artvisual_art.visual_art_mediumOrganic chemistryExtraction methodsBarkDiarylheptanoids
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CCDC 882133: Experimental Crystal Structure Determination

2012

Related Article: M.V.Leskinen, Kai-Tai Yip, A.Valkonen, P.M.Pihko|2012|J.Am.Chem.Soc.|134|5750|doi:10.1021/ja300684r

Methyl trans-2-(12-dimethyl-1H-indol-3-yl)-7-oxocycloheptanecarboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Inverse solvent effects in the heterogeneous and homogeneous epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica and meta-chl…

2014

The rate constants for the epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica (1a) and meta-chloroperbenzoic acid (mCPBA) (1b) in different solvents have been determined at temperatures in the −10 to 40 °C range. The heterogeneous epoxidation exhibits a dependence of the reaction rate on solvent polarity opposite to its homogeneous counterpart and anomalous activation parameters in n-hexane, which are interpreted in terms of the surface-promoted solvent structure at the solid–liquid interface. The results show that highly polar solvents can strongly inhibit heterogeneous reactions performed with silica-supported reagents or catalysts.

Organic ChemistryPhotochemistrySilicon DioxideBiochemistryHepteneCatalysisHeptanesSolventReaction rateChlorobenzoateschemistry.chemical_compoundKineticsReaction rate constantchemistryReagentSolventsPolarEpoxy CompoundsHexanesThermodynamicsPhysical and Theoretical ChemistrySolvent effectsOxidation-ReductionOrganicbiomolecular chemistry
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A Bioinspired Approach to Tri-nor-guaianes. Synthesis of (−)-Clavukerin A

2006

A bioinspired approach to tri-nor-guaianes by degradation of the C-7 side chain of related guaia-11-enes is described. In this approach (-)-clavukerin A (1) is obtained by selective ozonolysis-Criegge rearrangement of (+)-1alphaH,7alphaH,10alphaH-guaia-4,11-dien-3-one (4) to afford 7beta-hydroxy and 7beta-acetoxy tri-nor-guaiane derivatives 6 and 7, respectively, which after elimination and deoxygenation give the title compound. The starting guaiadienone is readily obtained from commercially available santonin or (+)-dihydrocarvone.

PharmacologyOzonolysisMolecular StructureOrganic ChemistryPharmaceutical ScienceStereoisomerismSesquiterpeneChemical synthesisAnalytical ChemistrySesquiterpenes Guaianechemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoverySide chainMolecular MedicineOrganic chemistryCycloheptanesPolycyclic Aromatic HydrocarbonsEnantiomerSelectivityDeoxygenationJournal of Natural Products
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Microwave radiation effect on the synthesis of cadmium sulphide nanoparticles in water in oil microemulsion: a preliminary study at different frequen…

2004

AbstractCadmium sulphide nanoparticles have been synthesised in water/sodium bis (2-ethylhexyl) sulfosuccinate (AOT)/n- heptane microemulsions kept at 30 °C by microwave irradiation coupled with water-cooling and in conventional thermostatic conditions at the same temperature. The study has been performed exposing the reaction media to microwave radiation at five different frequencies (2.45, 2.85, 8, 12 and 18 GHz). For each frequency, a suitable microwave exposure set-up has been assembled. During the growth process, the dimensions of the nanoparticles have been characterised by means of UV-Vis spectroscopy. At the end of the growth process, the surface morphology of the nanoparticles has …

PhotoluminescenceMorphology (linguistics)Materials scienceSodiumAnalytical chemistrychemistry.chemical_elementNanoparticle02 engineering and technology01 natural scienceschemistry.chemical_compound0103 physical sciencesOrganic chemistryGeneral Materials ScienceMicroemulsionSpectroscopySettore CHIM/02 - Chimica Fisica010302 applied physicsHeptaneMechanical Engineering021001 nanoscience & nanotechnologyCondensed Matter PhysicsNanoparticles synthesi Microwave irradiation Water in oil microemulsions Cadmium sulphidechemistryMechanics of Materials0210 nano-technologyMicrowave
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Structural Variation and Magneto-Structural Correlation in Two New Dinuclear Bis(µ2-Phenoxo)-Bridged CuII Schiff-Base Complexes: Catalytic Potential …

2010

Two new dinuclear bis(μ2-phenoxo)-bridged copper(ii) complexes [Cu(NCS)L1]2 (1) and [Cu(NCS)L2]2 (2) have been synthesized using two tridentate NNO-donor Schiff-base ligands, L1H (Me2N(CH2)3N=CHC6H3(OMe)(OH)) and L2H (Me2N(CH2)3N=C(CH3)C6H4(OH)), respectively. They have been characterized by elemental analyses, IR, UV-visible, and electron paramagnetic resonance (EPR) spectroscopy, cyclic voltammetry, and magnetic susceptibility measurements. X-Ray single-crystal structures reveal a central Cu2O2 core in each complex with an isothiocyanate ligand coordinated terminally to each metal centre. The coordination environments around the CuII ions in 1 and 2 are a distorted trigonal bipyramid and…

Schiff baseLigandSupramolecular chemistryGeneral ChemistryCrystal structurelaw.inventionchemistry.chemical_compoundTrigonal bipyramidal molecular geometryCrystallographychemistrylawSquare pyramidPhysical chemistryCycloheptaneElectron paramagnetic resonanceAustralian Journal of Chemistry
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