Search results for "Oxide"

showing 10 items of 6424 documents

Direct synthesis of methyl isobutyl ketone in gas-phase reaction over palladium-loaded hydroxyapatite

2005

Several compositions of palladium-loaded calcium hydroxyapatite Pd(x)/CaHAp were prepared and characterized by XRD, IR, and UV–visible spectroscopy and temperature-programmed reduction (TPR). The acid–base properties of the samples were studied with the use of butan-2-ol conversion and IR spectroscopy coupled with lutidine adsorption/desorption. Calcium hydroxyapatite bears Lewis acid sites of moderate strength and a limited number of Bronsted acid sites, which produce butenes by dehydration. The selectivity of the dehydrogenation reaction (formation of methyl ethyl ketone) is very limited in the absence of oxygen but indicates the existence on the surface of phosphate of basic sites that a…

chemistry.chemical_classificationKetoneChemistryInorganic chemistrychemistry.chemical_elementCatalysisCatalysisMethyl isobutyl ketonechemistry.chemical_compoundMesityl oxideAcetonePhysical and Theoretical ChemistryTemperature-programmed reductionBrønsted–Lowry acid–base theoryPalladium
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Inhibitoren der Korrosion 23 (1) - Gibt es eine Struktur- Wirkungs-Beziehung bei organischen Inhibitoren der Korrosion von Aluminium?

1978

Uber 400 organische Verbindungen wurden routinemasig darauf gepruft, ob sie die Auflosung des Aluminiums in In Salzsaure in Gegenwart von 2,5% NaCl und bei einer Konzentration von 10−2 Mol/l der zu prufenden Verbindung beeinflussen. Es wurde versucht, eine “Struktur-Wirkungs-Beziehung” zu erstellen. Eingehender diskutiert wurden folgende Verbindungsklassen: Arsenverbindungen, Phosphon- und Phosphinsauren, aromatische Aldehyde und Ketone, aromatische und aliphatische Carbonsauren, zweiwertige Phenole, Tetrazoliumsalze und formazane, Sulfoxide und aromatische Sulfonsauren, Sulfonamide und Sulfone. Bei einer Auswahl von Inhibitoren wurde die Abhangigkeit der Schutzwirkung von deren Konzentrati…

chemistry.chemical_classificationKetoneMechanical EngineeringMetals and Alloyschemistry.chemical_elementSulfoxideGeneral MedicineZincAldehydeMedicinal chemistryOrganic compoundSurfaces Coatings and FilmsSulfonamideSulfonechemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistryEnvironmental ChemistryPhenolsMaterials and Corrosion/Werkstoffe und Korrosion
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Enantioselective Protonation of the Lithium Transient Enolate of2-Methyltetralone with 2-Sulfinyl Alcohols

2005

A new catalytic cycle for the enantioselective protonation of cyclic ketone enolates with sulfinyl alcohols has been developed. An enol trifluoroacetate that can be easily obtained from the corresponding ketone is used for the first time as an enolate precursor of a cyclic ketone enolate. In this method, the achiral alcohol plays two roles: it is involved, as is usual in catalytic asymmetric protonation reactions, in the turnover of the chiral proton source and also in the generation of a transient enolate through the reaction of its corresponding alkoxide with the enol trifluoroacetate precursor. Stereoselectivity is highly dependent on the structure of the achiral alcohol. High levels of …

chemistry.chemical_classificationKetoneOrganic ChemistryEnantioselective synthesisCyclohexanolProtonationMedicinal chemistryEnolchemistry.chemical_compoundchemistryCatalytic cycleAlkoxideOrganic chemistryStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Radioactively labelled epoxides part II. (1) tritium labelled cyclohexene oxide, transstilbene oxide and phenanthrene 9,10-oxide

1980

Tritium labelled cyclohexene oxide, trans-stilbene oxide and phenanthrene 9,10-oxide were prepared with specific activities of 0.7 - 1.1 mCi per mmole starting with monoor diketo compounds. Tritium was introduced by reducing the ketone precursors with tritiated complex metal hydrides. The resulting alcohols were transformed to the epoxides by methods described for the unlabelled compounds. The syntheses require only two or three steps and yield cyclohexene oxide, trans-stilbene oxide and phenanthrene 9,10-oxide, important substrates for the study of epoxide hydratase and glutathione S-transferases in high radiochemical purity.

chemistry.chemical_classificationKetoneOrganic ChemistryOxidePhenanthreneBiochemistryAnalytical ChemistryMetalchemistry.chemical_compoundEpoxide Hydratasechemistryvisual_artYield (chemistry)Drug Discoveryvisual_art.visual_art_mediumOrganic chemistryRadiology Nuclear Medicine and imagingTritiumSpectroscopyCyclohexene oxideJournal of Labelled Compounds and Radiopharmaceuticals
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Enzyme-Responsive Controlled Release Using Mesoporous Silica Supports Capped with Lactose

2009

chemistry.chemical_classificationLactose metabolismHydrolysisLactoseGeneral ChemistryGeneral MedicineMesoporous silicaSilicon DioxideControlled releaseCatalysisGalactosidasesHydrolysischemistry.chemical_compoundEnzymechemistryX-Ray DiffractionOrganic chemistryRuthenium CompoundsLactoseAngewandte Chemie
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Tailoring the ligand structure to the reagent in the mandelamide-Ti(IV) catalyzed enantioselective addition of dimethyl- and diethylzinc to aldehydes

2007

Amides derived from (S)-(+)-mandelic acid in the presence of titanium isopropoxide catalyze the enantioselective addition of dimethyl- and diethylzinc to aldehydes with good yields and ee up to 90%. Because of the modular character of the mandelamides, the structure of the ligand can be tailored to obtain the best results with each reagent. Thus, best results with dimethylzinc are obtained with N-benzyl mandelamide while N-(pyridin-2-yl) mandelamide is the best ligand for the addition of diethylzinc.

chemistry.chemical_classificationLigandProcess Chemistry and TechnologyDimethylzincEnantioselective synthesisDiethylzincAlkylationAldehydeCombinatorial chemistryCatalysischemistry.chemical_compoundchemistryReagentOrganic chemistryPhysical and Theoretical ChemistryTitanium isopropoxideJournal of Molecular Catalysis A: Chemical
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Synthesis and Reaction Chemistry of Sb(ECH2CH2NMe2)3(E= O, S)

2012

The antimony aminoalkoxide and aminothiolates Sb(ECH 2CH 2NMe 2) 3 [E = O (1), S (2)] were synthesized and their ability to form adducts with other metal moieties investigated. Compound 1 forms 1:1 adducts with NiI 2 (3) and M(acac) 2 [M = Cd (4), Ni (5)], while 2 undergoes ligand exchange with AlMe 3 to afford Me 2AlSCH 2CH 2NMe 2 (6). The structures of 2-4 and 6 were determined. Compound 2 incorporates three S, N-chelating ligands though the interaction with nitrogen is weaker than in analogous alkoxide complexes. Product 3 reveals one iodine has migrated from nickel to antimony, and all three alkoxide ligands bridge the two metals through μ 2-O atoms. In contrast, in 4, only one alkoxide…

chemistry.chemical_classificationLigandStereochemistrychemistry.chemical_elementMedicinal chemistryCoordination complexAdductInorganic ChemistryMetalNickelchemistry.chemical_compoundchemistryAntimonyvisual_artAlkoxidevisual_art.visual_art_mediumChelationZeitschrift für anorganische und allgemeine Chemie
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Lauroyl peroxide as thermal initiator of lauryl methacrylate monolithic columns for CEC

2008

The preparation of lauryl methacrylate (LMA)-based monolithic columns for CEC using lauroyl peroxide (LPO) as thermal initiator of polymerization has been investigated. The influence of initiator amount and composition of porogenic solvent on the physical and electrochromatographic properties of the resulting LMA-based monoliths was evaluated. A comparison with LMA-based columns thermally polymerized with AIBN was performed. At a given porogenic solvent composition, LMA stationary phases initiated with LPO showed higher permeabilities and better efficiency values than those prepared using AIBN as initiator. The optimum polymerization mixture found for LPO initiator provided a minimum plate …

chemistry.chemical_classificationLipid PeroxidesChromatographyFree RadicalsPolymersChemistryClinical BiochemistryTemperatureLauric AcidsPolycyclic aromatic hydrocarbonRepeatabilityLauroyl peroxideBiochemistryAnalytical ChemistrySolventPolymerizationCapillary ElectrochromatographyNitrilesThermalMethacrylatesSolvent compositionLauryl methacrylateNuclear chemistryELECTROPHORESIS
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Polymeric Micelles and Liposomes as Potential Drug Carriers

1986

In the past, a whole aray of polymeric carriers for biologically active substances have been reported. In this field the main interest has focused on the use of randomly solubilized polymers. Naturally occuring amphiphilic transport proteins can be modelled by synthetic micellar solubilized polymers. Poly(ethylene oxide)-polypeptide block copolymers with hydrophobic and cyclophosphamide-containing side groups are described. These micellar systems are able to transport different hydrophobic drugs.

chemistry.chemical_classificationLiposomeEthylene oxidetechnology industry and agriculturemacromolecular substancesPolymerCombinatorial chemistryTransport proteinchemistry.chemical_compoundchemistryAmphiphileCopolymerNanocarriersDrug carrier
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1985

A block copolymer (6) with both hydrophilic and hydrophobic regions was synthesized, in order to examine its interaction with model membranes and its uptake by living cells. The copolymer comprised poly(ethylene oxide) and poly(L-lysine) with 50 mol-% substitution of the e-amino groups with palmitoyl groups. To permit 125I-labelling, p-methoxyphenyl residues (1–4 mol-%) were incorporated into the block copolymer and into a poly(ethylene oxide) used for comparison. Sudan Red 7 B solubilization studies indicated that the block copolymer, but not the homopolymer, forms micelles. Differential scanning calorimetry of dipalmitoyl-phosphatidylcholine liposomes indicated that the block copolymer in…

chemistry.chemical_classificationLiposomechemistry.chemical_compoundMembraneEthylene oxidechemistryPinocytosisPolymer chemistryCopolymerChemical modificationPolymerMicelleDie Makromolekulare Chemie
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