Search results for " Oxidation"

showing 10 items of 675 documents

Influence of gel composition in the synthesis of MoVTeNb catalysts over their catalytic performance in partial propane and propylene oxidation

2010

[EN] MoVTeNb mixed oxides catalysts have been prepared by a slurry method with different molar compositions (Mo/Te ratio from 2 to 6 and Nb/(V + Nb) ratio from 0 to 0.7) in the synthesis gel leading to different crystalline phases distribution and catalytic behaviour in the partial oxidation of both propane and propylene to acrylic acid. Chemical analysis indicates that the composition of samples before and after the heat-treatment changes, especially the Te-content, since a significant amount of Te is lost during the heat-treatment step when the amount of oxalate (from niobium oxalate) increases in the synthesis gel. Thus, the nature of the crystalline phases and the catalytic performance …

ChemistryStereochemistryOxalic acidAcroleinGeneral ChemistryCatalysisOxalateCatalysisPropeneAcrylic acidMo–V–Te–Nb–O mixed oxideschemistry.chemical_compoundLoss of telluriumChemical engineeringPropaneOxalic acidPartial oxidationSelective propane oxidationAcrylic acid
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Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)-Tagged 2,2,6,6-Tetramethylpiperidine 1-Oxyl

2013

Bis(imidazolium)-tagged 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) catalysts were adsorbed on different supports such as silica gel, silica gel modified with highly cross-linked polymeric imidazolium networks, and highly cross-linked polymeric imidazolium networks entrapping magnetic particles. These systems provided a convenient tool for the oxidation of both primary and secondary alcohols working as recyclable reservoirs for the bis(imidazolium)-tagged TEMPO catalysts. By using EPR spectroscopy it was demonstrated that the catalyst was released as the corresponding oxoammonium salt in the solution during the recycling step, thus promoting the oxidative process in a homogeneous fashion. …

ChemistryalcoholoxidationOrganic ChemistryketoneALCOHOLSSettore CHIM/06 - Chimica OrganicaRecyclable catalystCatalysisaldehydelaw.inventionInorganic Chemistry2 2 6 6 tetramethylpiperidine 1 oxyllawAlcohol oxidationKETONESOrganic chemistryPhysical and Theoretical Chemistrysupported catalystsElectron paramagnetic resonanceEPR spectroscopy
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Radioisotopic determination of l-carnitine content in foods commonly eaten in Western countries

2004

Abstract l -Carnitine is a vitamin-like nutrient essential for energy production and lipid metabolism in many organs and tissues such as skeletal muscle and heart. Even if l -carnitine can be synthesized, most of the carnitine present in human body is provided by food. Until now, no large study has been conducted where the content in l -carnitine of various foods was analyzed. The objective of this study was to determine the level of free l -carnitine present in food commonly consumed in Western countries. A radioisotopic assay was used to estimate l -carnitine content in raw and processed foods. From this study, it clearly appeared that meat products were the best sources for l -carnitine.…

Chemistrybusiness.industryLipid metabolismGeneral MedicineAnalytical ChemistryNutrientFood processingLarge studymedicineFish <Actinopterygii>Food scienceCarnitinebusinessBeta oxidationFood Sciencemedicine.drugFood Chemistry
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Gas chromatographic analysis of resveratrol in plasma, lipoproteins and cells after in vitro incubations

1998

Resveratrol is a trihydroxystilbene present in certain red wines. It may play a role in the inhibition of lipoprotein oxidation and platelet activity. We have developed the first method to measure resveratrol in animal and human samples and to study its incorporation in vitro. After adding epicoprostanol as an internal standard, samples are subjected to lipid extraction in the presence of antioxidant and under dim light to minimize both denaturation and isomerization of the trans-resveratrol to the cis-form. Extracts were purified by cold acetone precipitation and the resveratrol-containing acetone phase was evaporated under nitrogen. The resveratrol was analyzed as a trimethylsilyl derivat…

Chromatography GasErythrocytesAntioxidantendocrine system diseasesmedicine.medical_treatmentResveratrolSensitivity and Specificitychemistry.chemical_compoundStilbenesAcetonemedicineAnimalsHumansPlatelet activationLipoprotein oxidationDetection limitChromatographyorganic chemicalsReproducibility of Resultsfood and beveragesStereoisomerismGeneral ChemistryRatsLipoproteins LDLchemistryResveratrolCalibrationLinear ModelsGas chromatographyQuantitative analysis (chemistry)Platelet Aggregation InhibitorsJournal of Chromatography B: Biomedical Sciences and Applications
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Visible-light driven oxidation of gaseous aliphatic alcohols to the corresponding carbonyls via TiO2 sensitized by a perylene derivative

2013

Sensitized P25 TiO2 was prepared by wet impregnation with a home-prepared perylene dye, i.e., N,N?-bis(2-(1- piperazino)ethyl)-3,4,9,10-perylene-tetracarboxylic acid diimide dichloride (PZPER). Energy levels of PZPER were found to be compatible with those of TiO2 allowing fast electron transfer. The obtained catalyst has been characterized and used in the gas-phase partial oxidation of aliphatic primary and secondary alcohols, i.e., methanol, ethanol, and 2- propanol. The reaction was carried out under cut-off (?> 400 nm) simulated solar radiation in O2 atmosphere. The perylene derivative allowed a good absorbance of visible radiation thanks to its low optical energy gap (2.6 eV) which was …

Chromatography GasLightHealth Toxicology and MutagenesisInorganic chemistryFormaldehydeElectronsPhotochemistry..ImidesCatalysisCatalysischemistry.chemical_compoundDiimideEnvironmental ChemistryReactivity (chemistry)Partial oxidationVisible light photocatalysisPeryleneTitaniumSettore ING-IND/24 - Principi Di Ingegneria ChimicaMolecular StructureMethanolPerylene-sensitized TiO2General MedicinePollutionAliphatic alcohol oxidationchemistryYield (chemistry)MethanolPerylene-sensitized TiO2 Visible light photocatalysis Aliphatic alcohol oxidationOxidation-ReductionPerylene
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Carboxylated-xyloglucan and peptide amphiphile co-assembly in wound healing.

2021

Abstract Hydrogel wound dressings can play critical roles in wound healing protecting the wound from trauma or contamination and providing an ideal environment to support the growth of endogenous cells and promote wound closure. This work presents a self-assembling hydrogel dressing that can assist the wound repair process mimicking the hierarchical structure of skin extracellular matrix. To this aim, the co-assembly behaviour of a carboxylated variant of xyloglucan (CXG) with a peptide amphiphile (PA-H3) has been investigated to generate hierarchical constructs with tuneable molecular composition, structure, and properties. Transmission electron microscopy and circular dichroism at a low c…

Circular dichroismHYDROGELSwound healingSCAFFOLDSskin tissue engineeringBiomaterialsExtracellular matrixchemistry.chemical_compoundTissue engineeringDESIGNCIRCULAR-DICHROISM SPECTRAPeptide amphiphileABSORPTIONFORMULATIONSRELEASETEMPO-MEDIATED OXIDATIONintegumentary systemself-assemblyXyloglucanSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiPOLYSACCHARIDEchemistrypeptide nanofiberSelf-healing hydrogelsBiophysicsSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assemblyAcademicSubjects/SCI01410MEMBRANEhydrogelWound healingAcademicSubjects/MED00010Hydrogel Peptide nanofiber Self-assembly Skin tissue engineering Wound healingResearch ArticleRegenerative biomaterials
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Gas-phase selective oxidation of chloro- and methoxy-substituted toluenes on TiO2–Sepiolite supported vanadium oxides

2009

Abstract Catalytic behaviour of vanadium oxide systems (5–20 wt.% V2O5) supported on TiO2–Sepiolite (with titania loading around the theoretical monolayer, 12 wt.%, 12Ti–Sep) and, as reference, on Sepiolite calcined (Sepc) in the p-substituted toluene derivatives selective oxidation was studied. In all the catalysts studied p-chloro (p-ClBA) and p-methoxybenzaldehyde (p-MeOBA) were the main products. The yields to benzaldehydes obtained with %V/12Ti–Sep are comparable with some of those reported in the literature under similar kinetically controlled experimental conditions (Sp-ClBA = 70% and X = 19% were obtained at 653 K on 20 V/12Ti–Sep). The activity for benzaldehyde derivatives formatio…

Concerted reactionProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementMedicinal chemistryTolueneCatalysisVanadium oxideCatalysisBenzaldehydechemistry.chemical_compoundchemistryPartial oxidationMethyl groupApplied Catalysis A: General
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Intramolecular proton transfer boosts water oxidation catalyzed by a Ru complex

2015

We introduce a new family of complexes with the general formula [Run(tda)(py)2]m+ (n = 2, m = 0, 1; n = 3, m = 1, 2+; n = 4, m = 2, 32+), with tda2&ndash; being [2,2&prime;:6&prime;,2&Prime;-terpyridine]-6,6&Prime;-dicarboxylate, including complex [RuIV(OH)(tda-&kappa;-N3O)(py)2]+, 4H+, which we find to be an impressive water oxidation catalyst, formed by hydroxo coordination to 32+ under basic conditions. The complexes are synthesized, isolated, and thoroughly characterized by analytical, spectroscopic (UV&ndash;vis, nuclear magnetic resonance, electron paramagnetic resonance), computational, and electrochemical techniques (cyclic voltammetry, differential pulse voltammetry, coulometry), …

Coordination numberInorganic chemistryGeneral ChemistryElectrochemistryBiochemistryCatalysislaw.inventionCrystallographychemistry.chemical_compoundColloid and Surface ChemistryCatalytic oxidationchemistryOxidation statelawDifferential pulse voltammetryCarboxylateCyclic voltammetryElectron paramagnetic resonance
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Catalytic Oxidation of Alkanes and Alkenes by H 2 O 2 with a μ‐Oxido Diiron(III) Complex as Catalyst/Catalyst Precursor

2015

A new mu-oxo diiron(III) complex of the lithium salt of the pyridine-based unsymmetrical ligand 3-[(3-{[bis(pyridin-2-ylmethyl)amino]methyl}-2-hydroxy-5-methylbenzyl)(pyridin2-ylmethyl)amino] propanoate (LiDPCPMPP), [Fe-2(mu-O)(LiDPCPMPP)(2)](ClO4)(2), has been synthesized and characterized. The ability of the complex to catalyze oxidation of several alkanes and alkenes has been investigated by using CH3COOH/H2O2 (1:1) as an oxidative system. Moderate activity in cyclohexane oxidation (TOF = 33 h(-1)) and good activity in cyclohexene oxidation (TOF = 72 h(-1)) were detected. Partial retention of configuration (RC = 53%) in cis- and trans-1,2-dimethylcyclohexane oxidation, moderate 3 degrees…

Cyclohexane010405 organic chemistryAdamantaneCyclohexeneHomogeneous catalysis010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryCatalytic oxidationlithiumPyridineSelectivityta116European Journal of Inorganic Chemistry
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Interaction between peroxisomes and mitochondria in fatty acid metabolism

2012

Peroxisomes and mitochondria are ubiquitously found organelles. They both are dynamic structures able to divide, to fuse and to undergo autophagic processes. Their activities are dependent on proteins that are, for most (mitochondria) or all (peroxisome) of them, synthesized in the cytosol from the nuclear genome. Nevertheless, the membrane structures and the DNA content differ between these two organelles. Mitochondria possess a small circular genome while peroxisomes don’t. The control of their dynamic is dependent on specific factors even if some of those are able to affect both. These two organelles are metabolically connected: they are both involved in lipid metabolism. They are both a…

Cytosolchemistry.chemical_compoundFatty acid metabolismchemistryBiochemistryOrganelleAutophagyLipid metabolismMitochondrionPeroxisomeBiologyBeta oxidationCell biologyOpen Journal of Molecular and Integrative Physiology
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