Search results for "chemistry [Arsenates]"

showing 10 items of 2372 documents

Chemical evolution of ore-forming brines – Basement leaching, metal provenance, and the redox link between barren and ore-bearing hydrothermal veins.…

2019

Abstract Six mineralogically exemplary barren and mineralized hydrothermal veins (with Pb and Zn ores) of Jurassic-Cretaceous and Cenozoic age in the Schwarzwald mining district, SW Germany were chosen to shed light on the origin of their mineralogical diversity. The selection of the veins was guided by the fact that they represent the largest number of veins in the region, are very well known mineralogically and geochemically, and they provide nice examples of barren and mineralized veins of similar age. Fluid inclusion data from the individual veins overlap implying their diverse mineralogy is not caused by different fluid compositions participating during fluid mixing. LA-ICPMS data of s…

chemistry.chemical_classificationProvenanceMineralization (geology)010504 meteorology & atmospheric sciencesSulfideGeochemistryTrace elementGeology010502 geochemistry & geophysics01 natural sciencesHydrothermal circulationchemistryGeochemistry and PetrologyFluid inclusionsClay mineralsBase metalGeology0105 earth and related environmental sciencesChemical Geology
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New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

2014

Abstract The synthesis and photophysical properties of novel water-soluble phenol-based fluorophores derived from 3-benzothiazolyl-7-hydroxycoumarin and emitting in the range 485–631 nm are described. Further conversion into thiol-sensitive fluorogenic probes through the chemical modification of their hydroxyl group was next investigated. Depending on the type of thiol-reactive quenching moiety used (2,4-dinitrobenzenesulfonyl ester, 2,4-dinitrophenyl ether or benzoquinone-type Michael acceptors) and the water-solubilizing group(s) pre-introduced into the coumarin core, dramatic differences in the thiol-induced fluorescence activation of these pro-fluorophores under physiological conditions…

chemistry.chemical_classificationQuenching (fluorescence)[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringChemical modificationEther[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryCoumarinFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiolPhenolMoietyComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsDyes and Pigments
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Oxidation of N,N-Benzylalkylamines to Nitrones by Mo(VI) and W(VI) Polyperoxo Complexes

1996

Abstract Oxidation of N,N-benzylalkylamines in chloroform by Mo(VI) and W(VI) polyperoxo complexes (PPC) of general formula Q+3{PO4[MO(O2)2]4}3− (Q+ = onium ion) yield the corresponding nitrones as oxidized products quantitatively. Only in the case of N,N-benzylmethylamine the formation of nitrone is accompanied by 25% of benzaldoxime. Oxidation of N,N-benzyltertbutylamine and N,N-benzylisopropylamine follows second order kinetics. This finding does not disqualify the hypothesis that the reaction might occur by a rate determining nucleophilic attack of the amine onto the peroxide oxygens leading, through a Bartlett-type transition state, to the probable formation of the corresponding hydrox…

chemistry.chemical_classificationReaction mechanismLigandStereochemistryPolyperoxo complexesProcess Chemistry and TechnologyN-benzylalkylaminesNPolyperoxo complexes; NN-benzylalkylamines; OxidationMedicinal chemistryPeroxideCatalysisNitroneReaction coordinateAdductchemistry.chemical_compoundHydroxylaminechemistryNucleophileOxidationPhysical and Theoretical Chemistry
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Effect of ramp size and sample spinning speed on CPMAS 13C NMR spectra of soil organic matter

2011

Abstract Cross polarization (CP) magic angle spinning (MAS) 13C NMR spectroscopy is a solid state NMR technique widely applied to study the chemical composition of natural organic matter. In high magnetic fields (>7 T), fast sample spinning is required in order to reduce the influence of spinning sidebands underlying other chemical shift regions. As the spinning speed increases, the Hartmann–Hahn matching profiles break down into a series of narrow matching bands. In order to account for this instability variable amplitude cross polarization techniques (e.g. VACP, ramp-CP) have been developed. In the present study, we experimentally verified the stability of the Hartmann–Hahn condition unde…

chemistry.chemical_classificationSettore AGR/13 - Chimica AgrariaAnalytical chemistryCarbon-13 NMRSpectral lineMagnetic fieldAmplitudeSolid-state nuclear magnetic resonancechemistryGeochemistry and Petrologysoil organic matterCPMAS 13C NMRMagic angle spinningHumic acidSpinningOrganic Geochemistry
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Unexpectedly ambivalent O-2 role in the autocatalytic photooxidation of 2-methoxybenzyl alcohol in water

2015

An unusual autocatalytic photooxidation of 2-methoxybenzyl alcohol has been observed under UV irradiation in aqueous medium. The homogeneous oxidation is catalyzed by the corresponding aldehyde that is also the main oxidation product. The trend of alcohol disappearance rate matches the typical shape of an autocatalytic process, where a crucial and ambivalent role is played by the presence of molecular oxygen. Low oxygen concentrations give rise to a zero-order reaction since the beginning of irradiation, while higher amounts of oxygen reduce the alcohol oxidation rate until the aldehyde reaches a concentration high enough to speed up the alcohol's conversion. Experiments performed by varyin…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionAutocatalytic photooxidation 2-Methoxybenzyl alcohol 2-Methoxybenzaldehyd O2 quenchingHomogeneous photocatalysisProcess Chemistry and Technologychemistry.chemical_elementAlcoholSettore CHIM/06 - Chimica OrganicaPhotochemistryOxygenAldehydeCatalysisCatalysisAutocatalysischemistry.chemical_compoundchemistrySettore CHIM/03 - Chimica Generale E InorganicaAlcohol oxidationPhysical and Theoretical ChemistryAbsorption (chemistry)
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Temporal fatty acid profiles of human decomposition fluid in soil

2017

Abstract We studied the changes in concentration and relative abundance of human-derived fatty acids (FAs) in soil over a period of one year. The study is based on analysis of soil underneath a human body that lay on the soil surface for 18 days before it was discovered. Soil samples were taken when the body was removed, and also 358 days later. Large amounts of the total FA concentration at the start of the measurement period were still present one year after the removal of the body. The FA profile suggested that extensive saturated FA reduction occurred during the first 18 days after deposition. 10-Hydroxystearic acid and FA salts, which are characteristic of adipocere, were abundant in a…

chemistry.chemical_classificationSoil test010401 analytical chemistryMyristic acidFatty acidAdipocere01 natural sciencesDecomposition0104 chemical sciences03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDeposition (aerosol physics)chemistryGeochemistry and PetrologyEnvironmental chemistry030216 legal & forensic medicineGas chromatography–mass spectrometryRelative species abundanceOrganic Geochemistry
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d-Glucose as a multivalent chiral scaffold for combinatorial chemistry

2002

Due to their high density of functional groups and their availability in a variety of diastereomeric forms, monosaccharides are considered attractive scaffolds for combinatorial chemistry that allow the attachment and defined spatial alignment of up to five different pharmacophoric groups. For their application in combinatorial syntheses on solid phase, a set of selectively removable hydroxy protecting groups in combination with a cleavable anchor is required. Herein, we report on the construction and use of a versatile multivalent glucose building block for parallel synthesis on the solid phase.

chemistry.chemical_classificationSpectrometry Mass Electrospray IonizationScaffoldAlkylationMolecular StructureStereochemistryOrganic ChemistryDiastereomerHigh densityGeneral MedicineCrystallography X-RayBiochemistryCombinatorial chemistryAnalytical Chemistrychemistry.chemical_compoundCross-Linking ReagentsGlucosechemistryThioglycosidesD-GlucoseCombinatorial Chemistry TechniquesMonosaccharideChromatography High Pressure LiquidCarbohydrate Research
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Sulfide ore facies, fluid inclusion and sulfur isotope characteristics of the Tappehsorkh Zn-Pb ( ± Ag-Ba) deposit, South Esfahan, Iran

2020

International audience; The stratiform, stratabound Tappehsorkh Zn-Pb (± Ag-Ba) deposit, located in the southeastern part of the Malayer-Esfahan Metallogenic Belt of Iran, formed during Lower Cretaceous back-arc extension. Sulfide mi-neralization occurs within dolostone, black siltstone, and crystal lithic tuff and andesite associated with the Gushfil-Baghabrisham synsedimentary normal fault. Three sulfide ore facies (massive, bedded, and stockwork) occur in the deposit. Sulfide minerals are sphalerite, galena, tetrahedrite and pyrite with minor chalcopyrite and bornite, and gangue minerals are barite, dolomite and quartz. Sulfide mineralization textures are massive, replacement , vein-vein…

chemistry.chemical_classificationStockworkMineralization (geology)SulfideChalcopyriteGeochemistryengineering.material010502 geochemistry & geophysics01 natural sciencesSulfide mineralsGeophysicsSphaleritechemistryGeochemistry and PetrologyGalenavisual_artengineeringvisual_art.visual_art_mediumBorniteGeology0105 earth and related environmental sciences[SDU.STU.MI]Sciences of the Universe [physics]/Earth Sciences/Mineralogy
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Comparative effect of supercritical carbon dioxide and high pressure processing on structural changes and activity loss of oxidoreductive enzymes

2019

Abstract Due to the CO2 specific characteristics, it has been used as supercritical (Sc) fluid for several applications, including enzyme inactivation. The influence of Sc-CO2 (10–65 MPa/10–30 min/35–65 °C) on mushroom polyphenol oxidase (PPO) and horseradish peroxidase (POD) was evaluated and the results were compared with those found using high pressure processing (HPP) (200–900 MPa/5–45 °C/1–15 min). The free ion concentration was also studied to compare the enzymatic activity and changes in electrical conductivity. Additionally both enzymes, untreated or treated using either Sc-CO2 or HPP, were used as additives in the CuCl2 crystallization method. The resulting additive-specific CuCl2 …

chemistry.chemical_classificationSupercritical carbon dioxidebiologyChemistryProcess Chemistry and Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyphenol oxidaseHorseradish peroxidaseSupercritical fluid0104 chemical scienceslaw.inventionPascalizationPoint of deliveryEnzymelawbiology.proteinChemical Engineering (miscellaneous)Food scienceCrystallization0210 nano-technologyWaste Management and DisposalJournal of CO2 Utilization
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Influence of anthropogenic activity on the lead isotope signature of Thau Lake sediments (southern France): origin and temporal evolution

2000

Lead concentrations and isotopic compositions were determined on both bulk sediments deposited in the Thau lake in southern France during the last 200 years, and leachates derived from a series of sequential leachings of the sediments, making it possible to identify the sources, natural (i.e. indigenous lithologic) or anthropogenic, and to quantify the different inputs of Pb. Two distinct inputs of Pb could be distinguished. One of these corresponds to the terrigenous material entering the basin, representative of the local natural Pb ‘background’. Its supply remained steady most of the time with 206Pb/207Pb ratios of 1.200±0.003, except at the time of heavy storms producing voluminous and …

chemistry.chemical_classificationWatershedLithologyTerrigenous sedimentGeochemistryMineralogyStormStructural basinPollutionSilicatechemistry.chemical_compoundchemistryGeochemistry and PetrologyEnvironmental ChemistryOrganic matterLeachateGeologyApplied Geochemistry
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