Search results for "Anhydrous"

showing 10 items of 48 documents

Caffeine as a Gelator

2016

Caffeine (a stimulant) and ethanol (a depressant) may have opposite effects in our body, but under in vitro conditions they can “gel” together. Caffeine, being one of the widely used stimulants, continued to surprise the scientific community with its unprecedented biological, medicinal and physicochemical properties. Here, we disclose the supramolecular self-assembly of anhydrous caffeine in a series of alcoholic and aromatic solvents, rendering a highly entangled microcrystalline network facilitating the encapsulation of the solvents as illustrated using direct imaging, microscopy analysis and NMR studies. Peer reviewed

Polymers and Plasticsmedicine.drug_classSupramolecular chemistryBioengineeringDirect imaging02 engineering and technology010402 general chemistry01 natural sciencessupramolecular chemistrylcsh:ChemistryBiomaterialschemistry.chemical_compoundAnhydrous caffeinelcsh:General. Including alchemySupramolecularlcsh:Inorganic chemistrysupramolekulaarinen kemiamedicineOrganic chemistrylcsh:Scienceta116caffeinegeelitsolid state NMREthanolta114ChemistryCommunicationOrganic Chemistry021001 nanoscience & nanotechnologygelslcsh:QD146-1970104 chemical sciences3. Good healthMicrocrystallinelcsh:QD1-999kofeiiniAromatic solventslcsh:QDepressant0210 nano-technologyCaffeinelcsh:QD1-65Gels Caffeine SupramolecularGels
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Modeling of the Halloysite Spiral Nanotube

2015

A computational SCC-DFTB investigation dealing with the structure of hydrated and anhydrous halloysite nanotubes with a spiral geometry is reported. The peculiar characteristics of these systems are described in terms of tetrahedral and octahedral distortions, of hydrogen bonds geometries involving water molecules and the surfaces in the hydrated nanotube, and of the interlayer interactions in the anhydrous one. When the properties of the spiral nanotube are compared with those of the kaolinite sheet, a certain degree of intrinsic disorder in the halloysite systems is revealed, due to the intrinsic nature of the spiral folding. This is particularly evident in the hydrogen bonds network occu…

Quantitative Biology::BiomoleculesNanotubeMaterials scienceHydrogen bondElectronic Optical and Magnetic MaterialInorganic chemistrySurfaces Coatings and Filmengineering.materialCondensed Matter::Mesoscopic Systems and Quantum Hall EffectHalloysiteSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFolding (chemistry)Condensed Matter::Materials ScienceGeneral EnergyEnergy (all)OctahedronChemical physicsengineeringAnhydrousMoleculeKaolinitePhysics::Chemical PhysicsPhysical and Theoretical Chemistry
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ChemInform Abstract: Epoxidation of Olefins with a Silica-Supported Peracid in Supercritical Carbon Dioxide under Flow Conditions.

2012

Anhydrous 2-percarboxyethyl-functionalized silica (2b), a recyclable supported peracid, is a suitable reagent to perform the epoxidation of alkenes 1 in supercritical carbon dioxide at 250 bar and 40 °C under flow conditions. This procedure simplifies the isolation of the reaction products and uses only carbon dioxide as a solvent under mild conditions. The solid reagent 2b can be easily recycled by a reaction with 30% hydrogen peroxide in an acid medium.

Solventchemistry.chemical_compoundFlow conditionsSupercritical carbon dioxidechemistryChemical engineeringReagentCarbon dioxideAnhydrousGeneral MedicineHydrogen peroxideBar (unit)ChemInform
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Epoxidation of Olefins with a Silica-Supported Peracid in Supercritical Carbon Dioxide under Flow Conditions

2012

Anhydrous 2-percarboxyethyl-functionalized silica (2b), a recyclable supported peracid, is a suitable reagent to perform the epoxidation of alkenes 1 in supercritical carbon dioxide at 250 bar and 40 °C under flow conditions. This procedure simplifies the isolation of the reaction products and uses only carbon dioxide as a solvent under mild conditions. The solid reagent 2b can be easily recycled by a reaction with 30% hydrogen peroxide in an acid medium.

Solventchemistry.chemical_compoundFlow conditionsSupercritical carbon dioxidechemistryReagentOrganic ChemistryCarbon dioxideAnhydrousOrganic chemistryHydrogen peroxideThe Journal of Organic Chemistry
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Application of matrix solid-phase dispersion to the determination of a new generation of fungicides in fruits and vegetables.

2002

A method based on matrix solid-phase dispersion (MSPD) and gas chromatography to determine eight fungicides in fruits and vegetables is described. Fungicide residues were identified and quantified using nitrogen-phosphorus detection and electron-capture detection connected in parallel and confirmed by mass spectrometric detection. The method required 0.5 g of sample, C18 bonded silica as dispersant sorbent, silica as clean-up sorbent and ethyl acetate as eluting solvent. Recoveries from spiked orange, apple, tomato, artichoke, carrot and courgette samples ranged from 62 to 102% and relative standard deviations were less than 15% in the concentration range 0.05-10 mg kg(-1). Detection and qu…

SorbentChromatographyChromatography GasChemistryOrganic ChemistryEthyl acetateGeneral MedicineReference StandardsBiochemistrySensitivity and SpecificityAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundElectron capture detectorFruitVegetablesAnhydrousSample preparationSolid phase extractionGas chromatographyCaptanJournal of chromatography. A
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Influence of drying to the structure of lactitol monohydrate

1997

The purpose of this study is to find out the effect of the crystal water content on the crystal structure of lactitol monohydrate. Crystal water was removed by drying over silicagel at 40°C and by using phosphorus pentoxide as drying agent at 20°C. The amouts of water removals were identified by thermogravimetry, the melting points and the heat of fusions were calculated from the results of differential scanning calorimetry measurements and the structure of samples were identified by X-ray powder diffraction method. Over 23 w/w% of total water content could removed by gently drying until significant structural changes could be detected. The melting point of anhydrous lactitol obtained by dr…

ThermogravimetryCrystalchemistry.chemical_compoundCrystallographyDifferential scanning calorimetryLactitolchemistryAnhydrousMelting pointAnalytical chemistryPhosphorus pentoxideWater contentJournal of thermal analysis
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Hydration and dehydration kinetics of xylazine hydrochloride

2009

From the experiments where mixture of xylazine hydrochloride hydrate H and anhydrous X were held at constant conditions, the stable form of xylazine hydrochloride can be found out. To determine equilibrium relative humidity, the unstable form of xylazine hydrochloride was inserted in thermostated humidity chamber and its weight was recorded by weighing the sample outside the chamber. The kinetic model and the rate constant for each condition were determined. The rate constants give information regarding the speed of the process at every experimentally used relative humidity. Thus using the data in coordinates k – p for each temperature it is possible to determine the water vapor pressure of…

XylazineStereochemistryChemistry PharmaceuticalVapour pressure of waterEnthalpyAnalytical chemistryPharmaceutical ScienceXylazineReaction rate constantDrug StabilitymedicineRelative humidityDesiccationChemistryTemperaturefood and beveragesHumidityHumidityGeneral MedicinehumanitiesKineticsAnhydrousThermodynamicsCrystallizationHydrateAdrenergic alpha-Agonistsmedicine.drugPharmaceutical Development and Technology
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The relative stability of xylazine hydrochloride polymorphous forms

2009

All four known xylazine hydrochloride polymorphous forms were obtained and their relative stabilities were compared directly at three different temperatures. At higher temperatures, it is possible to determine the relative stability of all forms directly by measuring the changes in the composition of the mixtures of two polymorphous forms using powder x-ray diffraction methods. At lower temperatures, a solvent was added to the mixture and the changes in composition were determined. Polymorph transition temperatures were determined directly. To predict the transition temperature which was not found using the direct method, the polymorph melting data and determined transition temperatures wer…

XylazineVapor PressureVapor pressureStereochemistryChemistryTransition temperatureVapour pressure of waterTemperatureAnalytical chemistryWaterPharmaceutical ScienceGeneral Medicinelaw.inventionSolventDrug StabilityX-Ray DiffractionPolymorphism (materials science)lawX-ray crystallographySolventsAnhydrousTransition TemperatureCrystallizationCrystallizationAdrenergic alpha-AgonistsPharmaceutical Development and Technology
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Effects of the net charge on abundance and stability of supramolecular surfactant aggregates in gas phase

2011

Self-assembling of amphiphilic molecules under electrospray ionization (ESI) conditions is characterized by quite unexpected phenomenology. The noticeable differences with respect to the condensed phase are attributable to the absence of the surfactant-solvent interactions, the presence of net charge in the aggregates, and the strong deviation from equilibrium conditions. Aiming to investigate the effects of the net charge on abundance and stability of supramolecular surfactant aggregates, positively and negatively charged aggregates of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and sodium methane sulfonate (MetS), butane sulfonate (ButS) and octane sulfonate (OctS) have been studied by E…

anhydrous reverse micellechemistry.chemical_classificationself-assembling; anhydrous reverse micelles; electrospray ionization; energy-resolved mass spectrometry; DFT calculationsChemistryElectrospray ionizationenergy-resolved mass spectrometryelectrospray ionizationSupramolecular chemistryAnalytical chemistryMethane sulfonateDFT calculationsPhotochemistryMass spectrometryself-assemblingchemistry.chemical_compoundSulfonatePhase (matter)SpectroscopyAlkylOctane
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Epoxidation of Olefins with a Silica-Supported Peracid

2012

Anhydrous [2-percarboxyethyl] functionalized silica (2a) is an advantageous oxidant for performing the epoxidation of olefins 1. Epoxides 3 do not undergo the ring-opening reactions catalyzed by the acidic silica surface, except for particularly activated cases such as styrene oxide. The hydrophilic and acidic character of the silica surface does not interfere with the directing effects exerted by allylic H-bond acceptor substituents. The alkenes 1 carrying hydroxyl groups react with silica-supported peracid 2a faster than unsubstituted alkenes, thus reversing the trend known for reactions with soluble peracids. These results are attributed to the H-bond interactions of substrate 1 with the…

chemistry.chemical_classificationAllylic rearrangementMolecular StructureChemistryCarboxylic acidOrganic ChemistrySubstrate (chemistry)AlkenesSilicon DioxideAcceptorCatalysisSilanolchemistry.chemical_compoundStyrene oxideAnhydrousEpoxy CompoundsOrganic chemistryThe Journal of Organic Chemistry
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