Search results for "Solid"

showing 10 items of 3575 documents

Determination of soyasaponins I and βg in raw and cooked legumes by solid phase extraction (SPE) coupled to liquid chromatography (LC)-mass spectrome…

2013

Legumes contain a rich variety of phytochemicals as soyasaponins, triterpenoidal glycosides that possess multiple health-promoting properties, such as lowering of cholesterol. In this work, the quantification of soyasaponins I and βg in 60 raw and cooked legumes by using a solid phase extraction (SPE) coupled to a liquid chromatography (LC)-mass spectrometry (MS) method was carried out. Results showed that lentils are a good source of soyasaponins, with a content of soyasaponin I that ranged from 636 to 735 mg kg(-1) and of soyasaponin βg from 672 to 1807 mg kg(-1). The cooking process produced a small loss of soyasaponins in water, that is, 4.8-8.7%, and partially converted soyasaponin βg …

chemistry.chemical_classificationSoyasaponin IChromatographyCooking processSolid Phase ExtractionGlycosideBiological AvailabilityFabaceaeGeneral ChemistrySaponinsMass spectrometryIn vitro digestionMass SpectrometrychemistryLiquid chromatography–mass spectrometryHumansDigestionSolid phase extractionOleanolic AcidGeneral Agricultural and Biological SciencesDigestionChromatography High Pressure LiquidJournal of agricultural and food chemistry
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Amorphous Complexes MM (EDTA) (H2O)4 · 2H2O . LAXS and XPS Investigation of the Local Structure

1988

Abstract The amorphous MM (EDTA)(H2O)4·2 H2O (M = Ni,Co) substances are made up of infinite chains of alternating "hydrated" and "chelated" octahedra bridged by carboxylate groups: M(H2O)4 - M(EDTA)-M(H2O)4-... . XPS enables to ascertain that the coordination of the EDTA ligand in the amorphous phase is identical to that in the crystalline phase, i.e., hexacoordination toward the M atom and two bridging groups in the Ni -Ni, Co - Co compounds.

chemistry.chemical_classificationStereochemistryChemistryPhotoemission spectroscopyGeneral Physics and AstronomyAmorphous solidchemistry.chemical_compoundCrystallographyTransition metalX-ray photoelectron spectroscopyDiamineX-ray crystallographyMoleculePhysical and Theoretical ChemistryInorganic compoundMathematical PhysicsZeitschrift für Naturforschung A
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Diastereoselective formation of highly functionalised α-substituted amino acid derivatives via aldol addition

2005

Abstract Highly diastereoselective aldol additions of (2 R ,4 S )-3- tert -butyl 4-methyl 2- tert -butyloxazolidine-3,4-dicarboxylate ( 1 ) are reported. The utility of the highly substituted oxazolidines of type 1 for diastereoselective α-addition of the fully protected amino acid l -serine with achiral and chiral carbonyl compounds is demonstrated and the relative and absolute configuration of the aldol products are discussed on the basis of NOESY data and solid state structures of selected examples. The aldol products represent highly useful intermediates in the syntheses of sphingosine-related metabolites.

chemistry.chemical_classificationStereochemistryOrganic ChemistryAbsolute configurationSolid-stateAnalytical ChemistryAmino acidInorganic ChemistrySerineAldol reactionchemistrySubstituted Amino AcidTwo-dimensional nuclear magnetic resonance spectroscopySpectroscopyJournal of Molecular Structure
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Sterically controlled self-assembly of tetrahedral M(6)L(4) cages via cationic N-donor ligands.

2014

Tripodal cationic N-donor ligands exhibit sterically controlled self-assembly of tetrahedral M6L4 coordination cages that promote selective anion encapsulation (PF6(-)OTf(-)) in the solid state. The described method is a potential template for stepwise assembly of hetero-ligand coordination cages and polymers.

chemistry.chemical_classificationSteric effectsChemistryMetals and AlloysSolid-stateCationic polymerizationGeneral ChemistryPolymerCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMaterials ChemistryCeramics and CompositesTetrahedronSelf-assemblyta116Chemical communications (Cambridge, England)
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ChemInform Abstract: In situ DRIFT Spectroscopic Investigation on the Chemical Evolution of Zinc Phosphate Acid-Base Cement.

2010

Diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy has been used to follow the chemical evolution of zinc phosphate acid−base cement (ZPC), which has been prepared from unmodified, as well as from aluminum- and zinc-modified orthophosphoric acid. For the first time, amorphous dizinc cyclotetraphosphate octahydrate, Zn2P4O12·8H2O, although hydrolytically instable, has been observed as precursor phase prior to crystallization of α-hopeite, α-Zn3(PO4)2·4H2O, in both systems. Within minutes from onset of mixing the infrared spectrum of unmodified ZPC is dominated by the characteristic vibrations of α-hopeite, due to matrix crystallization. Setting of modified ZPC is strongly af…

chemistry.chemical_classificationSteric effectsDiffuse reflectance infrared fourier transformBase (chemistry)ChemistryInorganic chemistryZinc phosphateGeneral Medicinelaw.inventionAmorphous solidchemistry.chemical_compoundlawPhase (matter)CrystallizationSpectroscopyChemInform
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A new improved synthesis of the 110 K bismuth superconducting phase: freeze-drying of acetic solutions

1992

Abstract Metastability has greatly hindered the separated synthesis of the high-temperature superconducting phases represented as (Bi1−x, Pbx)2Sr2Can−1CunO4 + 2n (n = 2, 2-2-1-2, Tc≈80 K, and n = 3, 2-2-2-3, Tc≈110 K). By careful control of the synthetic variables, it becomes possible to obtain the 110 K phase as the only superconducting one through processing of freeze-dried acetic solutions. This technique leads to homogeneously sized (5–10 μm) micaceous platelets of the superconducting material.

chemistry.chemical_classificationSuperconductivityAqueous solutionMaterials scienceMechanical EngineeringInorganic chemistryAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsBismuthchemistryMechanics of MaterialsPhase (matter)MetastabilityGeneral Materials ScienceInorganic compoundStoichiometrySolid solutionMaterials Letters
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Stereocontrolled solid-phase synthesis of fluorinated partially-modified retropeptides via tandem aza-Michael/enolate-protonation

2003

N-Acylation of Wang resin-bound l-α-amino acids with 2-trifluoromethyl-propenoyl chloride, followed by asymmetric tandem aza-Michael/enolate-protonation by a series of l-α-amino esters and final release from the resin, afforded a representative library of partially-modified retropeptides incorporating a stereodefined trifluoroalanine surrogate. The stereocontrol can be dramatically improved (up to 15:1) by using apolar solvents like carbon tetrachloride and DABCO as base.

chemistry.chemical_classificationTandemBase (chemistry)Organic ChemistryProtonationDABCOBiochemistryMedicinal chemistryChloridechemistry.chemical_compoundSolid-phase synthesischemistryDrug DiscoverymedicineOrganic chemistrymedicine.drugTetrahedron Letters
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The effect of silica nanoparticles on the morphology, mechanical properties and thermal degradation kinetics of PMMA

2012

Abstract Silica–PMMA nanocomposites with different silica quantities were prepared by a melt compounding method. The effect of silica amount, in the range 1–5 wt.%, on the morphology, mechanical properties and thermal degradation kinetics of PMMA was investigated by means of transmission electron microscopy (TEM), X-ray diffractometry (XRD), dynamic mechanical analysis (DMA), thermogravimetric analyses (TGA), Fourier-transform infrared spectroscopy (FTIR), 13 C cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy ( 13 C{ 1 H} CP-MAS NMR) and measures of proton spin-lattice relaxation time in the rotating frame ( T 1 ρ ( H )), in the laboratory frame ( T 1 ( H )) a…

chemistry.chemical_classificationThermogravimetric analysisNanocompositeMaterials sciencePolymers and PlasticsPMMA Silica 13C{1H} CP-MAS NMR Degradation kineticsInfrared spectroscopyNuclear magnetic resonance spectroscopyDynamic mechanical analysisPolymerCondensed Matter PhysicsAmorphous solidChemical engineeringchemistryMechanics of MaterialsMaterials ChemistryFourier transform infrared spectroscopyComposite materialSettore CHIM/02 - Chimica Fisica
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Deformation recovery behavior of a solid polymer after tensile yielding

1984

In this work the deformation recovery behavior of an amorphous polymer after large tensile deformation is studied at different temperatures. The effect of three parameters other than temperature has been pointed out in previous works (1–3).

chemistry.chemical_classificationWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral ChemistryPolymerDeformation (meteorology)Amorphous solidchemistryResidual stressvisual_artUltimate tensile strengthMaterials ChemistryStress relaxationvisual_art.visual_art_mediumComposite materialPolycarbonatePolymer Engineering and Science
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Deformation recovery behaviour of a solid polymer after tensile yielding

1987

In this work the deformation recovery behavior of an amorphous polymer after large tensile deformation is studied at different temperatures. The effect of three parameters other than temperature has been pointed out in previous works (1–3). The data here presented indicate that the influence of all parameters, including temperature, on recovery behavior can be related to the residual stress, σ *, at the beginning of recovery test. This suggests to plot the recovery versus time curves, relative to different sets of parameters including temperature, by means of the same normalizing groups which were adopted in (2), thus shifting all curves towards a single master curve.

chemistry.chemical_classificationWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral ChemistryPolymerDeformation (meteorology)Condensed Matter PhysicsAmorphous solidchemistryResidual stressvisual_artUltimate tensile strengthMaterials Chemistryvisual_art.visual_art_mediumPolycarbonateComposite materialPolymer Bulletin
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