Search results for "Organo"

showing 10 items of 1460 documents

Influence of Physicochemical Interactions between Amylose and Aroma Compounds on the Retention of Aroma in Food-like Matrices

2002

In food matrices, where starch is often used as a gelling or texturing agent, the occurrence of amylose-aroma complexes and their effect on the release of aroma compounds are difficult to determine. Indeed, thick or gelled systems are known to reduce the diffusion rate of flavor molecules, resulting in an increase of retention. Moreover, interactions between aroma compounds and matrix components might increase the retention of aroma compounds. The complexing behavior of three aroma compounds with amylose was studied by DSC and X-ray diffraction to determine the relative importance of these two factors. Their interaction properties were different: two of them formed complexes, and the third …

Chemical PhenomenaStarchAmylopectinOrganolepticZea mays01 natural scienceschemistry.chemical_compoundViscosity0404 agricultural biotechnologyX-Ray DiffractionAmylose[SDV.IDA]Life Sciences [q-bio]/Food engineeringOrganic chemistryMoleculeComputingMilieux_MISCELLANEOUSAromaFlavorSolanum tuberosumCalorimetry Differential ScanningbiologyChemistry PhysicalViscosity010401 analytical chemistryfood and beveragesStarch04 agricultural and veterinary sciencesGeneral Chemistry[SDV.IDA] Life Sciences [q-bio]/Food engineeringbiology.organism_classification040401 food science0104 chemical scienceschemistryFoodAmylopectinOdorantsThermodynamicsAmyloseGeneral Agricultural and Biological SciencesGelsJournal of Agricultural and Food Chemistry
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Real-time time-dependent density functional theory implementation of electronic circular dichroism applied to nanoscale metal–organic clusters

2020

| openaire: EC/H2020/838996/EU//RealNanoPlasmon Electronic circular dichroism (ECD) is a powerful spectroscopy method for investigating chiral properties at the molecular level. ECD calculations with the commonly used linear-response time-dependent density functional theory (LR-TDDFT) framework can be prohibitively costly for large systems. To alleviate this problem, we present here an ECD implementation within the projector augmented-wave method in a real-time-propagation TDDFT framework in the open-source GPAW code. Our implementation supports both local atomic basis sets and real-space finite-difference representations of wave functions. We benchmark our implementation against an existin…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials Sciencemagneettiset ominaisuudetCondensed Matter - Mesoscale and Nanoscale PhysicsspektroskopiatiheysfunktionaaliteoriaMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesorganometalliyhdisteetoptiset ominaisuudetPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Physics::Atomic and Molecular Clustersnanohiukkaset
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Discrimination of nerve gases mimics and other organophosphorous derivatives in gas phase using a colorimetric probe array.

2012

A colorimetric array for the chromogenic discrimination of organophosphorous derivatives in gas phase has been developed. The array allows us to classify the nerve agent simulants DFP, DCP and DCNP.

Chemical warfare agentsNerve gasesSensitivity and SpecificityCatalysisGas phaseQUIMICA ORGANICAOrganophosphorus CompoundsMaterials ChemistryChemical Warfare AgentsChromogenic detectionPROYECTOS DE INGENIERIAChromatographyChemistryChromogenicSensorsQUIMICA INORGANICAMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsProbe arrayRecognitionMultivariate AnalysisCeramics and CompositesColorimetryGasesDCNPChemical communications (Cambridge, England)
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Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions

2007

Dehydropiperidinones stereoselectively obtained from N-arabinosyl imines were iodinated at the enaminone structure. Knochel iodine-magnesium exchange afforded Grignard compounds of these piperidinone derivatives which reacted, either directly or after transmetalation to zinc or copper intermediates, with alkyl-, aryl- or acylhalides to give correspondingly substituted piperidinones. Stereoselective conjugate allyl cuprate addition to a thus obtained 5-allyl dehydropiperidinone and ring-closing metathesis of the product gave a hydroquinolinone containing three stereogenic centers.

Chemistry OrganicMolecular ConformationStereoisomerismCrystallography X-RayMetathesisBiochemistryCoupling reactionStereocenterchemistry.chemical_compoundTransmetalationOrganometallic CompoundsOrganic chemistryMagnesiumPhysical and Theoretical ChemistryPiperidonesGroup 2 organometallic chemistryMolecular StructureChemistryArylOrganic ChemistryStereoisomerismZincModels ChemicalStereoselectivityIminesCopperIodineOrg. Biomol. Chem.
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Complexes of organometallic compounds XXVIII. The solution chemistry of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides

1971

Abstract The nature of methanol solutions of a series of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides has been studied by electronic and PMR spectroscopy and by osmometry and conductivity. Effectively complete dissociation to the free ligand and solvated organotin(IV) halide moieties is inferred.

ChemistryAcetylacetoneOrganic ChemistryHalideBiochemistryDissociation (chemistry)AdductInorganic Chemistrychemistry.chemical_compoundOsmometerPolymer chemistryMaterials ChemistryOrganic chemistryMethanolPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Prediction of acute toxicity of organophosphorus pesticides using topological indices

2007

Topological indices were used in the prediction of the acute toxicity (intraperitoneal and oral LD(50)) of organophosphorus pesticides on rats. Models with six variables for the prediction of LD(50)-i.p. (r = 0.849, Q(2) = 0.613) and eight variables for LD(50)-oral (r = 0.906, Q(2) = 0.701) were selected. External group and cross-validation by use of leave-n-out tests were also performed in order to assess the stability and the prediction performance of the selected topological models.

ChemistryAdministration OralQuantitative Structure-Activity RelationshipBioengineeringGeneral MedicineTopologyAcute toxicityRatsLethal Dose 50Organophosphorus CompoundsDrug DiscoveryAnimalsRegression AnalysisMolecular MedicineComputer SimulationPesticidesOrganophosphorus pesticidesInjections IntraperitonealSAR and QSAR in Environmental Research
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(-)-Isosteviol as a Versatile Ex-Chiral-Pool Building Block for Organic Chemistry (Eur. J. Org. Chem. 25/2013)

2013

ChemistryBlock (telecommunications)OrganocatalysisOrganic ChemistrySupramolecular chemistryOrganic chemistryPhysical and Theoretical ChemistryCombinatorial chemistryEuropean Journal of Organic Chemistry
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Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

ChemistryCatalyst supportOrganic ChemistryEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaChemical synthesisCatalysisAldol reactionOrganocatalysisOrganic chemistryDipeptide Organocatalysis Prolinamide Proline Supported catalystAldol condensationStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Preparation and structural studies on dibutyltin(IV) complexes with pyridine mono- and dicarboxylic acids

2004

Abstract A number of organotin(IV) complexes with pyridine mono- and dicarboxylic acids (containing ligating –COOH group(s) and aromatic {N} atoms) were prepared in the solid state. The bonding sites of the ligands were determined by means of FT-IR spectroscopic measurements. It was found that in most cases the –COO− groups form bridges between two central {Sn} atoms, thereby leading to polymeric (oligomeric) complexes. On this basis, the experimental 119Sn Mossbauer spectroscopic data were treated with partial quadrupole splitting approximations. The calculations predicted the existence of complexes with octahedral (oh) and trigonal-bipyramidal (tbp) structures, but the formation of comple…

ChemistryCrystal structureOrganic ChemistryInorganic chemistrySolid-stateQuadrupole splittingCrystal structureBiochemistryOrganotin(IV) compoundFT-IRM€ossbauerInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronGroup (periodic table)Mössbauer spectroscopyPyridineMaterials ChemistryNMR studiesPhysical and Theoretical ChemistryFourier transform infrared spectroscopyJournal of Organometallic Chemistry
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Hybrid Materials Formed by Two Molecular Networks. Towards Multiproperty Materials

1999

Abstract The possibilities offered by hybrid materials formed by two molecular networks in the context of the molecular magnets are illustrated. Molecule-based layered magnets are used as anionic hosts for electroactive molecules, with the aim of obtaining multiproperty materials exhibiting in addition to the cooperative magnetism other interesting properties according to the nature of the inserted molecules. In particular, hybrid molecular compounds containing molecular species giving rise to paramagnetic, conducting, or bi-stable properties are reported.

ChemistryMagnetismInorganic chemistryContext (language use)equipment and suppliesCondensed Matter PhysicsParamagnetismMolecular networkChemical physicsMagnetMoleculeHybrid materialhuman activitiesGroup 2 organometallic chemistry
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