Search results for " transfer"

showing 10 items of 3683 documents

Application of headspace analysis to the study of aroma compounds-lipids interactions

1998

Taking into account interactions between aroma compounds and food components is necessary to better manage the flavoring of food products. These interactions occur at a molecular level and reflect changes, at a macroscopic level, in thermodynamic equilibria, such as solubility or volatility. The rate of transfer of an aroma compound from the liquid to the vapor phase can be affected as well. The behavior of aroma compounds in water and lipid solutions was studied in two complementary ways, a thermodynamic and a kinetic approach (head-space analysis). The transfer rate of volatiles at the liquid-water interface does not only depend on the hydrophobicity of the aroma compounds. Vapor-liquid p…

chemistry.chemical_classificationActivity coefficientbiologyGeneral Chemical EngineeringOrganic Chemistryfood and beveragesbiology.organism_classificationGibbs free energyPartition coefficientchemistry.chemical_compoundsymbols.namesakechemistryComputational chemistryMass transfersymbolsAroma compoundOrganic chemistryVolatile organic compoundSolubilityAromaJournal of the American Oil Chemists' Society
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Identification and structural characterization of O-beta-ribosyl-(1"----2')-adenosine-5"-phosphate in yeast methionine initiator tRNA.

1990

We report in this paper on the complete structure determination of the modified nucleotide A*, now called Ar(p), that was previously identified in yeast methionine initiator tRNA as an isomeric form of O-ribosyl-adenosine bearing an additional phosphoryl-monoester group on its ribose2 moiety. By using the chemical procedure of periodate oxidation and subsequent beta-elimination with cyclohexylamine on mono- and dinucleotides containing Ar(p), we characterized the location of the phosphate group on the C-5" of the ribose2 moiety, and the linkage between the two riboses as a (1"----2')-glycosidic bond. Since the structural difference between phosphatase treated Ar(p) and authentic O-alpha-rib…

chemistry.chemical_classificationAdenosine monophosphateMethionineRNA Transfer MetStereochemistryChemical structurePhosphataseCyclohexylamineSaccharomyces cerevisiaeBiologyAdenosine Monophosphatechemistry.chemical_compoundchemistryBiochemistryTransfer RNAGeneticsMoietyNucleotideIndicators and ReagentsOxidation-ReductionChromatography High Pressure LiquidNucleic acids research
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Kinetics and Mechanisms in the Anionic Polymerization of Methacrylic Esters

1987

Under appropriate conditions the anionic polymerization of methacrylates proceeds in an ideal manner leading to polymers with narrow molecular weight distributions. From the kinetics of polymerization and from the microstructure of the polymers the existence of different active species is concluded, the most important one being a peripherally solvated contact ion pair. Depending on polymerization conditions two different modes of monomer addition can occur. Homo- and copolymerization experiments show that the influence of the ester group is mainly given by electronic effects. In non- polar solvents the polymerization of tert.-butyl methacrylate (in contrast to methyl methacrylate) leads to …

chemistry.chemical_classificationAnionic addition polymerizationchemistryPolymerizationPolymer chemistrytechnology industry and agricultureCopolymerChain transfermacromolecular substancesPolymerMethacrylateIonic polymerizationLiving anionic polymerization
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Extraction of short peptides using supported liquid membranes

2002

Studies of extraction of short peptides using supported liquid membranes containing Aliquat 336 as a carrier are presented. The extractions are carried out from an aqueous donor phase with pH ≥ 10 to an acceptor phase containing salt. The mass transfer is driven by the gradient of salt concentration between these phases. The extraction efficiency is dependent on the composition of water phases, the type and concentration of counter-ion in the stagnant acceptor phase and the flow rate of the donor phase. Moreover, it is also influenced by the concentration and structure of the examined peptides.

chemistry.chemical_classificationAqueous solutionChromatographyMechanical EngineeringGeneral Chemical EngineeringExtraction (chemistry)Aliquat 336Salt (chemistry)General ChemistryAliquat 336Acceptorchemistry.chemical_compoundMembranechemistryMass transferPhase (matter)peptidesextractionGeneral Materials Sciencesupported liquid membraneWater Science and TechnologyDesalination
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A Simple and Versatile Route to Stable Quantum Dot−Dye Hybrids in Nonaqueous and Aqueous Solutions

2008

Hybrid systems consisting of core/shell semiconductor quantum dots (QDs) and organic rylene dyes have been prepared and characterized. Complex formation is mediated by bidentate carboxylate moieties covalently linked to the dye molecules. The complexes were very stable with respect to time (at least months), dilution (sub nM), and precipitation. After preparation in organic solvent, complexes could be easily transferred into water. The strong quenching of QD emission by the dye molecules (transfer efficiencies up to 95%) was satisfactorily modeled by an FRET process. Single complexes immobilized in thin polymer films were imaged by confocal fluorescence microscopy.

chemistry.chemical_classificationAqueous solutionQuenching (fluorescence)Inorganic chemistryGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryFörster resonance energy transferchemistryCovalent bondQuantum dotMoleculeCarboxylateJournal of the American Chemical Society
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Fine tuning of the catalytic effect of a metal-free porphyrin on the homogeneous oxygen reduction.

2011

The catalytic effect of tetraphenylporphyrin on the oxygen reduction with ferrocene in 1,2-dichloroethane can be finely tuned by varying the molar ratio of the acid to the catalyst present in the solution. The mechanism involves binding of molecular oxygen to the protonated free porphyrin base, in competition with ion pairing between the protonated base and the acid anion present.

chemistry.chemical_classificationBase (chemistry)Inorganic chemistryMetals and AlloysProtonationGeneral ChemistryPhotochemistryPorphyrinCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferchemistryFerroceneTetraphenylporphyrinMaterials ChemistryCeramics and CompositesPerchloric acidChemical communications (Cambridge, England)
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A Versatile Grafting-to Approach for the Bioconjugation of Polymers to Collagen-like Peptides Using an Activated Ester Chain Transfer Agent

2009

DepartmentofMaterials Science and Engineering, University of Delaware, 201DuPont Hall, Newark, Delaware 19716,Received February 24, 2009Revised Manuscript Received April 24, 2009Biohybrid materials consisting of synthetic polymers andbiological moieties have gained more and more interest in therecent years.

chemistry.chemical_classificationBioconjugationPolymers and PlasticsChemistryScience and engineeringOrganic ChemistryRadical polymerizationChain transferPolymerGraftingInorganic Chemistrychemistry.chemical_compoundChemical couplingMaterials ChemistryPeptide synthesisOrganic chemistryMacromolecules
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Straightforward synthesis of bioconjugatable azo dyes. Part 2: Black Hole Quencher-2 (BHQ-2) and BlackBerry Quencher 650 (BBQ-650) scaffolds

2014

Abstract A further extension of the efficient synthetic methodology described in Part 1, to the aromatic bis-diazo scaffold of Black Hole Quencher-2 dye is presented. Bioconjugatable derivatives bearing either azido, terminal alkyne, or maleimide reactive group were easily obtained as well as the free-phenol form of BlackBerry® Quencher 650 (BBQ-650®) initially developed by Berry & Associates, Inc. Company. The efficient conjugation ability of azido- and maleimide-quenchers was demonstrated through the facile preparation of the first water-soluble and formylated BHQ-2 dyes and a FRET-based probe suitable for the in vitro/in cellulo detection of a cancer-associated protease namely urokinase-…

chemistry.chemical_classificationBioconjugation[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryAlkyne[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryBiochemistryCombinatorial chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundFörster resonance energy transferchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryDrug DiscoveryMaleimideComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsTetrahedron Letters
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Two-step polymerization of propylene over MgCl2-supported titanium catalyst

1998

The prepolymerization effect on propylene polymerization in the presence of a MgCl 2 -supported titanium catalyst was studied. The catalyst was pre-activated by polymerizing a small amount of propylene in the presence of Et 3 Al and cyclohexylmethyldimethoxysilane under mild conditions, and then it was used in a second step of propylene polymerization. Comparative studies of the polymerization process involving the investigated catalyst and its unmodified counterpart showed the rate-enhancement effect of prepolymerization and the same molecular weights, MWD's and isotacticities of the polymers obtained. Concentrations of active sites and propagation rate as well as transfer rate constants w…

chemistry.chemical_classificationChain propagationPolymers and PlasticsChemistryOrganic ChemistryChain transferPolymerCondensed Matter PhysicsCatalysisPolymerizationPolymer chemistryMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryZiegler–Natta catalystPrepolymerMacromolecular Chemistry and Physics
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