Search results for "Mono"

showing 10 items of 6843 documents

Ligands affecting silver antimicrobial efficacy on Listeria monocytogenes and Salmonella enterica

2013

Although silver is being extensively used in food or other applications as the key component to control microbial proliferation, many factors affecting its real potential are still unknown. In the present work, the presence of specific ligands or the contents in organic matter was correlated with silver speciation and its antibacterial performance. Silver was found to be only active in form of free silver ions (FSI). The presence of chloride ions produced an equilibrium of stable silver chloride complexes which were void of antimicrobial efficacy. However, even at relatively high concentrations of chlorides, a small fraction of FSI may still be present, producing a bactericidal effect with …

chemistry.chemical_classificationAqueous solutionInorganic chemistrySalmonella entericaSilver CompoundsGeneral MedicineBacterial growthLigandsAntimicrobialmedicine.disease_causeListeria monocytogenesChlorideAnti-Bacterial AgentsAnalytical ChemistryKineticsSilver chloridechemistry.chemical_compoundchemistryListeria monocytogenesThiolmedicineOrganic matterFood scienceFood Sciencemedicine.drugFood Chemistry
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Cyclodextrins in polymer synthesis: photocrosslinkable films via free radical copolymerization of methylated β-cyclodextrin-complexed styrene with so…

2001

The copolymerization of a methylated-β-cyclodextrin (m-β-CD) 1:1 host-guest compound of styrene (1a) with various molar ratios of sodium 4-(acrylamido)-phenyldiazosulfonate (2) is described. The copolymerization of complex 1a with 2 was carried out in water with 2,2′-azobis(N,N′-dimethyleneisobutyramidine)-dihydrochloride as the free radical initiator at 40°C. Depending on the amount of 2 incorporated in the copolymer, water- or DMF-soluble copolymers of high molar mass were obtained. Irradiation of the copolymers with UV light in solution resulted in rapid decomposition of the azo chromophore, and irradiation of the polymers as films led to crosslinking and thus to insolubility.

chemistry.chemical_classificationAqueous solutionMolar massMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringGeneral ChemistryPolymerInclusion compoundStyrenechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerRadical initiatorDesigned Monomers and Polymers
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Water-compatible molecularly imprinted polymers obtained via high-throughput synthesis and experimental design.

2003

A technique allowing high-throughput synthesis and evaluation of molecularly imprinted polymer sorbents at a reduced scale (mini-MIPs) was developed and used for the optimization of MIPs for use in pure aqueous environments. The technique incorporated a 4-port liquid-handling robot for the rapid dispensing of monomers, templates, solvents and initiator into the reaction vessels of a 96-well plate. A library of 80 polymers, each ca. 50 mg, could thus be prepared in 24 h. The MIP rebinding capacity and selectivity could be rapidly assessed in the batch mode by quantifying nonbound fractions in parallel using a UV monochromator plate reader. This allowed a complete evaluation of the binding ch…

chemistry.chemical_classificationAqueous solutionMolecularly imprinted polymerNanotechnologyGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryTemplateMonomerMolecular recognitionchemistryChemical engineeringMolecular imprintingSelectivityJournal of the American Chemical Society
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Cyclodextrins in polymer chemistry: Influence of methylated β-cyclodextrin as host on the free radical copolymerization reactivity ratios of isoborny…

1999

Methylated β-cyclodextrin (me-β-CD) was used to complex the hydrophobic monomers isobornyl acrylate (1) and butyl acrylate (2) yielding the water-soluble host/guest complexes isobornyl acrylate/me-β-CD (1a) and butyl acrylate/me-β-CD (2a). The included monomers were copolymerized in water by free-radical mechanism and the kinetics were studied. In order to evaluate these results, the corresponding uncomplexed monomers 1 and 2 were also copolymerized in organic solution. The reactivity ratios of 1a and 2a (r1a = 0.3, r2a = 1.7) differ significantly from the reactivity ratios of the corresponding uncomplexed acrylates 1 and 2 in organic solution (r1 = 1.3, r2 = 1.0). In addition, we found tha…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsCyclodextrinButyl acrylateOrganic ChemistryPolymerInclusion compoundchemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryReactivity (chemistry)Macromolecular Rapid Communications
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Consequences of linking charged and uncharged monomers to binary copolymers studied in dilute solution. Part II: Non-additivity effects in the viscom…

2017

Abstract Copolymers of ethylene oxide (EO) and N,N-dimethyl aminoethyl methacrylate (R) or [2-(methacryloyloxy)ethyl] trimethylammonium iodide (R+) were studied in dilute solution: P ( EO p – b – R n ) ( I ) , P(Rn(1−f) – ran – R+n f) ( II ) , and P ( EO p – b – R n + ) ( III ) ; n and p give the numbers of monomers and f is the degree of charging. For II (variable f) and III (variable n) the effects of charging on the intrinsic viscosities [η] are well described by Boltzmann sigmoids. The deviation of [ η ] from [ η ] add (calculated from the corresponding homopolymer data, assuming additivity of the individual contributions) are quantified by σ = [ η ] / [ η ] add - 1 measuring the segreg…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsEthylene oxideIntrinsic viscosityOrganic ChemistryIodideGeneral Physics and AstronomyBinary number02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundMonomerchemistryAdditive functionPolymer chemistryMaterials ChemistryCopolymerPhysical chemistry0210 nano-technologyEuropean Polymer Journal
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Suppression of new particle formation from monoterpene oxidation by NO<sub>x</sub>

2014

Abstract. The impact of nitrogen oxides (NOx = NO + NO2) on new particle formation (NPF) and on photochemical ozone production from real plant volatile organic compound (BVOC) emissions was studied in a laboratory setup. At high NOx conditions ([BVOC] / [NOx] < 7, [NOx] > 23 ppb) new particle formation was suppressed. Instead, photochemical ozone formation was observed resulting in higher hydroxyl radical (OH) and lower nitrogen monoxide (NO) concentrations. When [NO] was reduced back to levels below 1 ppb by OH reactions, NPF was observed. Adding high amounts of NOx caused NPF to be slowed by orders of magnitude compared to analogous experiments at low NOx conditions ([NOx] ~300 ppt)…

chemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesMonoterpeneRadicalPhotodissociation010501 environmental sciencesRate-determining stepPhotochemistry01 natural sciencesOrganic compoundchemistry.chemical_compoundchemistry13. Climate actionParticleHydroxyl radicalNOx0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Total synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone

1992

Abstract The first total stereodirected synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone from the same chiral starting product is described. A stereoselective, radical-mediated ring closure was the key step in both syntheses.

chemistry.chemical_classificationBicyclic moleculeChemistryMonoterpeneOrganic ChemistryTotal synthesisRing (chemistry)BiochemistryIsomintlactoneDrug DiscoveryOrganic chemistryStereoselectivityMINTLACTONELactoneTetrahedron
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Sponge aggregation factor: identification of the specific collagen-binding site by means of a monoclonal antibody.

1988

The aggregation factor (AF) from the sponge Geodia cydonium is known to be a complex proteinaceous particle, composed of a series of different (glyco)proteins (Mr lower than 150,000) around a 90S sunburst-like core structure. One of the low-Mr proteins is the 47-KD cell binding fragment. We describe a new monoclonal antibody (mAb), III1E6, raised against purified AF particles, which recognizes in tissue slices structures present both on the plasma membrane and in a network-like manner in the extracellular space. By applying immunoelectron microscopical, immunoblotting, and immunoaffinity chromatographical techniques, the mAb III1E6 was shown to recognize the core structure of the AF partic…

chemistry.chemical_classificationBinding SitesHistologyCell adhesion moleculeImmunoelectron microscopyAntibodies MonoclonalProteinsCell CommunicationAdhesionBiologyMolecular biologyPoriferachemistryCell–cell interactionCell surface receptorBiophysicsAnimalsCollagenAnatomyBinding siteCell adhesionGlycoproteinCell Adhesion MoleculesCell AggregationJournal of Histochemistry & Cytochemistry
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Bulk and interfacial properties in colloid-polymer mixtures

2005

Large-scale Monte Carlo simulations of a phase-separating colloid-polymer mixture are performed and compared to recent experiments. The approach is based on effective interaction potentials in which the central monomers of self-avoiding polymer chains are used as effective coordinates. By incorporating polymer nonideality together with soft colloid-polymer repulsion, the predicted binodal is in excellent agreement with recent experiments. In addition, the interfacial tension as well as the capillary length are in quantitative agreement with experimental results obtained at a number of points in the phase-coexistence region, without the use of any fit parameters.

chemistry.chemical_classificationBinodalMaterials scienceMonte Carlo methodThermodynamicsPolymerCondensed Matter::Soft Condensed MatterSurface tensionchemistry.chemical_compoundColloidMonomerCapillary lengthchemistryStatistical physicsPhysical Review E
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Novel diamine-bis(phenolate) Ti(IV) complexes – tuning the complex structure to control catalytic properties in α-olefin polymerization

2016

Abstract Four monomeric titanium(IV) dichloride complexes of amine-bis(phenolate) ligands having an extra donor arm (2a–2d) and one oxo-bridged complex 3 were successfully synthesized in the reaction of TiCl4 with a sodium salt of the appropriate ligand, and they were characterized by 1H NMR spectroscopy. The ligands had either a dimethylamino side‐arm donor and t-Bu substituents on both (1a) and one (1d) phenolate rings or a diisopropylamino side-arm donor and t-Bu (1b) and t-Bu along with OMe (1c) phenolate substituents. All complexes upon activation with [Ph3CB(C6F5)4] and MAO were used to catalyze polymerization of 1-octene (in liquid monomer) into poly(1-octene). Their activities as we…

chemistry.chemical_classificationBulk polymerization010405 organic chemistryLigandProcess Chemistry and TechnologyPoly(1-octene)microstructurePolymerZiegler-Natta polymerization010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundMonomerchemistryPolymerizationTacticityDiaminePolymer chemistrydiamine-bis(phenolate) ligandtitanium complexApplied Catalysis A : General : an International Journal Devoted to Catalytic Science and its Applications
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