Search results for "Polymerization"

showing 10 items of 1689 documents

Poly(N-vinylhalogenocarbazole). II. On the synthesis of some 1,3,6,8-tetrahalogenovinylcarbazoles

1976

This paper presents results of a research program in which several vinyl carbazole polymers containing chlorine and bromine atoms in their molecules were polymerized and characterized by IR spectroscopy and thermoanalysis. The compounds were synthesized by reacting 2-chloroethanol benzenesulfonate with the appropriate halogenocarbazoles (Clemo-Perkin method) obtaining in this way some halogen derivatives of 9-(2-chloroethyl)carbazole; these derivatives following dehydrochlorination produced relevant vinyl derivatives. Results are evaluated in terms of reaction mechanisms and molecular structures of polymers synthesized.

CHLORINE COMPOUNDS - PolymerizationChemistryGeneral EngineeringPOLYMERS - ChemistryGeneral Materials ScienceJournal of Polymer Science: Polymer Letters Edition
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In situ polymerization of soil organic matter by oxidative biomimetic catalysis

2017

Abstract Background Agricultural practices that enhance organic matter content in soil can play a central role in sequestering soil organic carbon (SOC) and reducing greenhouse gases emissions. Methods We used a water-soluble iron-porphyrin to catalyze directly in situ oxidative polymerization of soil organic matter in the presence of H2O2 oxidant, with the aim to enhance OC stabilization, and, consequently, reduce CO2 emissions from soil. The occurred SOC stabilization was assessed by monitoring soil aggregate stability, OC distribution in water-soluble aggregates, soil respiration, and extraction yields of humic and fulvic acids. Results Soil treatment with H2O2 and iron-porphyrin increas…

CO2 emissions Soil carbon sequestrate Soil organic matter Soil respiration Oxidative biomimetic catalysisSettore AGR/13 - Chimica Agraria010501 environmental sciencesCO2 emissions01 natural sciencesBiochemistrycomplex mixturesSoil respirationlcsh:AgricultureOrganic matter0105 earth and related environmental scienceschemistry.chemical_classificationSoil organic matterSoil organic matterlcsh:SSoil chemistry04 agricultural and veterinary sciencesSoil carbonMineralization (soil science)Soil respirationOxidative biomimetic catalysischemistryPolymerizationEnvironmental chemistrySoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesSoil carbon sequestrationAgronomy and Crop ScienceFood ScienceBiotechnologySettore AGR/16 - Microbiologia AgrariaChemical and Biological Technologies in Agriculture
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Interference of L-arginine analogues with L-arginine transport mediated by the y+ carrier hCAT-2B.

1997

The inducible human cationic amino acid transporter hCAT-2B was expressed in Xenopus laevis oocytes, and this system was used to test the effect of several NO synthase (NOS) inhibitors and/or L-arginine analogues on L-arginine transport by this y+ carrier. L-NG-Methyl-L-arginine (L-NMA), asymmetrical L-NG, NG-dimethyl-L-arginine (L-ADMA), L-N5-(1-iminoethyl)-ornithine (L-NIO), L-NG-nitro-L-arginine (L-NNA), and L-NG-nitro-L-arginine methyl ester (L-NAME) all inhibited the inducible NOS II extracted from RAW 264.7 macrophages induced with bacterial lipopolysaccharide. L-NMA, L-ADMA, and L-NIO also competed with L-arginine for transport by hCAT-2B, whereas L-NNA and L-NAME did not. The two L-…

Cancer ResearchArginineLipopolysaccharideMonosaccharide Transport ProteinsPhysiologyStereochemistryClinical BiochemistryNitric Oxide Synthase Type IIArginineBiochemistryCell Linechemistry.chemical_compoundMiceXenopus laevisAnimalsHumansAmino acid transporterEnzyme Inhibitorschemistry.chemical_classificationGlucose Transporter Type 1Arginine transportChemistryLysineCationic polymerizationSubstrate (chemistry)Membrane ProteinsTransporterBiological TransportRatsEnzymeGlucoseBiochemistryOocytesAmino Acid Transport Systems BasicNitric Oxide SynthaseCarrier ProteinsNitric oxide : biology and chemistry
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Acrylate ester-based monolithic columns for capillary electrochromatography separation of triacylglycerols in vegetable oils

2011

Abstract A simple and reliable method for the evaluation of triacylglycerols (TAGs) in vegetable oils by capillary electrochromatography (CEC) with UV–Vis detection, using octadecyl acrylate (ODA) ester-based monolithic columns, has been developed. The percentages of the porogenic solvents in the polymerization mixture, and the mobile phase composition, were optimized. The optimum monolith was obtained at the following ratios: 40:60% (wt/wt) monomers/porogens, 60:40% (wt/wt) ODA/1,3-butanediol diacrylate and 23:77% (wt/wt) 1,4-butanediol/1-propanol (14 wt% 1,4-butanediol in the polymerization mixture). A satisfactory resolution between TAGs was achieved in less than 12 min with a 65:35 (v/v…

Capillary electrochromatographyAcrylategeographyChromatographygeography.geographical_feature_categoryResolution (mass spectrometry)Organic ChemistryDiscriminant Analysis1-PropanolGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundMonomerVegetable oilAcrylateschemistryPolymerizationCapillary ElectrochromatographyMicroscopy Electron ScanningPlant OilsMonolithButylene GlycolsAmmonium acetateTriglyceridesJournal of Chromatography A
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Preparation and characterization of hexyl methacrylate monolithic columns for CEC

2008

The preparation of hexyl methacrylate (HMA) monolithic columns for CEC separations has been investigated with two initiation systems: (i) ammonium peroxodisulphate and TEMED to activate the polymerization reaction, and (ii) by thermal initiation with AIBN. For both initiators, the influence of composition of porogenic solvent on morphological and chromatographic properties of monoliths was investigated. Two porogenic solvent systems, aqueous and non-aqueous media, were also studied for monolithic beds polymerized with AIBN. Under optimal conditions, low minimum plate heights (9.6 mum for peroxodisulphate, 8.4 and 10.0 mum for AIBN in aqueous and non-aqueous porogenic solvents, respectively)…

Capillary electrochromatographyChromatographyAqueous solutionChemistryClinical BiochemistryAcrylic ResinsReproducibility of ResultsRepeatabilityEthylenediaminesMethacrylateBiochemistryAnalytical ChemistrySolventPolymerizationCapillary Electrochromatographyvisual_artMicroscopy Electron Scanningvisual_art.visual_art_mediumMethacrylatesAcrylic resinHexyl methacrylateELECTROPHORESIS
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Peroxodisulfate as a chemical initiator for methacrylate-ester monolithic columns for capillary electrochromatography

2008

Organic monolithic stationary phases for CEC were synthesized in situ in fused-silica capillaries. Polymerization mixtures were composed of butyl methacrylate, ethylene dimethacrylate, and [2-(methacryloyloxy)ethyl]trimethyl ammonium chloride in the presence of a porogenic solvent, using ammonium peroxodisulfate as chemical initiator, and N,N,N',N'-tetramethylethylenediamine to activate the reaction. The influence of the amount of initiator, temperature, and composition of porogenic solvent on the physical and chromatographic properties of monolithic stationary phases has been investigated. A minimum plate height of 14.5 microm was obtained at 18 wt% of 1,4-butanediol in the polymerization …

Capillary electrochromatographyChromatographySilicon dioxideClinical BiochemistryAcrylic ResinsAzobisisobutyronitrileEthylenediaminesSilicon DioxideMethacrylateBiochemistryAnalytical ChemistrySolventchemistry.chemical_compoundchemistryPolymerizationAmmonium SulfateCapillary ElectrochromatographyNitrilesMethacrylatesAmmoniumAmmonium chloridePorosityNuclear chemistryELECTROPHORESIS
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p–n Metallophosphor based on cationic iridium(iii) complex for solid-state light-emitting electrochemical cells

2011

An ionic transition-metal complex for improved charge transporting properties was designed, containing both n-type dimesitylboryl (BMes2) and p-type carbazole groups. The complex, [Ir(Bpq)2(CzbpyCz)]PF6 (1) (Bpq = 2-[4-(dimesitylboryl)phenyl] quinoline, CzbpyCz = 5,5′-bis(9-hexyl-9H-carbazol-3-yl)-2,2′-bipyridine) and its equivalent in which the BMes2 groups were substituted with carbazole moieties were evaluated on the photoluminescence and excited state properties in detail. According to the photophysical and electrochemical properties, we concluded that the BMes2 groups can increase the conjugation length of the cyclometalated C^N ligands and greatly enhance the phosphorescence efficienc…

CarbazoleQuinolineCationic polymerizationIonic bondingchemistry.chemical_elementGeneral ChemistryElectroluminescenceElectrochemistryPhotochemistrychemistry.chemical_compoundchemistryMaterials ChemistryIridiumPhosphorescenceJournal of Materials Chemistry
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Reversible coordination of dioxygen by tripodal tetraamine copper complexes incorporated in a porous silica framework.

2010

The present study reports the synthesis and rational design of porous structured materials by using a templating method. A tetraethoxysilylated tripodal tetraamine (TREN) was covalently incorporated in a silica framework with a double imprint: A surfactant template and a metal ion imprint. The presence of a cationic surfactant (CTAB) endowed the material with a high porosity, and the tripodal or square-pyramidal topology of the ligand was preserved thanks to the use of the silylated Cu(II) complex. After removal of the surfactant and de-metalation, the incorporated tetraamine was quantitatively complexed by CuCl(2) and the material has shown after thermal activation that a reversible bindin…

Carbon MonoxideSilicon dioxideLigandNitrogenMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCationic polymerizationElectron Spin Resonance Spectroscopychemistry.chemical_elementGeneral ChemistrySilicon DioxideCopperCatalysisAdductOxygenchemistry.chemical_compoundchemistryCoordination ComplexesTripodal ligandPolymer chemistryReactivity (chemistry)AminesPorosityCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Polymerization of diacetylene carbonic acid monolayers at the gas-water interface

1978

Carbonic acidchemistry.chemical_compoundDiacetylenechemistryPolymerizationMonolayerGeneral EngineeringGeneral Materials SciencePhotochemistryJournal of Polymer Science: Polymer Letters Edition
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Catechol-Initiated Polyethers: Multifunctional Hydrophilic Ligands for PEGylation and Functionalization of Metal Oxide Nanoparticles

2012

Bifunctional CA-PEG (catechol-poly(ethylene glycol)) and multifunctional CA-PEG-PGA/PEVGE (poly(glycidyl amine)/poly(ethylene glycol vinyl glycidyl ether)) ligands for the functionalization and solubilization of nanoparticles are introduced. Tunable polymers with polydispersities1.25 and molecular weights in the range 500-7700 g mol(-1) containing a catechol moiety for conjugation to metal oxide nanoparticles were prepared. The functional PEG ligands were synthesized starting from the acetonide-protected catechol initiator 2,2-dimethyl-1,3-benzodioxole-5-propanol (CA-OH) for oxyanionic polymerization. CA-OH was used both for homopolymerization of ethylene oxide (EO) as well as copolymerizat…

CatecholPolymers and PlasticsEthylene oxideChemistryCatecholstechnology industry and agricultureMetal NanoparticlesBioengineeringmacromolecular substancesLigandsPolyethylene GlycolsBiomaterialschemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryCopolymerPEGylationEpoxy CompoundsMoietyBifunctionalHydrophobic and Hydrophilic InteractionsEthylene glycolBiomacromolecules
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