Search results for "functional"

showing 10 items of 4822 documents

Normal-phase (temperature gradient) interaction chromatography – A powerful tool for the characterisation of high molecular weight chain-end function…

2015

Abstract We report here, for the first time, quantitative analysis of end-group functionalisation and the extent of end-group modification of polymers with molar mass up to 200,000 g mol −1 , using a combination of isothermal and temperature gradient interaction chromatography. At such high molecular weights, other common analytical techniques such as MALDI-ToF-MS and NMR spectroscopy are simply unable to offer any quantitative insight into the end-group functionality of polymers. Thus, normal phase isothermal interaction chromatography (NP-IIC) has been used to characterise a series of polystyrene samples, with identical molar mass (c. 90,000 g mol −1 ), each carrying a single chain-end fu…

chemistry.chemical_classificationMolar massChromatographyPolymers and PlasticsResolution (mass spectrometry)ChemistryElutionOrganic ChemistryAnalytical chemistryGeneral Physics and AstronomyPolymerNuclear magnetic resonance spectroscopyTemperature gradient interaction chromatography (TGIC)Primary alcoholEnd-functionalised polymers.Anionic polymerisationIsothermal processMaterials ChemistryProton NMRPolymer characterisation
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Photoaffinity cross-linking of F1ATPase from the thermophilic bacterium PS3 by 3′-arylazido-β-alanyl-2-azido ATP

1989

AbstractThe photoactivatable bifunctional 3′-arylazido-β-alanyl-2-azido ATP (2,3′-DiN3ATP) has been applied to study the localization of the nucleotide-binding sites of coupling factor 1 (F1ATPase, TF1) from the thermophilic bacterium PS3 by photoaffinity cross-linking. UV irradiation of TF1 in the presence of 2,3′-DiN3ATP results in the nucleotide-dependent formation of various higher molecular mass cross-links formed by two, three or even four α- and/or β-subunits. The differences observed upon photoaffinity cross-linking by the bifunctional 2-azido ATP or 8-azido ATP analog are discussed. They are probably due to the varied maximal distance between both azido groups, or to the different …

chemistry.chemical_classificationMolecular massbiologyStereochemistryProtein subunitNucleotide conformationBiophysicsCell Biologybiology.organism_classificationBiochemistrychemistry.chemical_compoundEnzymechemistryStructural BiologyGeneticsPhotoaffinity crosslinkingATPase F1-NucleotideNucleotide-binding siteBinding siteBifunctionalInterfacial localizationMolecular BiologyThermophilic bacterium PS3BacteriaFEBS Letters
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Production of soluble eukaryotic recombinant proteins in E. coli is favoured in early log-phase cultures induced at low temperature

2013

Abstract Background Producing recombinant plant proteins expressed in Escherichia coli produce in high yields and in a soluble and functional form can be difficult. Under overexpression conditions, proteins frequently accumulate as insoluble aggregates (inclusion bodies) within the producing bacteria. We evaluated how the initial culture density, temperature and duration of the expression stage affect the production of some eukaryotic enzymes in E. coli. Findings A high yield of active soluble proteins was obtained by combining early-log phase cultures and low temperatures for protein induction. When IPTG was added at OD600 = 0.1 and cultures were maintained at 4°C for 48-72 h, the soluble …

chemistry.chemical_classificationMultidisciplinarybusiness.industryShort Reportlac operonBiologymedicine.disease_causeFunctional proteinsInclusion bodiesBiotechnologylaw.inventionEnzymeBiochemistrychemistrylawProtein purificationmedicineRecombinant DNALow temperatureSoluble recombinant proteinsTarget proteinHeterologous expressionbusinessEscherichia coliEarly log phaseSpringerPlus
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Enhancing the mechanical performance of polymer based nanocomposites by plasma-modification of nanoparticles

2012

Abstract The possibility of enhancing the mechanical performance of two different polymer-based nanocomposites using polyamide 6 (PA6) and poly[ethylene-co-(vinyl acetate)] (EVA) as matrices was investigated. The nanofillers used were, respectively, either carbon nanotubes (CNTs) or an organically modified montmorillonite (Cloisite 15A), both previously modified by plasma treatment to introduce polar moieties. The nanofillers were fully characterized by Raman spectroscopy, XPS, FT-IR and XRD, demonstrating their effective modification with oxygenated groups. The nanocomposites were prepared by melt processing in order to obtain films and fibres. The mechanical tests carried out on the nanoc…

chemistry.chemical_classificationNanocompositeMaterials scienceNanocompositePolymers and PlasticsOrganic ChemistryNanoparticlePolymerCarbon nanotubeCarbon nanotubelaw.inventionCarbon nanotubes; Functionalization; Nanocomposite; Nanoclay; Nanoparticle; Plasma.chemistry.chemical_compoundNanoparticlechemistrylawPolyamideVinyl acetateNanoclaySurface modificationComposite materialFunctionalizationElastic modulusPlasma.
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Self-assembly of small gold colloids with functionalized gold nanorods.

2007

We present a general strategy to stabilize gold nanorod suspensions with mono- and bifunctional polyethylene glycol (PEG) and to attach a controlled number of nanoparticles or biomolecules. Characterization by gel electrophoresis, transmission electron microscopy (TEM), and optical dark-field microscopy show the specific binding of functionalized nanorods to their target while avoiding nonspecific binding to substrates, matrices, and other particles. Such nanorods are well suited for self-assembly of nanostructures and single-molecule labeling.

chemistry.chemical_classificationNanostructureMaterials scienceMechanical EngineeringBiomoleculeNanoparticleBioengineeringNanotechnologyGeneral ChemistryPolyethylene glycolCondensed Matter Physicschemistry.chemical_compoundchemistryTransmission electron microscopyGeneral Materials ScienceNanorodSelf-assemblyBifunctionalNano letters
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Functionalization of aliphatic polyesters by nitroxide radical coupling

2014

Functionalized poly(butylene succinate) (PBS) samples were prepared by a post-polymerization method based on the coupling reaction between TEMPO derivatives bearing different functionalities and PBS macroradicals generated by H-abstraction using a peroxide. 4-Benzoyloxy-2,2,6,6-tetramethylpiperidine-1- oxyl (BzO-TEMPO) and 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO), a pro-fluorescent nitroxide, were successfully grafted on PBS, as revealed by MALDI TOF MS and UV-Vis spectroscopy. The functionalization degrees were accurately determined by UV-Vis analysis and confirmed by 1H-NMR spectroscopy. The grafting site was identified by combining theoretical calculations with e…

chemistry.chemical_classificationNitroxide mediated radical polymerizationgenetic structuresPolymers and PlasticsOrganic ChemistrySide reactionBioengineeringPolymerBiochemistryPeroxideCoupling reactionlaw.inventionPolyesterchemistry.chemical_compoundaliphatic polyesterchemistrylawPolymer chemistrySurface modificationElectron paramagnetic resonancenitroxide radicalpolymer functionalizationPolymer Chemistry
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Reactivity of the carbon-carbon double bond towards nucleophilic additions. A dft analysis

2004

Abstract The global and local electrophilicity indexes have been used to characterize the reactivity pattern of the CC double bond towards nucleophilic addition reactions. A wide family of molecules including ketones, esters, anhydrides, nitriles and nitrocompounds containing appropriate substitution on the CC double bond have been classified within an unique scale of reactivity. The predictive capability of the theoretical model is tested against a series of benzylidenemalononitriles and substituted α-nitrostilbenes.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryReinforced carbon–carbonBiochemistrychemistryNucleophileComputational chemistryDrug DiscoveryElectrophileOrganic chemistryMoleculeDensity functional theoryReactivity (chemistry)
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A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
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The nucleophilic addition of nitrones to carbonyl compounds: insights on the nature of the mechanism of the l-proline induced asymmetric reaction fro…

2004

Abstract The mechanism of the l -proline induced asymmetric nitrone–aldol reaction of N -methyl- C -ethylnitrone with dimethyl ketomalonate has been studied by using density functional theory at B3LYP/6-31G** level. The reaction was initialized by the addition of l -proline to the nitrone to form an aminal, which by elimination of the hydroxylamine gave a chiral enamine. The nucleophilic addition of this chiral enamine to dimethyl ketomalonate corresponds to stereoselective C–C bond-formation step. Further nucleophilic addition of hydroxylamine to the zwitterionic intermediate formed in the enamine addition gave a second aminal, which by l -proline elimination afforded the corresponding β-h…

chemistry.chemical_classificationNucleophilic additionStereochemistryOrganic ChemistryCatalysisEnamineNitroneInorganic Chemistrychemistry.chemical_compoundHydroxylaminechemistryAminalDensity functional theoryStereoselectivityProlinePhysical and Theoretical ChemistryTetrahedron: Asymmetry
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Diene/olefin/polar monomer copolymerisation: unprecedented functional polymers from a rare earth catalyst

2002

An ansasamarocene allyl system is an efficient initiator which polymerises 1,3-dienes, copolymerises dienes and long-chain α-olefins or α,ω-dienes to give functionalisable polymers. It also polymerises caprolactone and allows the controlled diblock copolymerisation of isoprene or isoprene/ α-olefin copolymer and caprolactone.

chemistry.chemical_classificationOlefin fiberMaterials sciencePolymers and PlasticsDieneOrganic ChemistryPolymerchemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryFunctional polymersCaprolactoneIsoprenePolymer International
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