Search results for "Macro"

showing 10 items of 3471 documents

Riverine impacts on benthic biodiversity and functional traits: A comparison of two sub-Arctic fjords

2020

Abstract Climate change is leading to increases in freshwater discharge to coastal environments with implications for benthic community structure and functioning. Freshwater inputs create strong environmental gradients, which potentially affect the community structure of benthic infauna. In turn, changes in functional trait composition have the potential to affect the processing of terrestrially-derived nutrients and organic matter along the freshwater to marine continuum. We investigated the effects of riverine inputs on benthic community structure, functional traits, taxonomic and functional diversity, and utilization of terrestrial organic matter in two contrasting northern Norwegian fjo…

chemistry.chemical_classificationgeographygeography.geographical_feature_categoryEcologyCommunity structureBiodiversityClimate changeFjordVDP::Matematikk og Naturvitenskap: 400Aquatic ScienceOceanographyNutrientchemistryBenthic zoneMacrobenthosVDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470Environmental scienceOrganic matterVDP::Landbruks- og Fiskerifag: 900::Fiskerifag: 920VDP::Mathematics and natural science: 400
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Abstract Molecular recognition of aromatic hydrocarbons by four endo -functionalized molecular tubes has been studied by 1 H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅ π interactions.

chemistry.chemical_classificationhydrogen bond010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesmolecular dynamics0104 chemical sciencesMolecular recognitionmacrocycleschemistryhydrogenProton NMRhost-guest chemistryaromatic hydrocarbonhydrocarbonsmolecular recognitionAromatic hydrocarbonSpectroscopyHost–guest chemistryta116Binding selectivityChinese Chemical Letters
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Methyl-Substituted α-Cyclodextrin as Affinity Material for Storage, Separation, and Detection of Trichlorofluoromethane

2018

Abstract The severely ozone‐depleting trichlorofluoromethane is still appearing in several recycling processes or industrial applications. A simple and selective supramolecular complex formation of per‐methylated α‐cyclodextrin (1) with the highly volatile trichlorofluoromethane (2) is reported. This interaction moreover leads to thermally stable crystals. Per‐methylated α‐cyclodextrin is successfully exploited as a reversible and selective adsorption material for liquid and airborne trichlorofluoromethane as well as an affinity material for the chemical sensing and detection of this particular volatile organic component.

chemistry.chemical_classificationoptical sensorsCyclodextrinTrichlorofluoromethaneCFC‐11CommunicationComplex formationSupramolecular chemistrymacromolecular substances02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCommunicationssupramolecular chemistry0104 chemical scienceschemistry.chemical_compoundcyclodextrinchemistrySelective adsorptiontrichlorofluoromethaneOrganic component0210 nano-technologyGlobal Challenges
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Photooxidation and Stabilization of Photooxidized Polyethylene and of its Monopolymer Blends

2003

The increasing use of products from recycled polymers, or from blends with recycled polymers exposed to the outdoors, implies the need for good weathering resistance. This is particularly important when the recycled material comes, in turn, from products exposed during their lifetime to the sun. In this case the presence of C=O groups in the macromolecular chains strongly increases the photooxidative degradation kinetics of these secondary materials. In this work the change of the photooxidative degradation of blends of virgin and photooxidized polyethylene was evaluated as a function of the C=O content present in the material. As expected, the presence of the C=O groups strongly increases …

chemistry.chemical_classificationpolyethylene (PE)Materials sciencePolymers and PlasticsphotooxidationKineticsGeneral ChemistryPolymerPolyethylenemechanical propertiesphoto-oxidationSurfaces Coatings and Filmsstabilizationchemistry.chemical_compoundchemistryChemical engineeringpolymeric filmPolymer chemistryMaterials ChemistryPhotooxidative degradationPolymer blendHALSElongationMacromoleculeStabilizer (chemistry)
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A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush

2011

A new biorelevant polymer brush showing a polybenzofulvene backbone was synthesized by a ‘‘grafting through’’ approach based on click chemistry and spontaneous polymerization reactions. The easy polymerization of the relatively complex monomer (6-MOEG-9-TM-BF3k) suggests the existence of a particularly efficient recognition process capable of pre-organizing the monomer molecules for the spontaneous polymerization. 13C-NMR spectroscopy as well as UV-vis and fluorescence spectroscopy suggested for poly-6-MOEG-9-TM-BF3k the features of a vinyl (1,2) p-stacked polymer. The new polybenzofulvene derivative was found to interact with water at room temperature to give clear water solutions, but TEM…

chemistry.chemical_classificationpolymer brushPolymers and PlasticsOrganic ChemistryBioengineeringPolymerPolymer brushCell morphologyBiochemistryFluorescence spectroscopyNMRchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymerizationPolymer chemistryclick chemistryClick chemistryMacromolecule
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Polymerization of methyl and phenyl oxazoline initiated with alkyl chloroformates

2010

It has been shown that alkyl chloroformates are capable of initiating the polymerization of oxazolines. Esters itself initiate rather slowly and the polymerization proceeds via covalent growing species. Exchange of counter ions with triflate or iodide anions leads to faster initiation and higher reaction rates. The polymerization is of living character.

chemistry.chemical_classificationtechnology industry and agricultureChain transfermacromolecular substancesGeneral ChemistryOxazolinePhotochemistryLiving free-radical polymerizationchemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationPolymer chemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationAlkylBulletin des Sociétés Chimiques Belges
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Binding and Fluorescent Sensing of Dicarboxylates by a Bis(calix[4]pyrrole)-Substituted BODIPY Dye

2013

A bis(calix[4]pyrrole)-substituted BODIPY ditopic receptor 1 has been synthesised and characterised. The binding and sensing properties of 1 towards several aliphatic and aromatic dicarboxylates have been evaluated by using UV/Vis fluorescence and 1H NMR spectroscopy. The receptor strongly binds linear α,ω-dicarboxylates of appropriate lengths (C9 and C10) by acting as a cleft. For all dicarboxylates, the binding event is detected by a bathochromic shift in the UV/Vis spectra of the receptor and by strong quenching of its fluorescence.

chemistry.chemical_compound1h nmr spectroscopyQuenching (fluorescence)chemistryOrganic ChemistryBathochromic shiftmacromolecular substancesVis spectraPhysical and Theoretical ChemistryBODIPYPhotochemistryFluorescencePyrroleEuropean Journal of Organic Chemistry
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Acrylic Graft Copolymers Via Macromonomers

1995

Comb-shaped poly(methyl methacrylate) (PMMA) and PMMA grafted with poly(nbutyl acrylate) (PnBuA) were prepared by radical copolymerisation of ω-methacryloyl-PMMA with MMA and nBuA, respectively. The comb-shaped PMMA is characterised with respect to radius of gyration by using GPC equipped with a multi-angle laser light scattering detector. The radical copolymerisation of the macromonomer with nBuA in toluene follows complex kinetics. The dependence of the relative reactivity of the macromonomer on absolute concentration and on the ratio of comonomers may be explained by preferential solvation of comonomers by segments of their own kind (“bootstrap effect”) or even micelle formation. However…

chemistry.chemical_compoundAcrylateMaterials sciencechemistryButyl acrylatePolymer chemistryRadius of gyrationCopolymerMethyl methacrylateThermoplastic elastomerMacromonomerMicelle
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Pharmakologisch aktive polymere, 5. Modellreaktionen zur umsetzung von pharmaka und enzymen mit monomeren und polymeren reaktiven estern

1973

Die Darstellung reaktiver Ester der Acryl-, Methacryl- und N-Vinylcarbaminsaure wird beschrieben. Die Verbindungen sind im Gegensatz zu anderen reaktiven Saurederivaten wie Saurechloriden, -anhydriden und Isocyanaten kristalline Monomere, die gut zu handhaben sind. Sie lassen sich leicht zu unvernetzten, loslichen Polymeren homo- und copolymerisieren. Die Copolymerisationsparameter wurden bestimmt. Entsprechend wie die aus der Peptidchemie bekannten reaktiven Ester reagieren sie in monomerer wie in polymerer Form bei niedriger Temperatur selektiv und schonend mit Nucleophilen in guten Ausbeuten, z. B. mit Aminen in wasriger Losung. Dies eroffnet die Moglichkeit zur nebenreaktionsfreien Bind…

chemistry.chemical_compoundAqueous solutionMonomerNucleophilechemistryPolymer chemistryCopolymerPeptide chemistryReactivity (chemistry)macromolecular substancesDie Makromolekulare Chemie
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Effect of Monooxygenase Inducers on the Binding of Benzo-(A)Pyrene Metabolites to Cellular Macromolecules in Perfused Rat Lungs

1978

The irreversible binding of metabolically activated [3H]-benzo(a)pyrene (BP) to cellular macromolecules of isolated perfused rat lungs was studied. Lungs from differently pretreated animals were perfused in situ in a recirculating system without ventilation. BP with a specific activity of 10 mCi/μmol was added to 50 ml perfusion medium containing 40% washed bovine erythrocytes to a final concentration of 1 μM. DNA, RNA and protein fractions were isolated and assayed for irreversibly bound radioactivity.

chemistry.chemical_compoundBenzo(a)pyrenechemistryBiochemistryRNAPyreneInducerSpecific activityMonooxygenaseDNAMacromolecule
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