Search results for "MR"

showing 10 items of 3001 documents

Analysis of plasticization and reprocessing effects on the segmental cooperativity of polylactide by dielectric thermal spectroscopy

2021

Abstract In the present study, the dielectric properties of both neat and plasticized polylactide submitted to repeated extrusion and injection processes to simulate recycling were analysed. The dielectric relaxation spectrum, consisting of β and α relaxation, revealed the relevance of both acryl-PEG based plasticization and thermo-mechanical degradation induced by repeated extrusion and grinding-injection reprocessing cycles on polylactide (PLA). The β-relaxation has its origin in the intramolecular local motions of pendant groups of the PLA backbone, while the α-relaxation is representative of the intermolecular large-scale segmental motions of the PLA backbone. The addition of acryl-PEG …

chemistry.chemical_classificationPermittivityMaterials sciencePolymers and PlasticsOrganic ChemistryIntermolecular forceRelaxation (NMR)02 engineering and technologyDielectricPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCrystallinityChemical engineeringchemistryMaterials ChemistryExtrusion0210 nano-technologyGlass transitionPolymer
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Disordered charge distributions and dielectric loss in extra dense flint glasses

1990

The complex permittivities of some extra dense flint glasses (EDF glasses) have been studied. The dielectric features of the samples are dominated by their PbO content. Both refractive indices and dielectric losses exhibit a close relation to the concentration of Pb ions. The latter are located either at sites of the network atoms or filling the potential minima interstitially. They can be identified by their different relaxation mechanisms. The dispersion in the submillimeter wave and FIR area is characterized by a very broad distribution of comparably sharp resonant states. “Thermal lens” — or hysteresis effects can be excluded.

chemistry.chemical_classificationPermittivityPhysics and Astronomy (miscellaneous)Condensed matter physicsbusiness.industryRelaxation (NMR)General EngineeringPhysics::OpticsGeneral ChemistryDielectricIonCondensed Matter::Materials ScienceHysteresisOpticschemistryGeneral Materials ScienceDielectric lossbusinessInorganic compoundRefractive indexApplied Physics A Solids and Surfaces
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Phenolic and acetylenic metabolites from Artemisia assoana

1987

Abstract Nine flavones, three coumarins, two flavone glycosides, p-hydroxyacetophenone and methyl caffeate have been isolated from the aerial parts of Artemisia assoana. Six diacetylenic spiroketal enol-ethers, a mixture of n-alkyl p-coumarates and a new phenylpropanoid metabolite, sinapyl alcohol diisovalerate, have been isolated from root extracts of the same plant. 1H and 13C NMR spectra of some of these compounds are given and taxonomic aspects are discussed.

chemistry.chemical_classificationPhenylpropanoidChemistryStereochemistryMetabolitePlant ScienceGeneral MedicineHorticultureCarbon-13 NMRBiochemistryFlavoneschemistry.chemical_compoundSinapyl alcoholChemotaxonomyMethyl caffeateOrganic chemistryPhenolsMolecular BiologyPhytochemistry
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1H,13C and17O NMR spectroscopic study of four bicyclo [3.1.1]heptenes (derivatives of α-pinene) and four bicyclo[3.1.1]heptanes (derivatives of β-pin…

1992

Four derivatives of 2, 6, 6-trimethylbicyclo[3.1.1]hept-2-ene (α-pinene) and four derivatives of 2-methylene-6, 6-dimethylbicyclo[3.1.1]heptane (β-pinene) were synthesized and their 1H, 13C and 17O NMR spectra were measured, analysed and assigned. The 1H NMR spectral parameters were obtained by computer-aided analyses of the very complex multi-spin, second-order spectra. Some of the 13C NMR chemical shift assignments of these compounds reported in the literature should be changed, based on these accurate 1H NMR spectral analyses and carbon-proton chemical shift correlated spectra (COSY). The new assignments are supported by the 1J(C, H) values, which show a strong dependence on the bond ang…

chemistry.chemical_classificationPineneHeptaneKetoneBicyclic moleculeStereochemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRchemistry.chemical_compoundCrystallographyMolecular geometrychemistryProton NMRGeneral Materials ScienceMagnetic Resonance in Chemistry
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Polymer chains confined into tubes with attractive walls: A Monte Carlo simulation

1994

A bead-spring off-lattice model of a polymer chain with repulsive interactions among repeating units confined into straight tubes of various cross sections, DT2, is studied by Monte Carlo simulation. We are also varying the chain length from N = 16 to 128 and the strength of a short-range attractive interaction between the repeating units and the walls of the tube. Longitudinal and perpendicular static linear dimensions of the chains are analyzed, as well as the density profile of repeating units across the tube. These data are interpreted in terms of scaling concepts describing the crossover between three-dimensional and quasi-one-dimensional chain conformations and the adsorption transiti…

chemistry.chemical_classificationPolymers and Plastics530 PhysicsOrganic ChemistryMonte Carlo methodRelaxation (NMR)Polymer530 PhysikCondensed Matter PhysicsMolecular physicsInorganic ChemistrychemistryChain (algebraic topology)Materials ChemistryPerpendicularRadius of gyrationConfined spaceScalingSimulationMacromolecular Theory and Simulations
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Ferrocene-Containing Multifunctional Polyethers: Monomer Sequence Monitoring via Quantitative 13C NMR Spectroscopy in Bulk

2014

Ferrocenyl glycidyl ether (fcGE) and allyl glycidyl ether (AGE) are copolymerized via living anionic ring-opening polymerization to generate polyfunctional copolymers with molecular weights up to 40 300 g/mol and low molecular weight dispersities (Mw/Mn < 1.18). Copolymerizations were carried out in bulk at 100 °C and unexpectedly found to proceed without any isomerization of the allyl double bonds. The copolymerization behavior of fcGE and AGE was monitored by in situ quantitative 13C NMR kinetic measurements in bulk, evidencing the formation of random copolymers under these conditions, showing no gradient of comonomer incorporation. The redox-active behavior of the copolymers and homopoly…

chemistry.chemical_classificationPolymers and PlasticsAllyl glycidyl etherComonomerOrganic ChemistryPolymerCarbon-13 NMRInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationFerrocenePolymer chemistryMaterials ChemistryCopolymerMacromolecules
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Deuteron n.m.r. in relation to the glass transition in polymers

1985

Abstract 2H n.m.r. is introduced as a tool for investigating slow molecular motion in the glass transition region of amorphous polymers. In particular, we compare 2H spin alignment echo spectra of chain deuterated polystyrene with models for restricted rotational Brownian motion. Molecular motion in the polystyrene-toluene system has been investigated by analysing 2H n.m.r. of partially deuterated polystyrene and toluene, respectively. The diluent mobility in the mixed glass has been decomposed into ‘solid’ and ‘liquid’ components where the respective average correlation times differ by more than 5 decades.

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryRelaxation (NMR)Analytical chemistryPolymerAmorphous solidCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundNuclear magnetic resonanceDeuteriumMaterials ChemistrySpin echoPolystyrenePhysics::Chemical PhysicsGlass transitionRotational Brownian motionPolymer
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Poly(carbonate) copolymers with a tailored number of hydroxyl groups from glycidyl ethers and CO2

2014

Functional poly(carbonate)s with multiple hydroxyl functionalities have been prepared by copolymerization of carbon dioxide (CO2) with glycidyl methyl ether (GME) and benzyl glycidyl ether (BGE) in various ratios, using a diethylzinc–pyrogallol catalyst system. Subsequent catalytic hydrogenation was employed for removal of the benzyl protecting groups at the polymer backbone. A series of copolymers with varying comonomer fractions from 0 to 100% was obtained. The copolymers possessed a broad range of molecular weights from 9000 to 30 000 g mol−1 and showed polydispersities Mw/Mn between 2.4 and 3.6. The materials were characterized via1H and 13C NMR, SEC and differential scanning calorimetr…

chemistry.chemical_classificationPolymers and PlasticsComonomerOrganic ChemistryBioengineeringEtherPolymerCarbon-13 NMRBiochemistryCatalysischemistry.chemical_compoundDifferential scanning calorimetrychemistryPolymer chemistryCopolymerCarbonateOrganic chemistryPolym. Chem.
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Supramolecular Nanocycles Comprisingβ-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

2010

We applied 1,3-dipolar cycloaddition to bind ethynylferrocene onto 6I-azido-6I-deoxycyclomaltoheptaose under microwave assisted conditions. The process was investigated by (1) H NMR, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The ability of the synthesized compound to self-organize to cyclic supramolecular structures was investigated by dynamic light scattering measurements and cryo-transmission electron microscopy.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistrymacromolecular substancesCycloadditionInclusion compoundchemistry.chemical_compoundchemistryFerrocenePolymer chemistry13-Dipolar cycloadditionMaterials ChemistryProton NMROrganic chemistryMetalloceneMacromolecular Rapid Communications
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Synthesis and characterisation of novel chemical conjugates based on alpha, beta-polyaspartylhydrazide and beta-cyclodextrins

2006

A new family of supramolecular systems based on a synthetic polyaminoacid and cyclic oligosaccharides such as beta-cyclodextrins (beta-CDs) was synthesised. The pharmaceutical potential of these systems arises from the proper combination between the complexing properties of cyclodextrins and the particular pharmacokinetic profile that can be obtained by using macromolecular conjugates with a biocompatible backbone. Five supramolecular conjugates were synthesised by using alpha,beta-polyaspartylhydrazide (PAHy) as a polymeric component and various amounts of two P-CD derivatives. In particular, by reaction of PAHy with beta-CD monoaldehyde, samples named as A(1), A(2) and A(3), bearing, resp…

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinsupramolecular systemsOrganic ChemistrySupramolecular chemistryGeneral Physics and AstronomyChemical modificationConjugated systemCombinatorial chemistryInclusion compoundbeta-cyclodextrinchemistry.chemical_compoundchemistryMaterials ChemistryProton NMROrganic chemistryPAHyMacromoleculeConjugate
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