Search results for "SUBSTANCES"

showing 10 items of 1122 documents

Functional end groups for polymers prepared using ring-opening metathesis polymerization.

2011

The precise placement of functional groups on the chain-ends of macromolecules is a major focus of polymer research. Most common living polymerization techniques offer specific methods of end-functionalization governed by the active propagating species and the kinetics of the polymerization reaction. Ring-opening metathesis polymerization has established itself as one of the most functional-group-tolerant living polymerization techniques known, but this tolerance has limited the number of available functionalization reactions. Metathesis chemists have therefore been required to develop a variety of end-functionalizations, adapting each of them to the reactivity scheme of the particular cata…

chemistry.chemical_classificationMolybdenumPolymer scienceMolecular StructureMacromolecular SubstancesPolymersGeneral Chemical EngineeringGeneral ChemistryPolymerMetathesisCatalysisRutheniumchemistryPolymerizationOrganometallic CompoundsSurface modificationLiving polymerizationRing-opening metathesis polymerisationReactivity (chemistry)MacromoleculeNature chemistry
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Imaging of Keratin Dynamics during the Cell Cycle and in Response to Phosphatase Inhibition

2004

Publisher Summary The characterization and development of autofluorescent proteins, most prominently of the green florescent protein, have provided tools to label cellular structures such that they can be examined in living cells. This chapter highlights the potential of live cell imaging in providing novel and unprecedented insights into the dynamic organization of the keratin cytoskeleton and outlines the important aspects of this method. The live cell imaging experiments suggest that the driving force behind the vectorial and dynamic keratin distribution patterns relies both on microtubules and microfilaments and their associated factors. The studies on the dynamics of the keratin cytosk…

chemistry.chemical_classificationMotor proteinchemistryLive cell imagingMicrotubuleKeratinFluorescence recovery after photobleachingmacromolecular substancesBiologyIntermediate filamentCytoskeletonMicrofilamentCell biology
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Numerical model for composite material with polymer matrix reinforced by carbon nanotubes

2008

Due to the high stiffness and strength, as well as their ability to act as conductors, carbon nanotubes are under intense investigation as fillers in polymeric materials. The nature of the carbon nanotube/polymer bonding and the curvature of the carbon nanotubes within the polymer have arisen as particular factors in the efficacy of the carbon nanotubes to actually provide any enhanced stiffness or strength to the nanocomposite. Here the effects of carbon nanotube curvature and interface interaction with the matrix on the nanocomposite stiffness are investigated using nanomechanical analysis. In particular, the effects of poor bonding and thus poor shear lag load transfer to the carbon nano…

chemistry.chemical_classificationNanocompositeMaterials scienceMechanical EngineeringCarbon nanotube actuatorsComposite numbertechnology industry and agricultureMechanical properties of carbon nanotubesmacromolecular substancesPolymerCarbon nanotubeCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter PhysicsCarbon Nanotube Numerical Simulations Composite Materials Nanotechnology.law.inventionCarbon nanotube metal matrix compositesSettore ING-IND/14 - Progettazione Meccanica E Costruzione Di MacchineCondensed Matter::Materials ScienceCarbon nanobudchemistryMechanics of MaterialslawComposite materialMeccanica
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Recent advances on application of peptide nucleic acids as a bioreceptor in biosensors development

2019

Abstract The analogs of DNA are unique biomedical tools that are broadly utilized to develop different types of biosensors. Peptide nucleic acids (PNA) are an individual and notable class of nucleic acid analogs due to their unique, novel physicochemical and biochemical characteristics, stability and resistance to nuclease and protease enzymes, significant interactions with complementary strands and remarkable hybridization attributes. Therefore, they are employed in the preparation and fabrication of various types of functional biosensors. In other words, immobilization of PNA as an appropriate diagnostic probe on the surface of electrochemical and optical converters lead to the fabricatio…

chemistry.chemical_classificationNucleaseProteasePeptide nucleic acidbiologymedicine.medical_treatment010401 analytical chemistrytechnology industry and agricultureRNAPeptidemacromolecular substances01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryBiochemistrymedicinebiology.proteinNucleic acidBiosensorSpectroscopyDNATrAC Trends in Analytical Chemistry
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Determining the selective impregnation of waterlogged archaeological woods with poly(ethylene) glycols mixtures by differential scanning calorimetry

2012

The differential scanning calorimetry (DSC) technique was demonstrated to be a reliable and fast tool for the investigation of the selective impregnation of archaeological woods with poly(ethylene) glycols (PEGs) mixtures. To this aim, waterlogged archaeological woods were impregnated by using aqueous mixtures of PEG 4000 and PEG 400 as well as mixtures of these polymers in the melt state. The efficiency of the treatments was also estimated by determining the total consolidant content entrapped into the cavities of degraded wood by means of DSC and thermogravimetry.

chemistry.chemical_classificationPEG 400EthyleneMaterials scienceAqueous solutiontechnology industry and agriculturemacromolecular substancesPolymerCondensed Matter PhysicsArchaeologyThermogravimetryCultural Heritage Woodchemistry.chemical_compoundDifferential scanning calorimetrychemistryPEG ratioPhysical and Theoretical ChemistryPoly ethyleneSettore CHIM/02 - Chimica Fisica
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Chemical speciation of polycyclic aromatic hydrocarbons in sediments: partitioning and extraction of humic substances.

2010

The primary objective of this study was to examine the chemical speciation of polycyclic aromatic hydrocarbons (PAHs) found in sediments endowed with different characteristics. To achieve this purpose and because the nature of the sediments influences the distribution of PAHs, we have analyzed four different types of sediments. To study the role of organic matter in the sequestration of PAHs, we fractionated humic substances into humic acids and humin–mineral fractions. After their separation and purification, the humic components were examined for their sorptive reactivity by extracting them with organic solvents; these extracts were subsequently subjected to GC/MS analysis. Our results sh…

chemistry.chemical_classificationPollutionPersistent organic pollutantGeologic Sedimentsmedia_common.quotation_subjectExtraction (chemistry)Solid Phase ExtractionSedimentFraction (chemistry)PAHsChemical speciationHumicSandy and muddy sedimentsAquatic ScienceChemical FractionationOceanographyPollutionSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliGas Chromatography-Mass SpectrometrySpeciationHydrocarbonchemistryEnvironmental chemistryOrganic matterPolycyclic Aromatic HydrocarbonsHumic Substancesmedia_commonEnvironmental MonitoringMarine pollution bulletin
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Supramolecular Thermotropic Liquid Crystalline Materials with Nematic Mesophase Based on Methylated Hyperbranched Polyethylenimine and Mesogenic Carb…

2006

Supramolecular interaction of fully methylated hyperbranched polyethylenimines (PEI) with a mesogen-based carboxylic acid, 5-(p-cyanobiphenoxy)pentanoic acid, results in the formation of supramolecular complexes exhibiting thermotropic liquid crystalline (LC) mesophases. In contrast to the common smectic mesophases of most dendritic LC polymers, nematic LC phase were observed. The complexation of PEI and the mesogen units is due to electrostatic interaction between the carboxylate groups and the ammonium end groups of PEI. LC properties were investigated by a combination of differential scanning calorimetry, polarizing light optical microscopy, and X-ray diffractometry.

chemistry.chemical_classificationPolyethylenimineMaterials sciencePolymers and PlasticsMesogenCarboxylic acidOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryMesophasemacromolecular substancesThermotropic crystalchemistry.chemical_compoundchemistryLiquid crystalPolymer chemistryMaterials ChemistryCarboxylateMacromolecular Rapid Communications
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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, characterisation and properties of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide-graft-maleic anhydride precursors and their stimuli-responsiv…

2009

Abstract A family of poly(amino acid)-maleic anhydride hydrogels were designed and synthesized. Water soluble polymeric precursors were prepared by partially substituting the hydroxyl groups of the α,β-poly( N -2-hydroxyethyl)- dl -aspartamide backbone with maleic anhydride, so as to provide double bonds for crosslinking and carboxylic acid groups for pH and electric field responsiveness. Reaction conditions (reactive mixture composition and catalysis) were systematically varied in order to obtain PHEA–MA precursors with different and reliable graft-maleic anhydride levels. PHEA–MA precursors were characterised by titration, Nuclear Magnetic Resonance ( 1 H NMR), Fourier-Transformed Infrare…

chemistry.chemical_classificationPolymers and PlasticsGeneral Chemical EngineeringCarboxylic acidSize-exclusion chromatographyResponsive hydrogeltechnology industry and agricultureMaleic anhydrideChemical modificationAcid–base titrationGamma irradiationmacromolecular substancesGeneral ChemistryBiochemistryPolyelectrolytechemistry.chemical_compoundchemistryPolymer synthesiSelf-healing hydrogelsPolymer chemistryMaterials ChemistryEnvironmental ChemistryRadical initiatorSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSwellingReactive and Functional Polymers
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Comparison of living polymerization systems

1994

Recent developments in the field of living polymerization are surveyed. Comparison of the available mechanistic and kinetic information is made for living anionic, cationic, free radical, group transfer, ring-opening metathesis, Ziegler-Natta and immortal polymerizations. This evaluation indicates that the majority of living polymerizations involve quasiliving equilibrium between active (propagating) and dormant (nonpropagating) polymer chains. On the basis of the kinetics of a general model for quasiliving and ideal living polymerizations it is concluded that ideal living polymerization is a special subclass of quasiliving polymerizations. Classification of living polymerization systems is…

chemistry.chemical_classificationPolymers and PlasticsKinetic informationOrganic Chemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesPolymerCondensed Matter PhysicsMetathesisLiving free-radical polymerizationchemistryPolymer chemistryMaterials ChemistryLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationMacromolecular Symposia
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