Search results for "SUBSTANCES"

showing 10 items of 1122 documents

Thermo- and light responsive micellation of azobenzene containing block copolymers

2010

In this communication, the synthesis and characterization of thermo- and light responsive block copolymers is reported. PEO-b-PNIPAM polymers with azobenzene moieties were prepared and analyzed by turbidimetry, fluorescence, NMR and DLS measurements. A temperature controlled reversible formation as well as a light induced disruption and reformation of micellar structures in water was found.

chemistry.chemical_classificationMaterials scienceeducationtechnology industry and agricultureMetals and Alloysmacromolecular substancesGeneral ChemistryPolymerFluorescenceCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundLight responsivechemistryAzobenzeneChemical engineeringPolymer chemistryMaterials ChemistryCeramics and CompositesLight inducedCopolymerTurbidimetryChemical Communications
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MCM-41 and related materials as media for controlled polymerization processes

1994

The synthesis of mesoporous MCM-41 type materials based on transition metal oxides and the polymerization of several monomers within MCM-41 is presented with the aim to specifically investigate the effects of the interface and confinement on host-guest interactions. In addition to standard MCM-41, material based on transition metal oxides is obtained although template removal has been unsuccessful for such compounds until now. In situ polymerization of styrene, methyl methacrylate and vinyl acetate is possible within the mesopore system. The properties of some of the encapsulated polymers differ markedly with those obtained in the bulk.

chemistry.chemical_classificationMaterials sciencemacromolecular substancesPolymerchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryVinyl acetateCoordination polymerizationIn situ polymerizationMethyl methacrylateIonic polymerizationMesoporous material
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Emergence, evidence, and effect of junction clustering in supramolecular polymer materials

2021

A significant fraction of biomaterials consists of supramolecular polymers and networks formed by non-covalent interactions between associative motifs. They typically contain complex structures in which on top of binary associations, phase-separation and aggregation of associative junctions occur. Such hierarchical assemblies have significant influences on the dynamics as well as the physical and mechanical properties of the materials. Similar to supramolecular biomaterials, aggregation of associative junctions has also been frequently reported to occur in synthetic supramolecular polymers and networks. Engineering of such secondary structures in a sense to create and control the extent of …

chemistry.chemical_classificationMaterials sciencetechnology industry and agricultureSupramolecular chemistryNanotechnologymacromolecular substances02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSupramolecular polymerschemistryCharacterization methodsChemistry (miscellaneous)Deep knowledgeGeneral Materials ScienceThermoplastic elastomer0210 nano-technologyCluster analysisMaterials Advances
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Mesoscopic gel at low agarose concentration in water: a dynamic light scattering study

1995

Previous work in our laboratory has shown that at very low agarose concentration in water gelation still occurs within mutually disconnected, high concentration regions generated by spinodal demixing. The freely diffusing particles obtained in these conditions are studied in the present work by depolarized dynamic light scattering and probe diffusion experiments. These particles are found to behave as large (in fact, mesoscopic) polymer fibers entangled in a continuously rearranged mesh with scaling parameters typical of partially flexible, neutral chains. The present results allow specifying the notion of mesoscopic gelation. They also reveal that the same symmetry-breaking mechanism that …

chemistry.chemical_classificationMesoscopic physicsWork (thermodynamics)SpinodalLightMacromolecular SubstancesSepharoseDiffusionAnalytical chemistryBiophysicsPolymerBiophysical PhenomenaCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundDynamic light scatteringchemistryChemical physicsPercolationScattering RadiationAgaroseGelsResearch ArticleBiophysical Journal
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MODIFICATION OF HUMIC SUBSTANCES FOR DEVELOPMENT OF MATERIALS FOR ENVIRONMENTAL TECHNOLOGIES

2019

Humic substances are high molecular weight refractory polycationites formed during decay of living organic matter and through biosynthesis of low molecular weight organic substances (metabolites or decay products of living organisms). Presence of many functional groups in the structure of humic substances determines their ability to interact with metal ions forming stable complexes and influencing metal ion speciation in the environment and mobility, behaviour and speciation forms in the environment. Presently humic substances are a product of industrial scale and quantities in amounts of hundreds of tons are produced. The aim of this study is to analyse derivatization possibilities of humi…

chemistry.chemical_classificationMetal ions in aqueous solutionhumic substances; modification; functional groups; pollutants; remediationInner sphere electron transfercomplex mixturesMetalAcylationchemistry.chemical_compoundchemistryElemental analysisvisual_artFunctional groupvisual_art.visual_art_mediumOrganic chemistryOrganic matterDerivatizationENVIRONMENT. TECHNOLOGIES. RESOURCES. Proceedings of the International Scientific and Practical Conference
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Tuneable Transient Thermogels Mediated by a pH- and Redox-Regulated Supramolecular Polymerization.

2017

A multistimuli-responsive transient supramolecular polymerization of β-sheet-encoded dendritic peptide monomers in water is presented. The amphiphiles, which contain glutamic acid and methionine, undergo a glucose oxidase catalyzed, glucose-fueled transient hydrogelation in response to an interplay of pH and oxidation stimuli, promoted by the production of reactive oxygen species (ROS). Adjusting the enzyme and glucose concentration allows tuning of the assembly and the disassembly rates of the supramolecular polymers, which dictate the stiffness and transient stability of the hydrogels. The incorporation of triethylene glycol chains introduces thermoresponsive properties to the materials. …

chemistry.chemical_classificationMethioninebiologyStereochemistrytechnology industry and agricultureSupramolecular chemistrymacromolecular substances02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesRedoxCatalysis0104 chemical sciencesSupramolecular polymerschemistry.chemical_compoundMonomerPolymerizationchemistrySelf-healing hydrogelsbiology.proteinBiophysicsGlucose oxidase0210 nano-technologyAngewandte Chemie (International ed. in English)
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Ligand design for multidimensional magnetic materials: a metallosupramolecular perspective.

2008

The aim and scope of this review is to show the general validity of the ‘complex-as-ligand’ approach for the rational design of metallosupramolecular assemblies of increasing structural and magnetic complexity. This is illustrated herein on the basis of our recent studies on oxamato complexes with transition metal ions looking for the limits of the research avenue opened by Kahn's pioneering research twenty years ago. The use as building blocks of mono-, di- and trinuclear metal complexes with a novel family of aromatic polyoxamato ligands allowed us to move further in the coordination chemistry-based approach to high-nuclearity coordination compounds and high-dimensionality coordination po…

chemistry.chemical_classificationModels MolecularMolecular StructureChemistryMagnetismLigandMacromolecular SubstancesRational designMolecular electronicsNanotechnologyBridging ligandCrystallography X-RayLigandsCoordination complexInorganic ChemistryMagneticsMetals HeavyOrganometallic CompoundsMoleculeElectron configurationDalton transactions (Cambridge, England : 2003)
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Self-Assembling of Peptide/Membrane Complexes by Atomistic Molecular Dynamics Simulations

2007

Abstract Model biological membranes consisting of peptide/lipid-bilayer complexes can nowadays be studied by classical molecular dynamics (MD) simulations at atomic detail. In most cases, the simulation starts with an assumed state of a peptide in a preformed bilayer, from which equilibrium configurations are difficult to obtain due to a relatively slow molecular diffusion. As an alternative, we propose an extension of reported work on the self-organization of unordered lipids into bilayers, consisting of including a peptide molecule in the initial random configuration to obtain a membrane-bound peptide simultaneous to the formation of the lipid bilayer. This strategy takes advantage of the…

chemistry.chemical_classificationModels MolecularMolecular diffusionMembranesChemistryMacromolecular SubstancesMembrane FluidityBilayerLipid BilayersMolecular ConformationBiophysicsPeptideBiological membraneTransmembrane proteinMolecular dynamicsCrystallographyMembraneModels ChemicalQuantum TheoryComputer SimulationLipid bilayerPeptidesPhospholipidsBiophysical Journal
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Molecular characterization of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide derivatives as potential self-assembling copolymers forming polymeric micelles

2003

A family of graft copolymers derivatives obtained from α,β-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) have been studied as potential self-assembling macromolecules forming stable polymeric micelles at low critical micellar concentration. These polymers are obtained grafting on PHEA poly(ethylene glycol) (PEG) (Mw 5000 g/mol) (PHEA–PEG), hexadecylamine (PHEA–C16) or both moieties (PHEA–PEG–C16). The PHEA derivatives were characterised by a multi-angle light scattering (MALS) photometer on line to a size exclusion chromatography system in obtaining the molar mass distribution of the polymers. In addition, to investigate the capacity to form micellar aggregates in aqueous medium the MALS pho…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsOrganic ChemistrySize-exclusion chromatographytechnology industry and agriculturemacromolecular substancesPolymerMicellechemistry.chemical_compoundchemistryCritical micelle concentrationPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionlipids (amino acids peptides and proteins)Ethylene glycolPolymer
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Load-collapse-release cascades of amphiphilic guest molecules in charged dendronized polymers through spatial separation of noncovalent forces.

2012

The ability to pack guest molecules into charged dendronized polymers (denpols) and the possibility to release these guest molecules from subsequently densely aggregated denpols in a load-collapse-release cascade is described. Charged denpols, which constitute molecular objects with a persistent, well-defined envelope and interior, are capable of incorporating large amounts of amphiphilic guest molecules. Simultaneously, multivalent ions can coordinate to the surfaces of charged denpols, leading to counterion-induced aggregation of the already guest-loaded host structures. Thus, although the local guest concentration in denpol-based molecular transport might already be initially high due to…

chemistry.chemical_classificationMolecular StructureChemistryMacromolecular SubstancesPolymersOrganic ChemistryElectron Spin Resonance SpectroscopyNanotechnologymacromolecular substancesGeneral ChemistryPolymerCatalysisChemical physicsDivorceDendrimerAmphiphileMolecular TransportMoleculeHigh potentialMacromoleculeChemistry (Weinheim an der Bergstrasse, Germany)
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