Search results for "ionic"

showing 10 items of 2016 documents

Cooperative formation of inorganic-organic interfaces in the synthesis of silicate mesostructures.

1993

A model is presented to explain the formation and morphologies of surfactant-silicate mesostructures. Three processes are identified: multidentate binding of silicate oligomers to the cationic surfactant, preferential silicate polymerization in the interface region, and charge density matching between the surfactant and the silicate. The model explains present experimental data, including the transformation between lamellar and hexagonal mesophases, and provides a guide for predicting conditions that favor the formation of lamellar, hexagonal, or cubic mesostructures. Model Q(230) proposed by Mariani and his co-workers satisfactorily fits the x-ray data collected on the cubic mesostructure …

chemistry.chemical_classificationMultidisciplinaryCationic polymerizationMineralogyMesophasePolymerSilicatechemistry.chemical_compoundPulmonary surfactantchemistryPolymerizationChemical engineeringddc:540Lamellar structureGyroidScience (New York, N.Y.)
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Impact of non-functionalized and ionic liquid modified carbon nanotubes on mechanical and thermal properties of ethylene- octene copolymer nanocompos…

2016

In this article the development and characterization of composites made from metallocene based ethylene-octene copolymer (EOC) with 38% octene content, non-modified or modified multi walled carbon nanotubes (MWCNTs), covalently functionalised with long chain hexadecyl moiety imidazolium ionic liquid (IL-f-MWCNTs), is presented. The procedure of MWCNTs functionalization is discussed. In order to obtain a good dispersion of the filler, composites with MWCNTs and IL-f-MWCNTs in the concentration range of 0.5-12 wt.% were made by ultrasonication / thermoplastic mixing method. The results indicated improvement in mechanical properties with increase of the filler content. The methodology of the d…

chemistry.chemical_classificationNanocompositeThermoplasticMaterials science02 engineering and technologyCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistrylawIonic liquidCopolymerSurface modificationThermal stabilityOcteneComposite material0210 nano-technologyIOP Conference Series: Materials Science and Engineering
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Fabrication of soft-etched nanoporous polyimide membranes for ionic conduction and discrimination

2021

Abstract Ionic selectivity in nanopores is usually based either on steric or charge exclusion mechanisms. By simultaneously incorporating both mechanisms into a functionalized membrane, an improved control over selectivity can be achieved. We describe the fabrication and experimental characterization of alkali metal cation-selective nanopores in heavy ion-tracked polyimide (PI) membranes using the soft-etching (SE) technique. The latent ion tracks in the PI membrane are selectively dissolved by an organic solvent to form tiny pores without affecting the bulk material. The ionic transport properties of SE-PI membranes are characterized using different electrolyte solutions containing alkali …

chemistry.chemical_classificationNanoporousInorganic chemistryIonic bondingFiltration and Separation02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnologyAlkali metal01 natural sciencesBiochemistry0104 chemical sciencesDivalentSolventMembranechemistryIonic conductivityGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyJournal of Membrane Science
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Highly Defined, Colloid‐Like Ionic Clusters in Solution

2012

Many societal challenges at the beginning of the 21st century lead to an apparent and growing need for functional materials and novel ways of materials synthesis and assembly. Rising to the challenge, the utilization of small, self-assembling building blocks for the bottom-up construction of new types of polymers and nanostructures has enjoyed increasing popularity among materials researchers in the recent past. Supramolecular materials like foldamers, surface films, nanoparticles, etc. are created by exploiting noncovalent forces [1] leading to an ordered arrangement of nanoscale building blocks. [2] In the search for new polymers based on noncovalent molecular forces, we are motivated by …

chemistry.chemical_classificationNanostructureChemistrySupramolecular chemistryNanoparticleIonic bondingdynamic light scatteringNanotechnologyself-assemblyGeneral ChemistryPolymerCommunicationsmolecular dynamicsnanoscale electrostaticsMonte Carlo simulationsSupramolecular polymersMolecular dynamicsSelf-assemblyChemistryOpen
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Anionic tert-butyl-calix[4]arenes substituted at the narrow and wide rim by cobalt bis(dicarbollide)(1−) ions and CMPO-groups. Effect of stereochemis…

2013

Abstract Two ionic calix[4]arenes substituted at the narrow rim with an unpaired number ( n ) of cobalt bis(dicarbollide)(1−) anions ( 1 − ) ( n  = 1 and 3) and (4 −  n ) CMPO groups ( 3c , 4c ) have been synthesized via a three-step procedure based on nitrile substituted calix[4]arene precursors. Conjointly with them, the compound with a paired ratio of the groups, where n  = 2 and the same substituents are located in mutually adjacent 1,2-positions, is reported ( 5c ). Another compound with the paired ratio, but from a wide rim series ( 6c ) ( n  = 2) was successfully prepared starting from calix[4]arenes substituted with two nitro functions and two –OH sites available for further modific…

chemistry.chemical_classificationNitrileStereochemistryOrganic ChemistryNitro compoundIonic bondingBiochemistryInorganic Chemistrychemistry.chemical_compoundchemistryLiquid–liquid extractionCalixareneMaterials ChemistryNitroPhysical and Theoretical ChemistryHydrateConformational isomerismJournal of Organometallic Chemistry
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A new approach for the synthesis of magnetic materials based on nitroxide free radicals and inorganic coordination polymers

2001

The use of nitronyl nitroxide (NN) radicals as spectators inside extended inorganic magnetic lattices is described. Two possibilities are presently being explored, namely, the design of oxalato-bridged bimetallic networks by using cationic NN radicals of the N-alkylpyridinium type as templating agents, and the design of bimetallic lattices based on hexacyanometalates and nickel(II) diaminocomplexes incorporating anionic NN radicals of the carboxyphenyl type.

chemistry.chemical_classificationNitroxide mediated radical polymerizationMolecular magnetsRadicalCationic polymerizationchemistry.chemical_elementPolymerPhotochemistryInorganic ChemistryNickelchemistryMaterials ChemistryPhysical and Theoretical ChemistryBimetallic stripPolyhedron
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The effect of TMEDA on the kinetics of the anionic polymerization of methyl methacrylate in tetrahydrofuran using lithium as counterion

2000

The kinetics of the anionic polymerization of methyl methacrylate in presence of N,N,N', -tetramethylethylenediamine (TMEDA) in THF are investigated using 1,1-diphenyl-hexyllithium as initiator in a temperature range between -20°C and 0°C in a flow-tube reactor. The rate constants of propagation determined in the presence of TMEDA are compared to those obtained in the absence of a chelating agent. For propagation, the reaction order with respect to active centers is found to be 0.5 in both cases which indicates that the chelation of the lithium cation does not effectively perturb the aggregation of the enolate ion pair. Both the rate constants of propagation via non-aggregated ion pairs, k …

chemistry.chemical_classificationOrder of reactionPolymers and PlasticsOrganic ChemistrySolution polymerizationTetramethylethylenediamineCondensed Matter Physicschemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryPolymer chemistryMaterials ChemistryOrganic chemistryPhysical chemistryPhysical and Theoretical ChemistryCounterionTetrahydrofuranEquilibrium constant
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Universal Transients in Polymer and Ionic Transition Metal Complex Light-Emitting Electrochemical Cells

2012

Two types of light-emitting electrochemical cells (LECs) are commonly distinguished, the polymer-based LEC (p-LEC) and the ionic transition metal complex-based LEC (iTMC-LEC). Apart from marked differences in the active layer constituents, these LEC types typically show operational time scales that can differ by many orders of magnitude at room temperature. Here, we demonstrate that despite these differences p-LECs and iTMC-LECs show current, light output, and efficacy transients that follow a universal shape. Moreover, we conclude that the turn-on time of both LEC types is dominated by the ion conductivity because the turn-on time exhibits the same activation energy as the ion conductivity…

chemistry.chemical_classificationOrganic solar cellChemistryAnalytical chemistryIonic bonding02 engineering and technologyGeneral ChemistryPolymerConductivityElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesBiochemistryCatalysis0104 chemical sciencesElectrochemical cellIonColloid and Surface ChemistryChemical physicsIonic conductivity0210 nano-technologyJournal of the American Chemical Society
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Amino acid-based cholinium ionic liquids as sustainable catalysts for pet depolymerization

2021

Chemical recycling to monomers is one of the key strategies in tackling the issues deriving from persistent plastic pollution in the environment, and poly(ethylene terephthalate) (PET) is among the most used polymers in modern society. In this context, we herein describe the glycolysis of PET to bis-hydroxyethyl terephthalate (BHET), promoted by basic cholinium salts differing for the anions, also comprising amino acid anions. We investigated the optimal reaction conditions, finding that the best-performing catalyst is [Ch][Gly], in the presence of which a conversion of 85% and a yield of 51% are achieved at 150 °C after 6 h, from PET deriving from a clear water bottle. We used our protocol…

chemistry.chemical_classificationPet depolymerizationEthyleneRenewable Energy Sustainability and the EnvironmentDepolymerizationGeneral Chemical EngineeringTask-specific ionic liquidsGeneral ChemistrySettore CHIM/06 - Chimica OrganicaWaste valorizationCatalysisAmino acidBhetchemistry.chemical_compoundMonomerchemistryIonic liquidEnvironmental ChemistryOrganic chemistryCholinium saltsGlycolysis
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Two-Dimensional Assembly Formation of Hydrophobic Helical Peptides at the Air/Water Interface: Fluorescence Microscopic Study

1995

Monolayer formation of hydrophobic α-helical peptides, X-(Ala-Aib) 8 -Y (X=Boc-, HOOCCH 2 CH 2 CO-, biotinyl, biotinyl-(Sar) 3 -; Y=OMe, OBzl, OH), at the air/water interface was studied by the fluorescence microscopic method. Some peptides showed a mound in the π-A isotherm. When the monolayer containing a small amount of FITC-labeled peptide was held at the surface pressure corresponding to the top of the mound, bright and dark domains were observed by fluorescence microscopy. Domain formation was also observed by the addition of a cationic dye (DiIC 1 ) into the subphase underneath the peptide monolayer. The mound in the π-A isotherm is, therefore, ascribed to the phase transition from a…

chemistry.chemical_classificationPhase transitionStereochemistryfungiCationic polymerizationPeptideSurfaces and InterfacesCondensed Matter PhysicsSurface pressureFluorescencelaw.inventionCrystallographychemistrylawMonolayerElectrochemistryFluorescence microscopeGeneral Materials ScienceCrystallizationSpectroscopyLangmuir
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