Search results for "polymerization"

showing 10 items of 1689 documents

Silanization as a versatile functionalization method for the synthesis of polymer/magnetite hybrid nanoparticles with controlled structure

2016

We compare the use of different trimethoxysilane compounds for the surface functionalization of magnetite nanoparticles and their subsequent incorporation in hybrid particles formed by in situ polymerization. For the encapsulation of inorganic nanoparticles via miniemulsion polymerization, surface functionalization of the inorganic material is necessary to hydrophobize the otherwise hydrophilic inorganic material and to compatibilize it with the polymer. Hydrophobic magnetite nanoparticles are usually prepared by surface functionalization with oleic acid, which leads to effective hydrophobization, but offers only limited control over the structure of the hybrid particles. As an alternative,…

Materials scienceGeneral Chemical EngineeringNanoparticleJanus particles02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMiniemulsionChemical engineeringPolymerizationSilanizationPolymer chemistrySurface modificationIn situ polymerization0210 nano-technologyHybrid material
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Electrosynthesis and properties of poly(3,4-ethylenedioxythiophene) films functionalized with titanocene dichloride complex

2006

Synthesis of a titanocene dichloride derivative functionalized with 3,4-etylenedioxythiophene group, Tc1EDOT (Cl 2TiCpC5H4(CH2) (3,4ethylenedioxythiophene)) has been described. Redox behavior of the monomer in tetrahydrofuran (THF), dichloromethane (DCM) and acetonitrile (AN) at different scan rates has been discussed in terms of different ability of these solvents to coordination with the reduced titanocene (Tc) complex and the solvation of Cl − anions. Electrooxidation of Tc1EDOT to get a conducting polymer film with immobilized titanocene dichloride centers and electrochemical properties of its polymer matrix in background acetonitrile solution have been compared with those of non-substi…

Materials scienceGeneral Chemical EngineeringSTM02 engineering and technology010402 general chemistryElectrosynthesis01 natural scienceschemistry.chemical_compoundPEDOT:PSSPolymer chemistryElectrochemistryAcetonitrileComputingMilieux_MISCELLANEOUS[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]poly(3Titanocene dichloride021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/Polymers[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]chemistryPolymerizationelectrodepositionimmobilized titanocene dichloride centersCyclic voltammetry4-ethylenedioxythiophene)0210 nano-technologyEDOT-methanol derivativeMetallocenePoly(34-ethylenedioxythiophene)titanocene-EDOT derivative
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A fluorescent layered oxalato-based canted antiferromagnet

2018

We report the synthesis and characterization of the first fluorescent oxalato-based canted antiferromagnet. Compound [DOC][MnFe(C2O4)3] (1) (DOC = 3,3'-diethyloxacarbocyanine) combines the well-known canted antiferromagnetic [MnFe(C2O4)3]- honeycomb layers with a fluorescent cationic cyanine-type fluorescent dye. Besides the expected spin canted antiferromagnetic order in the oxalato layer at ca. 29 K, we show the key role played by the anionic oxalato lattice in the optical properties of the cation since it provides isolation of dye cations in the hexagonal cavities of the oxalato-based matrix. The emission of the DOC+ dye shows a redshift and a broadening of the emission as well as an inc…

Materials scienceHexagonal crystal systemCationic polymerization02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescence0104 chemical sciencesInorganic ChemistryCrystallographyLattice (order)AntiferromagnetismIsolation effect0210 nano-technologyDalton Transactions
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Preparation and conductivity of PEDOT encapsulated inside faujasites

2005

Poly[3,4-(ethylenedioxy)thiophene] (PEDOT) encapsulated inside the faujasite micropores has been prepared by polymerization of the monomer in partially Fe-exchanged faujasites. Faujasites containing PEDOT within the interior exhibit notable electrical conductivity compared to plain faujasite. This conductivity is attributed to the presence of polarons that have been detected by EPR spectroscopy.

Materials scienceInorganic chemistryGeneral Physics and AstronomyFaujasiteengineering.materialConductivitylaw.inventionchemistry.chemical_compoundMonomerchemistryPolymerizationPEDOT:PSSChemical engineeringlawThiopheneengineeringPhysical and Theoretical ChemistryElectron paramagnetic resonanceEthylenedioxyChemical Physics Letters
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On-surface synthesis on a bulk insulator surface

2018

On-surface synthesis has rapidly emerged as a most promising approach to prepare functional molecular structures directly on a support surface. Compared to solution synthesis, performing chemical reactions on a surface offers several exciting new options: due to the absence of a solvent, reactions can be envisioned that are otherwise not feasible due to the insolubility of the reaction product. Perhaps even more important, the confinement to a two-dimensional surface might enable reaction pathways that are not accessible otherwise. Consequently, on-surface synthesis has attracted great attention in the last decade, with an impressive number of classical reactions transferred to a surface as…

Materials scienceInsulator (electricity)02 engineering and technology010402 general chemistryF160 Organic Chemistry53001 natural sciencesChemical reactionUllmann reactionMetalchemistry.chemical_compoundGeneral Materials ScienceF200 Materials ScienceDiacetylene021001 nanoscience & nanotechnologyCondensed Matter PhysicsCycloaddition0104 chemical sciencesPolymerizationchemistryChemical physicsvisual_artvisual_art.visual_art_mediumF343 Computational PhysicsF320 Chemical PhysicsSupport surface0210 nano-technologyJournal of Physics: Condensed Matter
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Investigation of the swelling behavior of cationic exchange resins saturated with Na+ ions in a C3S paste

2015

Ion exchange resins (IERs) are widely used by the nuclear industry to decontaminate radioactive effluents. Spent products are usually encapsulated in cementitious materials. However, the solidified waste form can exhibit strong expansion, possibly leading to cracking, if the appropriate binder is not used. In this work, the interactions between cationic resins in the Na+ form and tricalcium silicate are investigated during the early stages of hydration in order to gain a better understanding of the expansion process. It is shown that the IERs exhibit a transient swelling of small magnitude due to the decrease in the osmotic pressure of the external solution. This expansion, which occurs jus…

Materials scienceIon exchangePrecipitation (chemistry)Cationic polymerizationBuilding and ConstructionMicrostructureChemical engineeringmedicineGeneral Materials ScienceCementitiousSwellingmedicine.symptomIon-exchange resinPorosityNuclear chemistryCement and Concrete Research
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An original 3D coordination polymer constructed from trinuclear nodes and tetracarboxylato spacers

2021

A novel 3D coordination polymer, ∞3[{Cu3(felden)}4(btec)3]·17H2O, has been assembled using cationic trigonal nodes, [CuII3(felden)]3+, generated by a tricompartmental ligand, H3felden, which results from the Schiff condensation reaction between 2,4,6-triformylphloroglucinol and N,N-dimethylethylenediamine. The tetraanion of the 1,2,4,5-benzenetetracaboxylic acid (H4btec) was employed as a spacer. The structure of 1 shows large icosahedral cavities and channels and the magnetic interaction between the copper(II) ions within the triangles is weak and antiferromagnetic.

Materials scienceLigandCoordination polymerIcosahedral symmetryCationic polymerizationchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsCondensation reactionCopperIonCrystallographychemistry.chemical_compoundchemistryAntiferromagnetismGeneral Materials ScienceCrystEngComm
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A deep-blue emitting charged bis-cyclometallated iridium(iii) complex for light-emitting electrochemical cells

2013

We report here a new cationic bis-cyclometallated iridium(III) complex, 1, with deep-blue emission at 440 nm and its use in Light-emitting Electrochemical Cells (LECs). The design is based on the 2′,6′-difluoro-2,3′-bipyridine skeleton as the cyclometallating ligand and a bis-imidazolium carbene-type ancillary ligand. Furthermore, bulky tert-butyl substituents are used to limit the intermolecular interactions. LECs have been driven both at constant voltage (6 V) and constant current (2.5 mA cm−2). The performances are significantly improved with the latter method, resulting overall in one of the best reported greenish-blue LECs having fast response (17 s), light intensity over 100 cd m−2 an…

Materials scienceLigandIntermolecular forceCationic polymerizationAnalytical chemistrychemistry.chemical_elementGeneral ChemistryPhotochemistryElectrochemical cellLight intensitychemistryMaterials ChemistryConstant currentIridiumDeep blueJ. Mater. Chem. C
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Nanostructuring with a crosslinkable discotic material.

2007

A high-yielding synthesis afforded a hexa-peri-hexabenzocoronene carrying acrylate units at the end of six attached alkyl spacers. The polymerization of these acrylate moieties could be initiated with thermal energy and through direct photoactivation without the addition of a photoinitiator. This allowed the organization of the liquid-crystalline material to be fixed in either the crystalline state or the mesophase, which preserved the organization in the respective phase. The use of a focused synchrotron beam permitted selected regions of a thin film to be rendered insoluble. After "developing" the film in this lithographic process by dissolving the soluble, unpolymerized material, defined…

Materials scienceMacromolecular SubstancesSurface PropertiesMolecular ConformationBiomaterialschemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials TestingNanotechnologyGeneral Materials ScienceParticle SizeAlkylchemistry.chemical_classificationTitaniumAcrylateMesophaseGeneral ChemistryLiquid CrystalsNanostructuresMembraneCross-Linking ReagentsPolymerizationchemistryAcrylatesMesoporous materialCrystallizationPhotoinitiatorBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Preparation of cholesteric particles from cellulose derivatives in a microfluidic setup

2011

A microfluidic setup was used to process lyotropic cholesteric liquid crystalline mixtures of cellulose derivatives into spherical particles in the micrometre scale. By the method of co-flowing injection, monodisperse droplets of the liquid crystal, dispersed in an aqueous carrier fluid, were prepared. Polymerization of the acrylic solvent with UV-light fixed the orientation obtained by the flowing motion. The resulting particles were characterized by polarizing optical microscopy.

Materials scienceMicrofluidicsCellulose derivatives02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionPhysics::Fluid DynamicsOptical microscopeLiquid crystallawLyotropic[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringPhysics::Chemical PhysicsChromatographyAqueous solutiontechnology industry and agricultureGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicseye diseases0104 chemical sciencesSolventCondensed Matter::Soft Condensed MatterPolymerizationChemical engineering0210 nano-technology
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