Search results for "cationic polymerization"

showing 10 items of 441 documents

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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Polymeric nanospheres as strategy to increase the amount of triclosan retained in the skin: passive diffusion vs. iontophoresis

2012

The aim of this study was to evaluate the passive and iontophoretic permeation of triclosan in human skin using a triclosan solution and triclosan-loaded cationic nanospheres in order to determine which of the two strategies is more effective in allowing the deposition of triclosan within the skin. Triclosan-loaded nanospheres were prepared by the emulsification-solvent displacement technique using aminoalkyl methacrylate (Eudragit® RL 100) as polymer matrix. Nanospheres of 261.0 ± 15.1 nm with a positive surface charge (Ψz = 26.0 ± 3.2 mV) were obtained. Drug loading was 62.0 ± 1.7%. Results demonstrated that the amount of triclosan retained within the skin was significantly greater (8.5-f…

Materials sciencePharmaceutical ScienceBioengineeringHuman skinMethacrylateDiffusionchemistry.chemical_compoundColloid and Surface ChemistryParticle SizePhysical and Theoretical ChemistrySolubilityChromatography High Pressure LiquidSkinChromatographyIontophoresisOrganic ChemistryCationic polymerizationIontophoresisPermeationControlled releaseTriclosanTriclosanSolubilitychemistryMicroscopy Electron ScanningNanospheresJournal of Microencapsulation
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PREPARATION OF OLIGOMERS WITH FUNCTIONAL END GROUPS BY POLYMERIZATION REACTIONS

1973

ABSTRACT The possibilities of preparing oligomers with functional end groups by cationic, anionic and radical polymerization are discussed. Special attention is given to oligomers with two functional end groups (telechelic oligomers). By use of efficient separation techniques, especially GPC, these oligomers can be separated and analyzed. The conclusions that can be drawn from the structure of these oligomers with respect to the elementary processes in polymerization reactions are critically examined.

Materials sciencePolymerizationPolymer chemistryRadical polymerizationCationic polymerizationfood and beveragesOrganic chemistry
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Reductive Decationizable Block Copolymers for Stimuli-Responsive mRNA Delivery

2016

Messenger ribonucleic acids (mRNAs) are considered as promising alternatives for transient gene therapy, but to overcome their poor pharmacokinetic properties, smart carriers are required for cellular uptake and stimuli-responsive release. In this work, a synthetic concept toward reductive decationizable cationic block copolymers for mRNA complexation is introduced. By combination of RAFT block copolymerization with postpolymerization modification, cationic block copolymers are generated with disulfide-linked primary amines. They allow effective polyplex formation with negatively charged mRNA and subsequent release under reductive conditions of the cytoplasm. In first in vitro experiments w…

Materials sciencePolymers and PlasticsCarrier systemPolymers02 engineering and technologyGene delivery010402 general chemistry01 natural sciencesMiceDrug Delivery SystemsGene expressionPolymer chemistryMaterials ChemistryCopolymerAnimalsReversible addition−fragmentation chain-transfer polymerizationRNA MessengerMessenger RNAOrganic ChemistryCationic polymerization3T3 CellsRaft021001 nanoscience & nanotechnology0104 chemical sciencesBiophysics0210 nano-technologyMacromolecular Rapid Communications
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A contribution to the kinetics of the polymerization of styrene with CF3SO3H as catalyst

1978

The time dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst can be formally described as being first-order with respect to monomer concentration [M]0. The reaction rate shows a third-order dependence in catalyst concentration [C]0. A high polymer and a low polymer polystyrene fraction are found at [M]0>0.2 mole · l−. The reaction rate of the high polymer fraction is proportional to [C] 0 3 , that of the low polymer fraction probably proportional to [C] 0 2 . The polymerization active species may thus be triple ions in the first and ion pairs in the second case.

Materials sciencePolymers and PlasticsCationic polymerizationSolution polymerizationGeneral ChemistryCondensed Matter PhysicsStyrenechemistry.chemical_compoundMonomerChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryAddition polymerPolystyrenePolymer Bulletin
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Synthesis and degradation of poly (2-hydroxyethyl methacrylate)-graft-poly (ε-caprolactone) copolymers

2004

Abstract Poly (e-caprolactone) macromonomers carrying a methacryloyl end groups were synthesized using different lanthanide derivatives as catalysts, and characterized by SEC and 1 H NMR. Hydrophilic–hydrophobic copolymers from macromonomers and 2-hydroxyethyl methacrylate (HEMA) were obtained by solution free radical polymerization. Depending on the feed ratio of the two components, different copolymer structures were obtained. The expected graft structure of the copolymers was confirmed by 1 H NMR. Thermal properties of the copolymers were determined by DSC and TGA. Hydrolytic and enzymatic degradations of the materials were performed. Poly (2-hydroxyethyl methacrylate)- graft -poly (e-ca…

Materials sciencePolymers and PlasticsRadical polymerizationtechnology industry and agricultureCationic polymerizationCondensed Matter PhysicsMethacrylateMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryMechanics of MaterialsPolycaprolactonePolymer chemistryMaterials ChemistryCopolymerCaprolactonePolymer Degradation and Stability
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One-pot synthesis and characterization of aliphatic poly(oxytetramethylene) ionene

2002

Abstract One-pot synthesis of poly(oxytetramethylene) ionene (POI) composed of one dimethylammonium group in each repeating unit is described. POI was prepared by using the cationic polymerization of tetrahydrofuran, followed by the chain extension reaction of living poly(oxytetramethylene) (POTM) chain with N , N -dimethylaminotrimethylsilane. The weight average molecular weight of the ionene with bromide counter-anion (POI–Br) was 48,000 g/mol and the molecular weight of POTM between the ionic sites was ca. 2100. POI–Br showed polyelectrolyte behavior in polar solvent. The elastomeric film of POI–Br was prepared: its tensile strength at break and elongation at break were ca. 11 MPa and ca…

Materials sciencePolymers and Plasticsliving polymerizationOrganic ChemistryCationic polymerizationRing-opening polymerizationpoly(oxytetramethylene)Polyelectrolyteionenechemistry.chemical_compoundDifferential scanning calorimetrychemistryBromidePolymer chemistryMaterials ChemistryMolar mass distributionLiving polymerizationTetrahydrofuranPOLYMER
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2016

Despite hundreds of cationic bis-cyclometalated iridium(III) complexes having been explored as emitters for light-emitting electrochemical cells (LEECs), uniformly their composition has been in the form of a racemic mixture of Λ and Δ enantiomers. The investigation of LEECs using enantiopure iridium(III) emitters, however, remains unprecedented. Herein, we report the preparation, the crystal structures, and the optoelectronic properties of two families of cyclometalated iridium(III) complexes of the form of [(C^N)2Ir(dtBubpy)]PF6 (where dtBubpy is 4,4′-di-tert-butyl-2,2′-bipyridine) in both their racemic and enantiopure configurations. LEEC devices using Λ and Δ enantiomers as well as the r…

Materials scienceStereochemistryCationic polymerizationchemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesElectrochemical cellEnantiopure drugchemistryRacemic mixtureGeneral Materials ScienceIridiumEnantiomer0210 nano-technologyACS Applied Materials & Interfaces
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Chitosan-based smart hybrid materials: a physico-chemical perspective.

2020

Chitosan is one of the most studied cationic polysaccharides. Due to its unique characteristics of being water soluble, biocompatible, biodegradable, and non-toxic, this macromolecule is highly attractive for a broad range of applications. In addition, its complex behavior and the number of ways it interacts with different components in a system result in an astonishing variety of chitosan-based materials. Herein, we present recent advances in the field of chitosan-based materials from a physico-chemical perspective, with focus on aqueous mixtures with oppositely charged colloids, chitosan-based thin films, and nanocomposite systems. In this review, we focus our attention on the physico-che…

Materials scienceSurface PropertiesBiomedical EngineeringBiocompatible Materialsmacromolecular substancesChitosanchemistry.chemical_compoundColloidGeneral Materials ScienceSolubilityParticle SizeChitosanNanocompositeAqueous solutiontechnology industry and agricultureCationic polymerizationTemperatureHydrogen BondingGeneral ChemistryGeneral Medicinecarbohydrates (lipids)chemistryChemical engineeringSolubilityHybrid materialMacromoleculeJournal of materials chemistry. B
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