Search results for "Small"

showing 10 items of 2441 documents

Degradable cationic nanohydrogel particles for stimuli-responsive release of siRNA.

2014

Well-defined nanogels have become quite attractive as safe and stable carriers for siRNA delivery. However, to avoid nanoparticle accumulation, they need to provide a stimuli-responsive degradation mechanism that can be activated at the payload's site of action. In this work, the synthetic concept for generating well-defined nanohydrogel particles is extended to incorporate disulfide cross-linkers into a cationic nanonetwork for redox-triggered release of oligonucleotide payload as well as nanoparticle degradation under reductive conditions of the cytoplasm. Therefore, a novel disulfide-modified spermine cross-linker is designed that both allows disassembly of the nanogel as well as removal…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyPolymers and PlasticsChemistryOligonucleotideSpermidineOrganic ChemistryCationic polymerizationNanoparticleNanogelsFluorescence correlation spectroscopyHydrogelsPolymerPolyethylene GlycolsNanotoxicologyCationsAgarose gel electrophoresisMaterials ChemistryBiophysicsPolyethyleneimineDisulfidesRNA Small InterferingNanogelMacromolecular rapid communications
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Minimizing geminate recombination losses in small-molecule-based organic solar cells

2019

Small-molecule-based organic solar cells (OSCs) are a recurrent alternative to polymer-based OSCs. Due to the higher purity and definition of small molecules compared to polymers, the morphological requirements can be more relaxed. Here, we present a series of novel rhodanine-based small-molecule electron donors and blend them with the standard acceptor PC70BM. By performing a target analysis on femtosecond spectroscopy data, we quantify the rates of geminate charge recombination. We are able to reproduce these rates by applying the Marcus–Levich–Jortner equation, using results from quantum chemical calculations. This shows that in a series of differently substituted compounds, one can corr…

chemistry.chemical_classificationMaterials scienceOrganic solar cellPhotovoltaic systemQuímica orgánicafood and beverages02 engineering and technologyGeneral ChemistryPolymerElectron010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesSmall moleculeAcceptor0104 chemical scienceschemistryChemical physicsMaterials ChemistryCyclic voltammetry0210 nano-technologyFemtochemistryJournal of Materials Chemistry C
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Hierarchically Structured Titania Films Prepared by Polymer/Colloidal Templating

2010

Hierarchically structured titania films for application in hybrid solar cells are prepared by combining microsphere templating and sol-gel chemistry with an amphiphilic diblock copolymer as a structure-directing agent. The films have a functional structure on three size scales: (1) on the micrometer scale a holelike structure for reduction of light reflection, (2) on an intermediate scale macropores for surface roughening and improved infiltration of a hole transport material, and (3) on a nanometer scale a mesoporous structure for charge generation. Poly(dimethyl siloxane)-block-methyl methacrylate poly(ethylene oxide) (PDMS-b-MA(PEO)) is used as a structure-directing agent for the prepara…

chemistry.chemical_classificationMaterials sciencePolymerHybrid solar cellMethacrylatelaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawPolymer chemistryCopolymerGrazing-incidence small-angle scatteringGeneral Materials ScienceCalcinationMethyl methacrylateMesoporous materialACS Applied Materials & Interfaces
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Preparation and determination of the structure of high-performance polymer blends by small-angle neutron scattering

1995

Amorphous blends from a deuterated polyaryletherketone and a polyetherimide have been prepared and investigated by neutron scattering. The used components differ remarkably in their structure antheir solution properties. The blends on the other hand are combinatorial mixtures : the scattering quantity Φ 1 Φ 2 /S(q) is independent of the composition of the blends if the polymer chains have the same length

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsScatteringOrganic ChemistryAnalytical chemistryPolymerNeutron scatteringFlory–Huggins solution theoryPolyetherimideSmall-angle neutron scatteringchemistry.chemical_compoundchemistryPolyaryletherketoneMaterials ChemistryRadius of gyrationComposite materialMacromolecular Rapid Communications
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Small angle X-ray scattering from amorphous polymers arising from heterogeneities

1973

The small angle X-ray scattering of glassy polymers (PET, PC, PVC, PMMA) and of polymer melts (PE) was studied. The dependence of the intensity scattered at small angles on the sample treatment suggests that neither the inherent structure of the pure polymer phase nor microholes are the origin of the scattering. In agreement with all experimental facts the scattering can be attributed to foreign particles such as for instance stabilizers in the polymer matrix. The consequence of this result is discussed with respect to the nodular structure of the amorphous phase and with respect to structural models of the amorphous phase. The nodular structure is not related to regions of different densit…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsScatteringSmall-angle X-ray scatteringPolymerAmorphous solidCondensed Matter::Soft Condensed MatterMatrix (mathematics)CrystallographyColloid and Surface ChemistrychemistryChemical physicsPhase (matter)Materials ChemistryPhysical and Theoretical ChemistryWide-angle X-ray scatteringIntensity (heat transfer)Kolloid-Zeitschrift und Zeitschrift für Polymere
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1995

Redoxactive liquid crystalline (LC) side group polymers were prepared by copolymerization of liquid crystalline acrylates and ferrocene-containing acrylates. The corresponding liquid crystalline ionomers were synthesized by a reversible redox reaction. The incorporation of tetra-alkylated ferrocene derivatives leads to LC polymers with reduced redox potential. These polymers can be oxidized under mild conditions to the corresponding ionomers, which are much more stable in solution than LC ionomers containing monoalkylated ferrocenium ions. Dynamic mechanical measurements and small angle X-ray scattering (SAXS) perfomed on LC ionomers prove the existence of ionic superstructures (clusters) w…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSmall-angle X-ray scatteringGeneral Chemical EngineeringIonic bondingPolymerchemistry.chemical_compoundchemistryLiquid crystalPhase (matter)Polymer chemistryPolymer blendPendant groupIonomerActa Polymerica
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Morphology, rheology, and mechanical properties of a new nanobiocomposite

2015

Nanobiocomposites are a new class of biodegradable polymer materials with an ultrafine phase dispersion of the order of a few nanometers in a biodegradable polymer matrix that shows very interesting properties often very different from those of conventional filled polymers. In this work the morphology and the rheological and mechanical properties of a new nanobiocomposite made of a biodegradable copolyester based blend with an organomodified montmorillonite have been investigated to evaluate its possible use in several applications. SAXS diffractograms and TEM micrographs show that the in both the adopted processing conditions an hybrid intercalated/exfoliated morphology is observed. Rheolo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsSmall-angle X-ray scatteringGeneral ChemistryPolymerBiomaterialBiodegradable polymerCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundMontmorillonitechemistryRheologyPhase (matter)Properties and characterizationMaterials ChemistryNanostructured polymerComposite materialRheologyElastic modulusJournal of Applied Polymer Science
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2019

Abstract The preparation method of a polymer composite and the filler loading are amongst the factors that influence the properties of the final composites. This article studies the effect of these factors on the thermal stability and thermal degradation kinetics of poly(methyl methacrylate) (PMMA)/mesoporous silica (MCM-41) composites filled with small amounts of MCM-41. The PMMA/MCM-41 composites were prepared through in situ polymerisation and melt mixing methods, with MCM-41 loadings of 0.1, 0.3, and 0.5 wt.%. The presence of MCM-41 increased the thermal stability of PMMA/MCM-41 composites prepared by melt mixing, but in the case of the in situ polymerised samples, the MCM-41 accelerate…

chemistry.chemical_classificationMaterials scienceRenewable Energy Sustainability and the EnvironmentSmall-angle X-ray scattering02 engineering and technologyPolymerActivation energyMesoporous silica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPoly(methyl methacrylate)0104 chemical sciencesBiomaterialschemistry.chemical_compoundPolymerizationchemistryvisual_artCeramics and Compositesvisual_art.visual_art_mediumThermal stabilityMethyl methacrylateComposite material0210 nano-technologyWaste Management and DisposalEmergent Materials
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The structure of high-performance polymer blends by small-angle neutron scattering

1997

Abstract Amorphous blends from a deuterated polyaryletherketone and a polyetherimide have been prepared and investigated by small-angle neutron scattering (SANS). The blends are combinatorial mixtures: the scattering quantity Φ1Φ2/S(q) is independant of the composition of the blends.

chemistry.chemical_classificationMaterials scienceScatteringPolymerNeutron scatteringCondensed Matter PhysicsPolyetherimideSmall-angle neutron scatteringElectronic Optical and Magnetic MaterialsAmorphous solidchemistry.chemical_compoundchemistryDeuteriumPolyaryletherketoneElectrical and Electronic EngineeringComposite materialPhysica B: Condensed Matter
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Relationship between structure of drawn polymers and molecular motion

1971

In order to study the relationship between structure and molecular motion, drawn polymers are more suitable than isotropic samples since their morphology can be characterized more easily by quantitative methods such as small angle X-ray scattering (SAXS) and electron microscopy (EM). The effects of changes in morphological structure on molecular motion are demonstrated by comparing the results of the SAXS and EM measurements with the dynamic mechanical behavior of drawn polyethylene. In addition the NMR broad line spectra of these samples were analyzed and the influence of annealing conditions and external stress was investigated.

chemistry.chemical_classificationMaterials scienceScatteringSmall-angle X-ray scatteringAnnealing (metallurgy)fungiIsotropyAnalytical chemistryPolymerPolyethyleneSpectral linelaw.inventionchemistry.chemical_compoundchemistryChemical physicslawElectron microscopeJournal of Polymer Science Part C: Polymer Symposia
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