Search results for "structure–property relationship"

showing 5 items of 5 documents

Homopolymerization of styrenic monomers and their copolymerization with ethylene using group 4 non‐metallocene catalysts

2020

Homopolymerization of styrenic monomers (St, p ‐Me‐St, p ‐t Bu‐St, p ‐t BuO‐St) and their copolymerization with ethylene, with the use of [( t Bu2O2NN′)ZrCl]2(μ‐O) (1 ) and ( t Bu2O2NN′)TiCl2 (2 ), where t Bu2O2NN′ = Me2N(CH2)2N(CH2‐2‐O−‐3,5‐t Bu2‐C6H2)2, is explored in the presence of MMAO and (i Bu)3Al/Ph3CB(C6F5)4. The ethylene/styrenic monomers copolymerization with 1 /MMAO produces exclusively copolymers with high activity and good comonomer incorporation whereas the other catalytic systems yield mixtures of copolymers and homopolymers. The use of p ‐alkyl styrene derivatives instead of styrene raises the catalytic activity, comonomer incorporation and molecular weights of the copolyme…

EthylenePolymers and Plasticsstructure–property relationshipsGeneral ChemistrypolystyrenecatalystsSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundMonomerchemistryGroup (periodic table)Polymer chemistryMaterials ChemistryCopolymercopolymersPolystyreneMetalloceneJournal of Applied Polymer Science
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Endocytotic uptake of HPMA-based polymers by different cancer cells: impact of extracellular acidosis and hypoxia.

2017

Daniel Gündel,1 Mareli Allmeroth,2 Sarah Reime,1 Rudolf Zentel,2 Oliver Thews1 1Institute of Physiology, Martin Luther University Halle-Wittenberg, Halle (Saale), 2Institute of Organic Chemistry, Johannes Gutenberg-University, Mainz, Germany Background: Polymeric nanoparticles allow to selectively transport chemotherapeutic drugs to the tumor tissue. These nanocarriers have to be taken up into the cells to release the drug. In addition, tumors often show pathological metabolic characteristics (hypoxia and acidosis) which might affect the polymer endocytosis.Materials and methods: Six different N-(2-hydroxypropyl)methacrylamide (HPMA)-based polymer structures (homopolymer as well as…

Materials sciencePolymersBiophysicsHPMA–LMA copolymersPharmaceutical ScienceBioengineering02 engineering and technologyEndocytosisMethacrylatestructure–property relationshipBiomaterials03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDrug Delivery SystemsInternational Journal of NanomedicineCell Line TumorDrug Discoverytumor linesMethacrylamideAnimalstumor microenvironmentOriginal ResearchAcrylamidesTumor hypoxiaPinocytosisOrganic ChemistryGeneral MedicineHydrogen-Ion Concentration021001 nanoscience & nanotechnologyEndocytosisRatsMolecular WeightBiochemistrychemistry030220 oncology & carcinogenesisDrug deliveryCancer cellMethacrylatesNanoparticlesTumor HypoxiaNanocarriers0210 nano-technologyAcidosisHydrophobic and Hydrophilic InteractionsInternational journal of nanomedicine
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Morphology, interfacial interaction, and thermal degradation of polycarbonate/MCM-41 (nano)composites

2017

ABSTRACTThis article reports on the morphology, interfacial interaction, thermal stability, and thermal degradation kinetics of polycarbonate (PC)/mesoporous silica (MCM-41) composites with various MCM-41 contents, prepared by melt compounding. The composites with low filler loadings (<0.3 wt%) maintained their transparency because of the well dispersed MCM-41 particles, but at higher filler loadings the composites lost their transparency due to the presence of agglomerates. The presence of agglomerates decreased the thermal stability of PC due to the reduced effectiveness of the particles to immobilize the polymer chains, free radicals, and volatile degradation products.

Mesoporous silica; nanocomposites; polycarbonate; structure–property relationship; thermal degradation; Analytical Chemistry; Chemical Engineering (all); Polymers and PlasticsMaterials sciencePolymers and PlasticsGeneral Chemical Engineering02 engineering and technologystructure–property relationship010402 general chemistry01 natural sciencesAnalytical ChemistryMCM-41nanocompositesChemical Engineering (all)Thermal stabilitythermal degradationPolycarbonateComposite materialchemistry.chemical_classificationNanocompositenanocompositePolymerMesoporous silica021001 nanoscience & nanotechnology0104 chemical sciencespolycarbonatechemistryAgglomerateCompoundingvisual_artvisual_art.visual_art_medium0210 nano-technologyMesoporous silicaInternational Journal of Polymer Analysis and Characterization
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Connections Between Topology and Macroscopic Mechanical Properties of Three-Dimensional Open-Pore Materials

2018

This work addresses a number of fundamental questions regarding the topological description of materials characterized by a highly porous three-dimensional structure with bending as the major deformation mechanism. Highly efficient finite-element beam models were used for generating data on the mechanical behavior of structures with different topologies, ranging from highly coordinated bcc to Gibson–Ashby structures. Random cutting enabled a continuous modification of average coordination numbers ranging from the maximum connectivity to the percolation-cluster transition of the 3D network. The computed macroscopic mechanical properties–Young's modulus, yield strength, and Poisson's ratio–co…

Work (thermodynamics)Materials sciencetopologyMaterials Science (miscellaneous)Coordination numberModulus02 engineering and technologyBendingPoisson distributionTopologystructure–property relationship01 natural scienceslcsh:Technologysymbols.namesakeApproximation error0103 physical sciencesTechnik [600]Topology (chemistry)ddc:620.11010302 applied physicslcsh:T600data mining021001 nanoscience & nanotechnologyelastic-plastic deformation behaviormachine learningopen-pore materialssymbols0210 nano-technologyReduction (mathematics)ddc:600Frontiers in Materials
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1,1,3,3-Tetraethyl-5-nitroisoindoline

2019

The title compound, C16H24N2O2, previously obtained as a yellow oil, exhibits a rather low melting point close to room temperature 297–298 K). In the molecule, the isoindoline ring system is approximately planar and coplanar to the nitro group, forming a dihedral angle of 5.63 (15)°. In the crystal, only weak N—H...O and C—H...π interactions are observed, linking molecules into chains parallel to the [101] direction.

crystal structurebiologyIsoindolineCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)biology.organism_classificationstructure–property relationshiporganic synthesis01 natural sciences0104 chemical sciencesCrystalCrystallographychemistry.chemical_compoundchemistryNitrolcsh:QD901-999TetraOrganic synthesislcsh:CrystallographyIUCrData
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