Search results for "Chemical physics"

showing 10 items of 2553 documents

Interaction of 5‐fluorouracil with β‐cyclodextrin: A density functional theory study with dispersion correction

2020

Detailed studies on the stability, interaction, and microstructure of host‐guest complexes in the vacuum of 5‐fluorouracil (5FU) with β‐cyclodextrin (βCD) were performed using B3LYP with the inclusion of Grimme's dispersion correction GD3 term and 6‐31+G(d,p) basis set. Among several studied 1:1 5FU‐βCD complexes, the one placing the keto tautomer of 5FU vertically in the host cavity and forming N‐H···OCD and CO···HOCD hydrogen bonds with hydroxyl groups of the smaller rim of βCD has the highest stability (Eint = −195 kJ/mol). Interestingly, there are no interactions with the inner hydrophobic part of the βCD host cavity. The strength of the intermolecular H‐bonds to the smaller rim of βC…

chemistry.chemical_classificationMaterials scienceCyclodextrinInteraction energyCondensed Matter Physics5‐fluorouracil (5FU)Atomic and Molecular Physics and OpticsDFT‐D3β‐cyclodextrin (βCD)chemistryChemical physicsDispersion (optics)Density functional theoryPhysical and Theoretical Chemistryinclusion complexinteraction energyInternational Journal of Quantum Chemistry
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Tracer diffusion in polymer and organic liquids close to the glass transition studied by forced rayleigh scattering

2007

Translational diffusion coefficients D of photochronic dye molecules have been measured by forced Rayleigh scattering in polymer diluent systems at compositions from pure polymer to pure diluent. D could be measured down to below the glass transition temperature T g. In the pure diluent, D(T g) was found typically about two decades below that in the pure polymer but still far above the Stokes-Einstein prediction extrapolated from high temperatures. Some experimental results are in contrast with predictions from free-volume theory.

chemistry.chemical_classificationMaterials scienceDiffusionPlasticizerThermodynamicsPolymerDiluentCondensed Matter::Soft Condensed MatterchemistryTRACEROrganic chemistryForced Rayleigh scatteringMoleculePhysics::Chemical PhysicsGlass transition
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The effect of free polymer on the interactions and the glass transition dynamics of microgel colloids.

2002

By studying the phase behaviour and the short range order of polystyrene microgel colloids in a good solvent we demonstrated that these particles can be considered as hard spheres or nearly hard spheres if the internal cross link density is made sufficiently high. A binary mixture of 1:50 crosslinked (1 crosslink per 50 monomers) particles with a size ratio R(small)/R(large) = 0.83 and a number ratio N(small)/N(large) = 2.7 was characterized with respect to the short range order and glass transition dynamics. We found that this mixture can be mapped onto a one-component hard sphere system with an effective polydispersity of 11%, even though for the particle interactions an inverse power pot…

chemistry.chemical_classificationMaterials scienceDispersityPolymer architecturePolymerHard spheresFlory–Fox equationchemistry.chemical_compoundchemistryChemical physicsPhase (matter)Polymer chemistryPolystyrenePhysical and Theoretical ChemistryGlass transitionFaraday discussions
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The effect of free polymer on the glass transition dynamics of microgel colloids

2002

Abstract From the phase behavior we establish that 1:10 crosslinked polystyrene microgel colloids in a good solvent can be considered as hard spheres whereas 1:50 crosslinked particles are slightly softer. Nevertheless, the glass transition dynamics of 1:10 microgels and a binary mixtures of 1:50 microgels can be described in both cases within the mode coupling theory for hard spheres. The only difference is that the increase of the polydispersity from about 7% to about 13% when going from the one-component system to the mixture is accompanied by a shift of the glass transition from ϕ g ≈0.56 to ϕ g ≈0.595. On addition of linear polystyrene to the 1:50 binary mixture we find a tremendous ac…

chemistry.chemical_classificationMaterials scienceDispersityPolymerHard spheresCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsColloidchemistry.chemical_compoundchemistryChemical physicsPhase (matter)Polymer chemistryMaterials ChemistryCeramics and CompositesPolystyreneGlass transitionStructure factorJournal of Non-Crystalline Solids
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Dynamics of weak interactions in the ligand layer of meta-mercaptobenzoic acid protected gold nanoclusters Au68(m-MBA)32 and Au144(m-MBA)40

2020

Atomically precise metal nanoclusters, stabilized and functionalized by organic ligands, are emerging nanomaterials with potential applications in plasmonics, nano-electronics, bio-imaging, nanocatalysis, and as therapeutic agents or drug carriers in nanomedicine. The ligand layer has an important role in modifying the physico-chemical properties of the clusters and in defining the interactions between the clusters and the environment. While this role is well recognized from a great deal of experimental studies, there is very little theoretical information on dynamical processes within the layer itself. Here, we have performed extensive molecular dynamics simulations, with forces calculated…

chemistry.chemical_classificationMaterials scienceDouble bondLigandHydrogen bond02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesNanoclustersMolecular dynamicschemistryChemical physicsCluster (physics)NanomedicineGeneral Materials ScienceDensity functional theory0210 nano-technologyNanoscale
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Structural and Gelation Characteristics of Metallo-Supramolecular Polymer Model-Network Hydrogels Probed by Static and Dynamic Light Scattering

2021

Supramolecular polymer gels are a promising class of materials whose polymer components are connected by transient bonds such as metal–ligand interactions, thereby spanning a dynamic network throug...

chemistry.chemical_classificationMaterials scienceDynamic network analysisPolymers and PlasticsOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistrySupramolecular polymerschemistryDynamic light scatteringChemical physicsSelf-healing hydrogelsMaterials ChemistryModel networkTransient (oscillation)0210 nano-technologyMacromolecules
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Segmental dynamics in polymer electrolytes

2002

Polymer dynamics in poly(ethylene oxide) (PEO)–salt mixtures is investigated by means of quasi-elastic neutron scattering (QENS). In a previous study, we reported QENS data from the NEAT spectrometer (BENSC) that evidenced, for the first time, a dynamic heterogeneity in PEO–salt mixtures induced by salt addition. This finding is supported by molecular dynamics (MD) simulations carried out by Borodin et al. In agreement with MD simulations, our QENS data revealed two distinct processes: a fast motion corresponding to the bulk polymer and a slower relaxation, which we attribute to formation of PEO–cation complexes. In this paper we present new QENS data from the high-resolution spectrometer I…

chemistry.chemical_classificationMaterials scienceEthylene oxideSpectrometerPolymer electrolytesDynamics (mechanics)Relaxation (NMR)General ChemistryPolymerNeutron scatteringCrystallographyMolecular dynamicschemistry.chemical_compoundchemistryChemical physicsGeneral Materials ScienceApplied Physics A: Materials Science & Processing
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Solvent Determines Nature of Effective Interactions between Nanoparticles in Polymer Brushes

2015

We study the effective interaction between two parallel rod-like nanoparticles in swollen and collapsed polymer brushes as a function of penetration depth by 2D self-consistent field calculations. In vertical direction, the interaction is always attractive. In lateral direction, the behavior under good and poor solvent conditions is qualitatively different. In swollen brushes (good solvent), nanoparticles always repel each other. In collapsed brushes (poor solvent), we identify two different regimes: an immersed regime, where the nanoparticles are fully surrounded by the brush, and an interfacial regime, where they are located in the interface between brush and solvent. In the immersed regi…

chemistry.chemical_classificationMaterials scienceField (physics)BrushNanoparticleNanotechnologyPolymerSurfaces Coatings and Filmslaw.inventionSolventchemistrylawChemical physicsVertical directionMaterials ChemistryPhysical and Theoretical ChemistryPenetration depthThe Journal of Physical Chemistry B
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Tuning of interfacial charge transport in polyporphine/phthalocyanine heterojunctions by molecular geometry control for an efficient gas sensor

2022

Abstract Owing to high interfacial conductivity, organic heterostructures hold great promises to augment the electrical performances of electronic devices. In this endeavor, the present work reports fabrication of novel polyporphine/phthalocyanine heterostructures and investigates the modulation of charge transport induced by structural change of polyporphine and its implication on ammonia sensing properties. Polyporphines materials are electrosynthesized by oxidation of zinc(II) porphine monomer that corresponds to the fully unsubstituted porphyrin. At less-positive anodic potential, low conducting meso,meso-singly-linked type-1 polymer (pZnP-1) is formed in which a monomer unit stays orth…

chemistry.chemical_classificationMaterials scienceGeneral Chemical EngineeringHeterojunction02 engineering and technologyGeneral ChemistryPolymerConductivity010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical sciencesAnodeDielectric spectroscopychemistry.chemical_compoundMonomerMolecular geometrychemistryChemical physicsPhthalocyanineEnvironmental Chemistry[CHIM]Chemical Sciences0210 nano-technologyComputingMilieux_MISCELLANEOUS
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Polymer Dynamics in a Polymer-Solid Interphase: Molecular Dynamics Simulations of 1,4-Polybutadiene At a Graphite Surface

2014

A chemically realistic model of 1,4-polybutadiene confined by graphite walls in a thin film geometry was studied by molecular dynamics simulations. The chemically realistic approach allows for a quantitative determination of a variety of experimentally accessible relaxation functions (e.g., dielectric, NMR, or neutron scattering responses). The simulations yield these experimental observables. Additionally, the simulations can be resolved as a function of distance to the solid interface on a much finer scale than experimentally possible, providing a detailed mechanistic picture of the segmental and large scale motions of polymers in the interfacial region between bulk polymer melts and soli…

chemistry.chemical_classificationMaterials scienceGeneral ChemistryDielectricPolymerNeutron scatteringCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterMolecular dynamicsCrystallographychemistryChemical physicsRelaxation (physics)General Materials ScienceInterphaseGraphiteGlass transitionSoft Materials
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