Search results for "molecular dynamics"

showing 10 items of 1075 documents

Bioinspired catechol-terminated self-assembled monolayers with enhanced adhesion properties

2013

The role of the catechol moiety in the adhesive properties of mussel proteins and related synthetic materials has been extensively studied in the last years but still remains elusive. Here, a simplified model approach is presented based on a self-assembled monolayer (SAM) of upward-facing catechols thiol-bound to epitaxial gold substrates. The orientation of the catechol moieties is confirmed by spectroscopy, which also showed lack of significant amounts of interfering o-quinones. Local force-distance curves on the SAM measured by atomic force microscopy (AFM) shows an average adhesion force of 45 nN, stronger than that of a reference polydopamine coating, along with higher reproducibility …

PolydopamineIndolesPolymersCatecholsBiocompatible MaterialsNanotechnologyMolecular Dynamics Simulationengineering.materialBiomimèticaMicroscopy Atomic ForceBiomaterialsMolecular dynamicschemistry.chemical_compound:Enginyeria química [Àrees temàtiques de la UPC]Coated Materials BiocompatibleCoatingMonolayerMoietyGeneral Materials ScienceMagnetite NanoparticlesAdhesive surfaceCatecholChemistrySAMsAdhesivenessSelf-assembled monolayerGeneral ChemistryAdhesionBiomimetic polymersChemical engineeringCatecholengineeringPrintingMagnetic nanoparticlesBiomimeticGoldBiotechnology
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Excess free energy of nanoparticles in a polymer brush

2008

Abstract We present an efficient method for direct determination of the excess free energy Δ F of a nanoparticle inserted into a polymer brush. In contrast to Widom's insertion method, the present approach can be efficiently implemented by Monte Carlo or Molecular Dynamics methods also in a dense environment. In the present investigation the method is used to determine the free energy penalty Δ F ( R , D ) for placing a spherical particle with an arbitrary radius R at different positions D between the grafting plane and the brush surface. Deep inside the brush, or for dense brushes, one finds Δ F  ∝  R 3 whereas for shallow nanoclusions Δ F  ∝  R 2 , regardless of the particle interaction (…

Polymer brushPolymers and PlasticsNanoinclusionsMonte Carlo methodNanoparticlePolymer brushdigestive systemMolecular physicslaw.inventionMolecular dynamicslawMaterials ChemistryStatistical physicsFree energyNanocolloidsMonte Carlochemistry.chemical_classificationQuantitative Biology::BiomoleculesChemistryOrganic ChemistryBrushPolymerRadiusCondensed Matter::Soft Condensed MatterComputer Science::GraphicsParticlePolymer
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Molecular Dynamics of a 1,4-Polybutadiene Melt. Comparison of Experiment and Simulation

1999

We have made detailed comparison of the local and chain dynamics of a melt of 1,4-polybutadiene (PBD) as determined from experiment and molecular dynamics simulation at 353 K. The PBD was found to have a random microstructure consisting of 40% cis, 50% trans, and 10% 1,2-vinyl units with a number-average degree of polymerization 〈Xn〉 = 25.4. Local (conformational) dynamics were studied via measurements of the 13C NMR spin−lattice relaxation time T1 and the nuclear Overhauser enhancement (NOE) at a proton resonance of 300 MHz for 12 distinguishable nuclei. Chain dynamics were studied on time scales up to 22 ns via neutron spin−echo (NSE) spectroscopy with momentum transfers ranging from q = …

Polymers and PlasticsChemistryOrganic ChemistryAnalytical chemistryCarbon-13 NMRDegree of polymerizationQuantum chemistryInorganic ChemistryMolecular dynamicsNuclear magnetic resonanceAtomMaterials ChemistryNeutronCenter of massSpectroscopyMacromolecules
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13C NMR Spin−Lattice Relaxation and Conformational Dynamics in a 1,4-Polybutadiene Melt

2001

We have performed molecular dynamics (MD) simulations of a melt of 1,4-polybutadiene (PBD, 1622 Da) over the temperature range 400-273 K. 13 C NMR spin-lattice relaxation times (T 1 ) and nuclear Overhauser enhancement (NOE) values have been measured from 357 to 272 K for 12 different resonances. The T 1 and NOE values obtained from simulation C-H vector P 2 (t) orientational autocorrelation functions were in good agreement with experiment over the entire temperature range. Analysis of conformational dynamics from MD simulations revealed that T 1 depends much less strongly on the local chain microstructure than does the mean conformational transition time. Spin-lattice relaxation for a give…

Polymers and PlasticsChemistryOrganic ChemistryAutocorrelationRelaxation (NMR)Spin–lattice relaxationThermodynamicsCarbon-13 NMRDihedral angleAtmospheric temperature rangeExponential functionInorganic ChemistryMolecular dynamicsNuclear magnetic resonanceMaterials ChemistryMacromolecules
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Study of the molecular origin of the mechanical and dielectric β relaxation of methyl methacrylate/isopropenyl methyl ketone copolymers

1988

Resultats de l'etude dielectrique, mecanique et par TSC en faveur d'une combinaison d'une barriere intra- et intermoleculaire dans la relaxation beta

Polymers and PlasticsChemistryOrganic ChemistryEnthalpyDielectricActivation energyCondensed Matter PhysicsMolecular dynamicschemistry.chemical_compoundTacticityPolymer chemistryMaterials ChemistryCopolymerStress relaxationMethyl methacrylateMakromolekulare Chemie. Macromolecular Symposia
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Structure of Polymer Brushes in Cylindrical Tubes: A Molecular Dynamics Simulation

2006

Molecular Dynamics simulations of a coarse-grained bead-spring model of flexible macromolecules tethered with one end to the surface of a cylindrical pore are presented. Chain length $N$ and grafting density $\sigma$ are varied over a wide range and the crossover from ``mushroom'' to ``brush'' behavior is studied for three pore diameters. The monomer density profile and the distribution of the free chain ends are computed and compared to the corresponding model of polymer brushes at flat substrates. It is found that there exists a regime of $N$ and $\sigma$ for large enough pore diameter where the brush height in the pore exceeds the brush height on the flat substrate, while for large enoug…

Polymers and PlasticsFOS: Physical sciencesSubstrate (electronics)Condensed Matter - Soft Condensed MatterInorganic ChemistryQuantitative Biology::Subcellular Processeschemistry.chemical_compoundColloidMolecular dynamicsPolymer chemistryMaterials Chemistrychemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesOrganic ChemistryPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterMonomerComputer Science::GraphicschemistryChemical physicsExcluded volumeSoft Condensed Matter (cond-mat.soft)Layer (electronics)Macromolecule
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The Role of Internal Rotational Barriers in Polymer Melt Chain Dynamics

2002

We present molecular dynamics simulations on 1,4-polybutadiene comparing the dynamics of melt chains between chemically realistic models and a freely rotating chain version of one of the models. These models exhibit the same liquid structure, as measured by the structure factor, and meso- to large-scale chain structure, as measured by the Rouse-mode amplitudes. We show that in this case the Rouse-like chain dynamics as observable in the momentum transfer range of neutron spin-echo experiments is the same for the chains with and without torsion barriers. Our results bear on a recent comparative neutron spin-echo study of the chain dynamics of two polymers with similar chain structure which r…

Polymers and PlasticsScatteringChemistryOrganic ChemistryMomentum transferTorsion (mechanics)ObservableCondensed Matter::Soft Condensed MatterInorganic ChemistryMolecular dynamicsChemical physicsComputational chemistryMaterials ChemistryRadius of gyrationNeutronStructure factorMacromolecules
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Single Molecules Probing the Freezing of Polymer Melts: A Molecular Dynamics Study for Various Molecule-Chain Linkages

2010

8 pages; International audience; We present molecular dynamics simulations of coarse-grained model systems of a glassforming polymer matrix containing fluorescent probe molecules. These probe molecules are either dispersed in the matrix or covalently attached to the center or the end of a dilute fraction of the polymer chains. We show that in all cases the translational and rotational relaxation of the probe molecules is a faithful sensor for the glass transition of the matrix as determined from a mode-coupling analysis or Vogel-Fulcher analysis of their R-relaxation behavior. Matrix and dumbbell related relaxation processes show a clear violation of the Stokes-Einstein-Debye laws. In accor…

Polymers and PlasticsSingle Molecules02 engineering and technologyMatrix (biology)Molecular dynamics010402 general chemistry01 natural sciencesInorganic Chemistry[PHYS.PHYS.PHYS-COMP-PH]Physics [physics]/Physics [physics]/Computational Physics [physics.comp-ph]Molecular dynamicsChain (algebraic topology)Materials ChemistryMoleculechemistry.chemical_classificationQuantitative Biology::BiomoleculesChemistryOrganic ChemistryPolymer021001 nanoscience & nanotechnologyFluorescence0104 chemical sciencesCondensed Matter::Soft Condensed MatterChemical physicsPhysical chemistry0210 nano-technologyGlass transition
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Conformations, Transverse Fluctuations and Crossover Dynamics of a Semi-Flexible Chain in Two Dimensions

2014

We present a unified scaling description for the dynamics of monomers of a semiflexible chain under good solvent condition in the free draining limit. We consider both the cases where the contour length $L$ is comparable to the persistence length $\ell_p$ and the case $L\gg \ell_p$. Our theory captures the early time monomer dynamics of a stiff chain characterized by $t^{3/4}$ dependence for the mean square displacement(MSD) of the monomers, but predicts a first crossover to the Rouse regime of $t^{2\nu/{1+2\nu}}$ for $\tau_1 \sim \ell_p^3$, and a second crossover to the purely diffusive dynamics for the entire chain at $\tau_2 \sim L^{5/2}$. We confirm the predictions of this scaling descr…

PolymersCrossoverMolecular ConformationGeneral Physics and AstronomyFOS: Physical sciencesMolecular Dynamics SimulationCondensed Matter - Soft Condensed MatterChain (algebraic topology)Statistical physicsPhysics - Biological PhysicsPhysical and Theoretical ChemistryScalingBrownian motionPhysicsPersistence lengthQuantitative Biology::BiomoleculesMathematics::Functional AnalysisModels TheoreticalSolutionsCondensed Matter::Soft Condensed MatterMean squared displacementLennard-Jones potentialBiological Physics (physics.bio-ph)SolventsBrownian dynamicsSoft Condensed Matter (cond-mat.soft)
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A Monte Carlo Study of Knots in Long Double-Stranded DNA Chains.

2016

We determine knotting probabilities and typical sizes of knots in double-stranded DNA for chains of up to half a million base pairs with computer simulations of a coarse-grained bead-stick model: Single trefoil knots and composite knots which include at least one trefoil as a prime factor are shown to be common in DNA chains exceeding 250,000 base pairs, assuming physiologically relevant salt conditions. The analysis is motivated by the emergence of DNA nanopore sequencing technology, as knots are a potential cause of erroneous nucleotide reads in nanopore sequencing devices and may severely limit read lengths in the foreseeable future. Even though our coarse-grained model is only based on …

PolymersMaterials by StructureMolecular biologyMaterials ScienceElectrophoretic techniquesDNA electrophoresisNucleotide SequencingMolecular Dynamics SimulationBiochemistryNanoporesSequencing techniquesMathematical and Statistical Techniquesstomatognathic systemGeneticsBiochemical SimulationsNanotechnologyDNA sequencingMaterials by AttributeNanomaterialsQuantitative Biology::BiomoleculesBiology and life sciencesMathematical Modelsfood and beveragesComputational BiologyDNAPolymer ChemistryMathematics::Geometric TopologyResearch and analysis methodsNucleic acidsChemistrysurgical procedures operativeMolecular biology techniquesMacromoleculesRandom WalkPhysical SciencesNucleic Acid ConformationEngineering and TechnologyMonte Carlo MethodResearch ArticlePLoS computational biology
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