Search results for " mechanics"

showing 10 items of 5066 documents

Spectrophotometric determinations of binding constants between cyclodextrins and aromatic nitrogen substrates at various pH values

2001

The inclusion capacity of native β-cyclodextrin (1) and mono-(6-amino-6-deoxy)-β-cyclodextrin (2) versus aromatic compounds having a nitro or an amino group or both has been investigated at three different pH values. Molecular interactions in inclusion complexes have also been investigated by means of molecular mechanics (MM2/QD) models. Electrostatic and van der Waals interactions and the formation of a hydrogen bond between the donor amino group and the oxygen atom of the secondary hydroxyl group seem to be the more important contributions in determining complex stability. The inclusion capacity of two different cyclodextrins versus aromatic compounds has been investigated at three differ…

chemistry.chemical_classificationMolecular interactionsChemistryHydrogen bondOrganic Chemistrychemistry.chemical_elementSettore CHIM/06 - Chimica OrganicaBiochemistryNitrogenMolecular mechanicscyclodextrins inclusion molecular mechanicssymbols.namesakeComputational chemistryGroup (periodic table)Drug DiscoveryNitrosymbolsOrganic chemistryNon-covalent interactionsvan der Waals forceTetrahedron
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Calculation of the Phase Behavior of Lipids

1998

The self-assembly of monoacyl lipids in solution is studied employing a model in which the lipid's hydrocarbon tail is described within the Rotational Isomeric State framework and is attached to a simple hydrophilic head. Mean-field theory is employed, and the necessary partition function of a single lipid is obtained via a partial enumeration over a large sample of molecular conformations. The influence of the lipid architecture on the transition between the lamellar and inverted-hexagonal phases is calculated, and qualitative agreement with experiment is found.

chemistry.chemical_classificationPartition function (quantum field theory)Quantitative Biology::BiomoleculesStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsChemistryFOS: Physical sciencesThermodynamics02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular conformationLarge sampleQuantitative Biology::Subcellular ProcessesCondensed Matter::Soft Condensed MatterHydrocarbonPhase (matter)0103 physical sciencesLamellar structurelipids (amino acids peptides and proteins)Lipid bilayer phase behavior0210 nano-technologyCondensed Matter - Statistical Mechanics
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Scaling theory of star polymers and general polymer networks in bulk and semi-infinite good solvents

1988

Theorie d'echelle utilisant l'equivalence entre la fonction generatrice du nombre total de configuration et la fonction de correlation a plusieurs spins du modele de Heisenberg classique a n composantes dans la limite n→0

chemistry.chemical_classificationPhysicsCorrelation function (statistical mechanics)Star polymerchemistrySemi-infiniteHeisenberg modelSolid-stateThermodynamicsField theory (psychology)PolymerScaling theoryJournal de Physique
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Third virial coefficient for 4-arm and 6-arm star polymers

2008

We discuss the computation of the third virial coefficient in polymer systems, focusing on an additional contribution absent in the case of monoatomic fluids. We determine the interpenetration ratio and several quantities that involve the third virial coefficient for star polymers with 4 and 6 arms in the good-solvent regime, in the limit of a large degree of polymerization.

chemistry.chemical_classificationPhysicsMonatomic gasStatistical Mechanics (cond-mat.stat-mech)Polymers and PlasticsOrganic ChemistryMonte Carlo methodFOS: Physical sciencesThermodynamicsPolymerStatistical mechanicsDegree of polymerizationCondensed Matter - Soft Condensed MatterCondensed Matter Physicsmonte carlo simulations; star polymers; statistical mechanics; statistical thermodynamics; virial expansionInorganic ChemistrychemistryVirial coefficientMaterials ChemistryVirial expansionSoft Condensed Matter (cond-mat.soft)Limit (mathematics)Condensed Matter - Statistical Mechanics
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Polymer dynamics in time-dependent periodic potentials.

2008

Dynamics of a discrete polymer in time-dependent external potentials is studied with the master equation approach. We consider both stochastic and deterministic switching mechanisms for the potential states and give the essential equations for computing the stationary state properties of molecules with internal structure in time-dependent periodic potentials on a lattice. As an example, we consider standard and modified Rubinstein-Duke polymers and calculate their mean drift and effective diffusion coefficient in the two-state non-symmetric flashing potential and symmetric traveling potential. Rich non-linear behavior of these observables is found. By varying the polymer length, we find cur…

chemistry.chemical_classificationPhysicsStatistical Mechanics (cond-mat.stat-mech)Equations of stateFOS: Physical sciencesObservablemolekyylitPolymerFlashingNonlinear systemClassical mechanicschemistryLattice (order)Master equationMoleculepolymeeritCondensed Matter - Statistical MechanicsdynamiikkaPhysical review. E, Statistical, nonlinear, and soft matter physics
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Scaling behavior of topologically constrained polymer rings in a melt

2014

Large scale molecular dynamics simulations on graphic processing units (GPUs) are employed to study the scaling behavior of ring polymers with various topological constraints in melts. Typical sizes of rings containing $3_1$, $5_1$ knots and catenanes made up of two unknotted rings scale like $N^{1/3}$ in the limit of large ring sizes $N$. This is consistent with the crumpled globule model and similar findings for unknotted rings. For small ring lengths knots occupy a significant fraction of the ring. The scaling of typical ring sizes for small $N$ thus depends on the particular knot type and the exponent is generally larger than 0.4.

chemistry.chemical_classificationPhysicsStatistical Mechanics (cond-mat.stat-mech)Mathematics::Commutative AlgebraCatenaneFOS: Physical sciencesGeometryPolymerCondensed Matter - Soft Condensed MatterCondensed Matter PhysicsMathematics::Geometric TopologyMolecular dynamicsKnot (unit)chemistryExponentSoft Condensed Matter (cond-mat.soft)General Materials ScienceScalingCondensed Matter - Statistical MechanicsJournal of Physics: Condensed Matter
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Stimuli-responsive brushes with active minority components: Monte Carlo study and analytical theory

2015

Using a combination of analytical theory, Monte Carlo simulations, and three dimensional self-consistent field calculations, we study the equilibrium properties and the switching behavior of adsorption-active polymer chains included in a homopolymer brush. The switching transition is driven by a conformational change of a small fraction of minority chains, which are attracted by the substrate. Depending on the strength of the attractive interaction, the minority chains assume one of two states: An exposed state characterized by a stem-crown-like conformation, and an adsorbed state characterized by a flat two-dimensional structure. Comparing the Monte Carlo simulations, which use an Edwards-…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodBrushFOS: Physical sciencesPolymerFlory–Huggins solution theoryCondensed Matter - Soft Condensed Matterlaw.inventionCondensed Matter::Soft Condensed MatterInorganic Chemistrysymbols.namesakelawThermalExcluded volumeMaterials ChemistrysymbolsDynamic Monte Carlo methodSoft Condensed Matter (cond-mat.soft)Statistical physicsHamiltonian (quantum mechanics)
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Adsorption Transition of a Polymer Chain at a Weakly Attractive Surface: Monte Carlo Simulation of Off-Lattice Models

2002

A bead-spring model of a polymer chain with one end attached to a wall is studied by Monte Carlo simulations for chain lengths 16 ≤ N ≤ 256. Two types of adsorption potentials, 9-3 and 10-4 Lennard-Jones (LJ) potentials, between the effective monomers and the wall are assumed. For both cases the adsorption transition where the chain changes its asymptotic statistical properties from a three-dimensional to a two-dimensional configuration is located using a scaling analysis. It is shown that the crossover exponent φ = 0.50 ± 0.02 is the same for both LJ potentials. This value is compatible with recent theoretical predictions and simulation results for lattice models with short-range wall pote…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodCrossoverThermodynamicsStatistical mechanicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterInorganic ChemistryAdsorptionLattice (order)Materials ChemistryExponentStatistical physicsScalingMacromolecular Theory and Simulations
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Anomalous Structure and Scaling of Ring Polymer Brushes

2011

A comparative simulation study of polymer brushes formed by grafting at a planar surface either flexible linear polymers (chain length $N_L$) or (non-catenated) ring polymers (chain length $N_R=2 N_L$) is presented. Two distinct off-lattice models are studied, one by Monte Carlo methods, the other by Molecular Dynamics, using a fast implementation on graphics processing units (GPUs). It is shown that the monomer density profiles $\rho(z)$ in the $z$-direction perpendicular to the surface for rings and linear chains are practically identical, $\rho_R(2 N_L, z)=\rho_L(N_L, z)$. The same applies to the pressure, exerted on a piston at hight z, as well. While the gyration radii components of ri…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesCondensed Matter - Materials ScienceMaterials scienceStatistical Mechanics (cond-mat.stat-mech)Monte Carlo methodGeneral Physics and AstronomyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterRing (chemistry)GyrationMolecular physicsCondensed Matter::Soft Condensed MatterMolecular dynamicsPlanarchemistryPerpendicularSoft Condensed Matter (cond-mat.soft)ScalingCondensed Matter - Statistical Mechanics
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Mechanical Properties of Single Molecules and Polymer Aggregates

2013

This chapter deals with the mechanical properties of single polymer chains, aggregates, and supramolecular complexes. The topics discussed cover a broad range from fundamental statistical mechanics of the equilibrium elastic properties of single polymer chains to details of the behavior of binding pockets in biomolecular assemblies as observed by force spectroscopy. The first section treats the equilibrium mechanical properties of single polymer chains in various environments, investigated via extensive simulations employing coarse-grained models that have proven extremely successful in many branches of polymer physics, namely the bond-fluctuation model and the self-avoiding walk model. Apa…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCatenaneForce spectroscopySupramolecular chemistryNanotechnologyPolymer adsorptionStatistical mechanicsPolymerMolecular dynamicschemistryChemical physicsPolymer physics
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