6533b7cefe1ef96bd1257a02
RESEARCH PRODUCT
Pearl-necklace structures of molecular brushes with rigid backbone under poor solvent conditions: A simulation study
Panagiotis E. TheodorakisWolfgang PaulKurt Bindersubject
chemistry.chemical_classificationMaterials scienceMolecular StructurePolymersTemperatureGeneral Physics and AstronomyPolymerMolecular Dynamics Simulationchemistry.chemical_compoundMolecular dynamicsMonomerChain (algebraic topology)chemistryChemical physicsComputational chemistrySolventsCluster (physics)Side chainCylinderPhysical and Theoretical ChemistryAxial symmetrydescription
Bottle-brush polymers, where flexible side chains containing N=20 to 50 effective monomers are grafted to a rigid backbone, are studied by molecular dynamics simulations, varying the grafting density σ and the solvent quality. Whereas for poor solvents and large enough σ the molecular brush is a cylindrical object, homogeneous in axial direction, for intermediate values of σ an axially inhomogeneous structure of "pearl-necklace" type is formed. The "pearls," however, have a strongly nonspherical ellipsoidal shape, due to the fact that several side chains cluster together in one pearl, qualitatively consistent with predictions of Sheiko et al. [Eur. Phys. J. E 13, 125 (2004)] We analyze the structure of these pearls and study both the transition to the axially uniform cylinder at high σ and to the trivial pearl-necklace structure at small σ, where each pearl contains a single collapsed chain only.
year | journal | country | edition | language |
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2010-09-21 | The Journal of Chemical Physics |