Rotational Symmetry Breaking of Complex Polymeric Macromolecules
ORAL
Abstract
A generalized version of Flory mean-field theory, supported by numerical simulations, indicates that polymeric macromolecules in good solvent with branches and cycles can show a sequence of spontaneous rotational symmetry breaking transitions as a function of increasing strength of the self-repulsion (J. Kelly, A. Grosberg and R. Bruinsma, submitted to PRL). We present here the analysis of the effect of including thermal fuctuations in the mean-field theory on the nature of these transitions for specific polymeric structures.
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Presenters
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Justin Little
Physics and Astronomy, University of California, Los Angeles
Authors
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Justin Little
Physics and Astronomy, University of California, Los Angeles
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Robijn Bruinsma
Physics and Astronomy, University of California, Los Angeles
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Alexander Grosberg
Department of Physics, New York University, New York University