Theory of Chiral Order in Random Copolymers
arXiv:cond-mat/9509099 · doi:10.1103/PhysRevLett.76.58
Abstract
Recent experiments have found that polyisocyanates composed of a mixture of opposite enantiomers follow a chiral ``majority rule:'' the chiral order of the copolymer, measured by optical activity, is dominated by whichever enantiomer is in the majority. We explain this majority rule theoretically by mapping the random copolymer onto the random-field Ising model. Using this model, we predict the chiral order as a function of enantiomer concentration, in quantitative agreement with the experiments, and show how the sharpness of the majority-rule curve can be controlled.
13 pages, including 4 postscript figures, uses REVTeX 3.0 and epsf.sty
Cited by in corpus (5)
- Cooperative Chiral Order in Copolymers of Chiral and Achiral Units
- Non-local correlations in the Haldane phase for an XXZ spin-1 chain: A perspective from infinite matrix product state representation
- Chiral and Antichiral Order in Bent-Core Liquid Crystals
- Chiral molecule adsorption on helical polymers
- Polymer-disordered liquid crystals: Susceptibility to electric field