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  • Enantioselective absorption of chirally doped liquid crystalline networks studied by the use of an electronic microbalance.

Enantioselective absorption of chirally doped liquid crystalline networks studied by the use of an electronic microbalance.

The journal of physical chemistry. B (2007-07-20)
G Palaprat, J-D Marty, D Langevin, H Finkelmann, M Mauzac
ABSTRACT

A polydomain cholesteric elastomer was obtained by cross-linking a nematic side-chain polysiloxane in the presence of a chiral dopant. After extraction of the chiral dopant, sorption experiments were performed, by the use of an electronic microbalance, in the presence of each enantiomer of a chiral amine molecule. The sorption kinetics corresponds to a Fickian diffusion behavior. They allowed us to determine the diffusion coefficients and to show that the doped polymer has a more pronounced affinity toward one of the enantiomers.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, purum, ≥98.0% (sum of enantiomers, GC)
Supelco
(R)-(+)-α-Methylbenzylamine, for chiral derivatization, LiChropur, ≥99.0%
Sigma-Aldrich
α-Methylbenzylamine, 99%
Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, 98%
Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, ChiPros®, produced by BASF, ≥99.0%
Sigma-Aldrich
(S)-(−)-α-Methylbenzylamine, 98%