A series of side-chain polyacrylates containing chiral, optically active sulfoxide substituents was prepared by the enantioselective oxidation of the corresponding prochiral polyacrylates containing prochiral sulfide substituents. A chiral sulfonyloxaziridine was used as the oxidant. The chemical modification was selective from chemical and stereochemical standpoints. The resulting polymers formed chiral nematic and/or smectic phases with a slightly decreased propensity to give stable and persistent mesophases with respect to the parent sulfide containing polymers.
Liquid-Crystalline Side-Chain Polyacrylates Containing Chiral Sulfoxide Substituents / Chiellini, E.; G., Galli; Angeloni, A. S.; M., Laus; S., Melone; Francescangeli, Oriano. - In: MOLECULAR CRYSTALS AND LIQUID CRYSTALS SCIENCE AND TECHNOLOGY. SECTION A, MOLECULAR CRYSTALS AND LIQUID CRYSTALS. - ISSN 1058-725X. - 266:(1995), pp. 189-196. [10.1080/10587259508033642]
Liquid-Crystalline Side-Chain Polyacrylates Containing Chiral Sulfoxide Substituents
FRANCESCANGELI, ORIANO
1995-01-01
Abstract
A series of side-chain polyacrylates containing chiral, optically active sulfoxide substituents was prepared by the enantioselective oxidation of the corresponding prochiral polyacrylates containing prochiral sulfide substituents. A chiral sulfonyloxaziridine was used as the oxidant. The chemical modification was selective from chemical and stereochemical standpoints. The resulting polymers formed chiral nematic and/or smectic phases with a slightly decreased propensity to give stable and persistent mesophases with respect to the parent sulfide containing polymers.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.