Synthesis and polymerization of a chiral liquid crystal diacrylate exhibiting smectic A* and C* phases

Citation
Bc. Baxter et Dl. Gin, Synthesis and polymerization of a chiral liquid crystal diacrylate exhibiting smectic A* and C* phases, MOL CRYST A, 332, 1999, pp. 2777-2782
Citations number
14
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
MOLECULAR CRYSTALS AND LIQUID CRYSTALS SCIENCE AND TECHNOLOGY SECTION A-MOLECULAR CRYSTALS AND LIQUID CRYSTALS
ISSN journal
1058725X → ACNP
Volume
332
Year of publication
1999
Pages
2777 - 2782
Database
ISI
SICI code
1058-725X(1999)332:<2777:SAPOAC>2.0.ZU;2-P
Abstract
The alignment and cross-linking of chiral liquid crystal (LC) phases has be en used to generate ordered noncentrosymmetric polymer networks with a vari ety of interesting optical and transducer properties. Examples of intrinsic ally chiral LC diacrylates which exhibit chiral smectic phases are rare bec ause of the difficulties associated with the design of such monomers. We ar e presenting the stereospecific synthesis and subsequent photopolymerizatio n of a chiral smectic diacrylate which is derived from (S)-ethyl lactate. T his monomer exhibits an enantiotropic smectic A* phase from 49 to 71 degree s C upon heating at 0.5 degrees C/min and from 71 to 39 degrees C upon cool ing at the same rate. The smectic A* phase of the chiral monomer can be hom eotropically and homogeneously aligned and subsequently photopolymerized to yield highly uniform, noncentrosymmetric polymer films of predefined symme try. Upon rapid cooling at 5 degrees C/min, the monomer also exhibits a met astable, monotropic ferroelectric smectic C* phase from approximately 35 to 33 degrees C. The cross-linking of this metastable phase will also be disc ussed.