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
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.