SYNTHESIS AND CURING OF NOVEL LC TWIN EPOXY MONOMERS FOR LIQUID-CRYSTAL THERMOSETS
Citation
A. Shiota et Ck. Ober, SYNTHESIS AND CURING OF NOVEL LC TWIN EPOXY MONOMERS FOR LIQUID-CRYSTAL THERMOSETS, Journal of polymer science. Part A, Polymer chemistry, 34(7), 1996, pp. 1291-1303
Categorie Soggetti
Polymer Sciences
SICI code
0887-624X(1996)34:7<1291:SACONL>2.0.ZU;2-B
Abstract
This article describes the synthesis and characterization of new liqui
d crystalline thermosets having a twin structure. Nematic epoxy-termin
ated monomers based on a phenyl benzoate twin mesogen connected by an
alkylene spacer were synthesized for these studies. In addition, an ep
oxy-terminated monomer based on a 1,4-bis(benzoyloxy)phenylene mesogen
was synthesized to determine the effect of the position of the mesoge
n on the final network structure. The diepoxy monomer made with phenyl
benzoate twin mesogens connected with an alkylene spacer formed a sme
ctic-like network when cured with diamines. This smectic organization
appeared even though the diepoxy monomer itself showed only a nematic
mesophase over a narrow temperature range. The presence of crosslinks
at both ends of the mesogens helped to retain a uniform spacing betwee
n crosslinking sites during the curing reaction, and aided formation o
f the smectic layer arrangement. The epoxy monomer possessing a 1,4-bi
s(benzoyloxy)phenylene mesogen and two epoxidized alkylene end groups
on both sides of the mesogen formed a stable nematic mesophase. Howeve
r, in contrast to the twin epoxies, the latter epoxy when reacted with
diamines tended to produce a nematiclike network which was retained a
s the crosslinking reaction proceeded. (C) 1996 John Wiley & Sons, Inc
.