Abstract
This article describes the synthesis and characterization of new liquid crystalline thermosets having a twin structure. Nematic epoxy-terminated monomers based on a phenyl benzoate twin mesogen connected by an alkylene spacer were synthesized for these studies. In addition, an epoxy-terminated monomer based on a 1,4-bis(benzoyloxy)phenylene mesogen was synthesized to determine the effect of the position of the mesogen on the final network structure. The diepoxy monomer made with phenyl benzoate twin mesogens connected with an alkylene spacer formed a smectic-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 between crosslinking sites during the curing reaction, and aided formation of the smectic layer arrangement. The epoxy monomer possessing a 1,4-bis(benzoyloxy)phenylene mesogen and two epoxidized alkylene end groups on both sides of the mesogen formed a stable nematic mesophase. However, in contrast to the twin epoxies, the latter epoxy when reacted with diamines tended to produce a nematic-like network which was retained as the crosslinking reaction proceeded. © 1996 John Wiley & Sons, Inc.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Polymer Science Part A: Polymer Chemistry
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.