Synthesis and characterization of novel polyimides bearing a side chain composed of stilbene mesogen and undecyl spacer and the alignment ability of nematic liquid-crystal molecules

Citation
Jh. Park et al., Synthesis and characterization of novel polyimides bearing a side chain composed of stilbene mesogen and undecyl spacer and the alignment ability of nematic liquid-crystal molecules, J POL SC PC, 39(10), 2001, pp. 1800-1809
Citations number
29
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
39
Issue
10
Year of publication
2001
Pages
1800 - 1809
Database
ISI
SICI code
0887-624X(20010515)39:10<1800:SACONP>2.0.ZU;2-9
Abstract
Four different polyimides with side chains containing undecyl spacers and 4 -fluorostilbene mesogen end groups were prepared, and their structures and the controllability of the liquid-crystal (LC) alignment with rubbing were investigated. From X-ray scattering and differential scanning calorimetry d ata, pyromellitic dianhydride (PMDA)-, benzophenone-3,3 ' ,4,4 ' -tetracarb oxylic dianhydride (BTDA)-, and 4,4 ' -oxydi(phthalic anhydride) (ODPA)-bas ed polyimides were shown to have layered structures and short-range orderin g. Pretilt angles of LCs on the rubbed surfaces were 1-9 degrees, depending on the rubbing density and backbone. In particular, the long undecyl space rs caused the mesogenic stilbene end groups to lie next to the main chain, resulting in a reduction in the pretilt angles. (C) 2001 John Wiley & Sons, Inc.