4.7 Article

Synthesis, structure and mesomorphism of new cholesteric monomers and smectic comblike polymers

Journal

EUROPEAN POLYMER JOURNAL
Volume 46, Issue 3, Pages 535-545

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2009.12.002

Keywords

Liquid crystalline polymers; Mesomorphism; Cholesteric phase; Smectic A phase

Funding

  1. Natural Science Foundation of China (NSFC) [50503005]
  2. Science and Technology Bureau of Shenyang

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Seven new cholesteric monomers (M-1-M-7) and the corresponding smectic comblike polymers containing cholesteryl groups (P-1-P-7) were synthesized. The chemical structures and purity were characterized by FT-IR. (1)H NMR, and elemental analyses. The specific optical rotations were evaluated with a polarimeter. The mesomorphism was investigated by polarizing optical microscopy, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction. The specific optical rotation values of these monomers and polymers with the same numbers of phenyl ring and terminal groups were nearly equal, however, they decreased with increasing the aryl numbers in the mesogenic core. M-1-M-7 showed oily streak texture and focal conic texture, or fingerprint texture, or spiral texture of cholesteric phase. P-1-P-7 showed the smectic A phase. The melting, clearing, and glass transition temperatures increased, and the mesophase temperature ranges widened with increasing the aryl number in the mesogenic core. Surprisingly, although the molecular structures of M-6 and M-7 were similar to those of M-4, namely the mesogenic cores contained three phenyl rings, their phase behavior had a considerable difference, and T(m), and T(i) of M-6 and M-7 were less than those of M-4. In addition, M-6 and M-7 also showed an obvious glass transition. TGA showed that all the polymers had good thermal stabilities. (C) 2009 Elsevier Ltd. All rights reserved.

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