Premium
Thermotropic liquid‐crystalline polyphosphate esters containing phenolphthalein moiety
Author(s) -
Srividhya D.,
Senthil S.,
Kannan P.
Publication year - 2004
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.13431
Subject(s) - phenolphthalein , thermotropic crystal , polymer , mesogen , differential scanning calorimetry , mesophase , polymer chemistry , moiety , glass transition , materials science , liquid crystal , condensation polymer , chemistry , organic chemistry , liquid crystalline , physics , optoelectronics , thermodynamics
Abstract A new series of thermotropic liquid‐crystalline (LC) polyphosphate esters containing phenolphthalein as a part of their mesogen has been synthesized by a solution polycondensation method. The even‐numbered methylene spacers were varied from 2–10, and ethyl phosphate was used as a phosphorus heterogeneity. Thermal analysis showed that these polymers are stable up to 275–342°C with high char yield. All of the polymers exhibited liquid‐crystalline properties except for Polymers I and VI. Differential scanning calorimetry (DSC) confirmed the mesophase formation of the polymers. The glass transition temperature ( T g ) and melting temperature ( T m ) of the polymers were considerably low. A polymer containing phenolphthalein alone as a rigid segment with decamethylene spacers was also synthesized, but it did not show birefringent melt properties. These results reveal that phenolphthalein alone cannot act as a mesogen, whereas phenolphthalein phenylester can. Molecular modeling studies and conformational analysis confirmed that the steric hindrance of phenylester and the conjugation effect could explain the promotion of mesogenic behavior by phenolphthalein phenylester. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 194–200, 2004