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New polymer syntheses, 88 . Thermosetting cholesterin oligocarbonates with propargyl endgroups
Author(s) -
Kricheldorf Hans R.,
Sun ShihJieh
Publication year - 1997
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.1997.030180704
Subject(s) - thermosetting polymer , propargyl , polymer chemistry , condensation polymer , mesogen , isosorbide , chloride , hydroquinone , materials science , chemistry , polymer , organic chemistry , liquid crystalline , catalysis
Thermosetting cholesteric oligocarbonates were prepared by polycondensation of mesogenic diphenols such as 4,4′‐dihydroxybiphenyl (DHB) or hydroquinone 4‐hydroxy‐benzoate (HQHB; system. name: 4‐hydroxyphenyl 4‐hydroxybenzoate) with methylhy‐droquinone and isosorbide. Trichloromethyl chloroformate served as condensing agent and propargyl alcohol (system. name of propargyl: 2‐propynyl), 4‐propargyloxybenzoyl chloride or 6‐propargyloxy‐2‐napthoyl chloride served as chain stoppers. Most oligocar‐bonates form a cholesteric phase over a broad temperature range. Depending on the mole fraction of isosorbide these oligocarbonates form Grandjean textures when sheared in the molten state.