Several novel mesogenic spiro-orthoester monomers such as 1,6,10trioxaspiro [4,5]decanes 4, containing biphenyl mesogens at the C-8 positions of the fiveand six-membered spirocyclic ring, through the alkylene spacers of different lengths were prepared by condensation reaction of the corresponding bi
Synthesis and characterization of crystalline poly(ethyleneimine)s with mesogenic side chains forming liquid crystals on quaternization
✍ Scribed by Patrick Masson; Benoit Heinrich; Yves Frègre; Philippe Gramain
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 652 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The synthesis and thermal properties of a new type of side‐chain liquid‐crystalline polysalts are described. The polymers are first obtained by partial or complete alkylation of a linear poly(ethyleneimine) with 6‐(4‐methoxy‐4′‐biphenylyloxy)hexyl bromide or 12‐(4‐methoxy‐4′‐biphenylyloxy)dodecyl bromide. In a second step, polysalts are prepared by partial or complete quaternization with acyl bromide or dimethyl sulfate. Differential scanning calorimetry, polarizing optical microscopy and X‐ray diffraction experiments show that the polymers and copolymers alkylated with the mesogenic groups are all crystalline. When quaternized, they exhibit thermotropic smectic A phases. This behaviour confirms the smectogenic function of the ammonium units located in the backbone, as already observed with poly(4‐vinylpyridinium) salts.
📜 SIMILAR VOLUMES
Side-chain liquid-crystalline polymers were synthesized using malonic acid esters with a mesogenic group (1) linked through a hexamethylene spacer and oligo(ethy1ene glycol) (2.) as a flexible mainchain spacer. Polymers derived from 1 with a mesogen such as p-nitrophenylazophenoxy (la) or 4-(4'-nitr