Synthesis and magnetic properties of mesogenic side-chain polymers containing stable radicals
✍ Scribed by Jürgen Allgaier; Heino Finkelmann
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 804 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
An amorphous and a liquid‐crystalline side‐chain polymer containing stable nitroxyl radicals are synthesized, the free radical being located either in a piperidine N‐oxyl or a 1,3‐oxazolidine N‐oxyl moiety. These polymers are available by reaction of precursor polymer having a formyl group in every repeating unit with low‐molecular‐weight nitroxyl free radicals functionalized with an amino group. The conversion of the polymer‐analogous reaction is nearly quantitative. Both the amorphous and the liquid‐crystalline polymer show paramagnetic behaviour in the temperature range from 6 to 300 K.
📜 SIMILAR VOLUMES
## Abstract Two novel optically active polymethacrylates bearing in the side chain a cyclic chiral group of one prevailing absolute configuration linked to the carbazole chromophore, deriving from the related monomers (__S__)‐(−)‐3‐methacryloyloxy‐__N__‐[3‐(9‐ethylcarbazolyl)]pyrrolidine [(__S__)‐(
The synthesis and characterization of side-chain liquid crystalline (LC) polyacrylates containing para-nitroazohenzene (Pn) as mesogenic groups were described. Homopolymers with 3 and 4 carbon atoms in the spacers were non-LC polymers; for homopolymers with 6 carbon atoms in the spacer, nematic LC b