Polymerization of acetylenes carrying precursors of aminyl radicals
✍ Scribed by Lothar Dulog; Peter Bognar
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 152 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
In the search for organic ferromagnets polymers with a conjugated backbone and pendant persistent radicals are one route of interest. The synthesis of poly[4‐(4‐ethynylphenyl)‐2′,4′,6′‐trinitro‐2,6‐diphenyldiphenylamine] (p‐3) and poly[4‐(3‐ethynylphenyl)‐2′,4′,6′‐trinitro‐2,6‐diphenyldiphenylamine] (m‐3) as precursors of polyradicals are described. A dinuclear rhodium cyclooctadiene chloride complex as polymerization catalyst was used to yield polymers with molecular weights (gel‐permeation chromatography) of 100 000 for m‐3 and 210 000 for p‐3.
📜 SIMILAR VOLUMES
l-(2-Aminophenyl)pent-l-yne 1 reacted with benzenethiol at 150 °C under radical conditions to give the thiol/alkyne adduct 2, the benzothiophene 4 and the indole 5. Reaction of l with henzenesulfanyl radicals produced from diphenyl disulfide in the absence of hydrogen donors gave only the indole 5 i