The kinetics of the homopolymerizations of styrene, N-(3-dimethylaminophenyl) maleimide (I) and N-(3-dimethylamino-6-methylphenyl) maleimide (I|) in benzene and dimethylformamide, and the molecular weights of the polymers were studied. N-(3-Dimethylaminophenyl) succinimide, regarded as a model for p
Polymerization of N-(2,3,4,5,6-pentafluorophenyl)-maleimide
✍ Scribed by Tokio Hagiwara; Naoyuki Kawashima; Hiroshi Hamana; Tadashi Narita
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 413 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
A novel fluorine‐containing polymer, poly[N‐(2,3,4,5,6‐pentafluorophenyl)maleimide], was prepared by the anionic polymerization of N‐(2,3,4,5,6‐pentafluorophenyl)maleimide (PFPMI). Anionic polymerization with alkali metal tert‐butoxides gave poly(PFPMI) in 14–32% yield. Phenyllithium and sec‐butyllithium also afforded poly(PFPMI). No polymer was obtained with a radical initiator such as 2,2′‐azoisobutyronitrile. The polymerization took place only via the vinylene group of PFPMI and no appreciable side‐reaction occurred. The obtained poly(PFPMI) shows unimodal molecular weight distribution and begins to decompose at 325°C.
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AbstractÐA variety of storable N-acyl-N-(2,3,4,5,6-penta¯uorophenyl)methanesulfonamides (4a±e) prepared from N-2,3,4,5,6-penta¯uorophenylmethanesulfonamide (3), have been developed after systematic research on the structure±reactivity relationship and were found to serve as N-acylation reagents exhi
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