Polymères porteurs de dérivés du glycérol, 1. Polymérisation du méthacrylate d'époxy-2,3 propyle et du méthacrylate-phényl-2 butyrate d'hydroxy-2 triméthylène
✍ Scribed by Brosse, Jean-Claude ;Mouity-Moussounda, François ;Soutif, Jean-Claude
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1983
- Weight
- 358 KB
- Volume
- 184
- Category
- Article
- ISSN
- 0025-116X
No coin nor oath required. For personal study only.
✦ Synopsis
Radical polymerizations and copolymerizations of 2,3-epoxypropyl methacrylate (1) and its reaction product with 2-phenylbutyric acid (2), 2-hydroxytrimethylene methacrylate 2-phenylbutyrate (3), were studied using 2,2 '-azodiisobutyronitrile, benzoyl peroxide, or H202 (with UV irradiation) as initiators, and also the influence of the experimental conditions (temperature, concentration, time) on the yield. Due to the reactivity of the oxirane moiety, poly(2,3-epoxypropyl methacrylate) can easily be modified by ring opening reactions, e. g. with carboxylic acids. a) Equipe de Recherche Associke au C.N.R.S. No 311.
📜 SIMILAR VOLUMES
## Abstract L'étude cinétique de réactions impliquant des dérivés du benzophéanthrène‐3,4, substitués en position 2, (solvolyses et échange S~N~2 avec l'iodure de potassium du chlorométhyl‐2‐benzophénanthrène‐3,4; hydrolyse basique du benzophénanthrène‐3,4‐carboxylate‐2 d'éthyle) niontre que la réa
## Abstract On décrit la synthèse, en quatre étapes a partir de l'acide dibromo‐ 4, 6‐isophtalique, de dérivés di‐ et tétraméthylés du cis‐fluorbnackne ([indéno‐2′, 1′: 2,3‐fluorkne]). Ce sont le diméthyl‐3,6‐cis‐fluorknacbne ou diméthyl‐6,6′‐[indho‐2′, 1′ : 2,3‐fluorène], le téraméhyl‐1, 3,6,8‐ ci
**Facile synthesis of derivatives of 2,4‐diphenyl‐3‐azabicyclo[3.3.1]nonane and 7,9‐diphenyl‐8‐azabicyclo[4.3.1]decane** The facile synthesis of hydantoins, cyanhydrins and aminonitriles derived from 2,4‐diphenyl‐3‐azabicyclo[3.3.1]nonanone and 7,9‐diphenyl‐8‐azabicyclo[4.3.1]decanone is described.
## Abstract The polymerization of 1‐(1‐cyclopentenyl)vinyl acetate (**1**) and (3‐methyl‐1,3‐butadien‐2‐yl) acetate (**7**) under radical conditions, leading to 1,4‐polymers, and the copolymerization with vinyl monomers were studied. The reactivity ratios are compared with those previously describe