Copolymerization of Fluorinated Monomers with Hydrophilic Monomers in Aqueous Solution in Presence of Cyclodextrin
✍ Scribed by Oliver Kretschmann; Helmut Ritter
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 120 KB
- Volume
- 207
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Summary: New fluorinated copolymers were synthesized by copolymerization of 1__H__,1__H__,2__H__,2__H‐__perfluorodecyl methacrylate (1) with hydrophilic comonomers methacrylic acid (3), 2‐acrylamido‐2‐methylpropane sulfonic acid (6), 3‐trimethylammonium propyl methacrylamide chloride (7) and N,N‐dimethylmethacrylamidopropyl‐N‐3‐sulfopropylammoniumbetaine (8). The reaction was carried out in water using randomly methylated β‐cyclodextrin (RAMEB) for solubilization of the fluorinated monomer by forming a host‐guest complex (1a). Polymerization kinetics were investigated and copolymerization parameters were determined. Additionally, a RAMEB complex of tert‐butyl methacrylate (2a) was copolymerized with 1a in water. For comparison, copolymerization of the uncomplexed monomers 1 and 2 were carried out in organic solvents. Evaluation of copolymerization kinetics and parameters showed significant differences in the relative reactivities of the free monomers and the monomer‐RAMEB complexes.
magnified image
📜 SIMILAR VOLUMES
Emulsion and miniemulsion copolymerizations were carried out with acrylic monomers (methyl methacrylate, butyl acrylate, and acrylic acid) in the presence of a n alkyd resin. Poly(methy1 methacrylate) was used as a hydrophobe or cosurfactant in the miniemulsion reactions. The results demonstrate tha
## Abstract We report on the first examples of the free radical polymerization of a fluorinated 2‐vinylcyclopropane **1** and its copolymerization with an alkyl 2‐vinylcyclopropane **2** in aqueous solution via their host‐guest complexation with a random methylated __β__‐cyclodextrin (RAMEB) using
## Abstract Ten hydrophobic, substituted, acetylene monomers were examined as to their abilities to form an inclusion complex with hydroxypropyl‐__β__‐cyclodextrin (HPCD). Only the monomers with suitable substitutents were found to form the monomer/HPCD complex, which was identified by NMR, FTIR, a