## Abstract Thermoresponsive poly(__N__‐isopropylacrylamide)/dextran hybrid particles were formed by surface‐initiated, aqueous atom transfer radical polymerization via the attachment of a polymerization initiator onto dextran microspheres and polymerization of __N__‐isopropylacrylamide. The result
Atom Transfer Radical Polymerization of N-Isopropylacrylamide
✍ Scribed by Giancarlo Masci; Laura Giacomelli; Vittorio Crescenzi
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 130 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
Summary: Controlled polymerization of N‐isopropylacrylamide (NIPAAM) was achieved by atom transfer radical polymerization (ATRP) using ethyl 2‐chloropropionate (ECP) as initiator and CuCl/tris(2‐dimethylaminoethyl)amine (Me~6~TREN) as a catalytic system. The polymerization was carried out in DMF:water 50:50 (v/v) mixed solvent at 20 °C. The first order kinetic plot was linear up to 92% conversion. Controlled molecular weights up to 2.2 × 10^4^ and low polydispersities (1.19) were obtained. The living character of the polymerization was also demonstrated by self‐blocking experiments. Block copolymers with N,N‐dimethylacrylamide (DMAAM) and 3‐sulfopropyl methacrylate (SPMA) were successfully prepared.
Molecular weights and polydispersities of polyNIPAAM versus NIPAAM conversion for two different degrees of polymerization.
imageMolecular weights and polydispersities of polyNIPAAM versus NIPAAM conversion for two different degrees of polymerization.
📜 SIMILAR VOLUMES
## Abstract **Summary:** The living polymerization of __N__,__N__‐dimethylacrylamide was achieved by atom transfer radical polymerization catalyzed by copper chloride complexed with a new ligand, __N__,__N′__‐bis(pyridin‐2‐ylmethyl 3‐hexoxo‐3‐oxopropyl)ethane‐1,2‐diamine (BPED). With methyl 2‐chlor
## Abstract ATRP of 2‐(__N,N__‐dimethylamino)ethyl acrylate (DMAEA) was investigated using CuBr or CuCl with different multidentate ligands. The catalyst was found active for DMAEA polymerization when ligated with tris[2‐(__N,N__‐dimethylamino)ethyl]amine. Good control over molecular weight was ach