## 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 c
Atom Transfer Radical Polymerization of N,N-Dimethylacrylamide
✍ Scribed by Shijie Ding; Maciej Radosz; Youqing Shen
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 200 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
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‐chloropropionate as the initiator, the polymerization reached high conversions (> 90%) at 80 °C and 100 °C, producing polymers with $\overline M _{\rm n}$ very close to theoretical values and low polydispersity. The ligand, temperature, and copper halide strongly affected the activity and control of the polymerization.
PDMA molecular weight and polydispersity dependence on the DMA conversion in the DMA bulk polymerizations at different temperatures: DMA/CuCl/MCP/BPED = 100/1/1/1, 100 °C (♦, ⋄); 80 °C (▴, ▵); 60 °C (▪, □); and DMA/CuCl/MCP/BPED = 100/1/1/2, 80 °C (•, ○).
imagePDMA molecular weight and polydispersity dependence on the DMA conversion in the DMA bulk polymerizations at different temperatures: DMA/CuCl/MCP/BPED = 100/1/1/1, 100 °C (♦, ⋄); 80 °C (▴, ▵); 60 °C (▪, □); and DMA/CuCl/MCP/BPED = 100/1/1/2, 80 °C (•, ○).
📜 SIMILAR VOLUMES
## 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
## 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