Reverse atom transfer radical polymerization of methyl methacrylate in imidazolium ionic liquids
β Scribed by Hongyang Ma; Xinhua Wan; Xiaofang Chen; Qi-Feng Zhou
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 207 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0032-3861
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β¦ Synopsis
Reverse atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) employing 2,2-azobisisobutyronitrile (AIBN)/CuCl 2 /bipyridine(bipy) as the initiating system was approached at 80 8C in two ionic liquids, 1-butyl-3-methylimidazolium tetrafluoroborate ([C 4 mim][BF 4 ]) and 1-dodecyl-3-methylimidazolium tetrafluoroborate ([C 12 mim][BF 4 ]), respectively. The polymerization in [C 12 mim][BF 4 ] proceeded in a well-controlled manner as evidenced by kinetic studies, end group analysis, chain extension, and block copolymerization results, but not in [C 4 mim][BF 4 ] presumably due to poor solubility of PMMA in it. The kinetic study of reverse ATRP of MMA in recycled [C 12 mim][BF 4 ] suggested that this ionic liquid could be re-used as reaction solvent after simple purification, without affecting the living nature of polymerization.
π SIMILAR VOLUMES
## Abstract The kinetics of methyl methacrylate (MMA) homopolymerization performed by atom transfer radical polymerization (ATRP) is investigated in detail using ethylβ2βbromopropionate (EPNβBr) as initiator, CuBr as catalyst, and pentamethyldiethylenetriamine (PMDETA) as ligand in ionic liquids (I
## Abstract The reverse atom transfer radical polymerization of methyl methacrylate was investigated in different solvents: xylene, __N,N__βdimethylformamide, and pyridine. The polymerizations were uncontrolled, using 2,2β²βbipyridine as a ligand in xylene and pyridine because the catalyst (CuBr~2~/