Well-defined poly(sulfobetaine) brushes prepared by surface-initiated ATRP using a fluoroalcohol and ionic liquids as the solvents
Well-defined poly(sulfobetaine) brushes prepared by surface-initiated ATRP using a fluoroalcohol and ionic liquids as the solvents
复制标题
DOI:
10.1021/ma102223y
复制
发表时间:
2011-01
期刊:
影响因子:
5.5
通讯作者:
Y. Terayama;M. Kikuchi;M. Kobayashi;A. Takahara
中科院分区:
文献类型:
--
作者:
Y. Terayama;M. Kikuchi;M. Kobayashi;A. Takahara
Surface-initiated atom transfer radical polymerization (ATRP) of 2-(N-2-methacryloyloxyethyl-N,N-dimethyl) ammonatoethanesulfonate) (MAES), 3-(N-2-methacryloyloxyethyl-N,N-dimethyl) ammonatopropanesulfonate) (MAPS), and 4-(N-2-methacryloyloxyethyl-N,N-dimethyl) ammonatobutanesulfonate) (MABS) was carried out in 2,2,2-trifluoroethanol (TFE) containing a small amount of 1-hexyl-3-methylimidazolium chloride at 60 °C to produce well-defined poly(sulfobetaine) brushes and the corresponding free polymers with predictable number-average molecular weight (Mn, 1 × 104 to 3 × 105 g mol−1) and narrow molecular weight distributions (Mw/Mn < 1.2). A first-order kinetic plot for ATRP of MAPS revealed a linear relationship between the monomer conversion index (ln([M]0/[M])) and polymerization time. The polymerization rates decreased with increasing ionic liquid concentration. The Mn of poly(MAPS) increased in proportion to the conversion. The sequential polymerization of MAPS initiated with the chain ends of poly(MAPS) ...