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Preparation of polyisobutene-graft-poly(methyl methacrylate) and polyisobutene-graft-polystyrene with different compositions and side chain architectures through atom transfer radical polymerization (ATRP)
被引:2
|作者:
Hong, SC
Pakula, T
Matyjaszewski, K
机构:
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Max Planck Inst Polymer Res, D-55021 Mainz, Germany
关键词:
atom transfer radical polymerization (ATRP);
controlled/living polymerization;
graft copolymers;
polyisobutene;
viscoelastic properties;
D O I:
10.1002/1521-3935(20011101)202:17<3392::AID-MACP3392>3.0.CO;2-4
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Polyisobutene-graft-poly(methyl methacrylate) and polyisobutene-graft-polystyrene with controlled compositions and side chain architectures were prepared through atom transfer radical polymerization (ATRP). Poly[isobutene-co-(p-methylstyrene)-co-(p-bromomethylstyrene)] (PIB) was used as a macroinitiator in the presence of CuCl or CuBr as a catalyst and dNbpy as a ligand. The compositions were controlled by the conversion of the monomer with polymerization time. The molecular weight distributions of the side chains were controlled through ATRP in the presence/absence of a halogen exchange reaction. DSC and DMA measurements showed that graft copolymers have two glass transition temperatures suggesting microphase separated behavior, which was also confirmed by SAXS measurements. The phase and dynamic mechanical behaviors were strongly affected by the compositions and/or the side chain architectures. The properties of the graft copolymers were controlled in a wide range leading to toughened glassy polymers or elastomers. © Wiley-VCH Verlag GmbH, 2001.
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页码:3392 / 3402
页数:11
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