Development of a universal alkoxyamine for "living" free radical polymerizations

被引:1007
作者
Benoit, D
Chaplinski, V
Braslau, R [1 ]
Hawker, CJ
机构
[1] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
[2] IBM Corp, Almaden Res Ctr, NSF, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USA
关键词
D O I
10.1021/ja984013c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Examination of novel alkoxyamines has demonstrated the pivotal role that the nitroxide plays in mediating the "living" or controlled polymerization of a wide range of vinyl monomers. Surveying a variety of different alkoxyamine structures led to alpha-hydrido derivatives based on a 2,2,5-trimethyl-4-phenyl-3-azahexane3-oxy,1, skeleton which were able to control the polymerization of styrene, acrylate, acrylamide, and acrylonitrile based monomers. For each monomer set, the molecular weight could be controlled from 1000 to 200 000 amu with polydispersities typically 1.05-1.15. Block and random copolymers based on combinations of the above monomers could also be prepared with similar control.:In comparison with 2,2,6,6-tetramethylpiperidinoxy (TEMPO), these new systems represent a dramatic increase in the range of monomers that can be polymerized under controlled conditions and overcome many of the limitations associated with nitroxide-mediated "living" free radical procedures. Monomer selection and functional group compatibility now approach those of ATRP-based systems.
引用
收藏
页码:3904 / 3920
页数:17
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