TY - JOUR
T1 - High-order multiblock copolymers via iterative Cu(0)-mediated radical polymerizations (SET-LRP): Toward biological precision
AU - Soeriyadi, Alexander H
AU - Boyer, Cyrille
AU - Nystrom, Fredrik
AU - Zetterlund, Per B
AU - Whittaker, Michael Raymond
PY - 2011
Y1 - 2011
N2 - We report a new approach for the facile synthesis of high-order multiblock copolymers comprising very short blocks. The approach entails sequential addition of different monomers via an iterative single electron transfer - living radical polymerization technique, allowing nearly perfect control of the copolymer microstructure. It is possible to synthesize high-order multiblock copolymers with unprecedented control, i.e., A-B-C-D-E-etc., without any need for purification between iterative 24 h block formation steps. To illustrate this concept, we report the synthesis of model P(MA-b-MA...) homopolymer and P(MA-b-nBuA-b-EA-b-2EHA-b-EA-b-nBuA) copolymer in extremely high yield. Finally, the halide end-group can be modified via click chemistry , including thiol - bromide click chemistry, sodium methanethiosulfonate nucleophilic substitution, and atom transfer radical nitroxide coupling reaction, to yield functional, structurally complex macromolecules.
AB - We report a new approach for the facile synthesis of high-order multiblock copolymers comprising very short blocks. The approach entails sequential addition of different monomers via an iterative single electron transfer - living radical polymerization technique, allowing nearly perfect control of the copolymer microstructure. It is possible to synthesize high-order multiblock copolymers with unprecedented control, i.e., A-B-C-D-E-etc., without any need for purification between iterative 24 h block formation steps. To illustrate this concept, we report the synthesis of model P(MA-b-MA...) homopolymer and P(MA-b-nBuA-b-EA-b-2EHA-b-EA-b-nBuA) copolymer in extremely high yield. Finally, the halide end-group can be modified via click chemistry , including thiol - bromide click chemistry, sodium methanethiosulfonate nucleophilic substitution, and atom transfer radical nitroxide coupling reaction, to yield functional, structurally complex macromolecules.
UR - http://pubs.acs.org/doi/pdfplus/10.1021/ja205080u
UR - https://www.scopus.com/pages/publications/79960579951
U2 - 10.1021/ja205080u
DO - 10.1021/ja205080u
M3 - Article
SN - 0002-7863
VL - 133
SP - 11128
EP - 11131
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 29
ER -