Synthesis of block copolymers viathe combination of RAFT and a macromolecular azo coupling reaction
We report a novel modular strategy for the synthesis of block copolymers viathe combination of a macromolecular azo coupling reaction and a reversible addition fragmentation chain transfer (RAFT) polymerization method. One block, with a terminus suitable for an azo coupling reaction, was obtained by...
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Published in | Polymer chemistry Vol. 4; no. 2; pp. 402 - 406 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.12.2012
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Subjects | |
Online Access | Get full text |
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Summary: | We report a novel modular strategy for the synthesis of block copolymers viathe combination of a macromolecular azo coupling reaction and a reversible addition fragmentation chain transfer (RAFT) polymerization method. One block, with a terminus suitable for an azo coupling reaction, was obtained by RAFT polymerization using a synthesized chain transfer agent (CTA) with the designed functional group. The other block, with a diazonium salt terminus, was obtained by the diazotization of aniline-functionalized PEG, which was prepared by a nucleophilic substitution reaction between the synthesized tosylate ended mPEG and p-aminobenzoic acid. The macromolecular azo coupling reaction between the above two polymer blocks was carried out in a polar organic solvent such as DMF under extremely mild conditions. Block copolymers with well-defined structures can be efficiently prepared through this approach. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/c2py20653f |