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Efficient synthesis and RAFT polymerization of the previously elusive N ‐[(cycloalkylamino)methyl]acrylamide monomer class
Author(s) -
Chalmers Benjamin A.,
Alzahrani Abdullah,
Hawkins Gerard,
Aldabbagh Fawaz
Publication year - 2017
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/pola.28607
Subject(s) - raft , chain transfer , reversible addition−fragmentation chain transfer polymerization , copolymer , cationic polymerization , monomer , polymerization , acrylamide , polymer chemistry , chemistry , salt (chemistry) , hydrochloride , methylene , living polymerization , polymer , organic chemistry , radical polymerization
Schiff base salts allowed the multigram preparation of methylene amino substituted acrylamide monomers. These, as well as the hydrochloride salt intermediates, were subjected to controlled/living polymerizations for the first time. One‐pot sequential reversible addition‐fragmentation chain transfer (RAFT) polymerizations resulted in well‐defined di‐ and triblock copolymers.

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