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Living Polymerization of 2-Ethylthio-2-oxazoline and Postpolymerization Diversification
Author(s) -
You-Chi Mason Wu,
Timothy M. Swager
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b06009
Subject(s) - chemistry , cationic polymerization , polymerization , copolymer , living polymerization , oxazoline , polymer , living cationic polymerization , nanomaterials , living anionic polymerization , polymer chemistry , combinatorial chemistry , ring opening polymerization , nanotechnology , anionic addition polymerization , organic chemistry , radical polymerization , catalysis , materials science
The postpolymerization modification of polymers produced by living polymerization is an attractive method to create precision nanomaterials. We describe the living cationic ring-opening polymerization of a 2-alkylthio-2-oxazoline to furnish a polythiocarbamate. The polythiocarbamate is activated toward substitution by N - and S -nucleophiles via oxidation of the S to an SO 2 . Mild substitution conditions provide broad functional group tolerance, constituting a versatile postpolymerization modification platform with access to a diversity of polyureas and polythiocarbamates. We further demonstrate the utility of this strategy by synthesizing and functionalizing block copolymers.

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