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Tailor Made Side‐Chain Functionalized Macromolecules by Combination of Controlled Radical Polymerization and Click Chemistry
Author(s) -
Krieg Andreas,
Becer C. Remzi,
Hoogenboom Richard,
Schubert Ulrich S.
Publication year - 2009
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200950109
Subject(s) - chain transfer , polymer chemistry , copolymer , reversible addition−fragmentation chain transfer polymerization , click chemistry , azide , chemistry , propargyl , polymer , polymerization , alkyne , radical polymerization , cycloaddition , methacrylate , functional polymers , organic chemistry , catalysis
Reversible addition‐fragmentation chain transfer polymerization of trimethylsilyl‐propargyl methacrylate (TMSPMA) was performed to obtain alkyne containing polymers with narrow molecular weight distributions (PDI < 1.3). Homopolymers of TMSPMA as well as random and block copolymers with methyl methacrylate were synthesized and subsequently deprotected. The obtained acetylene‐functionalized polymers were further functionalized using the copper(I) catalyzed alkyne‐azide cycloaddition reaction to obtain well‐defined glycopolymers, grafted copolymers and anthracene‐containing polymers (PDI = 1.08–1.28) that were characterized with GPC, MALDI‐TOF mass spectrometry and 1 H‐NMR‐spectroscopy.