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Rapid Synthesis of Well-Defined Polyacrylamide by Aqueous Cu(0)-Mediated Reversible-Deactivation Radical Polymerization
Author(s) -
Glen R. Jones,
Zai-Dong Li,
Athina Anastasaki,
Danielle J. Lloyd,
Paul Wilson,
Qiang Zhang,
David M. Haddleton
Publication year - 2016
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.5b01994
Subject(s) - polyacrylamide , copolymer , dispersity , acrylamide , disproportionation , atom transfer radical polymerization , monomer , chemistry , polymer chemistry , polymerization , aqueous solution , radical polymerization , molar mass distribution , solution polymerization , yield (engineering) , polymer , materials science , organic chemistry , catalysis , metallurgy
Atom transfer radical polymerization (ATRP) of acrylamide (AM) has proved challenging, typically exhibiting low conversions and broad molecular weight distributions (MWDs). Herein, we report the synthesis of well-defined polyacrylamide (both homo and block copolymers) via aqueous copper(0)-mediated reversible-deactivation radical polymerization (Cu(0)-RDRP), exploiting the in situ disproportionation of Cu(I)Br in the presence of Me6Tren to yield insoluble Cu(0) and Cu(II)Br2 which acts as a deactivator. Careful optimization of the levels of Cu(I)Br and Me6TREN allowed for the synthesis of polyacrylamide of a range of molecular weights (DPn = 20–640) proceeding to quantitative conversion within just a few minutes (typically full conversion is attained within 15 min of reaction time) and exhibiting narrow MWDs (Đ as low as 1.09), which represents a significant improvement over transitional-metal-mediated approaches previously reported in the literature. This optimized approach was subsequently utilized to p...

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