Ambient Temperature Transition-Metal-Free Dissociative Electron Transfer Reversible Addition–Fragmentation Chain Transfer Polymerization (DET-RAFT) of Methacrylates, Acrylates, and Styrene
Author(s) -
Pedro Maximiano,
Patrícia V. Mendonça,
João R. C. Costa,
Naomi L. Haworth,
Arménio C. Serra,
Tamaz Guliashvili,
Michelle L. Coote,
Jorge F. J. Coelho
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.5b02647
Subject(s) - chain transfer , raft , methacrylate , polymer chemistry , reversible addition−fragmentation chain transfer polymerization , styrene , polymerization , fragmentation (computing) , radical polymerization , chemistry , photochemistry , copolymer , living polymerization , materials science , polymer , organic chemistry , computer science , operating system
Inorganic sulfites as reducing agents were successfully used in combination with typical reversible addition–fragmentation chain transfer (RAFT) agents for the controlled DET-RAFT (DET: dissociative electron transfer) of methacrylates, methyl acrylate (MA), and styrene (Sty) near room temperature (30 °C). The polymerizations were first-order with respect to monomer conversion and polymers with narrow molecular weight distributions (Đ < 1.2), and “living” features were obtained. MALDI-TOF experiments demonstrated the integrity of the chain-ends and clearly showed the absence of SO2 in the polymer chains. Kinetic studies revealed that an increase of either temperature or concentration of sulfites provided faster reactions, without loss of control. Ab initio quantum chemistry calculations suggested that in the presence of the reducing agent the RAFT agent undergoes one-electron reduction to a stable radical anion that can then undergo fragmentation to yield the initiating carbon-centered radical. The new met...
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