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Termination Mechanism of the Radical Polymerization of Acrylates
Author(s) -
Nakamura Yasuyuki,
Lee Richmond,
Coote Michelle L.,
Yamago Shigeru
Publication year - 2016
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.201500677
Subject(s) - radical , disproportionation , chemistry , polymerization , radical polymerization , chain termination , radical disproportionation , cobalt mediated radical polymerization , photochemistry , intramolecular force , reaction mechanism , polymer , polymer chemistry , stereochemistry , organic chemistry , catalysis
The termination mechanism of the radical polymerization of acrylates, namely the selectivity of disproportionation (Disp) and combination (Comb) between polymer end radicals, is unambiguously determined by the reaction of polyacrylate end radicals generated from corresponding “living” organotellurium ω‐end polymer. While textbooks describe the occurrence of Comb, the reaction at 25 °C exclusively gives the Disp products. Ab initio molecular dynamics suggests that the products form by two pathways: The direct disproportionation reaction and a novel stepwise process that involves the initial formation of the C–O coupling product followed by intramolecular rearrangement. The termination at high temperature and low radical concentration increases the contribution of back‐biting reaction giving mid‐chain radicals, and complex reaction pathways of the mid‐chain radicals are clarified for the first time.
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