Related Experiment Video
Updated: Mar 26, 2026

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
Published on: January 19, 2016
Termination Mechanism of the Radical Polymerization of Acrylates
Yasuyuki Nakamura1, Richmond Lee2, Michelle L Coote2
1Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Abstract:
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.
More Related Videos
Related Concept Videos
Radical Chain-Growth Polymerization: Mechanism
Radical Chain-Growth Polymerization: Overview
Free-Radical Chain Reaction and Polymerization of Alkenes
Radical Chain-Growth Polymerization: Chain Branching
Cationic Chain-Growth Polymerization: Mechanism
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...

