Related Experiment Video
Updated: Nov 1, 2025

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
Switching from Single to Simultaneous Free-Radical and Anionic Polymerization with Enamine-Based Organic Electron
Yuxi Zhao1, Marion Rollet1, Laurence Charles1
1Aix Marseille Univ, CNRS, Institut de Chimie Radicalaire (ICR), 13013, Marseille, France.
Abstract:
Although most monomers can polymerize through different propagation pathways, polymerization-initiating systems that can switch from one mode to another are rare. In this study, we demonstrate that enamine-based organic electron donors (OEDs) constitute the first systems able to initiate either free-radical or anionic polymerization under simple, mild, and safe conditions. While direct electron-transfer reduction of monomers by OEDs results in the initiation of anionic chain-growth polymerization, introduction of a competing oxidant with a higher reduction potential than the monomer switches the former anionic propagation to a clean radical-propagation process. The benefit of this dual-mode activator is highlighted in the synthesis of an interpenetrating polymer network through simultaneous initiation of radical and anionic propagation processes.
Related Concept Videos
Free-Radical Chain Reaction and Polymerization of Alkenes
Radical Chain-Growth Polymerization: Overview
Radical Chain-Growth Polymerization: Mechanism
Radical Substitution: Allylic Bromination
Anionic Chain-Growth Polymerization: Overview
Cationic Chain-Growth Polymerization: Mechanism

