Diminishing catalyst concentration in atom transfer radical polymerization with reducing agents

TLDR

The study introduces continuous activator regeneration (ICAR) in ATRP to maintain Cu(I) activator levels at very low catalyst concentrations. ICAR ATRP uses a constant source of organic free radicals, supplemented by hydrazine and phenol derivatives in ARGET ATRP, with carefully chosen Cu ligands (Me6TREN, TPMA) and kinetic modeling to optimize activator regeneration and suppress side reactions. Using ICAR/ARGET ATRP, polystyrene, PMMA, and acrylate polymers were synthesized with Mw/Mn < 1.2 at catalyst loadings as low as 10–50 ppm, and the selected catalyst/reducing agent systems performed well in homo‑ and block copolymerizations.

Abstract

The concept of initiators for continuous activator regeneration (ICAR) in atom transfer radical polymerization (ATRP) is introduced, whereby a constant source of organic free radicals works to regenerate the Cu I activator, which is otherwise consumed in termination reactions when used at very low concentrations. With this technique, controlled synthesis of polystyrene and poly(methyl methacrylate) ( M w / M n &lt; 1.2) can be implemented with catalyst concentrations between 10 and 50 ppm, where its removal or recycling would be unwarranted for many applications. Additionally, various organic reducing agents (derivatives of hydrazine and phenol) are used to continuously regenerate the Cu I activator in activators regenerated by electron transfer (ARGET) ATRP. Controlled polymer synthesis of acrylates ( M w / M n &lt; 1.2) is realized with catalyst concentrations as low as 50 ppm. The rational selection of suitable Cu complexing ligands {tris[2-(dimethylamino)ethyl]amine (Me 6 TREN) and tris[(2-pyridyl)methyl]amine (TPMA)} is discussed in regards to specific side reactions in each technique (i.e., complex dissociation, acid evolution, and reducing agent complexation). Additionally, mechanistic studies and kinetic modeling are used to optimize each system. The performance of the selected catalysts/reducing agents in homo and block (co)polymerizations is evaluated.