Reversible Deactivation Radical Polymerization of Monomers Containing Activated Aziridine Groups.

Abstract

Polymers bearing activated aziridine groups are attractive precursors to α-substituted-β-amino-functionalized materials due to the enhanced reactivity of the pendant aziridine functionalities toward ring-opening by nucleophiles. Two aziridine-containing styrenic monomers, 2-(4-vinylphenyl)aziridine (VPA) and N-mesyl-2-(4-vinylphenyl)aziridine (NMVPA), were polymerized under a variety of reversible deactivation radical polymerization conditions. Low-catalyst-concentration atom transfer radical polymerization (LCC-ATRP) and reversible addition-fragmentation chain-transfer (RAFT) polymerization were ineffective at producing well-defined polymers from VPA due to side reactions between the aziridine functionalities and the agents controlling the polymerizations (catalysts or chain transfer agents). PolyVPA produced under nitroxide-mediated polymerization (NMP) conditions had narrow molecular weight distribution at low to moderate conversions of monomer, but branched and eventually cross-linked polymers were formed at higher conversions due to ring-opening reactions of the aziridine groups. Most of these undesirable side reactions were eliminated by attaching a methanesulfonyl (mesyl) group to the aziridine nitrogen atom, and well-defined linear homopolymers with targeted molecular weights were realized from NMVPA under RAFT and NMP conditions; however, side reactions between the aziridine groups and the catalyst in LCC-ATRP still occured and the polymerization was uncontrolled using this technique.