Nitroxide decomposition: Implications toward nitroxide design for applications in living free-radical polymerization

Abstract

Nitroxides bearing an α-hydrogen decompose upon heating in a bimolecular reaction. A new mechanism is proposed for the decomposition of t-butylisopropyl-phenyl nitroxide (TIPNO) involving the formation of a head-to-tail dimer, single electron transfer to form an oxammonium salt, epimerization to the corresponding nitrone, and elimination to form a conjugated oxime. This mechanism may provide insights into designing new nitroxides for use in controlled polymerization. © 2005 Wiley Periodicals, Inc.