Alkoxyamine-mediated "living" radical polymerization: MS investigation of the early stages of styrene polymerization initiated by cumyl-TEISO

• Main Authors: Cresidio, Salvacion P., Aldabbagh, Fawaz, Busfield, W. Ken, Jenkins, Ian D., Thang, San H., Holdsworth, Clovia Zayas-, Zetterlund, Per B.
• Format: text
• Published: Animo Repository 2001
• Subjects: Polymerization; Free radicals (Chemistry); Nitroxides; Styrene; Chemistry
• Online Access: https://animorepository.dlsu.edu.ph/faculty_research/4215
• Institution: De La Salle University

A new series of 1,1,3,3-tetraethylisoindoline-2-oxyl (TEISO)-based alkoxyamines was prepared. The half-lives for thermal dissociation indicated that the most sterically congested cumyl-TEISO alkoxymine had the greatest potential as an initiator for the polymerization of monomers at lower temperatures. The polymerization of styrene at 110 °C gave a linear evolution of Mn with conversion in the early stages. Further evidence for the "living" nature was given by the polydispersities of the polymers that remained low (Mw/Mn = 1.13-1.27) throughout the polymerization (up to 80% conversion). No polymer was formed for the styrene system in a reasonable time below 100 °C. High-performance liquid chromatographic/mass spectrometric investigations of the distribution of trapped oligomers containing one to nine monomer units formed at 60 °C revealed that the trapping of oligomeric cumyl-styryl radicals by TEISO is irreversible at this temperature. Methyl methacrylate polymerized with cumyl-TEISO at 60-70 °C, although the initial high rates of polymerization soon decreased to zero at low conversions (10-15%), and the high polydispersities (Mw/Mn = 1.42-1.73) indicated significant side reactions. © 2001 John Wiley & Sons, Inc.