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Improving the control of styrene polymerization at 60 °C using a dialkylated α‐hydrogenated nitroxide
Authors:Yohann Guillaneuf  Jean‐Philippe Lamps  Jean‐Marie Catala  Didier Gigmes  Eric Drockenmuller
Affiliation:1. Institut de Chimie Radicalaire, équipe CROPS, UMR 7273 CNRS, Aix‐Marseille Université, Campus de Saint Jér?me, avenue Escadrille Normandie‐Niemen, Case 542, 13397 Marseille Cedex 20, France;2. Institut Charles Sadron, CNRS, Université de Strasbourg, 23 rue du Loess, 67034 Strasbourg, France;3. Université Claude Bernard Lyon 1, Ingénierie des Matériaux Polymères, UMR CNRS 5223, 15 Boulevard Latarjet, 69622 Villeurbanne Cedex, France;4. Institut Universitaire de France (IUF)
Abstract:A new dialkylated α‐hydrogenated linear nitroxide and the corresponding 1‐phenylethyl alkoxyamine were synthesized in two and three steps, respectively. The alkoxyamine was involved in the polymerization of styrene at 60 °C, and the in situ concentration of nitroxide was monitored by electron spin resonance spectroscopy. The enhanced characteristics of these new alkylated alkoxyamine and nitroxide (kurn:x-wiley:0887624X:media:POLA26163:tex2gif-stack-1 = 1.5 × 10?4 s?1 and kurn:x-wiley:0887624X:media:POLA26163:tex2gif-stack-2 = 5.7 × 104 L mol?1 s?1) yielded a monomer consumption one order of magnitude higher than styrene thermal polymerization. This resulted in well‐defined polystyrenes up to 70,000 g mol?1 and the observation of a control occurring through the establishment of the radical persistent effect, that is, ln([M]0/[M]) = t2/3. Experimentally determined kinetic constants were involved in PREDICI modelings to investigate the influence of temperature and initial alkoxyamine concentration on the kinetics as well as on the livingness and the controlled character of the polymerization. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012
Keywords:alkoxyamine  kinetics (polym.)  nitroxide mediated polymerization (NMP)  polystyrene  radical polymerization  styrene
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