NMR studies on the mechanism of reverse iodine transfer polymerization of styrene
Date
2012
Authors
Wright T.
Chirowodza H.
Pasch H.
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
The evolution of chain transfer agents (CTAs) was studied for the polymerization of styrene by reverse iodine transfer polymerization (RITP). CTAs are formed during an inhibition period where the radical initiator reacts with molecular iondine. These compounds were studied using in situ
1H nuclear magnetic resonance (NMR) experiments. The molecular weight of polystyrene was evaluated with size exclusion chromatography (SEC) and
1H NMR. Structural analysis of the resulting polymers was done using
1H NMR spectroscopy and matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometry. The inhibition period of styrene polymerized by RITP was much shorter than expected. This is due to the consumption of iodine in the reaction between styrene and iodine which reversibly forms 1,2-diiodoethylbenzene leading to the subsequent formation of 1-phenylethyl iodide (1-PEI). For the first time the formation of 1,2-diiodoethylbenzene as an intermediate structure in RITP of styrene has been proven experimentally. The active role of 1-PEI in the polymerization process is documented through the detection of phenylethyl end groups by MALDI-ToF and
1H NMR. © 2012 American Chemical Society.
Description
Keywords
Chain transfer agents, End groups, H NMR spectroscopy, In-situ, Intermediate structures, MALDI-TOF, Matrix-assisted laser desorption/ionization time-of-flight, NMR studies, Polymerization process, Radical initiators, Transfer polymerization, Iodine, Mass spectrometry, Polymerization, Polymers, Polystyrenes, Styrene, Atom transfer radical polymerization
Citation
Macromolecules
45
7
2995
3003
45
7
2995
3003