Nitroxide-Mediated Polymerization of Vinyl Chloride at Low Temperature: Kinetic and Computational Studies
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Authors
Abreu, Carlos M. R.
Mendonça, Patrícia V.
Serra, Arménio C.
Noble, Dr Benjamin
Guliashvili, Tamaz
Nicolas, Julien
Coote, Michelle
Coelho, Jorge F. J.
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American Chemical Society
Abstract
The synthesis of poly(vinyl chloride) (PVC) by
nitroxide-mediated polymerization (NMP) using the SG1-
based BlocBuilder alkoxyamine at low temperature (30 and 42
°C) is reported. The reaction system was studied regarding the
nature of the solvent, the monomer-to-solvent ratio, the
polymerization temperature, and the target molecular weight.
First-order kinetics and linear evolutions of the molecular
weight with vinyl chloride (VC) conversion were obtained in
dichloromethane (DCM) and dimethyl sulfoxide (DMSO)
together with decreasing dispersities (Đ) down to 1.59−1.47.
The resulting PVC was fully characterized by
¹H nuclear
magnetic resonance spectroscopy (
¹H NMR), ³¹P NMR, and size exclusion chromatography (SEC). The
¹H NMR and ³¹P NMR
revealed the existence of very small content of structural defects and the presence of chain-end functional groups (∼91% SG1
chain-end functionality). Chain extension experiments were performed with VC, methyl methacrylate (MMA), and a mixture of
monomers (90% of MMA and 10% of styrene (S)) and confirmed the “livingness” of the PVC-SG1 macroinitiators, giving access
to different PVC-based block copolymers. High level ab initio molecular orbital calculations suggested that the C−O bond in the
PVC-SG1 alkoxyamine is too strong to mediate the NMP of VC by simple “classic” activation−deactivation equilibrium and is
possibly being mediated by a SG1-mediated dehydrochlorination mechanism. The results presented in this study established a
new route to afford a wide range of new complex macrostructures based on PVC segments.
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Macromolecules
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Open Access