Reversible addition-fragmentation chain transfer polymerization of vinyl chloride
Loading...
Date
Authors
Abreu, Carlos
Mendonça, Patrícia
Serra, Arménio
Coelho, Jorge
Popov, Anatoliy
Gryn'ova, Ganna
Coote, Michelle
Guliashvili, Tamaz
Journal Title
Journal ISSN
Volume Title
Publisher
American Chemical Society
Abstract
Controlled/"living" radical polymerization (CLRP) of vinyl chloride (VC) via the reversible addition-fragmentation chain transfer (RAFT) process is reported for the first time. The cyanomethyl methyl(phenyl) carbamodithioate (CMPCD) was found to be an efficient RAFT agent enabling the CLRP polymerization of VC monomer under certain experimental conditions. Two different radical initiators, having very distinct half-life times at room temperature, were employed in this study. The kinetic studies of RAFT polymerization of VC show a linear increase of the molecular weight with the monomer conversion and the lowest polydispersity (PDI) ever reported for poly(vinyl chloride) (PVC) synthesized with CLRP method (PDI ∼ 1.4). The resulting PVC was fully characterized using the matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS),1H nuclear magnetic resonance spectroscopy (1H NMR), and gel permeation chromatography (GPC) techniques. The1H NMR and MALDI-TOF-MS analysis of PVC prepared via RAFT polymerization method have shown the absence of structural defects and the presence of chain-end functional groups. The "livingness" of the PVC was also confirmed by a successful reinitiation experiment. The suitability of the RAFT agent was also confirmed via high-level ab initio molecular orbital calculations.
Description
Citation
Collections
Source
Macromolecules
Type
Book Title
Entity type
Access Statement
License Rights
Restricted until
2037-12-31
Downloads
File
Description