z-logo
Premium
A copper‐based reverse ATRP process for the living radical polymerization of methyl methacrylate
Author(s) -
Qin DongQi,
Qin ShuHui,
Qiu KunYuan
Publication year - 2001
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1661
Subject(s) - polymer chemistry , living free radical polymerization , reversible addition−fragmentation chain transfer polymerization , radical polymerization , atom transfer radical polymerization , copolymer , methyl methacrylate , living polymerization , polymerization , chain transfer , chemistry , end group , polymer , materials science , organic chemistry
The reverse atom transfer radical polymerization (RATRP) technique using CuCl 2 /bipyridine (bipy) complex as a catalyst was applied to the living radical polymerization of methyl methacrylate (MMA). A hexa‐substituted ethane thermal iniferter, diethyl 2,3‐dicyano‐2,3‐diphenylsuccinate (DCDPS), was used as the initiator in this copper‐based reverse ATRP initiation system. The reversible dissociation nature of DCDPS gives a more suitable amount of primary radical than formerly used conventional initiators, such as AIBN. High molecular weight and narrow molecular weight distribution ( M w /M n ≈ 1.20) of the resulting PMMA was obtained in bulk and in solution polymerization at 85°C. End‐group analysis result by 1 H‐NMR spectroscopy shows that the polymer obtained is ω‐functionalized by a chlorine group, which can be used as macroinitiator for chain extension and block copolymerization with a conventional ATRP catalyst. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 2237–2245, 2001

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom