Please use this identifier to cite or link to this item:
|Title:||Polystyrene-block-poly(methyl methacrylate): Initiation issues with block copolymer formation using ARGET ATRP|
|Keywords:||atom transfer radical polymerization|
|Citation:||Aitchison, T.J., Ginic-Markovic, M., Clarke, S., Valiyaveettil, S. (2012-01-16). Polystyrene-block-poly(methyl methacrylate): Initiation issues with block copolymer formation using ARGET ATRP. Macromolecular Chemistry and Physics 213 (1) : 79-86. ScholarBank@NUS Repository. https://doi.org/10.1002/macp.201100478|
|Abstract:||The synthesis, kinetics, and characterization of polystyrene and poly(methyl methacrylate) block copolymers produced by ARGET ATRP are discussed. Halogen exchange is used and the polymerization appears to be living in the generation of the second block. On further investigation, the GPC traces exhibit a shoulder, which suggests poor initiation of the macroinitiator. Previous reports suggest that to increase the initiation efficiency of the second block, 10% styrene monomer should be added to the mixture. Upon adding the 10% styrene for the second block ARGET ATRP polymerization, the appearance of a well-initiated polymer is observed. However, at greater conversions the results clearly demonstrate the production of a homopolymer/block copolymer mixture. A comprehensive exploration of ARGET ATRP for use in the formation of block copolymers is described. With polystyrene as the first block, the more reactive monomer methyl methacrylate is used to generate a second block using the halogen exchange technique and 10% comonomer. Issues with initiation efficiency and additional effects in the comonomer technique are discovered. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.|
|Source Title:||Macromolecular Chemistry and Physics|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Mar 20, 2019
WEB OF SCIENCETM
checked on Mar 5, 2019
checked on Jan 26, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.