Chain transfer to solvent in the radical polymerization of structurally diverse acrylamide monomers using straight-chain and branched alcohols as solvents
Magee, Christopher Sugihara, Yusuke Zetterlund, Per B. Aldabbagh, Fawaz
Magee, Christopher
Sugihara, Yusuke
Zetterlund, Per B.
Aldabbagh, Fawaz
Loading...
Identifiers
http://hdl.handle.net/10379/5729
https://doi.org/10.13025/15028
https://doi.org/10.13025/15028
Repository DOI
Publication Date
2014-01-02
Type
Article
Downloads
Citation
Christopher Magee, Yusuke Sugihara, Per B. Zetterlund, Fawaz Aldabbagh (2014) 'Chain transfer to solvent in the radical polymerization of structurally diverse acrylamide monomers using straight-chain and branched alcohols as solvents'. Polymer Chemistry, 5 :2259-2265.
Abstract
Chain transfer to solvent in conventional radical polymerizations of N-tert-butylacrylamide (TBAM) and N-(2-morpholin-4-ylethyl) acrylamide (MEA) in a range of alcohol solvents is investigated. Mayo analysis of polymerization of TBAM in linear alcohols (C-3-C-9) resulted in an approximately linear increase in chain transfer to solvent constant (C-tr,(S)) with the number of methylene (CH2) units in the solvent. The branched alcohol 3-methyl-3-pentanol gave the smallest C-tr,C-S (using Mayo analysis), and thus allowed attainment of higher molecular weights (MWs) in the nitroxide-mediated polymerizations (NMP) of TBAM. Overall, the data show that MEA is more prone to chain transfer to solvent than TBAM (higher C-tr,C-S), and further analysis of the conventional radical polymerization of MEA in 3-methyl-3-pentanol indicate chain transfer to monomer may also be occurring. The first controlled/ living polymerizations of MEA are detailed with chain transfer having a greater impact on maximum achievable MWs in NMP in comparison to TBAM.
Funder
Publisher
Royal Society of Chemistry
Publisher DOI
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland