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ID 115343
Author
Ishizu, Hideaki Tokushima University
Yamaoka, Ryosuke Tokushima University
Keywords
N-alkylacrylamides
Isotactic-specific radical polymerization
Hydrogen bonding
Content Type
Journal Article
Description
Radical polymerization of N-methylacrylamide (NMAAm), N-n-propylacrylamide, N-isopropylacrylamide (NIPAAm) and N-benzylacrylamide was investigated in CHCl3, CH2Cl2 and CH3CN, in the presence of 3,5-dimethylpyridine N-oxide (35DMPNO) to examine the effects of the N-substituent and the solvent on the isotactic specificity induced by 35DMPNO. With addition of 35DMPNO to radical polymerization of N-alkylacrylamides in CHCl3, isotactic specificity was significantly induced in NIPAAm polymerization but only slightly induced in NMAAm polymerization. Furthermore, mixed solvents of CH3CN and halomethanes such as CHCl3 and CH2Cl2 enhanced the ability of 35DMPNO to induce isotactic specificity, and poly(NIPAAm) with 74% meso dyad was obtained.
Journal Title
Polymer
ISSN
00323861
NCID
AA11537383
Publisher
Elsevier
Volume
50
Issue
15
Start Page
3522
End Page
3527
Published Date
2009-06-03
Rights
© 2009. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
EDB ID
DOI (Published Version)
URL ( Publisher's Version )
FullText File
language
eng
TextVersion
Author
departments
Science and Technology