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Copolymerization of N,N‐ Dimethylacrylamide with Styrene and Butadiene: The First Example of Polar Growing Chain End/Nonpolar Monomer Cross‐Initiation
Author(s) -
Nakhmanovich Boris I.,
Prudskova Tatya.,
ArestYakubovich Alexander A.,
Müller Axel H. E.
Publication year - 2001
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/1521-3927(20011001)22:15<1243::aid-marc1243>3.0.co;2-#
Subject(s) - copolymer , monomer , polar , polymer chemistry , styrene , chain (unit) , materials science , polymer science , chain transfer , chemistry , polymer , radical polymerization , organic chemistry , physics , astronomy
Living potassium poly( N,N ‐dimethylacrylamide) initiates the polymerization of styrene and butadiene, and adds 1,1‐diphenylethylene in THF solution. The model compound α ‐potassio‐ N,N ‐dimethylpropionamide also polymerizes styrene and butadiene in contrast to esterenolates, which are known to be incapable of such reactions. The IR spectra and SEC traces of the polymers obtained unequivocally prove that styrene and butadiene initiation proceeds directly via the amidoenolate anion. Apparently, this is the first case observed where the polymerization of a nonpolar monomer can be initiated by the growing chain end of a polar polymer.