A NOVEL THIOETHER POLYMER WITH PENDENT ESTER GROUPS FROM A READILY AVAILABLE ACRYLATE DERIVATIVE
Polymers and High Performance Materials
A thioether polymer with pendent ester groups was synthesized via nucleophilic substitution and Michael addition. Williamson ether synthesis conditions led to nucleophilic substitution at the alpha-methylene carbon of ethyl alpha-(chloromethyl)acrylate (ECMA, 1) and Michael addition at the activated vinyl group. Polymerization was rapid at room temperature to give a highly viscous, sticky product with intrinsic viscosity of 0.15 dL/g in chloroform at 24-degrees-C. C-13 solid-state and solution NMR were used to characterize the polymer and a model compound of the nucleophilic substitution product.
Mathias, L. J.,
(1992). A NOVEL THIOETHER POLYMER WITH PENDENT ESTER GROUPS FROM A READILY AVAILABLE ACRYLATE DERIVATIVE. POLYMER BULLETIN, 27(4), 395-398.
Available at: http://aquila.usm.edu/fac_pubs/6748