Abstract 2‐Vinyllhiolane‐1,1‐dioxide (Ia) and 2‐vinylthiane‐1,1‐dioxide(Ib) have been prepared and polymerized with free radical initiators to obtain poly(sulfonyl‐hex‐2‐enylene) (IIa) and poly(sulfonyl‐hept‐2‐enyIene‐co‐2‐vinylthiane‐1,1‐dioxide) (IIb), respectively, via a ring‐opening mechanism. Structures of the polymers are supported by infrared and 1H‐NMR spectroscopy. Poly(sulfonyl‐hex‐2‐enylene) was insoluble in ordinary organic solvents, but soluble in concentrated sulfuric acid or trifluoroacetic acid, and was white amorphous powder, softening at 168°C. Degradation occurred at 294°C under N2. Ia copolymerized with certain vinyl monomers, such as ethyl acrylate, but its copolymerization behavior was different from those of normal vinyl monomers.
No takes yet. Share an insight, caveat, or question.
Cho et al. (1986) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: