Mono‐ and dicationically living poly(1,3‐dioxolane) (pdxn) and poly (1,3‐dioxepane) (pdxp) were obtained with CF 3 SO 3 H (trifilic acid‐tfac) and (CF 3 SO 2 ) 2 O (triflic anhydride‐tfan), respectively. Concentration of the active species and living character of polymers were established by applying the ion‐trapping technique. Addition of a second cyclic acetal to the living bifunctional polyacetal (e. g. addition of dxn to pdxp) leads to the formation of a block copolymer (according to 13 C NMR), but before the second monomer polymerizes completely, the transacetalization process leads to the conversion of the internal homoblock to a more or less (depending on time) statictical copolymer. Thus, competition of the homopropagation and transacetalization is not in favor of formation of the block copolymers with pure homoblocks, at least when the second block, built on the already existing homoblock, is formed slower than the homoblock is reshuffled by transacetalization.
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Chwiałkowska et al. (1982) studied this question.
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