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Cyclopolymerization of diallylamides and diallylsulphonamides

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Summary

High resolution carbon−13 nuclear magnetic resonance spectroscopy is used to study the structure of N-amide and N-sulphonamide derivatives of polydiallylamines and shows that these have the poly(3,4-pyrrolidinediylethylene) structure common to most polydiallylamines, not the previously reported poly(3,5-piperidinediylmethylene) structure.

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Authors and Affiliations

  1. Division of Applied Organic Chemistry, CSIRO, G.P.O. Box 4331, 3001, Melbourne, Victoria, Australia

    J. H. Hodgkin, S. R. Johns & R. I. Willing

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  1. J. H. Hodgkin
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  2. S. R. Johns
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  3. R. I. Willing
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Hodgkin, J.H., Johns, S.R. & Willing, R.I. Cyclopolymerization of diallylamides and diallylsulphonamides. Polymer Bulletin 7, 353–359 (1982). https://doi.org/10.1007/BF00254290

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