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Highly efficient anionic ring-opening reactions of epoxide triggered by phosphide

  • 25-04-2024
  • ORIGINAL PAPER
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Abstract

The article presents a comprehensive study on the use of potassium diphenylphosphide (KPPh2) as a highly efficient initiator for the anionic ring-opening polymerization (ROP) of epoxides. Unlike traditional initiators, KPPh2 exhibits superior nucleophilicity, enabling rapid and controlled polymerization of glycidyl phenyl ether (GPE) without the need for additives. The resulting polymers display high molecular weights and narrow molecular weight distributions. Additionally, KPPh2 demonstrates exceptional catalytic ability in the addition of phenols to epoxides, showcasing its potential for applications in epoxy-phenol curing systems. The study provides valuable insights into the mechanisms of phosphide-initiated polymerization and addition reactions, paving the way for the development of new rapid-curing systems for epoxy resins.

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Title
Highly efficient anionic ring-opening reactions of epoxide triggered by phosphide
Authors
Tomoyuki Ariyoshi
Atsushi Sudo
Takeshi Endo
Publication date
25-04-2024
Publisher
Springer Berlin Heidelberg
Published in
Polymer Bulletin / Issue 13/2024
Print ISSN: 0170-0839
Electronic ISSN: 1436-2449
DOI
https://doi.org/10.1007/s00289-024-05256-3
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