End group characterization of poly(phthalaldehyde): Surprising discovery of a reversible, cationic macrocyclization mechanism

Joshua A. Kaitz, Charles E. Diesendruck, Jeffrey S. Moore

Research output: Contribution to journalArticlepeer-review

Abstract

End-capped poly(phthalaldehyde) (PPA) synthesized by anionic polymerization has garnered significant interest due to its ease of synthesis and rapid depolymerization. However, alternative ionic polymerizations to produce PPA have been largely unexplored. In this report, we demonstrate that a cationic polymerization of o-phthalaldehyde initiated by boron trifluoride results in cyclic PPA in high yield, with high molecular weight, and with extremely high cyclic purity. The cyclic structure is confirmed by NMR spectroscopy, MALDI-TOF mass spectrometry, and triple-detection GPC. The cyclic polymers are reversibly opened and closed under the polymerization conditions. Owing to PPA's low ceiling temperature, cyclic PPA is capable of chain extension to larger molecular weights, controlled depolymerization to smaller molecular weights, or dynamic intermixing with other polymer chains, both cyclics and end-capped linears. These unusual properties endow the system with great flexibility in the synthesis and isolation of pure cyclic polymers of high molecular weight. Further, we speculate that the absence of end groups enhances the stability of cyclic PPA and makes it an attractive candidate for lithographic applications.

Original languageEnglish (US)
Pages (from-to)12755-12761
Number of pages7
JournalJournal of the American Chemical Society
Volume135
Issue number34
DOIs
StatePublished - Aug 28 2013

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Fingerprint Dive into the research topics of 'End group characterization of poly(phthalaldehyde): Surprising discovery of a reversible, cationic macrocyclization mechanism'. Together they form a unique fingerprint.

Cite this