Free-radical chain generation of ketene during the synthesis of liquid crystalline aromatic polyesters

Mihaiela C. Stuparu, Juhua Xu, H. K. Hall*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

At the high temperatures used for the preparation of liquid crystalline aromatic polyesters (LCPs), ketene cleavage occurred from acetoxyarenes. Ketene is known to oligomerize to colored oligomers which may be responsible for an undesirable yellow color in LCPs. Thermolysis of the model compound p-acetoxybenzoate gave ketene oligomers and methyl p-hydroxybenzoate, which oligomerized. A free-radical chain reaction mechanism for ketene formation was demonstrated by the reaction of tributyltin hydride with haloacetoxyarenes.

Original languageEnglish
Pages (from-to)6743-6744
Number of pages2
JournalTetrahedron Letters
Volume50
Issue number49
DOIs
Publication statusPublished - Dec 9 2009
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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