Beilstein Journal of Organic Chemistry (Sep 2018)

Calixazulenes: azulene-based calixarene analogues – an overview and recent supramolecular complexation studies

  • Paris E. Georghiou,
  • Shofiur Rahman,
  • Abdullah Alodhayb,
  • Hidetaka Nishimura,
  • Jaehyun Lee,
  • Atsushi Wakamiya,
  • Lawrence T. Scott

DOI
https://doi.org/10.3762/bjoc.14.225
Journal volume & issue
Vol. 14, no. 1
pp. 2488 – 2494

Abstract

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Some of the least studied calixarenes are those that consist of azulene rings bridged by -CH2- groups. Since Lash and Colby’s discovery of a simple and convenient method for producing the parent all-hydrocarbon calix[4]azulene, there have been two other all-hydrocarbon calix[4]azulenes which have been synthesized in good yields by their method. This allowed studying their supramolecular properties. This report is of our latest work on the solution-state supramolecular complexation of one of these calix[4]azulenes, namely tetrakis(5,7-diphenyl)calix[4]azulene or “OPC4A”, with several electron-deficient tetraalkyammonium salts. As a result of more recent methods developed by us and others employing Suzuki–Miyaura cross-coupling reactions to produce additional functionalized azulenes, the promise of further greater functionalized calixazulenes lies in store to be investigated.

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