Efficient preparation and properties of triazole-linked corannulene derivatives

Mihaiela C. Stuparu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

In this study, we explore the potential of copper(I)-catalyzed cycloaddition reaction between azides and terminal alkynes to prepare corannulene-rich materials. For this purpose, a practical route is established to yield corannulene-based azide building blocks. The newly prepared corannulene-azides are then coupled with known corannulene-alkynes. The chemical yields of the dimerization reactions ranged from 80 to 90%. In this way, a number of triazole-linked corannulene derivatives varying in the geometry, length, and the triazole-content are prepared. These results suggest that alkyne-azide click reaction can serve as a useful synthetic tool in the preparation of corannulene-rich discrete oligomers as well as polymers.

Original languageEnglish
Pages (from-to)3527-3531
Number of pages5
JournalTetrahedron
Volume68
Issue number18
DOIs
Publication statusPublished - May 6 2012
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Keywords

  • Click reaction
  • Corannulenes
  • Oligomer synthesis

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