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 language | English |
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Pages (from-to) | 3527-3531 |
Number of pages | 5 |
Journal | Tetrahedron |
Volume | 68 |
Issue number | 18 |
DOIs | |
Publication status | Published - May 6 2012 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Keywords
- Click reaction
- Corannulenes
- Oligomer synthesis