Molecules (Jun 2017)

Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications

  • Ana F. R. Cerqueira,
  • Vítor A. S. Almodôvar,
  • Maria G. P. M. S. Neves,
  • Augusto C. Tomé

DOI
https://doi.org/10.3390/molecules22060994
Journal volume & issue
Vol. 22, no. 6
p. 994

Abstract

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This review covers the synthesis of coumarin–porphyrin, coumarin–phthalocyanine and coumarin–corrole conjugates and their potential applications. While coumarin–phthalocyanine conjugates were obtained almost exclusively by tetramerization of coumarin-functionalized phthalonitriles, coumarin–porphyrin and coumarin–corrole conjugates were prepared by complementary approaches: (a) direct synthesis of the tetrapyrrolic macrocycle using formylcoumarins and pyrrole or (b) by functionalization of the tetrapyrrolic macrocycle. In the last approach a range of reaction types were used, namely 1,3-dipolar cycloadditions, hetero-Diels–Alder, Sonogashira, alkylation or acylation reactions. This is clearly a more versatile approach, leading to a larger diversity of conjugates and allowing the access to conjugates bearing one to up to 16 coumarin units.

Keywords