Abstract
The dibenzofuran/dibenzothiophene-based nonaromatic hybrid macrocycles, exhibiting the features of both contracted macrocycles, subporphyrins and triphyrins, have been synthesized under simple reaction conditions using readily available precursors. The monoanionic new macrocyclic ligands with three donor atoms, such as two pyrrole nitrogens and one dibenzofuran oxygen or dibenzothiophene sulfur, readily form Re(I) complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 5924-5927 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 19 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - 2017 Nov 3 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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Cite this
Kumar, A., Rajeswara Rao, M., Lee, W. Z., & Ravikanth, M. (2017). Hybrid Macrocycles of Subporphyrins and Triphyrins. Organic Letters, 19(21), 5924-5927. https://doi.org/10.1021/acs.orglett.7b02919