We have developed a methodology that affords regioisomerically pure trans-A 2 B 2 -porphyrins bearing pyridyl substituents. The optimal conditions for their synthesis were identified by the modification of known conditions for the reaction of dipyrromethanes with aromatic aldehydes. A total of five
✦ LIBER ✦
Regiospecific aryl nitration of meso-substituted tetraarylporphyrins: a simple route to bifunctional porphyrins
✍ Scribed by Kruper, William J.; Chamberlin, Thomas A.; Kochanny, Monica
- Book ID
- 111871235
- Publisher
- American Chemical Society
- Year
- 1989
- Tongue
- English
- Weight
- 620 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-3263
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## Abstract __meso__‐Tetraarylporphyrinato complexes **1a**–**g** (Zn^II^, Cu^II^, and Ni^II^) bearing one or two nitro‐substituted aryl moieties react with 1,1,1‐trimethylhydrazinium iodide in the presence of ^__t__^BuOK in THF at 0–5° or in the presence of KOH in DMSO at 60–70° according to a nuc