## Abstract Acid‐catalyzed condensation of __meso__‐pentafluorophenyl dipyrromethane **1** (100 mM) and pentafluorobenzaldehyde **2** (100 mM) at 0 °C gave a series of expanded porphyrins with even number of pyrrolic subunits up to octadecaphyrin(1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1) **18** in impro
Facile Synthesis of Large meso-Pentafluorophenyl-Substituted Expanded Porphyrins (Eur. J. Org. Chem. 8/2008)
✍ Scribed by Yasuo Tanaka; Ji-Young Shin; Atsuhiro Osuka
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 516 KB
- Volume
- 2008
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
The cover picture shows the crystal structures and colors of meso‐pentafluorophenyl‐substituted expanded porphyrins. [18]Porphyrin, [26]hexaphyrin, [36]octaphyrin, [44]decaphyrin, [52]dodecaphyrin, [62]tetradecaphyrin, [72]hexadecaphyrin, and [80]octadecaphyrin were synthesized and characterized. As indicated, the absorption bands of these expanded porphyrins are redshifted as their size increases, and [80]octadecaphyrin shows its absorption maximum at 953 nm. Their solutions exhibit various colors, reflecting the macrocyclic conjugation like a rainbow. Details are discussed in the article by A. Osuka et al. on p. 1341 ff.
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